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C6

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By Targets:	11β-HSD (1) 5 alpha Reductase (1) 5-HT Receptor (4) ADC Linker (5) ADC Payload (1) Adenosine Deaminase (1) Adrenergic Receptor (4) Akt (3) Aldose Reductase (1) Amino Acid Derivatives (5) AMPK (2) Amylases (1) Anaplastic lymphoma kinase (ALK) (1) Androgen Receptor (2) Antibiotic (29) Apical Sodium-Dependent Bile Acid Transporter (1) Apoptosis (65) Aryl Hydrocarbon Receptor (1) Autophagy (40) Bacterial (49) Bcl-2 Family (2) Biochemical Assay Reagents (31) c-Kit (1) Calcium Channel (7) Carbonic Anhydrase (4) Cathepsin (1) Ceramidase (1) CFTR (4) CGRP Receptor (1) Chloride Channel (2) Cholinesterase (ChE) (1) CMV (3) Complement System (1) COX (22) Cytochrome P450 (5) Dengue Virus (1) Dihydroorotate Dehydrogenase (1) DNA/RNA Synthesis (2) Dopamine Receptor (3) Drug Derivative (3) Drug Intermediate (3) Drug Isomer (1) Drug Metabolite (11) Drug-Linker Conjugates for ADC (3) E3 Ligase Ligand-Linker Conjugates (42) EAAT (1) EGFR (5) Endogenous Metabolite (103) Endothelin Receptor (1) ERK (5) Estrogen Receptor/ERR (3) Ferroptosis (2) Filovirus (1) Flavivirus (1) FLT3 (1) Fluorescent Dye (15) Fungal (9) GABA Receptor (5) Gap Junction Protein (1) GCGR (5) GLP Receptor (1) Glycosidase (2) GlyT (2) GSK-3 (1) HDAC (2) Hexokinase (1) HIF/HIF Prolyl-Hydroxylase (2) Histamine Receptor (1) Histone Acetyltransferase (1) Histone Demethylase (1) HIV (7) HIV Integrase (1) HIV Protease (3) HMG-CoA Reductase (HMGCR) (1) HSP (2) HSV (2) IGF-1R (1) iGluR (3) IKK (1) Influenza Virus (2) Insulin Receptor (1) Interleukin Related (4) Isocitrate Dehydrogenase (IDH) (2) Isotope-Labeled Compounds (441) JNK (4) Keap1-Nrf2 (3) Ligands for E3 Ligase (3) Ligands for Target Protein for PROTAC (1) Liposome (5) LPL Receptor (2) MAP3K (3) MDM-2/p53 (4) MEK (3) Melanocortin Receptor (1) Microtubule/Tubulin (3) Mitochondrial Metabolism (3) Mitophagy (3) MMP (4) mTOR (2) NF-κB (4) NO Synthase (7) P-glycoprotein (2) P2Y Receptor (2) p38 MAPK (2) PAK (2) Parasite (17) PARP (3) PD-1/PD-L1 (1) PERK (1) Phosphodiesterase (PDE) (3) Photosensitizer (1) PKC (2) PKG (1) Potassium Channel (5) PPAR (5) PROTAC Linkers (26) PROTACs (3) Protease Activated Receptor (PAR) (2) Proteasome (1) Proton Pump (1) RAR/RXR (4) Reactive Oxygen Species (ROS) (15) Reference Standards (3) RET (1) Reverse Transcriptase (2) ROS Kinase (3) SARS-CoV (9) Ser/Thr Protease (3) SGLT (2) SHP2 (1) Sirtuin (2) Small Interfering RNA (siRNA) (6) Sodium Channel (3) Src (1) STAT (3) TGF-beta/Smad (2) Thrombin (2) Thyroid Hormone Receptor (5) Toll-like Receptor (TLR) (3) Topoisomerase (1) Trace Amine-associated Receptor (TAAR) (1) TRP Channel (2) VD/VDR (1) VEGFR (2) Virus Protease (4) WDR5 (2) YAP (2) α-synuclein (1) β-catenin (1)
By Research Areas:	Cancer (194) Cardiovascular Disease (33) Endocrinology (22) Infection (80) Inflammation/Immunology (71) Metabolic Disease (83) Neurological Disease (39)
Click Chemistry:	ADC Synthesis (2) DBCO (2) PROTAC Synthesis (8) Azide (11) Alkynes (4)
Oligonucleotides:	Aptamers (1) Rat Pre-designed siRNA Sets (1) Mouse Pre-designed siRNA Sets (1) Cationic Lipids (1) Human Pre-designed siRNA Sets (4) siRNAs (6)

707

Inhibitors & Agonists

Screening Libraries

Fluorescent Dye

Biochemical Assay Reagents

Peptides

Inhibitory Antibodies

Natural
Products

Recombinant Proteins

494

Isotope-Labeled Compounds

Antibodies

Click Chemistry

Oligonucleotides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-D1574

C6 NBD Sphingomyelin	Fluorescent Dye	Others
C6 NBD Sphingomyelin is a fluorescent short-chain analogue of Sphingomyelin (HY-113498). Chlamydia trachomatis acquires C6 NBD Sphingomyelin endogenously synthesizes from C6-NBD-ceramide and transportes to the chlamydial inclusion. C6 NBD Sphingomyelin can incorporate into the plasma membrane .

HY-D1577

C6 NBD Lactosylceramide	Fluorescent Dye	Cancer
C6 NBD Lactosylceramide is a derivative of lactosylceramides, and can be used in lactosylceramide synthase assay as a fluorescent acceptor substrate. C6 NBD Lactosylceramide can also be used in cancer research .

HY-W356117

C6 NBD Glucosylceramide	Fluorescent Dye	Others
C6 NBD Glucosylceramide is a glucosylceramide fluorescent derivative (Ex=466 nm, Em=535 nm). C6 NBD Glucosylceramide can be used to study the metabolism and internalization of glucosylceramide and also for the determination of glucosyl ceramide synthase activity .

HY-19542

C6 Ceramide 3 Publications Verification C6-Cer; N-Hexanoylsphingosine	Apoptosis	Cancer
C6 Ceramide (C6-Cer) is a short-chain, cell-permeable ceramide pathway activator with anticancer activity. C6 Ceramide-mediated miR-29b expression participates in the progression of multiple myeloma through suppressing the proliferation, migration and angiogenesis of endothelial cells by targeting Akt signal pathway. C6 Ceramide exhibits multiple anti-cancer properties including cell cycle arrest, Apoptosis, inhibition of tumor growth and enhances the effects of chemotherapy in drug-resistant cancer cells. C6-ceramide can be used as an adjuvant for chemotherapeutic agents, to enhance anti-tumor effects .

HY-W356116

C6 NBD Ceramide Nbd-ceramide	Fluorescent Dye	Others
C6 NBD Ceramide is a Golgi apparatus fluorescent probe with cell membrane permeability. C6 NBD Ceramide can be used for fast and convenient green fluorescent labeling of Golgi in living and fixed cells, and can be used to observe changes in Golgi morphology in living cells (Ex=466 nm, Em=536 nm). C6-NBD-ceramide is metabolized to fluorescent sphingomyelin and glucosylceramide, can be used for the study of sphingolipid transport and metabolic mechanism .

HY-D1576

C6 NBD L-threo-dihydroceramide	Fluorescent Dye	Others
C6 NBD L-threo-dihydroceramide is a dihydro-ceramide isomer labeled with a fluorescent group C6 nitrobenzoxadiazole (C6 NBD), can be used to detect ceramide.

HY-D1575

C6 NBD Galactosylceramide	Fluorescent Dye	Others
C6 NBD galactosylceramide is an active derivative of galactosylceramide that is tagged with fluorescent C6 nitrobenzoxadiazole (C6 NBD). C6 NBD galactosylceramide can be used as a substrate for neutral β-glycosylceramidase (GCase) to study intracellular localization and metabolism of galactosylceramide (Ex=nm, Em=525) .

HY-D1749

C6 NBD L-threo-ceramide	Fluorescent Dye	Others
C6 NBD L-threo-ceramide is a cell-permeable analog of ceramides that is tagged with a fluorescent group C6 nitrobenzoxadiazole (C6 NBD). It is rapidly transferred between liposomes, labels the Golgi apparatus, and is metabolized to C6 NBD sphingomyelin in BHK cells and V79 fibroblasts.

HY-158803

C6 Biotin glucosylceramide (d18:1/6:0) C6 Glucosylceramide-biotin; N-Hexanoyl-biotin-glucosylceramide	Biochemical Assay Reagents	Metabolic Disease
C6 Biotin glucosylceramide (d18:1/6:0) (C6 Glucosylceramide-biotin; N-Hexanoyl-biotin-glucosylceramide) is an ester product.

HY-116609

C6 L-threo Ceramide	Interleukin Related	Inflammation/Immunology
C6 L-threo Ceramide is a bioactive sphingolipid and cell-permeable analog of naturally occurring ceramides . C6 L-threo Ceramide significantly inhibits IL-4 production in T cells. Anti-allergic agents .

HY-D1573

C6 NBD Phytoceramide	Fluorescent Dye	Others
C6 NBD Phytoceramide is a fluorescently labeled short-chain ceramide analog that can be recognized by mammalian GlcCer synthase (GCS) .

HY-RS01752

C6 Human Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
C6 Human Pre-designed siRNA Set A contains three designed siRNAs for C6 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

C6 Human Pre-designed siRNA Set A C6 Human Pre-designed siRNA Set A

HY-RS16809

C6 Mouse Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
C6 Mouse Pre-designed siRNA Set A contains three designed siRNAs for C6 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

C6 Mouse Pre-designed siRNA Set A C6 Mouse Pre-designed siRNA Set A

HY-RS23249

C6 Rat Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
C6 Rat Pre-designed siRNA Set A contains three designed siRNAs for C6 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

C6 Rat Pre-designed siRNA Set A C6 Rat Pre-designed siRNA Set A

HY-147178

C-6 NBD-dihydro-Ceramide	Fluorescent Dye	Others
C-6 NBD-dihydro-Ceramide is a membrane-permeable ceramides. C-6 NBD-dihydro-Ceramide is a biologically active fluorescent analog of short chain .

HY-19542S1

C6 Ceramide-d11 C6-Cer-d₁₁; N-Hexanoylsphingosine-d₁₁	Apoptosis Isotope-Labeled Compounds	Cancer
C6 Ceramide-d₁₁ is deuterated labeled C6 Ceramide (HY-19542). C6-ceramide, a ceramide pathway activator, shows activity against a variety of cancer cell lines. C6-ceramide can be used as an adjuvant for chemotherapeutic agents, to enhance anti-tumor effects .

HY-139062

C6 Urea Ceramide C6 Ceramide (d18:1/6:0) Urea; Cer(d18:1/6:0) Urea; D-erythro-Urea-C6-Ceramide	Apoptosis Ceramidase Autophagy β-catenin	Cancer
C6 Urea Ceramide (Cer(d18:1/6:0) Urea) is an inhibitor of neutral ceramidase. C6 Urea Ceramide increases total ceramide levels in wild-type mouse embryonic fibroblasts (MEFs) and HT-29 colon cancer cells. C6 Urea Ceramide (5-10 μM) inhibits proliferation of HT-29 cells and induces apoptosis and autophagy, but is not toxic to non-cancerous cells. C6 Urea Ceramide decreases total and phosphorylated β-catenin levels in HT-29 and HCT116 cells, and induces colocalization of β-catenin with the 20S proteasome. C6 Urea Ceramide (1.25, 2.5, and 5 mg/kg) reduced tumor growth and increased C16, C18, C20, and C24 ceramide levels in tumor tissues in the HT-29 mouse xenograft model.

HY-116585

C6 D-Threo Ceramide (d18:1/6:0)	Liposome Interleukin Related	Neurological Disease
C6 D-Threo Ceramide (d18:1/6:0) is a bioactive sphingolipid and cell-permeable analog of ceramides. C6 D-Threo Ceramide (d18:1/6:0) enhances IL-4 production induced by Phorbol 12-myristate 13-acetate (HY-18739) in EL4 T cells .

HY-165087

C6 Biotin ceramide (d18:1/6:0) N-Hexanoyl-biotin-D-erythro-sphingosine	Biochemical Assay Reagents	Others
C6 Biotin ceramide (d18:1/6:0) is a biochemical reagent.

HY-W766368

C6 Ceramide-13C2,d2 C6-Cer-¹³C₂,d₂; N-Hexanoylsphingosine-¹³C₂,d₂	Isotope-Labeled Compounds Apoptosis	Cancer
C6 Ceramide- ¹³C₂,d₂ (C6-Cer- ¹³C₂,d₂) is the deuterium labeled and ¹³C-labeled C6 Ceramide (HY-19542). C6 Ceramide (C6-Cer) is a short-chain, cell-permeable ceramide pathway activator with anticancer activity. C6 Ceramide-mediated miR-29b expression participates in the progression of multiple myeloma through suppressing the proliferation, migration and angiogenesis of endothelial cells by targeting Akt signal pathway. C6 Ceramide exhibits multiple anti-cancer properties including cell cycle arrest, Apoptosis, inhibition of tumor growth and enhances the effects of chemotherapy in drug-resistant cancer cells. C6-ceramide can be used as an adjuvant for chemotherapeutic agents, to enhance anti-tumor effects .

HY-166282

C6 NBD-L-threo-dihydrosphingosine N-[6-[(7-Nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl]-L-threo-sphinganine	Biochemical Assay Reagents	Metabolic Disease
C6 NBD-L-threo-dihydrosphingosine (N-[6-[(7-Nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl]-L-threo-sphinganine) is an ester product.

HY-145517

C6-Phytoceramide	Apoptosis	Neurological Disease
C6-Phytoceramide is a cell-permeable analog of Phytoceramide. C6-Phytoceramide induces higher levels of apoptosis than C6-Ceramide (HY-19542) in neuroblastoma cells .

HY-141576

C6-NBD Sphinganine	Fluorescent Dye	Others
C6-NBD Sphinganine is a sphinganine analog and can be used as fluorescent dye for labeling fatty acid .

HY-W590666

N-Hexanoyldihydrosphingosine C6-dihydro-Ceramide (N-hexanoyl-)	Biochemical Assay Reagents	Metabolic Disease
N-Hexanoyldihydrosphingosine (C6-dihydro-Ceramide (N-hexanoyl-)) is an ester product.

HY-148153

C6-Amide-(PEG)n-CH3	Drug Derivative	Inflammation/Immunology
C6-Amide-(PEG)n-CH3 (n=310) is an active compound. C6-Amide-(PEG)n-CH3 is a small molecule moiety for PEGylation in Egaptivon pegol (HY-147079) that can be used for the research of platelet dysfunction disorders .

HY-141325

C6-Bis-phosphoramidic acid diethyl ester	PROTAC Linkers	Cancer
C6-Bis-phosphoramidic acid diethyl ester is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs .

HY-133685S

N-Hexanoyl-L-Homoserine lactone-d3 C6-HSL-d₃	Isotope-Labeled Compounds Bacterial	Infection Metabolic Disease
N-Hexanoyl-L-Homoserine lactone-d₃ (C6-HSL-d₃) is deuterium labeled N-Hexanoyl-L-homoserine lactone. N-Hexanoyl-L-homoserine lactone is a short-chained N-acyl homoserine lactone (AHL). Diatoms are frequently found in association with Proteobacteria, many members of which employ cell-to-cell communication via AHLs in aquatic habitats .

HY-E70163

Carbohydrate Sulfotransferase 3 EC:2.8.2.17; CHST3; C6ST1	Endogenous Metabolite	Cancer
Carbohydrate Sulfotransferase 3 (EC:2.8.2.17) can catalyze sulphate transfer to position 6 of GalNAc residue of chondroitin .

HY-114667

Lavendustin C6	EGFR	Others
Lavendustin C6 is a specific inhibitor of tyrosine kinase. Lavendustin C6 inhibits epidermal growth factor (EGF) receptor tyrosine kinase with an EC₅₀ value of 0.05 μg/mL. Lavendustin C6 inhibits platelet-derived growth factor (PDGF)-induced inositol phosphate formation .

HY-N8588

Methyl ganoderate C6	Others	Others
Methyl ganoderate C6 is a ganoderic acid. Methyl ganoderate C6 can be used for the research of various biochemical .

HY-N2461

Ganoderic acid C6	Aldose Reductase	Metabolic Disease
Ganoderic acid C6 has aldose reductase inhibitory activity .

HY-W1008621

GalNAc-THA C6 phosphoramidite	Biochemical Assay Reagents	Others
GalNAc-THA C6 phosphoramidite is a phosphoramidite derivative containing N-acetylgalactosamine (GalNAc) part linked to Trishexylamino (THA), which can be used for the synthesis of oligonucleotides.

HY-N6974

Ascr#2 Ascaroside C6	Endogenous Metabolite	Endocrinology
Ascr#2 (Ascaroside C6) is an ascaroside isolated from Caenorhabditis elegans, potently promotes dauer formation, and also acts as a potent male attractant combined with Ascr#3 (HY-N6977) at low concentration .

HY-132274

DMS(O)MT aminolink C6	Biochemical Assay Reagents	Others
DMS(O)MT aminolink C6 for oligonucleotide synthesis. DMS(O)MT is a special protective group similar to traditional MMT, but designed as an improved alternative to it. DMS(O)MT aminolink is fully compatible with standard coupling, deblock, and purification protocols.

HY-19542S

Ceramide C6-d7	Isotope-Labeled Compounds Apoptosis	Cancer
Ceramide C6-d₇ is the deuterium labeled Ceramide C6. Ceramide C6, a Ceramide pathway activator, is an exogenous short-chain ceramide which can induce apoptosis of multiple cancer cells .

HY-153542

AP-C6	PKG	Others
AP-C6 is a potent inhibitor of guanosine 3′,5′-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII) with a pIC₅₀ of 6.5. AP-C6 concentration-dependently inhibits human cGKII activity in vitro. AP-C6 potentiate cAMP signaling by PDE inhibition .

HY-121805

DBCO-C6-acid	ADC Linker	Cancer
DBCO-C6-acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). DBCO-C6-acid can be used in the synthesis of carmaphycin analogues . DBCO- C6- acid is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-161538

Lenalidomide-C6-Br	E3 Ligase Ligand-Linker Conjugates	Cancer
Lenalidomide-C6-Br is a conjugate of E3 ligase ligand and linker. Lenalidomide-C6-Br can be utilized for synthesis of PROTAC EGFR degrader 9 (HY-161536) .

HY-D2527

Biotin-PEG4-amide-PEG2-C6-Cl	Biochemical Assay Reagents	Others
Biotin-PEG4-amide-PEG2-C6-Cl is a biotinylated PEG4-amide-PEG2-C6-Cl.

HY-W008296

NH2-C6-NH-Boc	PROTAC Linkers	Cancer
NH2-C6-NH-Boc is a PROTAC linker which refers to the alkyl/ether composition. NH2-C6-NH-Boc can be used in the synthesis the Mcl-1 inhibitor based on PROTAC .

HY-W584531

VH032-C6-NH-Boc	E3 Ligase Ligand-Linker Conjugates	Cancer
VH032-C6-NH-Boc is a Boc-modified VH032 (HY-120217) that serves as a ligand for VHL and recruits von Hippel-Lindau (VHL) proteins. VH032-C6-NH-Boc will remove the protecting group under acidic conditions and be directly used in PROTAC molecule synthesis. VH032-C6-NH-Boc is a key intermediate in the synthesis of PROTAC based on VHL ligand.

HY-126683

Mal-C6-α-Amanitin	Drug-Linker Conjugates for ADC	Cancer
Mal-C6-α-Amanitin is a agent-linker conjugate for ADC with potent antitumor activity by using α-Amanitin (an RNA polymerase II inhibitor), linked via the ADC linker Mal-C6.

HY-155262

Pomalidomide-5-C6-NH2 hydrochloride	E3 Ligase Ligand-Linker Conjugates	Cancer
Pomalidomide-5-C6-NH2 hydrochloride is the Pomalidomide (HY-10984)-based cereblon (CRBN) ligand used in the recruitment of CRBN protein. Pomalidomide-5-C6-NH2 hydrochloride can be connected to the ligand for protein by a linker to form PROTAC .

HY-176167

mTOR ligand 1-C6-amino	Ligands for Target Protein for PROTAC	Cancer
mTOR ligand 1-C6-amino is a conjugate of a target protein ligand (HY-B0795) and a linker (HY-W008296). mTOR ligand 1-C6-amino can be used to synthesize PROTAC PD-M6 (HY-176166) .

HY-136006B

(S,R,S)-AHPC-C6-NH2 VH032-C6-NH2	E3 Ligase Ligand-Linker Conjugates	Cancer
(S,R,S)-AHPC-C6-NH2 (VH032-C6-NH2) is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used in?PROTAC?technology .

HY-136006

(S,R,S)-AHPC-C6-NH2 dihydrochloride VH032-C6-NH2 dihydrochloride	E3 Ligase Ligand-Linker Conjugates	Inflammation/Immunology Cancer
(S,R,S)-AHPC-C6-NH2 dihydrochloride (VH032-C6-NH2 dihydrochloride) is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used for AKT PROTAC degrader. (S,R,S)-AHPC-C6-NH2 dihydrochloride is XF038-161A, example 6, extracted from patent WO2019173516A1 .

HY-136006A

(S,R,S)-AHPC-C6-NH2 hydrochloride VH032-C6-NH2 hydrochloride	E3 Ligase Ligand-Linker Conjugates	Inflammation/Immunology Cancer
(S,R,S)-AHPC-C6-NH2 hydrochloride (VH032-C6-NH2 hydrochloride) is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used for AKT PROTAC degrader. (S,R,S)-AHPC-C6-NH2 hydrochloride is XF038-161A, example 6, extracted from patent WO2019173516A1 .

HY-150978

DDAO-C6	Fluorescent Dye	Others
DDAO-C6 is a cridone ester derivative, highly specific fluorescence for detecting human serum albumin (HSA). DDAO-C6 acts as an enzymatic activatable near-infrared fluorescent probe in visually sensing endogenous lipase from gut microbes (Ex/Em=600/658 nm) .

HY-153785

NH2-C6-ARC186 sodium	Complement System	Inflammation/Immunology
NH2-C6-ARC186 sodium is a modified ARC186 (HY-153098) with NH₂-C₆ that can be coupled to other peptides or molecules. ARC186 is a aptamer and a highly potent complement inhibitor that function by blocking the convertase-catalyzed activation of C5 .

HY-140314

DOTA-PEG5-C6-DBCO	PROTAC Linkers	Cancer
DOTA-PEG5-C6-DBCO is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . DOTA-PEG5-C6-DBCO is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N2461

Ganoderic acid C6	Triterpenes Classification of Application Fields Terpenoids Source classification Polyporaceae Metabolic Disease Plants Disease Research Fields	Aldose Reductase
Ganoderic acid C6 has aldose reductase inhibitory activity .

HY-N6974

Ascr#2 Ascaroside C6	Infection Structural Classification Natural Products Animals Classification of Application Fields Source classification Disease Research Fields	Endogenous Metabolite
Ascr#2 (Ascaroside C6) is an ascaroside isolated from Caenorhabditis elegans, potently promotes dauer formation, and also acts as a potent male attractant combined with Ascr#3 (HY-N6977) at low concentration .

HY-N6076

Tenuifoliside A	Triterpenes Structural Classification Monophenols Terpenoids Source classification Polygalaceae Phenols Plants Polygala tenuifolia Willd.	ERK
Tenuifoliside A is isolated from Polygala tenuifolia, has anti-apoptotic and antidepressant-like effects. Tenuifoliside A exhibits its neneurotrophic effects and promotes cell proliferation through the ERK/CREB/BDNF signal pathway in C6 cells .

HY-N1127

Tricin 3 Publications Verification	Infection Structural Classification Flavonoids Classification of Application Fields Flavones Agrostidoideae Source classification Phenols Polyphenols Plants Disease Research Fields Triticum aestivum L.	CMV
Tricin is a natural flavonoid found in large amounts in wheat. Tricin inhibits HCMV replication by inhibiting CDK9. Tricin inhibits the proliferation and invasion of C6 glioma cells by upregulating the expression of FAK-targeting microRNA-7 .

HY-N2038

3,5,6,7,8,3',4'-Heptemthoxyflavone	Structural Classification Flavonols Flavonoids Rutaceae Plants Citrus reticulata Blanco	Phosphodiesterase (PDE)
3,5,6,7,8,3',4'-Heptemthoxyflavone, a flavonoid from satsuma peel, is an orally available CREB activator with anti-tumor and anti-neuroinflammatory activity. 3,5,6,7,8,3',4'-Heptemthoxyflavone inhibits collagenase activity and increases the content of type I procollagen in human dermal fibroblast neoblast (HDFn) cells. 3,5,6,7,8,3',4'-Heptemthoxyflavone induces brain-derived neurotrophic factor (BDNF) expression through the cAMP/ERK/CREB signaling pathway and reduces phosphodiesterase activity in C6 glioma .

HY-N8588

Methyl ganoderate C6	Triterpenes Structural Classification Microorganisms Classification of Application Fields Terpenoids Other Diseases Disease Research Fields	Others
Methyl ganoderate C6 is a ganoderic acid. Methyl ganoderate C6 can be used for the research of various biochemical .

HY-N9454

Garcinoic acid	Monophenols other families Classification of Application Fields Ketones, Aldehydes, Acids Source classification Phenols Plants Disease Research Fields Cancer	Others
Garcinoic acid is the vitamin E analogue extracted from Garcinia Kola seeds. Garcinoic acid shows a marked antiproliferative effect on glioma C6 cancer cells .

HY-N7464

Jolkinolide E	Structural Classification Terpenoids Source classification Euphorbia rapulum Kar. et Kir. Diterpenoids Euphorbiaceae Plants	Others
Jolkinolide E is a casbane diterpenoid from the roots of Euphorbia rapulum. Jolkinolide E shows weak selective activity against HepG2, MCF-7, and C6 cell lines .

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-N1127R

Tricin (Standard)	Structural Classification Flavonoids Flavones Agrostidoideae Source classification Phenols Polyphenols Plants Triticum aestivum L.	Reference Standards CMV
Tricin (Standard) is the analytical standard of Tricin. This product is intended for research and analytical applications. Tricin is a natural flavonoid found in large amounts in wheat. Tricin inhibits HCMV replication by inhibiting CDK9. Tricin inhibits the proliferation and invasion of C6 glioma cells by upregulating the expression of FAK-targeting microRNA-7 .

HY-N2038R

3,?5,?6,?7,?8,?3',?4'-?Heptemthoxyflavone (Standard)	Structural Classification Flavonols Flavonoids Rutaceae Plants Citrus reticulata Blanco	Reference Standards Phosphodiesterase (PDE)
3,5,6,7,8,3',4'-Heptemthoxyflavone (Standard) is the analytical standard of 3,5,6,7,8,3',4'-Heptemthoxyflavone (HY-N2038). This product is intended for research and analytical applications. 3,5,6,7,8,3',4'-Heptemthoxyflavone, a flavonoid from satsuma peel, is an orally available CREB activator with anti-tumor and anti-neuroinflammatory activity. 3,5,6,7,8,3',4'-Heptemthoxyflavone inhibits collagenase activity and increases the content of type I procollagen in human dermal fibroblast neoblast (HDFn) cells. 3,5,6,7,8,3',4'-Heptemthoxyflavone induces brain-derived neurotrophic factor (BDNF) expression through the cAMP/ERK/CREB signaling pathway and reduces phosphodiesterase activity in C6 glioma .

HY-N7264

7α-Hydroxycholesterol 1 Publications Verification	Structural Classification Animals Classification of Application Fields Source classification Metabolic Disease Disease Research Fields Steroids	Others HMG-CoA Reductase (HMGCR) Toll-like Receptor (TLR) Akt Src ERK MDM-2/p53
7α-Hydroxycholesterol is a cholesterol oxide and can serve as a biomarker for oxidative stress and lipid peroxidation. 7α-Hydroxycholesterol has cytotoxic and pro-inflammatory activities. 7α-Hydroxycholesterol can also inhibit sterol synthesis and reduce the activity of HMG-CoA reductase. 7α-Hydroxycholesterol can be used in the research of diseases such as diabetes and atherosclerosis .

HY-N8462

6-O-Nicotinoylscutebarbatine G Scutebatin C	Structural Classification Alkaloids Other Alkaloids Labiatae Source classification Derris robusta Pyridine Alkaloids Plants	Others
6-O-Nicotinoylscutebarbatine G is an alkaloid that can be isolated from Scutellaria barbata.6-O-Nicotinoylscutebarbatine has cytotoxic activities against HONE-1, KB and HT29 cells with IC₅₀s of 3.1, 2.1 and 5.7 μM, respectively .

HY-N7147

Irisquinone	Structural Classification Natural Products Iridaceae Source classification Plants Iris latea pallasii	Others
Irisquinone, a natural product, is an anticancer agent. Irisquinone is also a radiation sensitizer for cancer. Irisquinone reduces GSH level and inhibits the repair of DNA singular strand breaks .

HY-N11137

3′-Omethyl-5′-hydroxydiplacone	Structural Classification Flavonoids Paulownia tomentosa (Thunb.) Steud. Flavonones Source classification Phenols Polyphenols Scrophulariaceae Plants	Bacterial
3′-Omethyl-5′-hydroxydiplacone (compound 2), an C-6-geranylflavonoid, can be isolated from the ethanol extract of Paulownia tomentosa fruits. 3′-Omethyl-5′-hydroxydiplacone has antibacterial activity against Gram-positive bacteria .

HY-N12396

Cyclosporin U	Structural Classification Microorganisms Antibiotics Cyclopeptides Source classification	Others
Cyclosporin U (SMP0V32C6L) is an cytostatic agent that plays an important role in preventing rejection of transplanted organs .

HY-N2037AR

Higenamine hydrochloride (Standard) Norcoclaurine hydrochloride (Standard)	Alkaloids Structural Classification Source classification Phenols Polyphenols Plants Lauraceae Isoquinoline Alkaloids Lindera aggregata (Sims) Kosterm.	MAP3K Reference Standards MDM-2/p53 ROS Kinase Apoptosis
Higenamine (hydrochloride) (Standard) is the analytical standard of Higenamine (hydrochloride). This product is intended for research and analytical applications. Higenamine hydrochloride is a selective LSD1 inhibitor (IC50=1.47 μM) that can be isolated from aconite. Higenamine hydrochloride has anti-inflammatory and antibacterial activity. Higenamine (Norcoclaurine) can attenuate IL-1β-induced Apoptosis through ROS-mediated PI3K/Akt signaling pathway. Higenamine hydrochloride protects brain cells from oxygen deprivation. Higenamine can promote bone formation in osteoporosis through the SMAD2/3 pathway. Higenamine hydrochloride can be used to study cancer, inflammation, cardiorenal syndrome and other diseases ^[6].

HY-N2037A

Higenamine hydrochloride 4 Publications Verification Norcoclaurine hydrochloride	Structural Classification Classification of Application Fields Source classification Plants Lindera aggregata (Sims) Kosterm. Alkaloids Phenols Polyphenols Lauraceae Isoquinoline Alkaloids Disease Research Fields Endocrinology Cancer	MAP3K MDM-2/p53 ROS Kinase Apoptosis
Higenamine hydrochloride is a selective LSD1 inhibitor (IC₅₀=1.47 μM) that can be isolated from aconite. Higenamine hydrochloride has anti-inflammatory and antibacterial activity. Higenamine (Norcoclaurine) can attenuate IL-1β-induced Apoptosis through ROS-mediated PI3K/Akt signaling pathway. Higenamine hydrochloride protects brain cells from oxygen deprivation. Higenamine can promote bone formation in osteoporosis through the SMAD2/3 pathway. Higenamine hydrochloride can be used to study cancer, inflammation, cardiorenal syndrome and other diseases ^[6].

HY-16594

Lactacystin 5 Publications Verification	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Proteasome Cathepsin Apoptosis
Lactacystin is a potent, orally active, irreversible, cell-permeable, selective 20S proteasome inhibitor (IC₅₀ = 4.8 μM). Lactacystin also inhibits the lysosomal enzyme cathepsin A. Lactacystin inhibits cell growth and induces apoptosisand cell cycle arrest, and has antiviral and antioxidative activity. Lactacystin induces neurite outgrowth and hypertension. Lactacystin has the potential for the research of cancer, Neurological Disease, hypertension and Malaria, and so on ^[2] ^[6] .

HY-N3622

Corchoionoside C (6S,9S)-Roseoside	Structural Classification Capparis spinosa L. Source classification Plants Capparidaceae Saccharides Monosaccharides	Others
Corchoionoside C ((6S,9S)-Roseoside), an ionone glucoside, can be isolated from Capparis spinosa. Corchoionoside C inhibits the antigen-antibody reaction induced histamine release from rat peritoneal exudate cells .

HY-N2037

Higenamine 4 Publications Verification Norcoclaurine; Demethyl-Coclaurine	Alkaloids Structural Classification Classification of Application Fields Ranunculaceae Source classification Phenols Polyphenols Aconitum carmichaeli Debx. Plants Isoquinoline Alkaloids Disease Research Fields Endocrinology	MAP3K MDM-2/p53 Adrenergic Receptor ROS Kinase Apoptosis
Higenamine (Norcoclaurine), a β2-AR agonist with antioxidant capability, is a key component of the Chinese herb aconite root that prescribes for treating symptoms of heart failure in the oriental Asian countries. Higenamine is also a α1-adrenergic receptor antagonist with hypotensive effect. is a selective LSD1 inhibitor (IC₅₀=1.47 μM) that can be isolated from aconite. Higenamine hydrochloride has anti-inflammatory and antibacterial activity. Higenamine protects myocyte Apoptosis and ischemia/reperfusion (I/R) injury through selective activation of beta2-adrenergic receptor (β2-AR). Higenamine also reduces I/R-induced myocardial infarction in mice. Higenamine can attenuate IL-1β-induced Apoptosis through ROS-mediated PI3K/Akt signaling pathway. Higenamine protects brain cells from oxygen deprivation. Higenamine can promote bone formation in osteoporosis through the SMAD2/3 pathway. Higenamine can be used to study cancer, inflammation, cardiorenal syndrome and other diseases ^[6] .

HY-N7140

Gamma-Linolenic acid 4 Publications Verification γ-Linolenic acid	Structural Classification Classification of Application Fields Source classification Endocrine diseases Metabolic Disease Tadehagi triquetrum (L.) Ohashi Plants Endogenous metabolite Microorganisms Ketones, Aldehydes, Acids Labiatae Disease markers Disease Research Fields	Endogenous Metabolite Apoptosis NF-κB ERK JNK
Gamma-linolenic acid (γ-Linolenic acid) is an orally active unsaturated fatty acid. Gamma-linolenic acid exerts anti-inflammatory effects by inhibiting the NF-κB pathway and the phosphorylation of ERK1/2 and JNK. At the same time, it exerts anticancer effects by inducing apoptosis (Apoptosis) in cancer cells. Additionally, Gamma-linolenic acid also has antioxidant and memory-improving effects. It holds promise for research in the fields of inflammation, neurology, and cancer diseases .

Cat. No.	Product Name	Chemical Structure

HY-19542S

Ceramide C6-d7
Ceramide C6-d₇ is the deuterium labeled Ceramide C6. Ceramide C6, a Ceramide pathway activator, is an exogenous short-chain ceramide which can induce apoptosis of multiple cancer cells .

HY-15330

Vitamin D2-d3
Vitamin D2-d₃ (Ergocalciferol-d₃) is the deuterium labeled vitamin D2 (HY-76542), where the C-6 and C-19 protons are replaced by deuterium. Vitamin D2 can be produced by plants and mushrooms in the presence of sunlight .

HY-P3003S

Cereulide-13C6
Cereulide-13C6 is the 13C6 labeled Cereulide.

HY-A0130S

Sulfalene-13C6
Sulfalene- ¹³C₆ is the ¹³C₆ labeled Sulfalene. Sulfalene (Sulfametopyrazine) is an antimalarial agent. Sulfalene is also a long-acting sulfonamide antibacterial .

HY-19542S1

C6 Ceramide-d11
C6 Ceramide-d₁₁ is deuterated labeled C6 Ceramide (HY-19542). C6-ceramide, a ceramide pathway activator, shows activity against a variety of cancer cell lines. C6-ceramide can be used as an adjuvant for chemotherapeutic agents, to enhance anti-tumor effects .

HY-W766368

C6 Ceramide-13C2,d2

C6 Ceramide- ¹³C₂,d₂ (C6-Cer- ¹³C₂,d₂) is the deuterium labeled and ¹³C-labeled C6 Ceramide (HY-19542). C6 Ceramide (C6-Cer) is a short-chain, cell-permeable ceramide pathway activator with anticancer activity. C6 Ceramide-mediated miR-29b expression participates in the progression of multiple myeloma through suppressing the proliferation, migration and angiogenesis of endothelial cells by targeting Akt signal pathway. C6 Ceramide exhibits multiple anti-cancer properties including cell cycle arrest, Apoptosis, inhibition of tumor growth and enhances the effects of chemotherapy in drug-resistant cancer cells. C6-ceramide can be used as an adjuvant for chemotherapeutic agents, to enhance anti-tumor effects .

HY-133685S

N-Hexanoyl-L-Homoserine lactone-d3
N-Hexanoyl-L-Homoserine lactone-d₃ (C6-HSL-d₃) is deuterium labeled N-Hexanoyl-L-homoserine lactone. N-Hexanoyl-L-homoserine lactone is a short-chained N-acyl homoserine lactone (AHL). Diatoms are frequently found in association with Proteobacteria, many members of which employ cell-to-cell communication via AHLs in aquatic habitats .

HY-N1127S

Tricin-d6
Tricin-d₆ is the deuterium labeled Tricin . Tricin is a natural flavonoid present in large amounts in Triticum aestivum. Tricin can inhibit human cytomegalovirus (HCMV) replication by inhibiting CDK9. Tricin inhibits the proliferation and invasion of C6 glioma cells via the upregulation of focal-adhesion-finase (FAK)-targeting microRNA-7 .

HY-W780150

1-Bromobenzene-13C6
1-Bromobenzene-13C6 is a deuterated labeled 1-Bromobenzene-13C6 .

HY-W156511S

Diacetylsulfanilamide-13C6
Diacetylsulfanilamide- ¹³C₆ is the ¹³C₆ labeled Diacetylsulfanilamide.

HY-146969S

Bisdesoxyquinoceton-13C6
Bisdesoxyquinoceton- ¹³C₆ is the ¹³C₆ labeled Bisdesoxyquinoceton.

HY-W280531S

DNSAH-13C6
DNSAH- ¹³C₆ is the ¹³C₆ labeled DNSAH.

HY-W278861S

Desoxy-Mequindox-13C6
Desoxy-Mequindox- ¹³C₆ is the ¹³C₆ labeled Desoxy-Mequindox.

HY-146968S

Alloerythro-Isoxsuprine-13C6 hydrochloride
Alloerythro-Isoxsuprine- ¹³C₆ (hydrochloride) is the ¹³C₆ labeled Alloerythro-Isoxsuprine (hydrochloride).

HY-N0455AS11

L-Arginine-13C6,d14 hydrochloride
L-Arginine-13C6,d14 hydrochloride ((S)-(+)-Arginine-13C6,d14 hydrochloride) is a deuterated derivative of L-Arginine hydrochloride (HY-N0455A) that is labeled with ¹³C6. L-Arginine hydrochloride ((S)-(+)-Arginine hydrochloride) serves as a nitrogen donor for the synthesis of nitric oxide and is a vasodilator .

HY-B0925S

Oxacillin-13C6 sodium
Oxacillin- ¹³C₆ (sodium) is the ¹³C₆ labeled Oxacillin (sodium). Oxacillin sodium salt is a narrow-spectrum β-lactam antibiotic of the penicillin class.

HY-W777681

Triflusal-13C6
Triflusal-13C6 is a C13-labeled Triflusal. Triflusal is a platelet aggregation inhibitor .

HY-112586S1

Sulfaethoxypyridazine-13C6
Sulfaethoxypyridazine- ¹³C₆ is the ¹³C₆ labeled Sulfaethoxypyridazine. Sulfaethoxypyridazine is a sulfonamide antibacterial agent. Sulfaethoxypyridazine is a sulfonamide that is used in veterinary medicine as feedstuffs.

HY-14538S3

Haloperidol-13C6
Haloperidol- ¹³C₆ is the ¹³C₆ labeled Haloperidol. Haloperidol is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic.

HY-W750888

(Z)-Chlorolefin-13C6
(Z)-Chlorolefin- ¹³C₆ is the ¹³C-labeled (Z)-Chlorolefin- ¹³C₆.

HY-131622S

7-Aminoclonazepam-13C6
7-Aminoclonazepam-13C6 is a deuterated labeled 7-Aminoclonazepam .

HY-B1436S1

Nifuroxazide-13C6
Nifuroxazide- ¹³C₆ is the ¹³C₆ labeled Nifuroxazide. Nifuroxazide is an effective inhibitor of STAT3, also exerts potent anti-tumor and anti-metastasis activity.

HY-B1267S1

Sulfaguanidine-13C6
Sulfaguanidine- ¹³C₆ is the ¹³C₆ labeled Sulfaguanidine. Sulfaguanidine is an orally active antimicrobial agent/antibiotic of sulfonamide class. Sulfaguanidine can be used for the research of enteric infections such as bacillary dysentery.

HY-146966S

2-NP-DNSAH-13C6
2-NP-DNSAH- ¹³C₆ is the ¹³C₆ labeled 2-NP-DNSAH.

HY-W778225

Vanillic acid-13C6
Vanillic acid- ¹³C6 is the ¹³C labeled isotope of Vanillic acid- ¹³C6(HY-N0708 ).Vanillic acid is a flavoring agent found in edible plants and fruits, and in the root of angelica. Vanillic acid inhibits NF-κB activation. It has anti-inflammatory and antimicrobial activities.

HY-114750S

Mebendazole-amine-13C6
Mebendazole-amine- ¹³C₆ is the ¹³C₆ labeled Mebendazole-amine. Mebendazole-amine is a metabolite of Mebendazole. Mebendazole is a broad-spectrum benzimidazole anti-helminthic agent.

HY-B0174AS

Olsalazine-13C6
Olsalazine- ¹³C₆ is the ¹³C labeled Olsalazine.

HY-121267S

Dicamba-13C6
Dicamba- ¹³C₆ is the ¹³C labeled Dicamba .

HY-122062S

Fenoxycarb-13C6
Fenoxycarb- ¹³C₆ is the ¹³C labeled Fenoxycarb .

HY-W777964

Phloroglucinol-13C6
Phloroglucinol- ¹³C₆ is ¹³C labeled Phloroglucinol .

HY-W770434

Octrizole-13C6
Octrizole- ¹³C₆ is ¹³C labeled Octrizole .

HY-W344468S

Adipate-13C6 sodium
Adipate- ¹³C₆ (sodium) is the ¹³C labeled Sodium adipate .

HY-B0493S1

Niflumic acid-13C6
Niflumic acid- ¹³C₆ is the ¹³C₆ labeled Niflumic acid. Niflumic acid, a Ca2+-activated Cl- channel blocker, is an analgesic and anti-inflammatory agent used in the treatment of rheumatoid arthritis.

HY-133694S

2-Aminoflubendazole-13C6
2-Aminoflubendazole- ¹³C₆ is the ¹³C₆ labeled 2-Aminoflubendazole. 2-Aminoflubendazole is the metabolite of Benzimidazoles. Benzimidazoles (BZ) are a class of agents with activities against fungi, protozoa, and helminthes.

HY-B0946S2

Sulfamonomethoxine-13C6
Sulfamonomethoxine- ¹³C₆ is the ¹³C₆ labeled Sulfamonomethoxine (HY-B0946). Sulfamonomethoxine is an orally active sulfonamide antibiotic for veterinary use. Sulfamonomethoxine is also an inhibitor of dihydropteroate synthetase, which can block the synthesis of folic acid. Sulfamonomethoxine has antibacterial activity .

HY-18341S3

L-Thyroxine-13C6,15N
L-Thyroxine- ¹³C₆, ¹⁵N is the ¹³C₆ ans ¹⁵N labeled L-Thyroxine (HY-18341) .

HY-W777457

Anthracene-13C6
Anthracene- ¹³C₆ (Anthracin- ¹³C₆) is ¹³C labeled Anthracene-13C6 (HY-W777457).

HY-136380S

Clodinafop-propargyl-13C6

Clodinafop-propargyl- ¹³C₆ is the ¹³C-labeled Clodinafop-propargyl. Clodinafop-propargyl, a main member of aryloxyphenoxy-propionate herbicides, is used for postemergence control of annual grasses in cereals, including Avena, Lolium, Setaria, Phalaris and Alopecurus spp . Clodinafop-propargyl-13C6 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-B1355AS1

Oxyphenbutazone-13C6
Oxyphenbutazone- ¹³C₆ is the ¹³C₆ labeled Oxyphenbutazone (HY-B1355A). Oxyphenbutazone is a phenylbutazone derivative, with anti-inflammatory effect. Oxyphenbutazone is a non-selective COX inhibitor. Oxyphenbutazone is the metabolite of Phenylbutazone (HY-B0230). Oxyphenbutazone selectively kills non-replicating Mycobaterium tuberculosis .

HY-17596S

Closantel-13C6
Closantel- ¹³C₆ is the ¹³C₆ labeled Closantel. Closantel is a halogenated salicylanilide with a potent anti-parasitic activity. Closantel is a potent and highly specific Onchocerca volvulus chitinase (OvCHT1) inhibitor with an IC50 of 1.6 μM and a Ki of 468 nM. Closantel inhibits the O. volvulus L3 to L4 molt of developing.

HY-113296S

Indoxyl sulfate-13C6 potassium
Indoxyl Sulfate Potassium Salt- ¹³C₆ is the ¹³C labeled Indoxyl Sulfate Potassium Salt .

HY-17598S

Rafoxanide-13C6
Rafoxanide ¹³C₆ is a labeled Rafoxanide (HY-17598). Rafoxanide is a salicylanilide used as an antiparasitic agent .

HY-W782153

Acetophenone-13C6
Acetophenone-13C6 is a deuterated labeled Acetophenone-13C6 .

HY-146972S

Zearalenone-14-O-β-glucoside-13C6
Zearalenone-14-O-β-glucoside- ¹³C₆ is the ¹³C₆ labeled Zearalenone-14-O-β-glucoside.

HY-125296S

Fipronil sulfone-13C6
Fipronil sulfone- ¹³C₆ is the ¹³C-labeled Fipronil sulfone .

HY-W014375S2

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

HY-176034S

GPAGPQGP-Arg(13C6,15N4) TFA
GPAGPQGP-Arg ( ¹³C₆, ¹⁵N₄) TFA is a peptide containing ¹³C₆ and ¹⁵N₄ labeled Arg.

HY-W001138S

4-Bromobenzaldehyde-13C6
4-Bromobenzaldehyde- ¹³C₆ is the ¹³C labeled 4-Bromobenzaldehyde .

HY-34428S

4-Fluorobenzonitrile-13C6
4-Fluorobenzonitrile- ¹³C₆ is the ¹³C labeled 4-Fluorobenzonitrile .

HY-133689AS

3-Nitrophenylhydrazine-13C6 hydrochloride
3-Nitrophenylhydrazine- ¹³C₆ (hydrochloride) is the ¹³C labeled 3-Nitrophenylhydrazine hydrochloride .

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