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- 抑制剂/受体激动剂
- PI3K/Akt/mTOR
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- JAK/STAT
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产品名字索引 B
- BMS-986195 (Catalog# : 20444, Cas# : 1912445 -55-6)
- Branebrutinib (Catalog# : 20428, Cas# : 1912445-55-6)Branebrutinib, also known as BMS-986195, is a potent, covalent, irreversible inhibito
- Bexotegrast ( PLN-74809 ) (Catalog# : 171680, Cas# : 2376257-44-0)Bexotegrast（同义词：PLN-74809）是一种小分子、双重选择性 αVβ1 / α
- 4-溴-2-氰基-6-甲氧基吡啶 (Catalog# : 171653, Cas# : 886372-53-8)4-溴-2-氰基-6-甲氧基吡啶, CAS 886372-53-8
- 1-(4-溴-6-甲基吡啶-2-基)乙-1-酮 (Catalog# : 171454, Cas# : 1060810-24-3)1-(4-溴-6-甲基吡啶-2-基)乙-1-酮, CAS 1060810-24-3.
- BGB 15025 ; BGB-15025 ; BGB15025 (Catalog# : 171452, Cas# : 2766481-17-6)BGB-15025 是一种有效的选择性 HPK1 抑制剂，在多种肿瘤模型中作为
- N-乙基-2-(4-甲酰基苯基)乙酰胺 (Catalog# : 20419, Cas# : 2477812-42-1)
- 497223-19-5 (Catalog# : 20403, Cas# : 497223-19-5)
- Benzeneacetic acid, 4-[[(2,4-dimethylbenzoyl)oxy]methyl]-, methyl ester (Catalog# : 20391, Cas# : 2097334-15-9)
- 497223-19-5 (Catalog# : 20386, Cas# : 497223-19-5)
- 1,10-BIS[4-AZA-1-AZONIABICYCLO[2.2.2]OCTAN-1-YL]DECANE DIBROMIDE (Catalog# : G20381, Cas# : 94630-53-2)
- 6-(苄氧基)-3,4-二氢萘-2(1H)-酮 (Catalog# : 20372, Cas# : 885280-42-2)
- BIBF0775 (Catalog# : L20357, Cas# : 334951-90-5)BIBF0775 is an inhibitor of the transforming growth factor β receptor I (TGFβRI). X
- Blarcamesine HCl (Catalog# : 6111905, Cas# : 195615-84-0)Anavex2-73 is a muscarinic/σ1 ligand. ANAVEX2-73 (0.01-3.0 mg/kg i.p.) alleviated th
- Bunamidine hydrochloride (Catalog# : 20271, Cas# : 1055-55-6)Bunamidine is a anti-parasitic drug, which was approved by FDA for the treatment of t
- BIT225 (Catalog# : 20270, Cas# : 917909-71-8)BIT-225 is a NCp7 zinc finger inhibitor potentially for the treatment of HCV infectio
- BI-3406 (Catalog# : 21234, Cas# : 2230836-55-0)BI-3406 is Potent & Selective SOS1::KRAS Inhibitor (IC50=5 nM), which Opens a New
- BI-187004 (Catalog# : 21224, Cas# : 1303515-32-3)BI-187004, also known as VTP-34072, is an 11β-hydroxysteroid dehydrogenase 1 inhibit
- Bafetinib (Catalog# : 2021221, Cas# : 887650-05-7)Bafetinib, also known as INNO-406 and NS187, is an orally bioavailable 2-phenylaminop
- BRD0705 (Catalog# : 202112701, Cas# : 2056261-41-5)BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor. BRD0705 ca
- BLU-782 (Catalog# : 20121701, Cas# : 2141955-96-4)
- (2S,5R)-5-氨基-2-甲基哌啶-1-甲酸苄酯盐酸盐 (Catalog# : 20103006, Cas# : 1207853-23-3)
- Benpyrine racemate (Catalog# : 2091907, Cas# : 1333714-43-4)(Rac)-Benpyrine is a racemate of Benpyrine. (Rac)-Benpyrine is a potent and orally ac
- BAY-2416964 (Catalog# : 2091906, Cas# : 2242464-44-2)BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist
- BI-894999 (Catalog# : 2091902, Cas# : 1660117-38-3)BI-894999 is a potent and selective BET inhibitor potentially useful for the Treatmen
- 4-溴-(2-丁氧基乙氧基)苯 (Catalog# : 2091206, Cas# : 39255-24-8)
- 4-(2-丁氧基乙氧基)苯基硼酸 (Catalog# : 2091203, Cas# : 279262-28-1)
- 6-BROMO-2-ETHYL-N,8-DIMETHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE (Catalog# : 2091201, Cas# : 1628264-07-2)
- BCH001 (Catalog# : 208192, Cas# : 384859-58-9)BCH001是一种特异性PAPD5抑制剂，可在DC患者诱导的多能干细胞中恢
- BMS-1166 (Catalog# : 2073102, Cas# : 1818314-88-3)BMS-1166是一种有效的PD-1 / PD-L1相互作用抑制剂，IC50为1.4 nM，可拮抗
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
- TRPM4-IN-2 (Catalog# : 24147, Cas# : 667411-04-3)TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
- Isolithocholic Acid (Catalog# : 24146, Cas# : 1534-35-6)Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
- H2-Gamendazole (Catalog# : 24145, Cas# : 877768-84-8)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
- CPI-455 HCl (Catalog# : 24144, Cas# : 2095432-28-1)CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
- KH-3 (Catalog# : 24143, Cas# : 1215115-03-9)KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
- Stafib-2 (Catalog# : 24142, Cas# : 2097938-74-2)Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
- TCRS-417 (Catalog# : 24141, Cas# : 2032123-28-5)TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
- PST3 1a (Catalog# : 24140, Cas# : 1096144-06-7)PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
- YTX-465 (Catalog# : 24139, Cas# : 2225824-53-1)YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
- CAY10566 (Catalog# : 10403, Cas# : 944808-88-2)Coming soon!