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rac Metoprolol Hemi ( )-Tartrate-d<sub>6</sub>

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Click Chemistry:	Labeling and Fluorescence Imaging (1) PROTAC Synthesis (1) BCN (1) Azide (3) Alkynes (17)
Oligonucleotides:	Rat Pre-designed siRNA Sets (4) Mouse Pre-designed siRNA Sets (4) Phospholipids (10) Human Pre-designed siRNA Sets (4) siRNAs (12)

5073

Inhibitors & Agonists

Fluorescent Dye

Biochemical Assay Reagents

Peptides

MCE Kits

Inhibitory Antibodies

Natural
Products

Recombinant Proteins

4372

Isotope-Labeled Compounds

Antibodies

Click Chemistry

Oligonucleotides

Targets Recommended: SOS1 P-glycoprotein

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-17503B

**Metoprolol tartrate** 10+ Cited Publications	Adrenergic Receptor Apoptosis	Infection Cardiovascular Disease Endocrinology Cancer
Metoprolol tartrate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol tartrate shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-W769272

rac Metoprolol Hemi (+)-Tartrate-d6	Isotope-Labeled Compounds	Others
rac Metoprolol Hemi (+)-Tartrate-d₆ is the deuterium labeled rac Metoprolol Hemi (+)-Tartrate.

HY-90010S

*Tolterodine tartrate-d14* Kabi-2234-d<sub>14sub>; PNU-200583E-d<sub>14sub>	Isotope-Labeled Compounds mAChR	Neurological Disease Cancer
Tolterodine tartrate-d₁₄ (Kabi-2234-d₁₄) is deuterium labeled Tolterodine (tartrate). Tolterodine Tartrate (Kabi-2234; PNU-200583E) is a potent muscarinic receptor antagonist and shows selectivity for the urinary bladder over salivary glands in vivo.

HY-17503BR

Metoprolol tartrate (Standard)	Reference Standards Adrenergic Receptor Apoptosis	Infection Cardiovascular Disease Endocrinology Cancer
Metoprolol (tartrate) (Standard) is the analytical standard of Metoprolol (tartrate). This product is intended for research and analytical applications. Metoprolol tartrate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol tartrate shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-A0024AS

(Rac)-Tolterodine-d14 tartrate (rac)-PNU-200583-d<sub>14sub> Tartrate	mAChR Isotope-Labeled Compounds	Others
(Rac)-Tolterodine-d₁₄ (tartrate) is the deuterium labeled (Rac)-Tolterodine tartrate .

HY-W654154

*Dexmedetomidine-d4 L-tartrate (-d4-major)*	Isotope-Labeled Compounds	Others
Dexmedetomidine-d₄ L-tartrate (-d₄-major) is deuterium labeled Dexmedetomidine L-tartrate (-d4-major) .

HY-17503BS

**Metoprolol-d6 tartrate**	Isotope-Labeled Compounds Adrenergic Receptor	Infection Cardiovascular Disease Endocrinology Cancer
Metoprolol-d₆ (tartrate) is the deuterium labeled Metoprolol tartrate. Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-146227

DNA topoisomerase II inhibitor 1	Topoisomerase Apoptosis	Cancer
DNA topoisomerase II inhibitor 1 (compound 8ed) is a potent DNA topoisomerase II inhibitor. DNA topoisomerase II inhibitor 1 shows anti-proliferative activity. DNA topoisomerase II inhibitor 1 induces apoptosis and cell cycle arrest at sub G1 phase .

HY-RS13999

SUB1 Human Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
SUB1 Human Pre-designed siRNA Set A contains three designed siRNAs for SUB1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

SUB1 Human Pre-designed siRNA Set A SUB1 Human Pre-designed siRNA Set A

HY-RS18793

Sub1 Mouse Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
Sub1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Sub1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

Sub1 Mouse Pre-designed siRNA Set A Sub1 Mouse Pre-designed siRNA Set A

HY-RS25282

Sub1 Rat Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
Sub1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Sub1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

Sub1 Rat Pre-designed siRNA Set A Sub1 Rat Pre-designed siRNA Set A

HY-17368S1

*(Rac)-Rivastigmine-d6* (rac)-ENA 713-d<sub>6sub> free base; (rac)-SDZ-ENA 713-d<sub>6sub> free base	Isotope-Labeled Compounds Cholinesterase (ChE)	Neurological Disease
(Rac)-Rivastigmine-d₆ is a labelled racemic Rivastigmine. Rivastigmine (ENA 713 free base) is an orally active and potent cholinesterase (ChE) inhibitor and inhibits butyrylcholinesterase (BChE) and acetylcholinesteras (AChE) with IC₅₀s of 0.037 μM , 4.15 μM, respectively. Rivastigmine can pass the blood brain barrier (BBB). Rivastigmine is a parasympathomimetic or cholinergic agent used for the research of mild to moderate dementia of the Alzheimer's type and dementia due to Parkinson's disease .

HY-109506S2

*(Rac)-DPPC-d6* (rac)-129Y83-d<sub>6sub>	Isotope-Labeled Compounds	Others
(Rac)-DPPC-d6 is a deuterated labeled DPPC . DPPC (129Y83) is a phosphoglyceride that can be used to prepare lipid monolayers, bilayers, and liposomes. DPPC is the main lipid component of pulmonary surfactant. Dppc-liposome can be effectively used as a delivery vector to induce an immune response against GSL antigen in mice ^[6].

HY-N15188

hemi-Oxanthromicin A	Endogenous Metabolite	Others
hemi-Oxanthromicin A is a polyketide which can be extracted from Streptomyces .

HY-76570S

*(Rac)-5-Hydroxymethyl Tolterodine-d14* (rac)-Desfesoterodine-d<sub>14sub>; (rac)-PNU-200577-d<sub>14sub>	Isotope-Labeled Compounds mAChR	Neurological Disease
(Rac)-5-Hydroxymethyl Tolterodine-d₁₄ is the deuterium labeled (Rac)-5-Hydroxymethyl Tolterodine. (Rac)-5-Hydroxymethyl Tolterodine ((Rac)-Desfesoterodine), an active metabolite of Tolterodine, is a mAChR antagonist (Ki values of 2.3 nM, 2 nM, 2.5 nM, 2.8 nM, and 2.9 nM for M1, M2, M3, M4, and M5 receptors, respectively). (Rac)-5-Hydroxymethyl Tolterodine can be used for overactive bladder research .

HY-113904S1

*(Rac)-Tenofovir-d7* (rac)-GS 1278-d<sub>7sub>; (rac)-PMPA-d<sub>7sub>	Isotope-Labeled Compounds	Others
(Rac)-Tenofovir-d₇ is the deuterium labeled (Rac)-Tenofovir .

HY-158254S

*(Rac)-Trandolaprilate-d5* (rac)-Trandolaprilat-d<sub>5sub>; (rac)-RU 44403-d<sub>5sub>	Isotope-Labeled Compounds	Others
rac-Trandolaprilat-d₅ is deuterium labeled rac-Trandolaprilat .

HY-107370AS1

*(Rac)-Atomoxetine-d5 hydrochloride* (rac)-Tomoxetine-d<sub>5sub> hydrochloride; (rac)-LY 139603-d<sub>5sub>	Isotope-Labeled Compounds	Others
(Rac)-Atomoxetine-d₅ (hydrochloride) is the deuterium labeled (Rac)-Atomoxetine hydrochloride .

HY-B1205S

*(Rac)-Atropine-d3* 1 Publications Verification (rac)-Tropine tropate-d<sub>3sub>; (rac)-Hyoscyamine-d<sub>3sub>	mAChR Endogenous Metabolite Isotope-Labeled Compounds	Others
(Rac)-Atropine-d₃ is the deuterium labeled (Rac)-Atropine[1].

HY-144154S

(Rac)-Rivastigmine-d6 tartrate	Isotope-Labeled Compounds	Others
(Rac)-Rivastigmine-d₆ (tartrate) is the deuterium labeled (Rac)-Rivastigmine tartrate .

HY-W062703S

*(Rac)-Ruxolitinib-d9* (rac)-INCB18424-d<sub>9sub>; Ruxotinib racemate-d<sub>9sub>	Isotope-Labeled Compounds JAK	Cancer
(Rac)-Ruxolitinib D9 ((Rac)-INCB18424 D9) is the deuterium labeled (Rac)-Ruxolitinib. (Rac)-Ruxolitinib is a JAK2 inhibitor .

HY-107370AS

*(Rac)-Atomoxetine-d7 hydrochloride* (rac)-Tomoxetine d<sub>7sub> hydrochloride; (rac)-LY 139603 d<sub>7sub>	Serotonin Transporter Sodium Channel Isotope-Labeled Compounds	Neurological Disease
(Rac)-Atomoxetine-d₇ (hydrochloride) is a deuterium labeled (Rac)-Atomoxetine hydrochloride. (Rac)-Atomoxetine hydrochloride is a racemic form of Atomoxetine hydrochloride. Atomoxetine hydrochloride is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5 nM, 77 nM and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively) .

HY-144162S

*(Rac)-Selegiline-d5 hydrochloride* (rac)-Deprenyl-d<sub>5sub> hydrochloride; (±)-Selegiline-d<sub>5sub> hydrochloride; (±)-Deprenyl-d<sub>5sub> hydrochloride	Isotope-Labeled Compounds	Others
(Rac)-Selegiline-d₅ (hydrochloride) is the deuterium labeled (Rac)-Selegiline hydrochloride .

HY-17503R

Metoprolol (Standard)	Reference Standards Adrenergic Receptor Apoptosis	Infection Cardiovascular Disease Endocrinology Cancer
Metoprolol (Standard) is the analytical standard of Metoprolol. This product is intended for research and analytical applications. Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-141749S

*(Rac)-Clopidogrel carboxylic acid-d4* (rac)-CLPM-d<sub>4sub>; (rac)-SR 26334-d<sub>4sub>	Isotope-Labeled Compounds	Others
(Rac)-Clopidogrel carboxylic acid-d₄ is the deuterium labeled (Rac)-Clopidogrel carboxylic acid .

HY-B1178S

*(Rac)-Cotinine-d3* (±)-Cotinine-d<sub>3sub>; (rac)-NIH-10498-d<sub>3sub>	Endogenous Metabolite Isotope-Labeled Compounds	Others
(Rac)-Cotinine-d₃ is the deuterium labeled (Rac)-Cotinine .

HY-B1178S1

*(Rac)-Cotinine-d4* (±)-Cotinine-d<sub>4sub>; (rac)-NIH-10498-d<sub>4sub>	Endogenous Metabolite Isotope-Labeled Compounds	Others
(Rac)-Cotinine-d₄ is the deuterium labeled (Rac)-Cotinine .

HY-131589

Metoprolol acid Atenolol acid	Endogenous Metabolite	Others
Metoprolol acid (Atenolol acid) is a urinary metabolite with no pharmacological activity. Metoprolol acid does not exert its pharmacological effects in vivo. Metoprolol acid can be detected by solid phase extraction and reversed phase high performance liquid chromatography. The analysis of metoprolol acid requires specific conditions, such as the use of fluorescence detection and specific eluents .

HY-134670

a-Hydroxymetoprolol	Drug Metabolite	Others
a-Hydroxymetoprolol is a metabolite of metoprolol. The adrenoreceptor blocking effect of a-Hydroxymetoprolol on metoprolol is almost zero .

HY-W062703S1

*(Rac)-Ruxolitinib-d8* (rac)-INCB18424-d<sub>8sub>; Ruxotinib racemate-d<sub>8sub>	Isotope-Labeled Compounds	Others
(Rac)-Ruxolitinib-d₈ is deuterium labeled (Rac)-Ruxolitinib.

HY-17503AS

Metoprolol-d7 hydrochloride	Isotope-Labeled Compounds Adrenergic Receptor	Infection Cardiovascular Disease Endocrinology Cancer
Metoprolol-d₇ (hydrochloride) is the deuterium labeled Metoprolol. Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-17503S3

Metoprolol-d5	Apoptosis Adrenergic Receptor	Cancer
Metoprolol-d₅ is the deuterium labeled Metoprolol . Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-167580

*18:1 Hemi* BMP (S,R)**	Biochemical Assay Reagents
18:1 Hemi BMP (S,R) is a kind of biochemical reagent.

HY-14773S

*(Rac)-Mirabegron-d5* (rac)-YM178-d<sub>5sub>	Isotope-Labeled Compounds Adenosine Receptor	Metabolic Disease
(Rac)-Mirabegron-d₅ is a deuterium labeled (Rac)-Mirabegron. (Rac)-Mirabegron is the racemate of Mirabegron. Mirabegron is a selective β3-adrenoceptor agonist .

HY-131589R

Metoprolol acid (Standard) Atenolol acid (Standard)	Endogenous Metabolite Reference Standards	Others
Metoprolol acid (Standard) is the analytical standard of Metoprolol acid. This product is intended for research and analytical applications. Metoprolol acid (Atenolol acid) is a urinary metabolite with no pharmacological activity. Metoprolol acid does not exert its pharmacological effects in vivo. Metoprolol acid can be detected by solid phase extraction and reversed phase high performance liquid chromatography. The analysis of metoprolol acid requires specific conditions, such as the use of fluorescence detection and specific eluents .

HY-17503

*Metoprolol* 10+ Cited Publications	Adrenergic Receptor Apoptosis	Infection Cardiovascular Disease Endocrinology Cancer
Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-17503D

Metoprolol Hydrochloride	Adrenergic Receptor Apoptosis	Cardiovascular Disease Inflammation/Immunology Cancer
Metoprolol Hydrochloride is an orally active and selective β1-adrenoceptor antagonist. Metoprolol Hydrochloride exhibits anti-inflammatory, antitumor, and anti-angiogenic properties .

HY-D1490

*Fast red TR salt hemi(zinc chloride)*	Fluorescent Dye	Others
Fast red TR salt hemi (zinc chloride) is a diazonium dye with red color .

HY-17503AR

Metoprolol succinate (Standard)	Reference Standards Adrenergic Receptor Apoptosis	Cardiovascular Disease Endocrinology Cancer
Metoprolol (succinate) (Standard) is the analytical standard of Metoprolol (succinate). This product is intended for research and analytical applications. Metoprolol succinate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol succinate shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-17503S

Metoprolol-d7	Isotope-Labeled Compounds Adrenergic Receptor	Cardiovascular Disease Endocrinology
Metoprolol-d₇ is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2].

HY-W654270A

*(rac)-Calcium N5-methyltetrahydrofolate-d3* (rac)-NSC173328-d<sub>3sub>; (rac)-5-Methyl THF calcium-d<sub>3sub>	Isotope-Labeled Compounds	Others
(rac)-Calcium N5-methyltetrahydrofolate-d₃ ((rac)-NSC173328-d₃) is a deuterium labeled (rac)-Calcium N5-methyltetrahydrofolate.

HY-132446S

Metoprolol Acid-d5	Isotope-Labeled Compounds	Others
Metoprolol Acid-d₅ is the deuterium labeled Metoprolol Acid .

HY-143859S

Metoprolol dimer-d10	Isotope-Labeled Compounds	Others
Metoprolol dimer-d₁₀ is the deuterium labeled Metoprolol dimer .

HY-17503AS1

Metoprolol-d6 succinate	Isotope-Labeled Compounds Adrenergic Receptor Apoptosis	Cardiovascular Disease Endocrinology Cancer
Metoprolol-d₆ (succinate) is deuterium labeled Metoprolol (succinate). Metoprolol succinate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol succinate shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-B1178S2

*(Rac)-Cotinine-d7* (±)-Cotinine-d<sub>7sub>; (rac)-NIH-10498-d<sub>7sub>	Isotope-Labeled Compounds Endogenous Metabolite	Others
(Rac)-Cotinine-d₇ is deuterium labeled Cotinine.

HY-134670R

a-Hydroxymetoprolol (Standard)	Drug Metabolite Reference Standards	Others
a-Hydroxymetoprolol (Standard) is the analytical standard of a-Hydroxymetoprolol. This product is intended for research and analytical applications. a-Hydroxymetoprolol is a metabolite of metoprolol. The adrenoreceptor blocking effect of a-Hydroxymetoprolol on metoprolol is almost zero .

HY-109541S6

*(Rac)-Colfosceril miristate-d72* (rac)-DMPC-d<sub>72sub>; (rac)-1,2-Dimyristoyl-sn-glycero-3-phosphocholine-d<sub>72sub>	Isotope-Labeled Compounds	Others
(Rac)-1,2-Dimyristoyl-sn-glycero-3-phosphocholine-d₇₂ is deuterium labeled (Rac)-1,2-Dimyristoyl-sn-glycero-3-phosphocholine. 1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) is a synthetic phospholipid used in liposomes. 1,2-Dimyristoyl-sn-glycero-3-ph

HY-17503S2

*(S)-Metoprolol-d7*	Isotope-Labeled Compounds Adrenergic Receptor	Cardiovascular Disease Endocrinology
(S)-Metoprolol-d₇ is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2].

HY-17503S1

*(R)-Metoprolol-d7*	Isotope-Labeled Compounds Adrenergic Receptor	Cardiovascular Disease Endocrinology
(R)-Metoprolol-d₇ is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2].

HY-17503A

Metoprolol succinate 10+ Cited Publications	Adrenergic Receptor Apoptosis	Cardiovascular Disease Endocrinology Cancer
Metoprolol succinate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol succinate shows anti-inflammation, antitumor and anti-angiogenic properties .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-17503

*Metoprolol* 10+ Cited Publications	Classification of Application Fields Disease Research Fields Endocrinology	Adrenergic Receptor Apoptosis
Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-125833

Alpha-Naphthoflavone 5+ Cited Publications	Flavonoids Flavones Source classification Indigofera heterantha Wall. ex Brand. Plants Compositae Disease Research Fields Cancer	Cytochrome P450 Aryl Hydrocarbon Receptor Apoptosis
Alpha-Naphthoflavone is an orally active flavonoid that is a potent, competitive inhibitor of aromatase< b>aromatase. < b > IC < sub > 50 < / sub > < / b > and < b > K < sub > I < / sub > < / b > value were 0.5 and 0.2 microns. Alpha-Naphthoflavone can inhibit cell proliferation and induce apoptosis .

HY-N0585

*(Rac)-Norcantharidin* 1 Publications Verification (rac)-NCTD	Structural Classification Natural Products Classification of Application Fields Source classification Endogenous metabolite Disease Research Fields Cancer	Apoptosis
(Rac)-Norcantharidin ((Rac)-NCTD) is the racemic form of Norcantharidin. Norcantharidin is a demethylated derivative of Cantharidin (HY-N0209) and has antitumor activity .

HY-N15188

hemi-Oxanthromicin A	Structural Classification Microorganisms Source classification Phenols Polyphenols	Endogenous Metabolite
hemi-Oxanthromicin A is a polyketide which can be extracted from Streptomyces .

HY-125833R

Alpha-Naphthoflavone (Standard)	Flavonoids Flavones Source classification Indigofera heterantha Wall. ex Brand. Plants Compositae	Cytochrome P450 Aryl Hydrocarbon Receptor Apoptosis
Alpha-Naphthoflavone (Standard) is the analytical standard of Alpha-Naphthoflavone. This product is intended for research and analytical applications. Alpha-Naphthoflavone is an orally active flavonoid that is a potent, competitive inhibitor of aromatase< b>aromatase. < b > IC < sub > 50 < / sub > < / b > and < b > K < sub > I < / sub > < / b > value were 0.5 and 0.2 microns. Alpha-Naphthoflavone can inhibit cell proliferation and induce apoptosis .

HY-N11799

Neochilenin 3-O-Methylquercetin 4′-O-glucoside	Structural Classification Flavonoids Source classification Plants Compositae Other Flavonoids	Others
Neochilenin (3-O-Methylquercetin 4 '-O-glucoside) is a glycoside of 3-O-methylquercetin, which can be isolated from the sub-family Cereoideae (Cactaceae). .

HY-N6030

*(Rac)-Dencichine* (rac)-Dencichin; (rac)-ODAP	other families Classification of Application Fields Source classification Other Diseases Amino acids Plants Disease Research Fields	HIF/HIF Prolyl-Hydroxylase
(Rac)-Dencichine ((Rac)-Dencichin) is the racemate of Dencichin. Dencichin is a non-protein amino acid originally extracted from Panax notoginseng, and can inhibit HIF-prolyl hydroxylase-2 (PHD-2) activity .

HY-N0585R

*(Rac)-Norcantharidin (Standard)*	Structural Classification Natural Products Source classification Endogenous metabolite	Reference Standards Apoptosis
(Rac)-Norcantharidin (Standard) is the analytical standard of (Rac)-Norcantharidin (HY-N0585). This product is intended for research and analytical applications. (Rac)-Norcantharidin ((Rac)-NCTD) is the racemic form of Norcantharidin. Norcantharidin is a demethylated derivative of Cantharidin (HY-N0209) and has antitumor activity .

HY-N3422A

*(rac)-Khellactone*	Thymus serpyllum L. Structural Classification Natural Products Source classification Umbelliferae Plants	Drug Isomer
(rac)-Khellactone is the racemic form of Khellactone. (rac)-Khellactone is a type of coumarin, and its derivatives are expected to be used in the research of the anti-cancer field .

HY-N0075R

*(Rac)-Byakangelicin (Standard)*	Structural Classification Ruta graveolens Linn. Source classification Rutaceae Coumarins Phenylpropanoids Plants	Reference Standards Others
(Rac)-Byakangelicin (Standard) is the analytical standard of (Rac)-Byakangelicin. This product is intended for research and analytical applications. (Rac)-Byakangelicin is a racemate of Byakangelicin mainly isolated from the genus Angelica. Byakangelicin is an aldose-reductase inhibitor with an IC₅₀ value of 6.2 μM .

HY-N8547A

*(Rac)-Sclerone*	Structural Classification Natural Products Juglandaceae Carya illinoinensis (Wangenheim) K. Koch Source classification Plants	Cholinesterase (ChE)
(Rac)-Sclerone is a natural product, that can be isolated from the green husk of Carya illinoinensis. (Rac)-Sclerone shows appreciable inhibition of AChE, with an IC₅₀ of 192.65 ± 10.12 μg/mL .

HY-N6004

*(Rac)-Shikonin* Shikalkin	Structural Classification Natural Products other families Classification of Application Fields Source classification Phenols Polyphenols Plants Disease Research Fields Cancer	Others
(Rac)-Shikonin (Shikonin) possesses anti-tumor activity. (Rac)-Shikonin (Shikonin) circumvents cancer agent resistance by induction of a necroptotic death .

HY-W011474

Geranylgeraniol	Structural Classification Natural Products Microorganisms	NF-κB
Geranylgeraniol is an orally acitve vitamin K₂ sub-type, an intermediate of the mevalonate pathway. Geranylgeraniol targets NF-kB signaling pathway and could alleviate LPS-induced microglial inflammation in animal model .

HY-N5112

*(Rac)-Arnebin 1* (rac)-β,β-Dimethylacrylalkannin; (rac)-β,β-Dimethylacrylshikonin	Quinones Structural Classification Classification of Application Fields Source classification Other Diseases Phenols Polyphenols Plants Lithospermum canescens Lehm. Naphthalene Quinones Boraginaceae Disease Research Fields	HIF/HIF Prolyl-Hydroxylase
(Rac)-Arnebin 1 ((Rac)-β,β-Dimethylacrylalkannin) is the racemate of β,β-Dimethylacrylalkannin and/or β,β-Dimethylacrylshikonin. β,β-Dimethylacrylalkannin and β,β-Dimethylacrylshikonin are napthoquinones isolated from Arnebia nobilis. β,β-Dimethylacrylshikonin has anti-tumor activity .

HY-122448A

*(Rac)-Sativan*	Structural Classification Flavonoids Leguminosae Source classification Trifolium pratense Linn. Plants	Bacterial Fungal
(Rac)-Sativan is an isoflavanoid with a broad spectrum of antimicrobial activity against bacteria and phytopathogenic fungi. (Rac)-Sativan exhibits antituberculosis activity against Mycobacterium tuberculosis H37Rv, with MIC values of 50 µg/mL .

HY-N0278A

*(Rac)-Anemonin* (rac)-Pulsatilla camphor; (rac)-Anemonine	Structural Classification Natural Products Ranunculaceae Source classification Clematis crassifolia Benth. Plants	PKC NO Synthase
(Rac)-Anemonin ((Rac)-Pulsatilla camphor) is the diastereoisomer of Anemonin (HY-N0278). Anemonin (Pulsatilla camphor), a selective iNOS inhibitor, is also a PKC-θ inhibitor. Anemonin can significantly inhibit the translation or protein stability of PKC-θ protein. Anemonin also ameliorates dextran sodium sulfate-induced acute ulcerative colitis (UC) in mice. Anemonin can be used in the research of inflammation-related diseases .

HY-N0106R

*(Rac)-Salvianic acid A sodium (Standard)* (rac)-Danshensu sodium (Standard); (rac)-Tanshinol sodium (Standard)	Structural Classification Simple Phenylpropanols Labiatae Samanea saman (Jacq.) Merr. Source classification Phenols Polyphenols Phenylpropanoids Plants	Reference Standards Keap1-Nrf2 NF-κB Mitochondrial Metabolism Apoptosis
(Rac)-Salvianic acid A (sodium) (Standard) is the analytical standard of (Rac)-Salvianic acid A (sodium). This product is intended for research and analytical applications. (Rac)-Salvianic acid A sodium is the racemic form of Salvianic acid A (HY-N1913). Salvianic acid A is an orally active phenolic compound that induces Nrf2/HO-1 activation and inhibits the NF-κB pathway, and it also activates the mitochondrial antioxidant defense system (Mitochondrial Metabolism). Salvianic acid A exhibits anti-inflammatory, antioxidant, and anti-apoptotic properties (Apoptosis), demonstrating potential for research into inflammation and cardiovascular diseases ^[6] .

HY-N1166A

*(Rac)-Tephrosin*	Structural Classification Flavonoids Leguminosae Isoflavanones Source classification Plants Tephrosia purpurea (L.) Pers.	Others
(Rac)-Tephrosin is a natural product that can be found in Tephrosia purpurea .

HY-W720042A

*(rac)-Zeaxanthin dimethyl ether*	Structural Classification Natural Products Microorganisms Source classification	Biochemical Assay Reagents
(rac)-Zeaxanthin dimethyl ether is the racemate of Zeaxanthin dimethyl ester. Zeaxanthin is a type of xanthophyll. (rac)-Zeaxanthin dimethyl ether has applications as pharmaceuticals and nutraceuticals and in the food industry .

HY-N3036

*(Rac)-Isovalerylshikonin*	Quinones Structural Classification Alkanna tinctoria (L.) Tausch Source classification Plants Naphthalene Quinones Boraginaceae	Others
(Rac)-Isovalerylshikonin (compound 372) is a naphthoquinone pigment present in hexane extracts of safflower roots .

HY-N7199

*(Rac)-Hydnocarpin*	Structural Classification Caprifoliaceae Classification of Application Fields Flavones Lonicera japonica Thunb. Source classification Hydnocarpus anthelminthica Pierr. ex Gagnep. Plants Flavonoids Phenols Polyphenols Flacourtiaceae Disease Research Fields Cancer	Drug Isomer
(Rac)-Hydnocarpin is a flavonoid isolated from Hydnocarpus anthelminthica, and exhibits moderate cytotoxic on cancer cells .

HY-N15356

9-Oxooctadecanedioic acid	Structural Classification Ketones, Aldehydes, Acids Source classification Plants Quercus suber L. Fagaceae	Bacterial
9-Oxooctadecanedioic acid is an α,ω-dicarboxylic fatty acid monomer found in the cork suberin of Quercus suber. It contributes to the formation of the hydrophobic barrier structure in plant cell walls and may play an important role in functions such as water resistance and protection against microbial penetration .

HY-129155

*(Rac)-Germacrene D*	Bursera copallifera (Moc. & Sessé ex DC.) Bullock Source classification Plants Burseraceae	Bacterial Fungal Drug Isomer
(Rac)-Germacrene D is a natural product that can be isolated from the genus Bursera .

HY-N8038

Isoanthricin (rac)-Deoxypodophyllotoxin	Classification of Application Fields Source classification Centaurea ornata Lignans Other Diseases Phenylpropanoids Plants Umbelliferae Disease Research Fields	Others
Isoanthricin ((Rac)-Deoxypodophyllotoxin) is the racemate of Deoxypodophyllotoxin. Deoxypodophyllotoxin is a potent antitumor and anti-inflammatory agent .

HY-113261A

*(Rac)-Oleoylcarnitine*	Microorganisms Source classification	GlyT
(Rac)-Oleoylcarnitine is an endogenous acylcarnitine and a potential noncompetitive inhibitor of glycine transporter 2 (GLYT2) that can be used as a pain suppressant.

HY-N0075

*(Rac)-Byakangelicin*	Classification of Application Fields Source classification Ruta graveolens Linn. Rutaceae Coumarins Metabolic Disease Phenylpropanoids Plants Disease Research Fields	Others
(Rac)-Byakangelicin is a racemate of Byakangelicin mainly isolated from the genus Angelica. Byakangelicin is an aldose-reductase inhibitor with an IC₅₀ value of 6.2 μM .

HY-W040821R

DL-Homocysteine (Standard)	Structural Classification Ketones, Aldehydes, Acids Source classification Disease markers Endocrine diseases Nervous System Disorder Endogenous metabolite Cardiovascular System Disorder	Reference Standards Endogenous Metabolite
Metoprolol acid (Standard) is the analytical standard of Metoprolol acid. This product is intended for research and analytical applications. Metoprolol acid (Atenolol acid) is a urinary metabolite with no pharmacological activity. Metoprolol acid does not exert its pharmacological effects in vivo. Metoprolol acid can be detected by solid phase extraction and reversed phase high performance liquid chromatography. The analysis of metoprolol acid requires specific conditions, such as the use of fluorescence detection and specific eluents .

HY-P2274

Argifin	Infection Structural Classification Natural Products Microorganisms Classification of Application Fields Source classification Disease Research Fields	Parasite
Argifin is a sub-nanomolar chitinase inhibitor produced by soil microorganisms, with IC₅₀s of 0.025 μM, 6.4 μM , 1.1 μM and 4.5 μM for SmChiA (Serratia marcescens chitinaese A), SmChiB, Aspergillus fumigatus chitinase B1 and human chitotriosidase, respectively .

HY-N7606

*(Rac)-β-Chamigrenic acid*	Classification of Application Fields Terpenoids Sesquiterpenes Source classification Other Diseases Plants Schisandraceae Disease Research Fields Schisandra chinensis (Turcz.) Baill.	Others
(Rac)-β-Chamigrenic acid is a racemate of β-Chamigrenic acid. β-Chamigrenic acid is a sesquiterpenoid isolated from S.chinensis

HY-N1274

*(rac)-Secodihydro-hydramicromelin B*	Structural Classification Source classification Rutaceae Other Phenylpropanoids Micromelum integerrimum (Buch.-Ham.) Roem. Phenylpropanoids Plants	Others
(rac)-Secodihydro-hydramicromelin B is a natural product that can be isolated from Equisetum hyemale L .

HY-N0168AR

*(Rac)-Hesperetin (Standard)*	Structural Classification Flavonoids other families Flavonones Source classification Phenols Polyphenols Plants	Reference Standards p38 MAPK Apoptosis Autophagy Reactive Oxygen Species (ROS) Bcl-2 Family NF-κB
(Rac)-Hesperetin (Standard) is the analytical standard of (Rac)-Hesperetin. This product is intended for research and analytical applications. (Rac)-Hesperetin is the racemate of Hesperetin. Hesperetin is a natural flavanone that can be found in citrus, and acts as a potent and orally active broad-spectrum inhibitor against human UGT activity. Hesperetin induces apoptosis via p38 MAPK activation. Hesperetin displays a range of bioactivities including antioxidant, anti-inflammatory, and anti-cancer. Hesperetin is found to induce cell-cycle arrest at G2/M phase. Hesperetin can reduce Bcl-2 and enhance BaxM. Hesperetin induces apoptosis through inhibiting NF-κB receptor .

HY-W011474R

Geranylgeraniol (Standard)	Structural Classification Natural Products Microorganisms	Reference Standards NF-κB
Geranylgeraniol (Standard) is the analytical standard of Geranylgeraniol. This product is intended for research and analytical applications. Geranylgeraniol is an orally acitve vitamin K2 sub-type, an intermediate of the mevalonate pathway. Geranylgeraniol targets NF-kB signaling pathway and could alleviate LPS-induced microglial inflammation in animal model [4].

HY-N10192

Aculene D	Infection Microorganisms Classification of Application Fields Terpenoids Sesquiterpenes Source classification Disease Research Fields	Endogenous Metabolite Bacterial
Aculene D, a fungal metabolite, shows quorum sensing (QS) inhibitory activity against Chromobacterium violaceum CV026, and could significantly reduce violacein production in N-hexanoyl-l-homoserine lactone (C6-HSL) induced C. violaceum CV026 cultures at sub-inhibitory concentrations .

HY-107383

Tetrahydrobiopterin 1 Publications Verification (rac)-Sapropterin	Alkaloids Structural Classification Classification of Application Fields Other Alkaloids Source classification Disease markers Endogenous metabolite Inflammation/Immunology Disease Research Fields Cardiovascular System Disorder	NO Synthase Endogenous Metabolite
Tetrahydrobiopterin ((Rac)-Sapropterin) is a cofactor of the aromatic amino acid hydroxylases enzymes and also acts as an essential cofactor for all nitric oxide synthase (NOS) isoforms.

HY-108776

*(Rac)-sn-Glycerol 3-phosphate sodium* DL-α-Glycerol phosphate sodium	Structural Classification Natural Products Human Gut Microbiota Metabolites Classification of Application Fields Source classification Endogenous metabolite Inflammation/Immunology Disease Research Fields	Endogenous Metabolite
(Rac)-sn-Glycerol 3-phosphate sodium is an a-site substrate analogue. (Rac)-sn-Glycerol 3-phosphate sodium is bound to the a-site, the rate of reaction of indole and nucleophilic indole analogues with E(A-A) is strongly inhibited .

HY-113128C

*(Rac)-sn-Glycerol 3-phosphate* DL-α-Glycerol phosphate	Structural Classification Natural Products Classification of Application Fields Source classification Other Diseases Endogenous metabolite Disease Research Fields	Endogenous Metabolite
(Rac)-sn-Glycerol 3-phosphate is an a-site substrate analogue. (Rac)-sn-Glycerol 3-phosphate is bound to the a-site, the rate of reaction of indole and nucleophilic indole analogues with E(A-A) is strongly inhibited .

HY-N0662

Amentoflavone 5+ Cited Publications Didemethyl-ginkgetin	Structural Classification Flavonoids Classification of Application Fields Source classification Phenols Polyphenols Selaginellaceae Plants Biflavones Selaginella tamariscina (P. Beauv.) Spring Disease Research Fields Cancer	Reactive Oxygen Species (ROS) Apoptosis Bacterial Fungal RSV GABA Receptor
Amentoflavone (Didemethyl-ginkgetin) is a potent and orally active GABA(A) negative modulator. Amentoflavone also shows anti-inflammatory, antioxidative, anti-viral, anti-tumor, anti-radiation, anti-fungal, antibacterial activity. Amentoflavone induces apoptosis and cell cycle arrest at sub-G1 phase .

HY-N7240

*(Rac)-Juvenile hormone III*	Structural Classification Natural Products Animals Source classification	Others
(Rac)-Juvenile hormone III, a natural compound that can be isolated from farnesoic acid ,is the most widely distributed Juvenile hormone homologue .

HY-N11060

*(Rac)-Dehydrovomifoliol* PBI 344	Structural Classification Other Monoterpenes Terpenoids Source classification Euphorbia peplus Linn. Euphorbiaceae Plants	Others
(Rac)-Dehydrovomifoliol (PBI 344) is a bisnorsesquiterpene compound that can be found in Euphorbia peplus .

HY-113145

*(Rac)-Salvianic acid A* (rac)-Danshensu; (rac)-Tanshinol	Structural Classification Classification of Application Fields Ketones, Aldehydes, Acids Labiatae Samanea saman (Jacq.) Merr. Source classification Other Diseases Phenols Polyphenols Plants Disease Research Fields	Drug Isomer
(Rac)-Salvianic acid A is the racemate of Salvianic acid A (HY-N1913). Salvianic acid A, an orally active phenolic compound, can induce Nrf2/HO-1 activation and inhibition of NF-κB pathway. Danshensu has anti-oxidation, anti-apoptosis, anti-lung inflammatory and has the potential for COVID-19, cardiovascular and cerebrovascular diseases research .

HY-N10872

*(Rac)-Phorbol-12-(2-methylbutyrate)*	Structural Classification Terpenoids Croton tiglium Linn. Source classification Diterpenoids Euphorbiaceae Plants	Others
(Rac)-Phorbol-12-(2-methylbutyrate) is a nature product that could be isolated form croton oil .

HY-N0608A

*(Rac)-Myrislignan*	Monophenols Classification of Application Fields Source classification Phenols Myristicaceae Plants Myristica fragrans Houtt. Disease Research Fields Inflammation/Immunology	NF-κB
(Rac)-Myrislignan is the racemate of Myrislignan. Myrislignan, a lignan isolated from Myristica fragrans Houtt, possesses anti-inflammatory activities. Myrislignan attenuates LPS-induced inflammation reaction in murine macrophage cells through inhibition of NF-kB signalling pathway activation .

HY-N0106

*(Rac)-Salvianic acid A sodium* (rac)-Danshensu sodium; (rac)-Tanshinol sodium	Structural Classification Classification of Application Fields Simple Phenylpropanols Labiatae Samanea saman (Jacq.) Merr. Source classification Phenols Polyphenols Phenylpropanoids Plants Disease Research Fields Cancer	Keap1-Nrf2 NF-κB Mitochondrial Metabolism Apoptosis
(Rac)-Salvianic acid A sodium is the racemic form of Salvianic acid A (HY-N1913). Salvianic acid A is an orally active phenolic compound that induces Nrf2/HO-1 activation and inhibits the NF-κB pathway, and it also activates the mitochondrial antioxidant defense system (Mitochondrial Metabolism). Salvianic acid A exhibits anti-inflammatory, antioxidant, and anti-apoptotic properties (Apoptosis), demonstrating potential for research into inflammation and cardiovascular diseases ^[6] .

HY-N15496

Fusaproliferin FUS	Structural Classification Microorganisms Terpenoids Sesquiterpenes Source classification	Reactive Oxygen Species (ROS) NO Synthase Interleukin Related TNF Receptor p38 MAPK ERK IKK NF-κB
Fusaproliferin is a sesterterpene mycotoxin isolated from Fusarium solani. Fusaproliferin reverse Lipopolysaccharides (HY-D1056) stimulation and the NF-κB and MAPKs signaling pathways contribute to the anti-inflammatory process. Fusaproliferin exhibits affinity for the TLR4 protein with K_D values of 28.6 μM. Fusaproliferin shows cytotoxicity against pancreatic cancer cell with rapid and sub-micromolar IC₅₀ .

HY-W011370

Pelargonidin chloride 1 Publications Verification	Structural Classification Anthocyans Flavonoids Classification of Application Fields Leguminosae Source classification Other Diseases Phenols Polyphenols Plants Phaseolus vulgaris Linn. Disease Research Fields	Quinone Reductase Reactive Oxygen Species (ROS)
Pelargonidin chloride is an anthocyanidin and also is a scavenger of nitric oxide radical and has antioxidant activities. Pelargonidin inhibits cell viability and induces cell cycle arrest at sub-G1 phase. Pelargonidin chloride increases the mRNA and protein expression of HO-1, NQO1, Nrf2. Pelargonidin chloride improves Aβ-induced memory and learning impairment .

HY-157732

*1,2-Dimyristoyl-3-palmitoyl-rac-glycerol*	Structural Classification Natural Products Classification of Application Fields Source classification Metabolic Disease Endogenous metabolite Disease Research Fields	Endogenous Metabolite
1,2-Dimyristoyl-3-palmitoyl-rac-glycerol (MMP) is a triacylglycerol that contains myristic acid and palmitic acid .

HY-N9086A

*(rac)-Poriol* 5,7,4'-Trihydroxy-6-methylflavanone	Structural Classification Flavonoids Flavonones Source classification Plants Cephalotaxaceae Cephalotaxus oliveri Mast.	NO Synthase COX Interleukin Related
(rac)-Poriol (5,7,4'-Trihydroxy-6-methylflavanone) exhibits antioxidant activity, and scavenges free radical DPPH with an IC₅₀ of 0.18 µg/mL. (rac)-Poriol inhibits the LPS (HY-D1056)-induced NO generation in RAW264.7 (98.35% inhibition rate at 10 μM), and exhibits anti-inflammatory activity. (rac)-Poriol exhibits good binding affinity with iNOS, COX-1, COX-2, TNF-α, and IL-1β .

HY-N12224

*1-Heptadecanoyl-rac-glycerol* MG(17:0/0:0/0:0); 1-Heptadecanoin	Apocynaceae Structural Classification Natural Products Source classification Plants Trachelospermum jasminoides (Lindl.) Lem.	NO Synthase
1-Heptadecanoyl-rac-glycerol (1-Heptadecanoin) is a glyceride compound with anti-inflammatory activity. 1-Heptadecanoyl-rac-glycerol inhibits the occurrence of inflammation by suppressing the expression of inducible nitric oxide synthase (iNOS) related to inflammation. 1-Heptadecanoyl-rac-glycerol can be used for research on diseases related to inflammation .

HY-18061

Ochromycinone 3 Publications Verification (rac)-STA-21	Infection Quinones Structural Classification Monophenols Microorganisms Classification of Application Fields Anthraquinones Source classification Phenols Disease Research Fields	Antibiotic STAT Bacterial
Ochromycinone ((Rac)-STA-21) is a natural antibiotic and a STAT3 inhibitor. Ochromycinone can inhibits STAT3 DNA binding activity, STAT3 dimerization. Ochromycinone has anticancer and antimicrobial activity .

HY-P2274R

Argifin (Standard)	Structural Classification Natural Products Microorganisms Source classification	Reference Standards Parasite
Argifin (Standard) is the analytical standard of Argifin. This product is intended for research and analytical applications. Argifin is a sub-nanomolar chitinase inhibitor produced by soil microorganisms, with IC50s of 0.025 μM, 6.4 μM , 1.1 μM and 4.5 μM for SmChiA (Serratia marcescens chitinaese A), SmChiB, Aspergillus fumigatus chitinase B1 and human chitotriosidase, respectively[1].

Cat. No.	Product Name	Chemical Structure

HY-17368S1

(Rac)-Rivastigmine-d6

(Rac)-Rivastigmine-d₆ is a labelled racemic Rivastigmine. Rivastigmine (ENA 713 free base) is an orally active and potent cholinesterase (ChE) inhibitor and inhibits butyrylcholinesterase (BChE) and acetylcholinesteras (AChE) with IC₅₀s of 0.037 μM , 4.15 μM, respectively. Rivastigmine can pass the blood brain barrier (BBB). Rivastigmine is a parasympathomimetic or cholinergic agent used for the research of mild to moderate dementia of the Alzheimer's type and dementia due to Parkinson's disease .

HY-W769272

rac Metoprolol Hemi (+)-Tartrate-d6
rac Metoprolol Hemi (+)-Tartrate-d₆ is the deuterium labeled rac Metoprolol Hemi (+)-Tartrate.

HY-90010S

*Tolterodine tartrate-d14*
Tolterodine tartrate-d₁₄ (Kabi-2234-d₁₄) is deuterium labeled Tolterodine (tartrate). Tolterodine Tartrate (Kabi-2234; PNU-200583E) is a potent muscarinic receptor antagonist and shows selectivity for the urinary bladder over salivary glands in vivo.

HY-A0024AS

(Rac)-Tolterodine-d14 tartrate
(Rac)-Tolterodine-d₁₄ (tartrate) is the deuterium labeled (Rac)-Tolterodine tartrate .

HY-W654154

*Dexmedetomidine-d4 L-tartrate (-d4-major)*
Dexmedetomidine-d₄ L-tartrate (-d₄-major) is deuterium labeled Dexmedetomidine L-tartrate (-d4-major) .

HY-17503BS

**Metoprolol-d6 tartrate**
Metoprolol-d₆ (tartrate) is the deuterium labeled Metoprolol tartrate. Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-109506S2

*(Rac)-DPPC-d6*
(Rac)-DPPC-d6 is a deuterated labeled DPPC . DPPC (129Y83) is a phosphoglyceride that can be used to prepare lipid monolayers, bilayers, and liposomes. DPPC is the main lipid component of pulmonary surfactant. Dppc-liposome can be effectively used as a delivery vector to induce an immune response against GSL antigen in mice ^[6].

HY-76570S

(Rac)-5-Hydroxymethyl Tolterodine-d14

(Rac)-5-Hydroxymethyl Tolterodine-d₁₄ is the deuterium labeled (Rac)-5-Hydroxymethyl Tolterodine. (Rac)-5-Hydroxymethyl Tolterodine ((Rac)-Desfesoterodine), an active metabolite of Tolterodine, is a mAChR antagonist (Ki values of 2.3 nM, 2 nM, 2.5 nM, 2.8 nM, and 2.9 nM for M1, M2, M3, M4, and M5 receptors, respectively). (Rac)-5-Hydroxymethyl Tolterodine can be used for overactive bladder research .

HY-113904S1

*(Rac)-Tenofovir-d7*
(Rac)-Tenofovir-d₇ is the deuterium labeled (Rac)-Tenofovir .

HY-158254S

*(Rac)-Trandolaprilate-d5*
rac-Trandolaprilat-d₅ is deuterium labeled rac-Trandolaprilat .

HY-107370AS1

*(Rac)-Atomoxetine-d5 hydrochloride*
(Rac)-Atomoxetine-d₅ (hydrochloride) is the deuterium labeled (Rac)-Atomoxetine hydrochloride .

HY-B1205S

*(Rac)-Atropine-d3* 1 Publications Verification
(Rac)-Atropine-d₃ is the deuterium labeled (Rac)-Atropine[1].

HY-144154S

(Rac)-Rivastigmine-d6 tartrate
(Rac)-Rivastigmine-d₆ (tartrate) is the deuterium labeled (Rac)-Rivastigmine tartrate .

HY-W062703S

*(Rac)-Ruxolitinib-d9*
(Rac)-Ruxolitinib D9 ((Rac)-INCB18424 D9) is the deuterium labeled (Rac)-Ruxolitinib. (Rac)-Ruxolitinib is a JAK2 inhibitor .

HY-107370AS

*(Rac)-Atomoxetine-d7 hydrochloride*
(Rac)-Atomoxetine-d₇ (hydrochloride) is a deuterium labeled (Rac)-Atomoxetine hydrochloride. (Rac)-Atomoxetine hydrochloride is a racemic form of Atomoxetine hydrochloride. Atomoxetine hydrochloride is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5 nM, 77 nM and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively) .

HY-144162S

*(Rac)-Selegiline-d5 hydrochloride*
(Rac)-Selegiline-d₅ (hydrochloride) is the deuterium labeled (Rac)-Selegiline hydrochloride .

HY-141749S

*(Rac)-Clopidogrel carboxylic acid-d4*
(Rac)-Clopidogrel carboxylic acid-d₄ is the deuterium labeled (Rac)-Clopidogrel carboxylic acid .

HY-B1178S

*(Rac)-Cotinine-d3*
(Rac)-Cotinine-d₃ is the deuterium labeled (Rac)-Cotinine .

HY-B1178S1

*(Rac)-Cotinine-d4*
(Rac)-Cotinine-d₄ is the deuterium labeled (Rac)-Cotinine .

HY-W062703S1

*(Rac)-Ruxolitinib-d8*
(Rac)-Ruxolitinib-d₈ is deuterium labeled (Rac)-Ruxolitinib.

HY-17503AS

Metoprolol-d7 hydrochloride
Metoprolol-d₇ (hydrochloride) is the deuterium labeled Metoprolol. Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-17503S3

Metoprolol-d5
Metoprolol-d₅ is the deuterium labeled Metoprolol . Metoprolol is an orally active, selective β1-adrenoceptor antagonist. Metoprolol shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-14773S

*(Rac)-Mirabegron-d5*
(Rac)-Mirabegron-d₅ is a deuterium labeled (Rac)-Mirabegron. (Rac)-Mirabegron is the racemate of Mirabegron. Mirabegron is a selective β3-adrenoceptor agonist .

HY-17503S

Metoprolol-d7
Metoprolol-d₇ is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2].

HY-W654270A

*(rac)-Calcium N5-methyltetrahydrofolate-d3*
(rac)-Calcium N5-methyltetrahydrofolate-d₃ ((rac)-NSC173328-d₃) is a deuterium labeled (rac)-Calcium N5-methyltetrahydrofolate.

HY-132446S

Metoprolol Acid-d5
Metoprolol Acid-d₅ is the deuterium labeled Metoprolol Acid .

HY-143859S

Metoprolol dimer-d10
Metoprolol dimer-d₁₀ is the deuterium labeled Metoprolol dimer .

HY-17503AS1

Metoprolol-d6 succinate
Metoprolol-d₆ (succinate) is deuterium labeled Metoprolol (succinate). Metoprolol succinate is an orally active, selective β1-adrenoceptor antagonist. Metoprolol succinate shows anti-inflammation, antitumor and anti-angiogenic properties .

HY-B1178S2

*(Rac)-Cotinine-d7*
(Rac)-Cotinine-d₇ is deuterium labeled Cotinine.

HY-109541S6

*(Rac)-Colfosceril miristate-d72*
(Rac)-1,2-Dimyristoyl-sn-glycero-3-phosphocholine-d₇₂ is deuterium labeled (Rac)-1,2-Dimyristoyl-sn-glycero-3-phosphocholine. 1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) is a synthetic phospholipid used in liposomes. 1,2-Dimyristoyl-sn-glycero-3-ph

HY-17503S2

*(S)-Metoprolol-d7*
(S)-Metoprolol-d₇ is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2].

HY-17503S1

*(R)-Metoprolol-d7*
(R)-Metoprolol-d₇ is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2].

HY-66011BS

(Rac)-Moxifloxacin-d4

(Rac)-Moxifloxacin-d₄ ((Rac)-BAY 12-8039-d₄ (free base)) is deuterium labeled (Rac)-Moxifloxacin. (Rac)-Moxifloxacin ((Rac)-BAY 12-8039 free base) is the isoform of Moxifloxacin Hydrochloride (HY-66011), which is an oral 8-methoxyquinolone antimicrobial for use in the treatment of acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, and community-acquired pneumonia .

HY-12142S

rac-Vofopitant-d3
rac-Vofopitant-d₃ (rac-GR 205171-d₃) is the deuterium labeled Vofopitant (HY-12142) . Vofopitant is potent tachykinin NK₁ receptor antagonist, with pK_is of 10.6, 9.5, and 9.8 for human, rat and ferret NK₁ receptor, respectively .

HY-12085S2

*(Rac)-Apremilast-d5*
(Rac)-Apremilast-d₅ is a deuterium labeled (R)-Apremilast. (R)-Apremilast ((R)-CC-10004) is a enantiomer of Apremilast .

HY-B0592S2

rac-Trandolapril-d5

rac-Trandolapril-d₅ (rac-RU44570-d₅) is deuterium labeled Trandolapril. Trandolapril (RU44570) is a nonsulfhydryl proagent that is hydrolysed to the active diacid Trandolaprilat. Trandolapril is an orally administered angiotensin converting enzyme (ACE) inhibitor that has been used in the treatment of hypertension and congestive heart failure (CHF), and after myocardial infarction (MI) .

HY-19489S1

*(Rac)-Levomepromazine-d3 hydrochloride*
(Rac)-Levomepromazine-d₃ (hydrochloride) is a labelled racemic Methotrimeprazine, which is a phenothiazine which has antagonist actions at multiple neurotransmitter receptor sites, including dopaminergic, cholinergic, serotonin and histamine receptors .

HY-10844S1

Pretomanid-d5
Pretomanid-d₅ is deuterated labeled Pretomanid (HY-10844). Pretomanid (PA-824) is an antibiotic used for the research of multi-drug-resistant tuberculosis affecting the lungs. Pretomanid exhibits a sub-micromolar MIC against M. tuberculosis (MTB). The MIC values of PA-824 against a panel of MTB pan-sensitive and Rifampin mono-resistant clinical isolates range from 0.015 to 0.25 μg/mL.

HY-18204S3

*(Rac)-Valsartan-d9*
(Rac)-Valsartan-d₉ is deuterium labeled Valsartan. Valsartan (CGP 48933) is an angiotensin II receptor antagonist and has the potential for high blood pressure and heart failure research .

HY-Y1039S1

*1-Stearoyl-rac-glycerol-d35*
1-Stearoyl-rac-glycerol-d₃₅ is the deuterium labeled 1-Stearoyl-rac-glycerol.

HY-W752055

*(Rac)-Nebivolol-d4 hydrochloride*
(Rac)-Nebivolol-d4 hydrochloride is a labelled racemic Nebivolol. Nebivolol selectively inhibits β1-adrenergic receptor with an IC₅₀ of 0.8 nM .

HY-Y1039S

*1-Stearoyl-rac-glycerol-d40*
1-Stearoyl-rac-glycerol-d₄₀ is the deuterium labeled 1-Stearoyl-rac-glycerol .

HY-15394S1

(Rac)-Rotigotine-d3 hydrochloride

(Rac)-Rotigotine-d₃ hydrochloride is a deuterium labeled (Rac)-Rotigotine (hydrochloride) (HY-15394). (Rac)-Rotigotine hydrochloride is a racemate of Rotigotine. Rotigotine is a full agonist of dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor, with K_is of 0.71 nM, 4-15 nM, and 83 nM for the dopamine D3 receptor and D2, D5, D4 receptors, and dopamine D1 receptor.

HY-15394S

(Rac)-Rotigotine-d7 hydrochloride

(Rac)-Rotigotine-d₇ (hydrochloride) is deuterium labeled (Rac)-Rotigotine (hydrochloride). (Rac)-Rotigotine hydrochloride is a racemate of Rotigotine. Rotigotine is a full agonist of dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor, with Kis of 0.71 nM, 4-15 nM, and 83 nM for the dopamine D3 receptor and D2, D5, D4 receptors, and dopamine D1 receptor.

HY-B0203BS2

(Rac)-Nebivolol-d2,15N

(Rac)-Nebivolol-d₂, ¹⁵N is ¹⁵N and deuterated labeled (Rac)-Nebivolol (HY-B0203B). (Rac)-Nebivolol ((Rac)-R 065824) is a racemic isomer of Nebivolol. Nebivolol is a selective β1-adrenergic receptor antagonist with an IC₅₀ value of 0.8 nM. Nebivolol can prevent up-regulation of Nox2/NADPH oxidase and lipoperoxidation in the early stages of ethanol-induced cardiac toxicity. Vasodilatory activity .

HY-17494S

(Rac)-Timolol-d5 maleate

rac Timolol-d₅ (maleate) is a labelled racemic (S)-Timolol maleate. (S)-Timolol Maleate (L-714,465 Maleate) is a non-cardioselective hydrophilic β-adrenoceptor blocker. (S)-Timolol Maleate is widely used as standard medication for intraocular pressure (glaucoma) by preventing the production of aqueous humor. (S)-Timolol Maleate can be used for hypertension, angina pectoris and myocardial infarction .

HY-W777286

rac-Lenalidomide-13C5
rac Lenalidomide- ¹³C₅ is a ¹³C-labeled rac Lenalidomide .

HY-134670S

*α-Hydroxy Metoprolol-d5 (Mixture of Diastereomers)*
α-Hydroxy Metoprolol-d₅ (Mixture of Diastereomers) is the deuterium labeled α-Hydroxy Metoprolol Mixture of Diastereomers .

HY-W778189

rac-2-Linoleoyl-3-chloropropanediol-d5,95%
rac-2-Linoleoyl-3-chloropropanediol-d₅,95% (2-Linoleoyl-3-chloropropanediol-d₅) is deuterium labeled rac-2-Linoleoyl-3-chloropropanediol,95% .

HY-B0161ES

(±)-Duloxetine-d3 hydrochloride
(±)-Duloxetine-d₃ (hydrochloride) is deuterium labeled (±)-Duloxetine (hydrochloride). (±)-Duloxetine ((Rac)-Duloxetine) hydrochloride is the racemate of Duloxetine hydrochloride. Duloxetine hydrochloride, a serotonin-norepinephrine reuptake inhibitor, can be used for diabetic neuropathic pain and fibromyalgia as well as major depressive disorder research .

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