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- Inhibitors & Agonists
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- Anti-infection
- Apoptosis
- Autophagy
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- Cytoskeleton
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- Epigenetics
- GPCR & G Protein
- Immunology & Inflammation
- JAK/STAT
- MAPK
- Membrane Transporter/Ion Channel
- Metabolism
- Neuronal Signaling
- NF-κB
- Protein Tyrosine Kinase
- Proteases
- PI3K/Akt/mTOR
- Stem Cells & Wnt
- TGF-beta/Smad
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Name Index Z
- Zanubrutinib (Catalog# : 18577, Cas# : 1691249-45-2)Zanubrutinib, aslo known as BGB-3111, is a potent and highly selective small molecule
- ZM241385 (Catalog# : 17022714, Cas# : 139180-30-6)ZM241385 is an adenosine A2A-receptor antagonist. ZM241385 enhances neuronal survival
- ZINC00881524 (ROCK inhibitor) (Catalog# : 17021304, Cas# : 557782-81-7)ZINC00881524 is a ROCK inhibitor.
- ZLN005 (Catalog# : 16122852, Cas# : 49671-76-3)ZLN005 is a PGC-1 Transcriptional Regulator, which shoed some beneficialfEffects on d
- ZL006 (Catalog# : 16122851, Cas# : 1181226-02-7)ZL006 is a PSD95-nNOS protein-protein interaction inhibitor. ZL006 (EC50: 12.88 M) di
- ZK-756326 dihydrochloride (Catalog# : 16122850, Cas# : 1780259-94-0)ZK-756326 is a potent, selective and non-peptide CCR8 chemokine receptor agonist. ZK
- Z-IETD-FMK (Catalog# : 16122771, Cas# : 210344-98-2)Z-IETD-FMK is a specific Caspase-8 inhibitor.Z-IETD-FMK, which inhibits the cleavage
- ZK756326 (Catalog# : 16122725, Cas# : 874911-96-3)ZK756326 is a full agonist of CCR8Chemokine receptor 8 with an IC50 of 1.8 M, dose-re
- ZLN024 hydrochloride (Catalog# : 611814, Cas# : 1883548-91-1)ZLN024 Hcl is a novel AMPK allosteric activator; activated 111 and 211 by around 2C2.
- Zotarolimus (Catalog# : 161009018, Cas# : 221877-54-9)It is a semi-synthetic derivative of rapamycin. It was designed for use in stents wit
- ZSTK474 (Catalog# : 160926006, Cas# : 475110-96-4)Combination treatment using X-rays then ZSTK474 given orally for 8 days, starting 2
- Z-Vad-fmk, non-methylated (Catalog# : 16071403, Cas# : 161401-82-7)Z-Vad-fmk, non-methylated
- Z-DEVD-FMK (Catalog# : 16062112, Cas# : 210344-95-9)Z-DEVD-FMK(Caspase-3 Inhibitor) is a specific, irreversible Caspase-3 inhibitor, and
- Z-FA-FMK (Catalog# : 16062111, Cas# : 105637-38-5)Z-FA-FMK
- Z-VAD(OH)-FMK (Catalog# : 16062110, Cas# : 634911-81-2)Z-VAD(OH)-FMK
- Zibotentan (Catalog# : 011908, Cas# : 186497-07-4)Zibotentan is an orally available selective antagonist of the endothelin-A (ET-A) rec
- ZM 306416 (Catalog# : 122923, Cas# : 690206-97-4)ZM-306416 is a VEGFR inhibitor that inhibits Flk-1 (KDR) (IC50=100 nM) and Flt (IC50
- ZM 323881 hydrochloride (Catalog# : 122214, Cas# : 324077-30-7) ZM323881 is a potent and selective inhibitor of VEGF-R2 tyrosine kinase in vitr
- Zucapsaicin (Catalog# : 121415, Cas# : 25775-90-0)Comig soon!
- ZM323881 hydrochloride (Catalog# : 111008, Cas# : 193000-39-4)ZZZM 323881 Hcl is a potent and selective VEGFR2 inhibitor with IC50 of <2 nM, alm
- Z-VAD-FMK (Catalog# : 110604, Cas# : 187389-52-2)Z-VAD-FMK is a cell-permeable, irreversible broad-spectrum caspase inhibitor, blocks
- 1088965-37-0 (Catalog# : 101201, Cas# : 1088965-37-0)Coming soon!
- ZCL278 (Catalog# : 52555, Cas# : 587841-73-4)ZCL278 is a Cdc42 small molecule modulator that directly binds to Cdc42 (Kd=11.4 uM)
- ZM 336372 (Catalog# : 52239, Cas# : 208260-29-1)ZM 336372 is a potent and selective c-Raf inhibitor with IC50 of 70 nM, 10-fold selec
- Zosuquidar trihydrochloride (Catalog# : 52003, Cas# : 167465-36-3)zosuquidar trihydrochloride is adifluorocyclopropyl quinoline. Zosuquidar trihydrochl
Products Catalog
- ---- VEGFR
- ---- JAK
- ---- EGFR
- ---- PDGFR
- ---- FLT3
- ---- FGFR
- ---- Src
- ---- ALK
- ---- Syk
- ---- HIF
- -- Anti-infection
- ---- CMV
- ---- Filovirus
- ---- HBV
- ---- HCV
- ---- HIV
- ---- HSV
- ---- Influenza Virus
- ---- RSV
- ---- SARS-CoV
- ---- Antibacterial
- ---- Antifungal
- ---- Parasite
- -- Apoptosis
- ---- PD-1
- ---- PD-L1
- ---- Bcl-2
- ---- Caspase
- ---- TNF-alpha
- ---- Survivin
- ---- IAP
- ---- PERK
- ---- p53
- ---- Mdm2
- ---- E1/E2/E3 Enzyme
- -- Autophagy
- ---- LRRK2
- ---- CXCR
- ---- Autophagy
- -- Cell Cycle
- ---- CDK
- ---- PD-1
- ---- PD-L1
- ---- Chk
- ---- ROCK
- ---- PLK
- ---- APC
- ---- Wee1
- ---- DYRK
- ---- c-Myc
- ---- Aurora Kinase
- ---- ROCK inhibitor
- ---- Eukaryotic Initiation Factor (eIF)
- -- Cytoskeleton
- ---- HSP
- ---- Kinesin
- ---- Integrin
- ---- Dynamin
- ---- Wnt
- ---- β-catenin
- ---- Gap Junction Protein
- -- DNA Damage
- ---- PARP
- ---- DNA/RNA Synthesis
- ---- Sirtuin
- ---- Topoisomerase
- ---- DNA-PK
- ---- Telomerase
- ---- RAD51
- ---- HDAC
- ---- ATM
- ---- DNA alkylator
- ---- Mps1
- -- Epigenetics
- ---- PARP
- ---- JAK
- ---- Pim
- ---- PKC
- ---- PKD
- ---- Sirtuin
- ---- Histone Demethylase
- ---- Histone Acetyltransferase
- ---- HDAC
- ---- HIF-PH
- ---- Aurora Kinase
- ---- Histone Methyltransferase
- ---- METTL3
- ---- Epigenetic Reader Domain
- -- GPCR & G Protein
- ---- Histamine Receptor
- ---- Dopamine Receptor
- ---- Opioid Receptor
- ---- Endothelin Receptor
- ---- SGLT
- ---- OX Receptor
- ---- CaSR
- ---- CXCR
- ---- Vasopressin Receptor
- ---- Glucagon Receptor
- ---- Prostaglandin Receptor
- ---- 5-HT Receptor
- ---- Adrenergic Receptor
- ---- Cannabinoid Receptor
- ---- Sphingosine 1 Phosphate Receptor
- ---- PKA
- ---- Adenosine Receptor
- ---- GnRH
- ---- LPL Receptor
- ---- Ras
- ---- Cholecystokinin Receptor
- ---- Melanocortin Receptor
- ---- RXFP Receptor
- ---- Bradykinin Receptor
- -- Immunology & Inflammation
- ---- PD-1
- ---- PD-L1
- ---- COX
- ---- CCR
- ---- Histamine Receptor
- ---- TLR
- ---- CXCR
- ---- MALT
- ---- TDO
- ---- NOS
- ---- NADPH-oxidase
- ---- IDO
- ---- Thrombopoietin Receptor(TPO)
- ---- NLR inhibitor
- ---- Interleukin Related
- ---- CD73
- ---- Complement System
- ---- Aryl Hydrocarbon Receptor
- ---- Kallikrein
- ---- IRAK
- -- JAK/STAT
- ---- JAK
- ---- STAT
- ---- Pim
- ---- EGFR
- -- MAPK
- ---- MEK
- ---- Raf
- ---- p38 MAPK
- ---- ERK
- ---- MNK
- ---- Mixed Lineage Kinase
- ---- JNK
- ---- MAP4K
- -- Membrane Transporter/Ion Channel
- ---- BCRP
- ---- CFTR
- ---- EAAT2
- ---- GABA Receptor
- ---- HCN Channel
- ---- Monoamine Transporter
- ---- Na+/Ca2+ Exchanger
- ---- Na+/K+ ATPase
- ---- nAChR
- ---- Calcium Channel
- ---- Chloride Channel
- ---- CRAC Channel
- ---- GlyT1
- ---- iGluR
- ---- P2X Receptor
- ---- P-glycoprotein
- ---- Amino acid transporter
- ---- Monocarboxylate Transporter
- ---- Potassium Channel
- ---- Proton Pump
- ---- Potassium Channel
- -- Metabolism
- ---- PPAR
- ---- P450
- ---- HSP
- ---- PDE
- ---- Factor Xa
- ---- Phospholipase
- ---- FAAH
- ---- CETP
- ---- Lipoxygenase
- ---- HMG-CoA Reductase
- ---- Fatty Acid Synthase
- ---- FXR
- ---- NAMPT
- ---- TDO
- ---- Carbonic Anhydrase
- ---- Monoamine Oxidase
- ---- IDO
- ---- Mitochondrial Metabolism
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- RAR/RXR
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Ketohexokinase(KHK)
- -- Neuronal Signaling
- ---- COX
- ---- Histamine Receptor
- ---- Dopamine Receptor
- ---- Opioid Receptor
- ---- GABA Receptor
- ---- OX Receptor
- ---- Amyloid-β
- ---- 5-HT Receptor
- ---- γ-secretase
- ---- Adrenergic Receptor
- ---- NMDA Receptor
- ---- GlyT1
- ---- Beta-secretase
- ---- Sigma Receptor
- ---- mAChR
- ---- α-Synuclein
- ---- Tau Protein
- ---- Cannabinoid Receptor
- ---- Transthyretin (TTR)
- ---- Melanocortin Receptor
- ---- Glucosylceramide Synthase (GCS)
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- ---- Keap1-Nrf2
- -- Protein Tyrosine Kinase
- ---- VEGFR
- ---- EGFR
- ---- PDGFR
- ---- IGF-1R
- ---- FLT3
- ---- FGFR
- ---- c-Kit
- ---- Src
- ---- ALK
- ---- Ephrin receptor
- ---- BTK
- ---- Trk receptor
- ---- c-Met/HGFR
- ---- Syk (Spleen tyrosine kinase)
- ---- TAM Receptor
- ---- ULK1
- ---- CSF-1R
- ---- TYK2
- ---- ROS Kinase
- ---- Bcr-Abl
- ---- FAK
- ---- RET
- ---- Phosphoglycerate Kinase (PGK)
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- ---- Methionine Adenosyltransferase (MAT)
- ---- Lipase
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- -- TGF-beta/Smad
- ---- PKC
- ---- ROCK
- ---- TGF-beta/Smad
- -- Ubiquitin
- ---- Proteasome
- ---- p97
- ---- Deubiquitinase
- ---- DUB
- -- Vitamin D Related
- ---- VD/VDR
- -- PROTAC
- ---- Molecular Glues
- ---- PROTACs
- -- Antibody-drug Conjugate/ADC Related
- -- Microbiology
- -- Others
- ---- PKK
- ---- Others modulator
- ---- Estrogen Receptor/ERR
- ---- ChoKα
- ---- Newest added products
- -- Aldehydes
- -- Amines
- -- Amino Acids
- -- Anilines
- -- Boronic Acids
- -- Bromides
- -- Carboxes
- -- Catalysts
- -- Chiral Compounds
- -- Deuterated
- -- Fluorides
- -- Imidazoles
- -- Indoles and Oxindoles
- -- Iodos
- -- Nitro Compounds
- -- Oxazoles
- -- Peg Linkers
- -- Phenols
- -- Piperidines
- -- Pyridines
- -- Pyrimidines
- -- Quinolines
- -- Sulfonamides
- -- Thiazoles
- -- Trifluoroborates
- -- Other Azoles
- -- Other Heterocycles
- -- Other Building Blocks
- -- On Sale
Latest Products
- Dabogratinib ( TYRA-300 ) (Catalog# : 24073, Cas# : 2800223-30-5)Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the
- AF710B (Catalog# : 25205, Cas# : N/A)AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
- MAT2A inhibitor 5 (Catalog# : 25204, Cas# : 2957874-18-7)MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit
- (Rac)-AF710B (Catalog# : 24083, Cas# : 1235733-73-9)AF-710B is an agonist of sigma and M1 muscarinic receptors; AF710B is an enantiomer o
- Flurpiridaz-nonradiolabeled (Catalog# : 25203, Cas# : 863888-33-9)Flurpiridazis a promising novel cardiac PET imaging tracer formed by the radiolabelin
- Flurpiridaz-Precursor (Catalog# : 25202, Cas# : 863888-32-8)Flurpiridaz-Precursor in stock.
- KL1333 (Catalog# : 25201, Cas# : 1800405-30-4)KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon
- Palupiprant ( E7046 ) (Catalog# : 24055, Cas# : 1369489-71-3)E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece
- Oveporexton ( TAK-861 ) (Catalog# : 25194, Cas# : 2460722-04-5)Oveporexton isan oral small molecule selective orexin type-2 receptor (OX2R) agonist.
- VT-3989 (Catalog# : 25200, Cas# : 2506273-81-8)VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran