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<i>Lagotis alutacea<_i> W. W. Smith

" in MedChemExpress (MCE) Product Catalog:

By Targets:	11β-HSD (1) 17β-HSD (1) 5 alpha Reductase (10) 5-HT Receptor (19) AAK1 (1) Acetolactate Synthase (ALS) (1) Acetyl-CoA Carboxylase (3) Ack1 (1) Acyltransferase (4) ADAMTS (2) ADC Antibody (1) ADC Cytotoxin (45) ADC Linker (6) Adenosine Deaminase (1) Adenosine Receptor (7) Adenylate Cyclase (7) Adrenergic Receptor (37) AIM2 (2) Akt (22) Amino Acid Decarboxylase (1) Amino Acid Derivatives (31) Aminopeptidase (3) Aminotransferases (Transaminases) (2) AMPK (14) Amylases (5) Amyloid-β (14) Anaplastic lymphoma kinase (ALK) (6) Androgen Receptor (19) Angiotensin Receptor (29) Angiotensin-converting Enzyme (ACE) (38) Annexin A (1) Antibiotic (92) Antibody-Drug Conjugates (ADCs) (11) AP-1 (1) Apelin Receptor (APJ) (1) Apical Sodium-Dependent Bile Acid Transporter (1) Apolipoprotein (2) Apoptosis (318) Aquaporin (1) Arenavirus (2) Arginase (6) Aryl Hydrocarbon Receptor (8) Atg8/LC3 (3) ATM/ATR (7) ATTECs (2) Aurora Kinase (10) AUTACs (1) Autophagy (97) AUTOTACs (1) Bacterial (168) 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Stain (2) DNA-PK (4) DNA/RNA Synthesis (95) Dopamine Receptor (4) Dopamine Transporter (2) Drug Derivative (25) Drug Intermediate (21) Drug Isomer (4) Drug Metabolite (40) Drug-Linker Conjugates for ADC (42) Dynamin (11) E1/E2/E3 Enzyme (5) E3 Ligase Ligand-Linker Conjugates (15) EAAT (1) EBV (2) EGFR (25) Elastase (3) Endogenous Metabolite (302) Endonuclease (2) Endoplasmic Reticulum Oxidoreductase 1 (ERO1) (1) Endothelin Receptor (8) Enterovirus (1) Epigenetic Reader Domain (62) Epoxide Hydrolase (2) ERK (14) Estrogen Receptor/ERR (15) Eukaryotic Initiation Factor (eIF) (1) FAAH (1) Factor Xa (5) Factor XI (1) FAK (2) FAP (3) Farnesyl Transferase (7) Fat Mass and Obesity-associated Protein (FTO) (1) Fatty Acid Synthase (FASN) (3) Fc Receptor (FcR) (1) Ferroptosis (16) FGFR (11) Filovirus (3) FKBP (5) FLAP (1) Flavivirus (4) FLT3 (12) Fluorescent Dye (176) Formyl Peptide Receptor (FPR) (2) Free Fatty Acid Receptor (1) Fungal (61) FXR (3) G protein-coupled Bile Acid Receptor 1 (1) G Protein-coupled Receptor Kinase (GRK) (2) G-quadruplex (1) GABA Receptor (8) GCGR (5) GGTase (6) GHSR (3) GLP Receptor (9) Glucokinase (1) Glucosylceramide Synthase (GCS) (5) GLUT (6) Glutaminase (2) Glutathione Peroxidase (9) Glutathione S-transferase (2) Glycosidase (16) Glycosyltransferase (1) Glyoxalase (GLO) (11) GlyT (4) GnRH Receptor (3) GPR119 (1) GSK-3 (11) Guanylate Cyclase (2) HBV (7) HCV (13) HDAC (63) Herbicide (4) HIF/HIF Prolyl-Hydroxylase (11) Hippo (MST) (1) Histamine Receptor (9) Histone Acetyltransferase (3) Histone Demethylase (5) Histone Methyltransferase (18) HIV (55) HIV Integrase (1) HIV Protease (4) HMG-CoA Reductase (HMGCR) (1) HPV (3) HSP (11) HSV (18) IAP (3) IFNAR (16) IGF-1R (7) iGluR (20) IKK (27) IKZF Family (1) Imidazoline Receptor (29) IMPDH (1) Indoleamine 2,3-Dioxygenase (IDO) (4) Influenza Virus (17) Insecticide (11) Insulin Receptor (8) Integrin (5) Interleukin Related (27) IRAK (10) IRE1 (1) Isocitrate Dehydrogenase (IDH) (1) Isotope-Labeled Compounds (443) Itk (1) JAK (21) JNK (7) Keap1-Nrf2 (4) LAG-3 (3) Leukotriene Receptor (1) Ligands for E3 Ligase (3) Ligands for Target Protein for PROTAC (5) LIM Kinase (LIMK) (2) Lipase (1) Liposome (4) Lipoxygenase (4) LOX-1 (1) LPL Receptor (6) LRRK2 (2) LXR (2) mAChR (8) MAGL (2) Malate Dehydrogenase (MDH) (1) MAP3K (6) MAP4K (5) MARCKS (1) MDM-2/p53 (10) MEK (2) Melanocortin Receptor (4) Melatonin Receptor (1) Methionine Adenosyltransferase (MAT) (1) mGluR (19) MHC (17) MicroRNA (46) Microtubule/Tubulin (10) Mineralocorticoid Receptor (2) Mitochondrial Metabolism (36) Mitophagy (12) Mitosis (1) Mixed Lineage Kinase (3) MMP (24) Molecular Glues (5) Monoamine Oxidase (15) Monoamine Transporter (2) Mps1 (2) mTOR (21) Mucin (1) MyD88 (2) Myosin (4) Na+/K+ ATPase (5) nAChR (16) NADPH Oxidase (1) Natriuretic Peptide Receptor (NPR) (1) Necroptosis (5) NEKs (1) Neprilysin (1) Neurokinin Receptor (5) Neuropeptide B/W Receptor (6) Neuropeptide Y Receptor (5) Neurotensin Receptor (2) NF-κB (81) NKCC (1) NO Synthase (20) NOD-like Receptor (NLR) (5) Notch (3) NTPDase (1) Nuclear Hormone Receptor 4A/NR4A (1) Nucleoside Antimetabolite/Analog (67) Oct3/4 (2) Olfactory Receptor (1) Opioid Receptor (12) Organoid (16) Orphan Receptor (1) Orthopoxvirus (3) Oxidative Phosphorylation (11) Oxytocin Receptor (1) P-glycoprotein (8) P2X Receptor (3) P2Y Receptor (4) p38 MAPK (12) p62 (1) p97 (2) PACAP Receptor (6) PAK (2) Paraptosis (1) Parasite (69) PARP (15) PCSK9 (2) PD-1/PD-L1 (5) PDGFR (6) PDK-1 (2) Peptide-Drug Conjugates (PDCs) (1) PERK (2) PGE synthase (2) Phosphatase (4) Phosphodiesterase (PDE) (21) Phospholipase (2) Photosensitizer (2) Phytohormone (1) PI3K (41) PI4P5K (1) Piezo Channel (2) Pim (4) PIN1 (2) PKA (22) PKC (19) PKD (2) PKG (8) Platelet-activating Factor Receptor (PAFR) (5) Polo-like Kinase (PLK) (2) Potassium Channel (31) PPAR (7) Prion Protein (1) Prostaglandin Receptor (15) PROTAC Linkers (7) PROTACs (214) Protease Activated Receptor (PAR) (4) Proteasome (30) Protein Arginine Deiminase (2) Protein Prenyltransferase (2) Protoporphyrinogen IX oxidase (4) PSMA (6) PTEN (1) Pyroptosis (2) Pyruvate Kinase (2) Quinone Reductase (3) Radionuclide-Drug Conjugates (RDCs) (3) Raf (5) RAR/RXR (1) Ras (25) Reactive Oxygen Species (52) Reference Standards (46) Renin (4) RET (3) Reverse Transcriptase (6) RIP kinase (10) RNA MTase (1) ROCK (12) ROR (4) ROS Kinase (5) RSV (2) RUNX (1) Salt-inducible Kinase (SIK) (1) SARS-CoV (19) Scavenger Receptor Class B type I (SR-BI） (2) Ser/Thr Kinase (2) Ser/Thr Protease (7) Serine Racemase (SR) (1) Serotonin Transporter (3) Sex Pheromone (2) SF3B1 (1) SHMT (1) SHP2 (2) Sigma Receptor (1) Sirtuin (3) Small Interfering RNA (siRNA) (38) SNIPERs (1) SOD (6) Sodium Channel (28) Somatostatin Receptor (2) SOS1 (8) SphK (3) Src (5) STAT (22) Stearoyl-CoA Desaturase (SCD) (1) Steroid Sulfatase (1) STING (22) Succinate Dehydrogenase (1) Survivin (5) SWI/SNF Complex (2) Syk (1) TAM Receptor (3) Target Protein Ligand-Linker Conjugates (1) Taste Receptor (1) Tau Protein (2) TGF-beta/Smad (10) TGF-β Receptor (36) Thrombin (1) Thymidylate Synthase (2) Thyroid Hormone Receptor (3) TMV (2) TNF Receptor (30) Toll-like Receptor (TLR) (19) Topoisomerase (218) Transferrin Receptor (1) Transketolase (1) Transmembrane Glycoprotein (9) Transthyretin (TTR) (4) Trk Receptor (5) TROP2 (1) TRP Channel (10) TrxR (3) Tyrosinase (18) URAT1 (2) VD/VDR (4) VEGFR (18) Virus Protease (2) VKOR (1) WDR5 (2) Wee1 (1) Wnt (9) Xanthine Oxidase (2) YAP (6) α-synuclein (5) β-catenin (9) γ-secretase (1)
By Research Areas:	Cancer (1475) Cardiovascular Disease (266) Endocrinology (119) Infection (414) Inflammation/Immunology (478) Metabolic Disease (380) Neurological Disease (385)
Click Chemistry:	ADC Synthesis (1) TCO (1) DBCO (2) PROTAC Synthesis (1) Azide (25) Tetrazine (2) Alkynes (20)
Oligonucleotides:	miRNA mimics (12) Solvents (1) miRNA antagomirs (10) Nucleosides and their Analogs (33) Thickeners (1) Nucleoside Phosphoramidites (5) Flavoring Agents (1) Rat Pre-designed siRNA Sets (10) miRNA inhibitors (10) Phospholipids (2) Solubilizing Agents (1) mRNA (1) Antisense Oligonucleotides (2) Bases (1) siRNAs (37) miRNA agomirs (10) MicroRNAs (42) Aptamers (5) Emulsifiers (1) Mouse Pre-designed siRNA Sets (9) Human Pre-designed siRNA Sets (18) Polymers (1)

3676

Inhibitors & Agonists

Screening Libraries

163

Fluorescent Dye

116

Biochemical Assay Reagents

274

Peptides

MCE Kits

Inhibitory Antibodies

536

Natural
Products

391

Recombinant Proteins

477

Isotope-Labeled Compounds

167

Antibodies

Click Chemistry

132

Oligonucleotides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-P990832

Anti-MHC Class I Antibody (W6/32)	MHC	Others
Anti-MHC Class I Antibody (W6/32) is a kind of mouse IgG2a, κ chimeric antibody, targeting to human MHC Class I. The recommend isotype control of Anti-MHC Class I Antibody (W6/32): Mouse IgG2a kappa, Isotype Control (HY-P99978).

HY-16992A

W-54011 5 Publications Verification	Complement System Reactive Oxygen Species	Inflammation/Immunology
W-54011 is a potent and orally active non-peptide C5a receptor antagonist. W-54011 inhibits the binding of ¹²⁵I-labeled C5a to human neutrophils with a K_i value of 2.2 nM. W-54011 also inhibits C5a-induced intracellular Ca ²⁺ mobilization, chemotaxis, and generation of ROS in human neutrophils with IC₅₀s of 3.1 nM, 2.7 nM, and 1.6 nM, respectively .

HY-100911

W-5 hydrochloride	Calmodulin	Neurological Disease
W-5 hydrochloride is a calmodulin antagonist. W-5 hydrochloride inhibits phosphodiesterase activation with an IC₅₀ value of 240 µM. W-5 hydrochloride can be used as a negative control for W-7 (HY-100912) .

HY-100913

W-7 isomer hydrochloride	Calmodulin	Cancer
W-7 isomer hydrochloride is an isomer of W-7 hydrochloride (HY-100912). W-7 hydrochloride is a selective calmodulin antagonist .

HY-100912

W-7 hydrochloride 5 Publications Verification	Phosphodiesterase (PDE) Myosin Apoptosis Calmodulin Potassium Channel	Cancer
W-7 hydrochloride is a selective calmodulin antagonist. W-7 hydrochloride inhibits the Ca ²⁺-calmodulin-dependent phosphodiesterase and myosin light chain kinase with IC₅₀ values of 28 μM and 51 μM, respectively. W-7 hydrochloride induces apoptosis and has antitumor and vascular relaxing activity. W-7 hydrochloride is a blocker of Kv4.3 and can be used for research of arrhythmias .

HY-100910

W-13 hydrochloride	CaMK	Cancer
W-13 hydrochloride is a calmodulin antagonist. W-13 hydrochloride can inhibit Tamoxifen (HY-13757A)-resistant human breast cancer cell growth .

HY-163106

W000113414_I13	Ceramidase	Cancer
W000113414_I13 is an acid ceramidase (AC) inhibitor. W000113414_I13 exhibits dose-dependent inhibition of AC with an IC₅₀ value of 6.6?μM. W000113414_I13 can be used for the research of cancer .

HY-P10951

(R)-Zadavotide guraxetan (R)-PSMA I&T; (R)-PNT-2002	PSMA	Cancer
Zadavotide guraxetan (PSMA I&T; PNT-2002) is a prostate-specific membrane antigen (PSMA) inhibitor. Zadavotide guraxetan has antitumor activity and can be used in prostate cancer-targeted research .

HY-130368

W-7	Calmodulin Potassium Channel Phosphodiesterase (PDE) Myosin Apoptosis	Cardiovascular Disease
W-7 is a selective calmodulin antagonist. W-7 inhibits the Ca ²⁺-calmodulin-dependent phosphodiesterase and myosin light chain kinase with IC₅₀ values of 28 μM and 51 μM, respectively. W-7 induces apoptosis and has antitumor and vascular relaxing activity. W-7 is a blocker of Kv4.3 and can be used for research of arrhythmias .

HY-Y0407A

Tetrapropylammonium hydroxide (40% w/w in water) TPAOH (40% w/w in water)	Biochemical Assay Reagents	Others
Tetrapropylammonium hydroxide (40% w/w in water)It is a compound belonging to the class of quaternary ammonium compounds and is a strong base with cationic properties. Tetrapropylammonium hydroxide (40% w/w in water)It is usually used as a phase transfer catalyst to promote the transfer of reactants between immiscible phases in various organic synthesis reactions. It is also used in the production of semiconductors, especially the manufacture of thin-film transistors and other electronic devices.

HY-173020

W23-1006	Anaplastic lymphoma kinase (ALK) Apoptosis	Cancer
W23-1006 is a selective and covalent ALKBH5 inhibitor. W23-1006 binds to the ALKBH5 C200 residue with an IC₅₀ value of 3.848 μM. W23-1006 shows ~30- and 8-fold stronger inhibitory activity than that against FTO and ALKBH3, respectively. W23-1006 can be used for the study of triple-negative breast cancer (TNBC) .

HY-145012S

W-19-d4 hydrochloride	Isotope-Labeled Compounds	Others
W-19-d₄ (hydrochloride) is the deuterium labeled W-19 hydrochloride .

HY-145482

W36017	Drug Metabolite	Neurological Disease
W3601 is the impurity of Lidocaine. W3601 exhibits nerve blocking activity with the pK_a of 7.4 .

HY-145415

W13	Bacterial	Infection
W13 is a potent MsbA inhibitor. W13 is an ATPase stimulator with an EC₅₀ of 5.5 µM .

HY-107928B

Iron–Dextran(Fe 35-40% w/w)	Biochemical Assay Reagents	Others
Iron–Dextran(Fe 35-40% w/w) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-163192

W6134	ROR	Cancer
W6134 is highly potent and selective RORγ covalent inhibitor with IC₅₀ of 0.21 μM. W6134 exhibits superior activity ini nhibiting the proliferation and colony formation and inducing apoptosis. W6134 can be used for the research of cancer .

HY-100979

W-84 dibromide HDMPPA	mAChR	Others
W-84 (dibromide) is a potent allosteric modulator of M2-cholinoceptors, which retards [ ³H]N-methylscopolamine dissociation. W-84 dibromide can stabilize cholinergic antagonist-receptor complexes. W-84 (dibromide) is a non-competitive muscarinic acetylcholine receptors antagonist with allosteric effects. W-84 (dibromide) protects over additively against an organophosphate-intoxication when applied in combination with atropine .

HY-18731

1400W Dihydrochloride 15+ Cited Publications	NO Synthase Apoptosis	Cardiovascular Disease Inflammation/Immunology Cancer
1400W dihydrochloride is the dihydrochloride form of 1400W (HY-18730). 1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a K_d value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .

HY-168035

W4275	Histone Methyltransferase	Cancer
W4275 (Compound 42) is a selective NSD2 inhibitor with oral activity, showing an IC₅₀ value of 17 nM. W4275 exhibits antiproliferative activity with an IC₅₀ of 230 nM against RS411 cells and significantly inhibits tumor growth in the RS411 tumor xenograft model. Pharmacokinetic analysis in mice demonstrates that W4275 has good oral bioavailability (F of 27.34%). W4275 holds promise for use in cancer research .

HY-N8097

Kushenol W	Bacterial	Infection
Kushenol W is a prenylated flavonoid that can be isolated from the root of Sophora flavescens. Kushenol W has antimicrobial effect, with a MIC of 10 μg/mL for Staphylococcus aureus .

HY-18730

1400W W1400	NO Synthase Apoptosis	Cardiovascular Disease Inflammation/Immunology Cancer
1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a K_d value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .

HY-P3844

Biotinyl-neuropeptide W-23 (human)	Transmembrane Glycoprotein Neuropeptide B/W Receptor	Neurological Disease
Biotinyl-neuropeptide W-23 (human) is a biotinylated neuropeptide W-23 (human) (HY-P1035). Neuropeptide W-23 (human) is an agonist of NPBW1 (GPR7) and NPBW2 (GPR8) .

HY-153190

W1131	Oxidative Phosphorylation STAT Ferroptosis	Cancer
W1131 is a potent STAT3 inhibitor, triggering ferroptosis. W1131 suppresses cancer progression in gastric cancer cell subcutaneous xenograft model, organoids model, and PDX model. W1131 effectively alleviates chemical resistance of cancer cells to 5-FU (HY-90006). W1131 regulates cell cycle, DNA damage response, and oxidative phosphorylation, including IL6-JAK-STAT3 pathway and ferroptosis pathway .

HY-19282A

(5R)-BW-4030W92	Sodium Channel	Neurological Disease
(5R)-BW-4030W92 is the R enantiomer of BW-4030W92. BW-4030W92 is a non-selective, voltage-, and use-dependent sodium channel antagonist.

HY-N15011

Ganoderic acid W	Others	Cancer
Ganoderic acid W is a natural product with anti-tumor activity .

HY-153190A

W1131 TFA	Ferroptosis STAT	Cancer
W1131 TFA is a potent STAT3 inhibitor that induces ferroptosis. W1131 inhibits cancer progression in subcutaneous xenograft, organoid, and PDX models of gastric cancer. W1131 effectively alleviates cancer cell chemoresistance to 5-FU (HY-90006). W1131 regulates the cell cycle, DNA damage response, and oxidative phosphorylation, including the IL6-JAK-STAT3 pathway and the ferroptosis pathway .

HY-U00204

Nisobamate W1015	Drug Derivative	Neurological Disease
Nisobamate (W1015) is a tranquilizer.

HY-N14602

Rifamycin W	Bacterial	Infection
Rifamycin W has anti-Gram-positive bacterial activity .

HY-118311

(Z)-W 3699 (Z)-Probilin; (Z)-Secrebil; (Z)-Piprozolin	Others	Metabolic Disease
(Z)-W 3699 is a potential choleretic. (Z)-W 3699 can increase the solubility of cholesterol in the gallbladder by altering the secretion of micellar bile acids. (Z)-W 3699 can prevent the formation of cholesterol-containing gallstones in dogs.

HY-116088

W123	LPL Receptor	Inflammation/Immunology
W123, a FTY720 analog, is a competitive sphingosine 1-phosphate type 1 (S1P1) receptor antagonist. W123 is measured by GTPγS activation, MAPK recruitment, cell migration, and ligand-induced receptor internalization .

HY-171790

W-2451 NSC 294839	5-HT Receptor	Neurological Disease
W-2451 (NSC 294839) is a selective serotonin 5-HT₂ receptor antagonist. W-2451 is promising for research of neurological disorders .

HY-N5154

Sanggenon W	Others	Others
Sanggenon W is an isoprenyl flavonoid extracted from mulberry root bark .

HY-19264

264W94	Apical Sodium-Dependent Bile Acid Transporter	Metabolic Disease
264W94 is a potent ileal bile acid transporter (IBAT) inhibitor and a new cholesterol lowering agent. 264W94 has CYP7A1 induction, and antilipemic action .

HY-P1175

L-R4W2	TRP Channel	Neurological Disease
L-R4W2 is a potent antagonist of vanilloid receptor 1 (VR1, TRPV1), with an IC₅₀ of 0.1 μM. L-R4W2 may act as a potent analgesic .

HY-106537

W 3699 Probilin; Secrebil; Piprozolin	Others	Metabolic Disease
W 3699 (Probilin; Secrebil; Piprozolin) is a choleretic agent that can be used in the study of biliary diseases .

HY-N11531

Kuwanon W	Others	Others
Kuwanon W is a natural product that can be isolated from the root bark of Morus lhou .

HY-N7294

Taxuspine W	Others	Others
Taxuspine W is a natural product, that can be isolated from the Japanese Yew Taxus cuspidata .

HY-N1262

Scutebarbatine W Scutehenanine B	Others	Inflammation/Immunology
Scutebarbatine W is a 13-spiro subtype neo-clerodane diterpenoid. Scutebarbatine W inhibits NO production with an IC₅₀ value of 34.7 μM .

HY-100174

W-2429 NSC294836	Others	Neurological Disease
W-2429 (NSC294836) is considerably more effective than acetylsalicylic acid in inhibiting carrageenan-induced edema and in reducing brewer's yeast-induced fever in rats .

HY-P3087

Tyr-W-MIF-1	Opioid Receptor	Neurological Disease
Tyr-W-MIF-1 is an opioid tetrapeptide with opiate and antiopiate activity. Tyr-W-MIF-1 can induce analgesia .

HY-143665S

Nor-W-18-d4	Isotope-Labeled Compounds	Others
Nor-W-18-d₄ is the deuterium labeled Nor-W-18 .

HY-B2056

Triforine CELA W 524	Fungal	Infection Inflammation/Immunology
Triforine (CELA W 524), a systemic fungicide, was shown to display a moderate to distinct fungitoxic activity in vitro towards several pathogenic and non-pathogenic fungi .

HY-107094

MT-7716 hydrochloride W-212393 hydrochloride	Opioid Receptor	Neurological Disease
MT-7716 hydrochloride (W-212393 hydrochloride) is a selective non-peptide nociceptin receptor (NOP) agonist and promising potential treatment drug for alcohol abuse and relapse prevention .

HY-N14733

31-Homorifamycin W	Antibiotic Bacterial	Infection
31-Homorifamycin W is an antibiotic found in Amycolatopsis mediterranei .

HY-122491

Dimethyl-W84 dibromide	mAChR	Neurological Disease
Dimethyl-W84 (dibromide) modulates M2 muscarinic acetylcholine receptors. Dimethyl-W84 (dibromide) can be used in nervous system related research .

HY-P1035

Neuropeptide W-23 (human) NPW-23	Neuropeptide B/W Receptor	Neurological Disease
Neuropeptide W-23 (human) (NPW-23), the active form of Neuropeptide W, is an endogenous agonist of NPBW1 (GPR7) and NPBW2 (GPR8) .

HY-B2081

Etozolin W-2900A	Others	Cardiovascular Disease Metabolic Disease
Etozolin (W-2900A) is a diuretic agent. Etozolin inhibits fluid and electrolyte reabsorption in the loop of Henle. Etozolin can be used in research of congestive heart failure, hypertension and edema .

HY-174066

SI-W052	mTOR Autophagy Interleukin Related	Neurological Disease Inflammation/Immunology
SI-W052 is an orally active, brain-penetrant and selective small-molecule inhibitor targeting mTOR and TEX264. SI-W052 activates autophagy by inhibiting mTOR phosphorylation and enhances TEX264 expression to promote ER turnover, suppressing LPS-induced release of inflammatory factors (TNF-α, IL-6). SI-W052 is promising for research of Alzheimer’s disease (AD)-associated neuroinflammation .

HY-P1175A

L-R4W2 TFA	TRP Channel	Neurological Disease
L-R4W2 TFA is a potent antagonist of vanilloid receptor 1 (VR1, TRPV1), with an IC₅₀ of 0.1 μM. L-R4W2 TFA may act as a potent analgesic .

HY-B0184A

Felbamate hydrate W-554 hydrate; ADD-03055 hydrate	iGluR	Neurological Disease
Felbamate hydrate (W-554 hydrate) is a potent nonsedative anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA) .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N11531

Kuwanon W	Structural Classification Flavonoids Flavones Source classification Plants Moraceae Morus alba Linn.	Others
Kuwanon W is a natural product that can be isolated from the root bark of Morus lhou .

HY-122949

Momordicine I	Triterpenes Structural Classification Terpenoids Source classification Cucurbitaceae Plants Momordica charantia Linn.	DGK
Momordicine I, a triterpenoid compound extracted from momordica charantia L. Momordicine I alleviates isoproterenol-induced cardiomyocyte hypertrophy through suppression of PLA2G6 and DGK-ζ .

HY-N8097

Kushenol W	Infection Flavonoids Classification of Application Fields Leguminosae Flavonones Source classification Phenols Polyphenols Plants Sophora flavescens Aiton Disease Research Fields	Bacterial
Kushenol W is a prenylated flavonoid that can be isolated from the root of Sophora flavescens. Kushenol W has antimicrobial effect, with a MIC of 10 μg/mL for Staphylococcus aureus .

HY-N15011

Ganoderic acid W	Structural Classification Natural Products Microorganisms Source classification	Others
Ganoderic acid W is a natural product with anti-tumor activity .

HY-N14602

Rifamycin W	Structural Classification Natural Products Microorganisms Source classification	Bacterial
Rifamycin W has anti-Gram-positive bacterial activity .

HY-N5154

Sanggenon W	Structural Classification Flavonoids Flavones Source classification Plants Moraceae Morus alba Linn.	Others
Sanggenon W is an isoprenyl flavonoid extracted from mulberry root bark .

HY-N7294

Taxuspine W	Structural Classification Taxus cuspidata Siebold & Zucc. Ketones, Aldehydes, Acids Source classification Taxaceae Plants	Others
Taxuspine W is a natural product, that can be isolated from the Japanese Yew Taxus cuspidata .

HY-N1262

Scutebarbatine W Scutehenanine B	Structural Classification Terpenoids Labiatae Source classification Derris robusta Diterpenoids Plants	Others
Scutebarbatine W is a 13-spiro subtype neo-clerodane diterpenoid. Scutebarbatine W inhibits NO production with an IC₅₀ value of 34.7 μM .

HY-N14733

31-Homorifamycin W	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Bacterial
31-Homorifamycin W is an antibiotic found in Amycolatopsis mediterranei .

HY-N14457

Platenomycin W2	Structural Classification Microorganisms Ketones, Aldehydes, Acids Source classification	Antibiotic Bacterial
Platenomycin W2 is a macrolide antibiotic with anti-Gram-positive bacteria activities .

HY-N12370

Tenaxin I	Structural Classification Flavonoids Flavones Labiatae Source classification Plants Medicago truncatula Gaertn.	Others
Tenaxin I is a component extracted from Radix Scutellariae with neuraminidase inhibitory activity .

HY-N12073

Monofucosyllacto-N-hexaose I MFLNH I	Structural Classification Polysaccharides Animals Source classification Saccharides	Others
Monofucosyllacto-N-hexaose I (MFLNH I) is a composition of human milk oligosaccharide .

HY-P3055

Dendrotoxin-I DTX-I	Structural Classification Animals Cyclopeptides Source classification Animal Venoms	Potassium Channel
Dendrotoxin-I (DTX-I) is a potent K ⁺ channels blocker with IC₅₀s of 0.13-50 nM for voltage-gated potassium channel subunits K_V1.1, K_V1.2 and K_V1.6, respectively. Dendrotoxin-I, a neurotoxin, has the potential for cancer research .

HY-N11172

Schibitubin I	Structural Classification Source classification Lignans Schisandra bicolor Cheng Phenylpropanoids Plants Schisandraceae	Others
Schibitubin I is a lignin. Schibitubin I has neuroprotective activity. Schibitubin I can be isolated from the fruits of Schisandra bicolor var. tuberculata .

HY-N12316

Goshuyuamide I	Structural Classification Alkaloids Source classification Evodia rutaecarpa (Juss.) Benth. Rutaceae Plants Indole Alkaloids	Others
Goshuyuamide-I (compound 4) is a kind of alkaloid. Goshuyuamide-I can be isolated from the fruits of Euodia rutaecarpa. Goshuyuamide-I can be used in the research of analgesics .

HY-N5196

Nocathiacin I Nocathiacine I	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Bacterial
Nocathiacin I (Nocathiacine I) is highly resistant to Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), penicillin-resistant Streptococcus pneumoniae (PRSP) and multidrug resistant Enterococcus faecalis (MREF) .

HY-107301

Dehydrosoyasaponin I Soyasaponin Be; DHS-I	Structural Classification Polysaccharides Leguminosae Source classification Plants Saccharides Medicago sativa L.	Potassium Channel
Dehydrosoyasaponin I (Soyasaponin Be;DHS-I), a triterpene glycoside, is a potent and reversible calcium-activated potassium (maxi-K) channels activator .

HY-N0407R

Picroside I (Standard)	Structural Classification Iridoids Terpenoids Source classification Scrophulariaceae Plants Picrorhiza scrophulariiflora Pennell	STAT
Picroside I (Standard) is the analytical standard of Picroside I. This product is intended for research and analytical applications. Picroside I is the major ingredient of Picrorhiza scrophulariiflora. Picrorhiza scrophulariiflora is a high value medicinal herb due to rich source of hepatoprotective metabolites, Picroside-I and Picroside-II . Picroside I is a promising agent for the management of asthma. Picroside I reduces the inflammation significantly at its higher dose. Picroside I also downregulates pSTAT6 and GATA3 expressions. Picroside I dose-dependently increases the serum levels of IFN-γ .

HY-N1628

1β-Hydroxybaccatin I 1-Hydroxybaccatin I	Structural Classification Terpenoids Source classification Taxaceae Diterpenoids Plants Taxus wallichiana Zucc.	Others
1β-Hydroxybaccatin I (1-Hydroxybaccatin I) can be extracted from Taxus wallichiana .

HY-N11430

F1839-I	Structural Classification Monophenols Microorganisms Source classification Phenols	HIV
F1839-I is a compound that can be isolated from Stachybotrys. F1839-I has weak cytotoxicity and anti-HIV activity with an IC₅₀ value of 15.6 μM .

HY-N10076

Ganomycin I	Structural Classification Microorganisms Source classification Phenols Polyphenols	HMG-CoA Reductase (HMGCR) Glycosidase HIV Protease
Ganomycin I is a dual inhibitor of α-Glucosidase and HMG-CoA reductase. Ganomycin I can also inhibits HIV protease. Ganomycin I exhibits anti-diabetic and anti-osteoclastogenesis effects .

HY-N14084

Monamycin I	Structural Classification Microorganisms Macrolide Antibiotics Antibiotics Source classification	Antibiotic Bacterial
Monamycin I is an ester peptide antibiotic. Monamycin I has activity against Gram-positive bacteria .

HY-N11455

Lacto-N-difucohexaose I LDFH I	Structural Classification Polysaccharides Microorganisms Source classification Saccharides	Others
Lacto-N-difucohexaose I (LNDFH I), a linker, could be used to combine oligosaccharides containing Lewis b sugar chain to water insoluble polysaccharide .

HY-N3340

Macrocarpal I	Structural Classification Terpenoids Sesquiterpenes Source classification Phenols Polyphenols Myrtaceae Plants Eucalyptus globulus Labill.	Fungal
Macrocarpal I is a phloroglucinol coupled sesquiterpenoid with antifungal activity. Macrocarpal I against C. glabrata with an IC₅₀ value of 0.75 μg/mL. Macrocarpal I can be isolated from the juvenile leaves of E. maideni .

HY-N7141R

Spiramycin I (Standard)	Structural Classification Microorganisms Macrolide Antibiotics Antibiotics Source classification Anti-parasitic Disease Research	Antibiotic Parasite Bacterial
Spiramycin I (Standard) is the analytical standard of Spiramycin I. This product is intended for research and analytical applications. Spiramycin I is a macrolide antibiotic and antiparasitic .

HY-N15386

Hericenone I	Structural Classification Microorganisms Ketones, Aldehydes, Acids Source classification	Drug Intermediate
Hericenone I (Compound 24) is an aromatic compound, which is found in Hericium erinaceum. Hericenone I can be biosynthetically generated from hericenone A via acid-catalyzed cyclization. Hericenone I is promising for research of neurodegenerative diseases .

HY-N8511

Acremine I	Structural Classification Natural Products Microorganisms Source classification	Fungal
Acremine I is a fungi inhibitor and also a metabolite of the endophytic fungus Acremonium byssoides. Acremine I can effectively inhibit Plasmopara viticola. Acremine I can be used for research on plant diseases, such as grape downy mildew .

HY-120860

Sporidesmolide I	Structural Classification Microorganisms Cyclopeptides Source classification	Others
Sporidesmolide I can be found in Sporidesmium bakeri. Sporidesmolide I is promising for research into diseases such as mammalian facial eczema .

HY-N8293

Eupalinolide I	Structural Classification Melilotus albus Desr. Terpenoids Sesquiterpenes Source classification Plants Compositae	Others
Eupalinolide I inhibits the viability of breast cancer cells. Eupalinolide I can be isolated from Eupatorium lindleyanum .

HY-B1411R

i-Inositol (Standard)	Structural Classification Natural Products Human Gut Microbiota Metabolites Immune System Disorder Microorganisms Source classification Disease markers Endocrine diseases Endogenous metabolite	Endogenous Metabolite
i-Inositol (Standard) is the analytical standard of i-Inositol. This product is intended for research and analytical applications. i-Inositol (myo-Inositol) is a compound of sugar alcohols. i-Inositol is involved in a series of biological processes such as insulin signal transduction and cytoskeletal transduction. i-Inositol mainly exists in glial cells and plays an osmotic role .

HY-N0612R

Siamenoside I (Standard)	Triterpenes Structural Classification Terpenoids Source classification Cucurbitaceae Siraitia grosvenorii (Swingle) C. Jeffrey ex Lu et Z. Y. Zhang Plants	Others
Siamenoside I (Standard) is the analytical standard of Siamenoside I. This product is intended for research and analytical applications. Siamenoside I is one of the mogrosides that has several kinds of bioactivities.

HY-N0331

Ziyuglycoside I	Triterpenes Structural Classification Classification of Application Fields Sanguisorba officinalis Linn. Terpenoids Source classification Rosaceae Plants Disease Research Fields Cancer	MDM-2/p53 Apoptosis
Ziyuglycoside I isolated from S. officinalis root, has anti-wrinkle activity, and increases the expression of type I collagen. Ziyuglycoside I could be used as an active ingredient for cosmetics . Ziyuglycoside I triggers cell cycle arrest and apoptosis mediated by p53, it can be a potential agent candidate for treating triple-negative breast cancer (TNBC) .

HY-N12127

Gymnoside I	Orchidaceae Gymnadenia conopsea (L.) R. Br. Source classification Plants	Others
Gymnoside I (compound 1) is a glycosidoxybenzyl 2-isobutylmalic acid. Gymnoside I shows antiallergic activity in passive cutaneous allergic reaction (PCA) in mice. Gymnoside I can be used in research to treat asthma, neurasthenia and chronic hepatitis .

HY-N2541

Gymnemic acid I	Triterpenes Structural Classification Classification of Application Fields Terpenoids Source classification Asclepiadaceae Metabolic Disease Plants Disease Research Fields Gymnema sylvestre (Retz.) Schult.	Taste Receptor mTOR Autophagy Apoptosis
Gymnemic acid I is a bioactive triterpene saponin found in Gymnema sylvestre. Gymnemic acid I is an antisweetness inhibitor via human sweet receptor type 1 receptor 2 (T1R2) and T1R3. Gymnemic acid I is a ribosomal protein biosynthesis inhibitor. Gymnemic acid I has antidiabetic effects. Gymnema acid I induces autophagy-protected MIN-6 cells from apoptosis under high glucose stress by inhibiting the phosphorylation activity of mTOR .

HY-N8614

Peucedanocoumarin I	Structural Classification Natural Products Chrysanthemum × morifolium (Ramat.) Hemsl. Source classification Plants Umbelliferae	Others
Peucedanocoumarin I (compound 1) is a kind of dihydropyranocoumarin. Peucedanocoumarin I can be isolated from the root of f Peucedanum praeruptorum .

HY-N12718

Campneoside I	Structural Classification Source classification Phenols Polyphenols Bignoniaceae Plants Incarvillea compacta Maxim.	Others
Campneoside I is a bitter phenyl propanoid glycoside. Campneoside I can be isolated from the roots of Incarvillea compacta .

HY-N7218

Lysolipin I	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Bacterial
Lysolipin I is a lipophilic antibiotic from Streptomyces violaceoniger. Lysolipin I is active against Gram-positive and Gramnegative bacteria .

HY-N0331R

Ziyuglycoside I (Standard)	Triterpenes Structural Classification Sanguisorba officinalis Linn. Terpenoids Source classification Rosaceae Plants	MDM-2/p53 Apoptosis
Ziyuglycoside I (Standard) is the analytical standard of Ziyuglycoside I. This product is intended for research and analytical applications. Ziyuglycoside I isolated from S. officinalis root, has anti-wrinkle activity, and increases the expression of type I collagen. Ziyuglycoside I could be used as an active ingredient for cosmetics . Ziyuglycoside I triggers cell cycle arrest and apoptosis mediated by p53, it can be a potential agent candidate for treating triple-negative breast cancer (TNBC) .

HY-W019806

Lacto-N-fucopentaose I LNFP I	Infection Structural Classification Natural Products Polysaccharides Classification of Application Fields Animals Inflammation/Immunology Disease Research Fields Saccharides	Endogenous Metabolite CDK Reactive Oxygen Species Apoptosis Enterovirus Bacterial
Lacto-N-fucopentaose I (LNFPI) is a human milk oligosaccharide (HMO), possessing antiviral and antibacterial activity. Lacto-N-fucopentaose I can reduce capsid protein VP1 to block virus adsorption, promote CDK2 and reduce cyclin E to recover cell cycle S phase block. Lacto-N-fucopentaose I inhibits ROS production and apoptosis in virus-infected cells. Lacto-N-fucopentaose I can also regulate intestinal microbiota to affect immune system development .

HY-N15368

Pradimicinone I	Quinones Structural Classification Microorganisms Anthraquinones Source classification	Antibiotic Bacterial
Pradimicinone I (Compound 10), a Pradimicin A (HY-132191) analog, is an antibiotic. Pradimicinone I is promising for research of antibacterial agents .

HY-N0432R

Astragaloside I (Standard)	Triterpenes Structural Classification other families Leguminosae Terpenoids Source classification Astragalus membranaceus var. mongholicus (Bunge)P.K.Hsiao Plants	Wnt β-catenin
Astragaloside I (Standard) is the analytical standard of Astragaloside I. This product is intended for research and analytical applications. Astragaloside I, one of the main active ingredients in Astragalus membranaceus, has osteogenic properties. Astragaloside I stimulates osteoblast differentiation through the Wnt/β-catenin signaling pathway .

HY-N7022R

Eclalbasaponin I (Standard)	Triterpenes Structural Classification other families Terpenoids Source classification Plants	Others
Eclalbasaponin I (Standard) is the analytical standard of Eclalbasaponin I. This product is intended for research and analytical applications. Eclalbasaponin I is isolated from Eclipta prostrata L with antitumor activity. Eclalbasaponin I inhibits the proliferation of hepatoma cell smmc-7721 with an IC₅₀ value of 111.1703 μg/ml .

HY-122530

Juvocimene I	Structural Classification Natural Products Labiatae Source classification Plants Helenium arizonicum S.F.Blake	Insecticide
Juvocimene I is a potent juvenile hormone mimic. Juvocimene I can be isolated from the essential oil of sweet basil,Ocimum basilicum L .

HY-N2013

Aristolactam I 1 Publications Verification Aristololactam; Aristolactam	Structural Classification Natural Products other families Classification of Application Fields Source classification Plants Inflammation/Immunology Disease Research Fields	Drug Metabolite Aquaporin Cadherin TGF-beta/Smad
Aristolactam I is an AQP1 inhibitor and Aristolochic acid I metabolite. Aristolactam I can be isolated from Aristolochia plants. Aristolactam I downregulates Twist1 expression, increases E-cadherin expression, and activates the TGF-β/Smad signaling pathway. Aristolactam I has anticancer activity against breast cancer. Aristolactam I is nephrotoxic. Aristolactam I is mainly used in the study of breast cancer and kidney diseases such as renal interstitial fibrosis .

HY-N0360R

Dihydrotanshinone I (Standard)	Quinones Structural Classification Labiatae Samanea saman (Jacq.) Merr. Source classification Plants Phenanthrenequinones	SARS-CoV
Dihydrotanshinone I (Standard) is the analytical standard of Dihydrotanshinone I. This product is intended for research and analytical applications. Dihydrotanshinone I is a natural compound extracted from Salvia miltiorrhiza Bunge which has been widely used for treating cardiovascular diseases. Dihydrotanshinone I exhibits entry-blocking effect for MERS-CoV.

HY-126476

Justicisaponin I	Justicia rotundifolia Nees Triterpenes Structural Classification Acanthaceae Terpenoids Source classification Plants	Others
Justicisaponin I can be used as an anti-fertility agent. Justicisaponin I stabilizes the acrosome membrane of sperm, and inhibits the release of acid hydrolase and sperm proteins .

HY-N15545

Thaigranatumin I	Structural Classification Natural Products Xylocarpus granatum J. Koenig Source classification Plants Meliaceae	Drug Derivative
Thaigranatumin I is a limonoid compound found in the seeds of the Thai mangrove (Xylocarpus granatum). Thaigranatumin I is promising for research of neurodegenerative diseases such as Parkinson's diseases .

HY-N1939R

Icariside I (Standard)	Flavonols Structural Classification Monophenols Flavonoids Source classification Phenols Epimedium brevicornu Maxim. Plants Berberidaceae	Others
Icariside I (Standard) is the analytical standard of Icariside I. This product is intended for research and analytical applications. Icariside I is a metabolite of Icarlin, which could regulate bone remodeling and is recognized as an effective agent for the treatment of osteoporosis.

HY-N8355

Beauveriolide I	Infection Alkaloids Structural Classification Microorganisms Classification of Application Fields Source classification Disease Research Fields	Endogenous Metabolite
Beauveriolide I is the metabolite of Entomopathogenic Fungi Beauveria sp.. Beauveriolide I (1) exhibits moderate insecticidal activities against Spodoptera litura and Callosobruchus chinensis .

HY-N0047R

Polyphyllin I (Standard)	Structural Classification Liliaceae Paris polyphylla Smith Plants Saccharides Steroids	JNK mTOR Akt PDK-1 Autophagy Apoptosis
Polyphyllin I (Standard) is the analytical standard of Polyphyllin I. This product is intended for research and analytical applications. Polyphyllin I is a bioactive constituent extracted from Paris polyphylla, has strong anti-tumor activity. Polyphyllin I is an activator of the JNK signaling pathway and is an inhibitor of PDK1/Akt/mTOR signaling. Polyphyllin I induces autophagy, G2/M phase arrest and apoptosis .

Cat. No.	Product Name	Chemical Structure

HY-16305S1

Maribavir-d6 TFA
Maribavir-d6 TFA (1263W94-d6 TFA; BW1263W94-d6 TFA; GW257406X-d6 TFA) is a deuterium labeled Maribavir (HY-16305). Maribavir is an orally active antiviral agent for cytomegalovirus (CMV) through inhibition of protein kinase UL97 and the following CMV DNA replication .

HY-16305S

Maribavir-d6
Maribavir-d₆ (1263W94-d₆) is a deuterium labeled Maribavir (HY-16305). Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC₅₀ of 3 nM .

HY-W653982

Coproporphyrin I-15N4
Coproporphyrin I- ¹⁵N₄ is a ¹⁵N-labeled Coproporphyrin I (HY-113318). Coproporphyrin I is an endogenous metabolite present in urine and blood that can be used for the research of liver disease and porphyria .

HY-143623S

Neo Spiramycin I-d3
Neo Spiramycin I-d₃ is the deuterium labeled Neo Spiramycin I (HY-143623) . Neo Spiramycin I (NSPI) is the active metabolite of Spiramycin (SPI) with antimicrobial activity. Neo Spiramycin is widely used in veterinary medicine .

HY-W010452S1

3-Hydroxybutyric acid-13C4 sodium
3-Hydroxybutyric acid- ¹³C₄ (sodium) is the ¹³C labeled 3-Hydroxybutyric acid sodium (HY-W010452). 3-Hydroxybutyric acid sodium is a metabolite that is elevated in type I diabetes, and can modulate the properties of membrane lipids[1].

HY-145012S

W-19-d4 hydrochloride
W-19-d₄ (hydrochloride) is the deuterium labeled W-19 hydrochloride .

HY-143665S

Nor-W-18-d4
Nor-W-18-d₄ is the deuterium labeled Nor-W-18 .

HY-W890109S

Spiramycin I-d3-1
Spiramycin I-d₃-1 is deuterium-labeled Spiramycin I .

HY-124211S

Dibenzo(a,i)pyrene-d14
Dibenzo(a,i)pyrene-d₁₄ is the deuterium labeled Dibenzo(a,i)pyrene .

HY-W010452S2

3-Hydroxybutyric acid-13C2 sodium
3-Hydroxybutyric acid- ¹³C₂ (sodium) is the ¹³C labeled 3-Hydroxybutyric acid sodium (HY-W010452). 3-Hydroxybutyric acid sodium is a metabolite that is elevated in type I diabetes, and can modulate the properties of membrane lipids[1].

HY-W008452S

H-Tyr(3-I)-OH-13C6
H-Tyr(3-I)-OH- ¹³C₆ is the ¹³C-labeled H-Tyr(3-I)-OH. H-Tyr(3-I)-OH is a potent and effective tyrosine hydroxylase inhibitor. H-Tyr(3-I)-OH is an intermediate in the production of thyroid hormones and has a role as a human or mouse metabolite[1][2].

HY-W019776

Sudan I-d5
Sudan I-d₅ is a the deuterated Sudan I. Sudan I is a diazo-conjugate red dye and can be used as an additive to products such as oils, solvents or polishes. Sudan I inhibits growth of bacterial strains Clostridium perfringens and L. rhamnosus[1].

HY-W743804

Aclidinium-d5 bromide
Aclidinium-d₅ (LAS 34273-d₅; LAS-W 330-d₅) bromide is deuterium-labeled Aclidinium Bromide (HY-14144) .

HY-P1032S2

Angiotensin I-13C6,15N (human, mouse, rat) TFA
Angiotensin I-13C6,15N (human, mouse, rat) TFA is ¹³C and ¹⁵N labeled Angiotensin I (human, mouse, rat) TFA. Angiotensin I-13C6,15N (human, mouse, rat) TFA is a precursor of angiotensin II and is cleaved into angiotensin II by angiotensin converting enzyme (ACE) .

HY-B0674S1

Ebastine-d6
Ebastine-d₆ is deuterated labeled Ebastine (HY-B0674). Ebastine (LAS-W 090) is an orally active, second-generation histamine H1 receptor antagonist. Ebastine can be used for the symptoms of allergic rhinitis and chronic idiopathic urticaria research .

HY-B1411S1

i-Inositol-d1
i-Inositol-d is the deuterium labeled i-Inositol .

HY-B1411S

i-Inositol-d6
i-Inositol-d₆ is the deuterium labeled i-Inositol. i-Inositol is a chemical compound, associated lipids are found in many foods, in particular fruit, especially cantaloupe and oranges.

HY-B0175S

Toltrazuril-d3
Toltrazuril-d₃ is deuterated labeled Toltrazuril. Toltrazuril (BAY-i 9142) is an antiprotozoal agent that acts upon Coccidia parasites.

HY-P1032S

Angiotensin I-13C19,15N3 (human, mouse, rat)

Angiotensin I- ¹³C₁₉, ¹⁵N₃ (human, mouse, rat) is the ¹³C and ¹⁵N labeled Angiotensin I (human, mouse, rat) (HY-P1032). Cellulose (Pectin glycosidase) is a natural high molecular weight polysaccharide found in many plants and organisms. It is widely used in manufacturing industries, such as in paper making, textiles, food and medicine, etc. As a renewable resource, Cellulose is biodegradable and sustainable, and can also be used to manufacture chemicals such as Cellulose Esters, Cellulose Acetate and Cellulose Nitrate. In addition, Cellulose is often used as a food additive to increase the stability and quality of food .

HY-W015851S

3-Hydroxybutanoic acid-13C sodium
3-Hydroxybutanoic acid-13C- ¹³C (sodium) is the ¹³C labeled 3-Hydroxybutanoic acid sodium (HY-W010452). 3-Hydroxybutyric acid sodium (β-Hydroxybutyric acid sodium) is a metabolite that is elevated in type I diabetes. 3-Hydroxybutyric acid sodium can modulate the properties of membrane lipids .

HY-B0184S

Felbamate-d4
Felbamate-d₄ (W-554-d4) is the deuterium labeled Felbamate. Felbamate (W-554) is a potent anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA).

HY-13458S1

Droxidopa-13C2,15N hydrochloride
Droxidopa- ¹³C₂, ¹⁵N (hydrochloride) is deuterium labeled Droxidopa. Droxidopa(L-DOPS), the mixture of Droxidopa (w/w80%) and Pharmaceutical starch (w/w20%), acts as a proagent to the neurotransmitters norepinephrine (noradrenaline) and epinephrine (adrenaline); Droxidopa(L-DOPS) is capable of crossing the protective blood-brain barrier .

HY-B0184S1

Felbamate-d5
Felbamate-d₅ is the deuterium labeled Felbamate . Felbamate (W-554) is a potent nonsedative anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA) .

HY-W010248S

2-Phenylglycine-d5
2-Phenylglycine-d₅ is the deuterium labeled 2-Phenylglycine. 2-Phenylglycine (DL-α-Phenylglycine) is a metabolite in breast milk during the W2 to W4 lactation period[1].

HY-W588193S

Cortol-d5
Cortol-d₅ is deuterium-labeled Cortol (HY-W588193) .

HY-W110148S

Amitrole-13C,15N2
Amitrole- ¹³C, ¹⁵N₂ is the deuterium labeled Amitrole (HY-W027592) .

HY-W014375S3

Arginine-d7 hydrochloride
Arginine-d₇ hydrochloride is deuterium labeled Arginine (hydrochloride) (HY-W014375). Arginine hydrochloride is an arginine derivative.

HY-W654119

CMPF-d3
CMPF-d3 is the deuterium labeled CMPF-d3 (HY-W654119) .

HY-W710540

Guanidine-15N3 hydrochloride
Guanidine- ¹⁵N₃ hydrochloride is the ¹⁵N-labeled Guanidine Hydrobromide (HY-W710540) .

HY-W643348

4-Bromoiodobenzene-d4
4-Bromoiodobenzene-d₄ is the deuterium labeled 4-Bromoiodobenzene (HY-W086988).

HY-W744599

Desoxymetasone-d5
Desoxymetasone-d5 is the deuterium labeled Desoxymetasone-d5 (HY-W744599) .

HY-W009455S

9-Bromoanthracene-d9
9-Bromoanthracene-d₉ is the deuterium labeled 9-Bromoanthracene (HY-W009455).

HY-W750155

Tetramethrin-d6
Tetramethrin-d6 is the deuterium labeled Tetramethrin-d6 (HY-W750155) .

HY-W747795

Digitoxin-d3
Digitoxin-d3 is the deuterium labeled Digitoxin-d3 (HY-W747795) .

HY-W007537S

2-Bromonaphthalene-d7
2-Bromonaphthalene-d7 is the deuterium labeled 2-Bromonaphthalene(HY-W007537) .

HY-W709575

Spermidine-d6 trihydrochloride
Spermidine-d6 trihydrochloride is the deuterium labeled Spermidine-d6 (trihydrochloride) (HY-W709575) .

HY-W701834S

4-Hydroxymethylambrisentan-d5
4-Hydroxymethylambrisentan-d₅ is deuterium-labeled 4-Hydroxymethylambrisentan (HY-W701834) .

HY-W741222S

N-Desmethyl Olopatadine-d6
N-Desmethyl Olopatadine-d₆ is deuterium-labeled N-Desmethyl Olopatadine (HY-W741222) .

HY-W020678S

2-Methylbutanal-13C2
2-Methylbutanal- ¹³C₆ is ¹³C labeled 2-Methylbutanal (HY-W020678).

HY-W700866S

4-Hydroxyclonidine-d4 acetate
4-Hydroxyclonidine-d4 acetate is the deuterium labeled 4-Hydroxyclonidine hydrochloride (HY-W700866) .

HY-W014375S2

Arginine-13C6 hydrochloride
Arginine- ¹³C₆ hydrochloride is ¹³C-labeled Arginine (hydrochloride) (HY-W014375). Arginine hydrochloride is an arginine derivative.

HY-W088178S

N,N-Dimethylbenzenesulfonamide-d2
N,N-Dimethylbenzenesulfonamide-d2 is the deuterium labeled N,N-Dimethylbenzenesulfonamide (HY-W088178) .

HY-18600AS

Azimilide-d8 dihydrochloride
Azimilide-d₈ (dihydrochloride) is the deuterium labeled Azimilide dihydrochloride. Azimilide Dihydrochloride (NE-10064 Dihydrochloride) is a class III antiarrhythmic compound, inhibits I(Ks) and I(Kr) in guinea-pig cardiac myocytes and I(Ks) (minK) channels expressed in Xenopus oocytes.

HY-W143071S

1-(Methylthio)-pentane-d3
1-(Methylthio)-pentane-d3 is the deuterium labeled Amyl methyl sulfide (HY-W143071) .

HY-W013998S

Glycyl-L-phenylalanine-d2
Glycyl-L-phenylalanine-d₂ is a deuterium labeled Glycyl-L-phenylalanine (HY-W013998). Glycyl-L-phenylalanine is a phenylalanine derivative.

HY-W725480

Carfentrazon-ethyl-d5
Carfentrazon-ethyl-d5 is the deuterium labeled Carfentrazon-ethyl-d5 (HY-W725480) .

HY-W008440S

DL-Cycloserine-15N,d3
DL-Cycloserine- ¹⁵N,d₃ is the deuterium labeled DL-Cycloserine (HY-W008440) .

HY-W357090S

L-Idose-13C-3
L-Idose- ¹³C-3 is the ¹³C labeled L-Idose (HY-W357090)[1].

HY-W012837S

Benzylmethylether-d2
Benzylmethylether-d2 (Methoxymethylbenzene-d2) is the deuterium labeled (Methoxymethyl)benzene (HY-W012837) .

HY-W750265

Dexamethasone Phosphate-d5
Dexamethasone Phosphate-d5 is the deuterium labeled Dexamethasone Phosphate-d5 (HY-W750265) .

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