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- 抑制剂/受体激动剂
- PI3K/Akt/mTOR
- Epigenetics
- Protein Tyrosine Kinase
- Angiogenesis
- Apoptosis
- Autophagy
- JAK/STAT
- MAPK
- Cytoskeletal Signaling
- Cell Cycle
- TGF-beta/Smad
- DNA Damage
- Stem Cells & Wnt
- Ubiquitin
- Neuronal Signaling
- NF-κB
- GPCR & G Protein
- Metabolism
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产品名字索引 A
- AZD6738 (Catalog# : 110906, Cas# : 1352226-88-0)AZD6738 is an orally available morpholino-pyrimidine-based inhibitor of ataxia telang
- 3-Amino-2,6-dibromopyridine (Catalog# : 110217, Cas# : 39856-57-0)Coming soon!
- 2-Amino-4-(trifluoromethyl)pyridine (Catalog# : 110214, Cas# : 106447-97-6)Coming soon!
- 1-aminocyclopropanecarboxylic acid (Catalog# : 110211, Cas# : 22059-21-8)Coming soon!
- 3-Amino-1-propanesulfonic acid (Catalog# : 110207, Cas# : 3687-18-1)Coming soon!
- Alda 1 (Catalog# : 102702, Cas# : 349438-38-6)Alda 1 is a cell-permeable benzamide compound that selectively enhances the activity
- ACTB-1003 (Catalog# : 102619, Cas# : 939805-30-8)ACTB-1003 is a potent inhibitor of FGFR1 with IC50 <10 nM in FGFR-1 biochemical as
- ABT-751 (Catalog# : 102613, Cas# : 141430-65-1)ABT-751 is a novel bioavailable tubulin-binding and antimitotic sulfonamide agent wit
- AZD1981 (Catalog# : 102604, Cas# : 802904-66-1)AZD1981 is a potent and selective CRTh2 antagonist; displaces radio-labelled PGD2 fro
- AL 082D06 (Catalog# : 101921, Cas# : 256925-03-8)AL 082D06(D-06) is the first selective, nonsteroidal glucocorticoid receptor (GR) ant
- ANA-12 (Catalog# : 101910, Cas# : 219766-25-3)ANA-12 is aTrkB receptor antagonist, which showed direct and selective binding to Trk
- (3aR,5S)-3a,4,5,7-tetrahydro-5-methyl-3H-pyrano[3,4-c]isoxazole (Catalog# : 91823, Cas# : 1613393-51-3)Coming soon!
- (3aR,5R)-3a,4,5,7-tetrahydro-5-methyl-3H-pyrano[3,4-c]isoxazole (Catalog# : 91803, Cas# : 1220327-45-6)Coming soon!
- Amoxanox (Catalog# : 91411, Cas# : 68302-57-8)Amlexanox inhibits mast cell release of allergic mediators, which is also an antialle
- (3aR,4S,7R,7aS)-Hexahydro-4,7-methanoisobenzofuran-1,3-dione (Catalog# : 91404, Cas# : 14166-28-0)The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3
- (3aR,4S,7R,7aS)-Hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione (Catalog# : 91401, Cas# : 14805-29-9)The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3
- AZD3759 (Catalog# : 901301, Cas# : 1626387-80-1)AZD3759 isan orally available inhibitor of the epidermal growth factor receptor (EGFR
- 3-(4-Acetoxyphenyl)propanoic acid (Catalog# : 90702, Cas# : 7249-16-3)Coming soon!
- 3-(3-Aminophenyl)propanoic acid (Catalog# : 90607, Cas# : 1664-54-6)Coming soon!
- 3-Azetidinecarboxylic Acid (Catalog# : 90102, Cas# : 36476-78-5)Coming soon!
- 1-aminocyclohexane-1-carboxylic acid (Catalog# : 83110, Cas# : 2756-85-6)Coming soon!
- 2-amino-2-ethylbutanoic acid (Catalog# : 83109, Cas# : 2566-29-2)Coming soon!
- 8-(2-aminoethyl)-5-hydroxy-4H-1,4-benzoxazin-3-one,hydrochloride (Catalog# : 82801, Cas# : 1035229-35-6)Coming soon!
- Aliskiren (Catalog# : 82708, Cas# : 173334-57-1)Aliskiren(CGP 60536) is a direct renin inhibitor with IC50 of 1.5 nM.
- Abiraterone (Catalog# : 82706, Cas# : 154229-19-3)Abiraterone is a potent steroidal cytochrome P450 17alpha-hydroxylase-17,20-lyase (CY
- AT7519 Hydrochloride (Catalog# : 82702, Cas# : 902135-91-5)AT7519 hydrochloride is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10
- AZ191 (Catalog# : 82405, Cas# : 1594092-37-1)AZ191 selectively inhibits DYRK1B serine/threonine kinase activity with no effect on
- 4-Amino-2,3-dihydro-1H-inden-1-one (Catalog# : 81940, Cas# : 51135-91-2)Coming soon!
- 6-Aminoindan-1-one (Catalog# : 81928, Cas# : 69975-65-1)Coming soon!
- 4-Amino-Piperidine-1-Carboxylic Acid Benzyl Ester (Catalog# : 81805, Cas# : 120278-07-1)Coming soon!
产品分类
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- -- Epigenetics
- ---- PARP
- ---- JAK
- ---- Pim
- ---- PKC
- ---- PKD
- ---- Sirtuin
- ---- Histone Demethylase
- ---- Histone Acetyltransferase
- ---- HDAC
- ---- HIF-PH
- ---- Aurora Kinase
- ---- Histone Methyltransferase
- ---- METTL3
- ---- Epigenetic Reader Domain
- -- 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
- -- Angiogenesis
- ---- VEGFR
- ---- JAK
- ---- EGFR
- ---- PDGFR
- ---- FLT3
- ---- FGFR
- ---- Bcr-Abl
- ---- Src
- ---- ALK
- ---- Syk
- ---- FAK
- ---- BTK
- ---- HIF
- -- Apoptosis
- ---- PD-1
- ---- PD-L1
- ---- Bcl-2
- ---- Caspase
- ---- TNF-alpha
- ---- Survivin
- ---- IAP
- ---- PERK
- ---- p53
- ---- Mdm2
- ---- E1/E2/E3 Enzyme
- -- Autophagy
- ---- LRRK2
- ---- CXCR
- ---- Autophagy
- -- JAK/STAT
- ---- JAK
- ---- STAT
- ---- Pim
- ---- EGFR
- -- MAPK
- ---- MEK
- ---- Raf
- ---- p38 MAPK
- ---- ERK
- ---- MNK
- ---- Mixed Lineage Kinase
- ---- JNK
- ---- MAP4K
- -- Cytoskeletal Signaling
- ---- Akt
- ---- Bcr-Abl
- ---- PKC
- ---- FAK
- ---- HSP
- ---- Kinesin
- ---- Integrin
- ---- Dynamin
- ---- Wnt
- ---- β-catenin
- -- Cell Cycle
- ---- CDK
- ---- PD-1
- ---- PD-L1
- ---- Chk
- ---- ROCK
- ---- PLK
- ---- APC
- ---- Wee1
- ---- DYRK
- ---- c-Myc
- ---- Aurora Kinase
- ---- ROCK inhibitor
- -- TGF-beta/Smad
- ---- Bcr-Abl
- ---- PKC
- ---- ROCK
- ---- TGF-beta/Smad
- -- DNA Damage
- ---- PARP
- ---- DNA/RNA Synthesis
- ---- Sirtuin
- ---- Topoisomerase
- ---- DNA-PK
- ---- Telomerase
- ---- RAD51
- ---- HDAC
- ---- ATM
- ---- DNA alkylator
- ---- Mps1
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- -- Ubiquitin
- ---- Proteasome
- ---- p97
- ---- Deubiquitinase
- -- 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
- ---- α-Synuclein
- ---- Tau Protein
- ---- Cannabinoid Receptor
- ---- Transthyretin (TTR)
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- -- 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
- ---- Sigma Receptor
- ---- Ras
- ---- mAChR
- ---- Cholecystokinin Receptor
- ---- Melanocortin Receptor
- ---- RXFP Receptor
- -- 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
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- RAR/RXR
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- -- Anti-infection
- ---- CMV
- ---- Filovirus
- ---- HBV
- ---- HCV
- ---- HIV
- ---- HSV
- ---- Influenza Virus
- ---- RSV
- ---- SARS-CoV
- ---- Antibacterial
- ---- Antifungal
- ---- Parasite
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Mitochondrial Metabolism
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- -- 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
- -- Vitamin D Related
- ---- VD/VDR
- -- 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
- -- others
- ---- PKK
- ---- Others modulator
- ---- Estrogen Receptor/ERR
- ---- ChoKα
- -- PROTAC
- ---- Molecular Glues
- -- 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
最新产品
- VVD-130037 ( BAY-3605349 ) (Catalog# : 24110, Cas# : 3034880-93-5)VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
- INDEX NAME NOT YET ASSIGNED (Catalog# : 25002, Cas# : 2891709-58-1)
- HC-5404 抑制剂 (Catalog# : 25001, Cas# : 2247396-91-2)HC-5404 是一种新型、高选择性、有效的PERK抑制剂。
- HC-5404-FU (Catalog# : 24112, Cas# : 3034479-99-4)HC-5404-FU 是一种新型、高选择性、有效的PERK抑制剂。
- CMP-5 2HCl (Catalog# : 24161, Cas# : 2309409-79-6)CMP-5 is a potent, specific, and selective PRMT5 inhibitor, while displays no activit
- Wu-5 (Catalog# : 24160, Cas# : 2630378-05-9)Wu-5 is a USP10 inhibitor that can inhibit FLT3 and AMPK pathways, induce FLT3-ITD de
- VU-29 (Catalog# : 24159, Cas# : 890764-36-0)VU 29 is a potent allosteric potentiator at the rat mGlu5 receptor (EC50 = 9 nM); bin
- ML-202 (Catalog# : 24158, Cas# : 1221186-52-2)ML-202 is an activator of pyruvate kinase M2 (PKM2).
- BTA-EG4 hydrate (Catalog# : 24157, Cas# : 921193-28-4)BTA-EG4 is a catalase-amyloid interaction inhibitor, which can significantly enhance
- CYD19 (Catalog# : 24156, Cas# : 2415281-52-4)CYD19 is a potent Snail/HDAC dual target inhibitor.