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Name Index B

• BQR695 (Catalog# : 184218, Cas# : 1513879-21-4)BQR695,也被称为NVP-BQR695, 是一种有效且具有选择性的PI4K抑制剂。
• BAY1143572 (Catalog# : 181242, Cas# : 1414943-88-6)Atuveciclib，也被称为BAY1143572，是一种具有高度选择性、有效和口服
• BAY-1436032 (Catalog# : 181181, Cas# : 1803274-65-8)BAY-1436032 is a potent, selective and orally available inhibitor of mutant Isocitrat
• BGB-283 (Catalog# : 17101620, Cas# : 1446090-77-2;1446090-79-4)BGB-283, also known as Beigene-283 or Lifirafenib, is a Novel potent and selective RA
• Belizatinib (Catalog# : 17101619, Cas# : 1357920-84-3)Belizatinib, also known as TSR-011, is an orally available inhibitor of both the rece
• Bioymifi (Catalog# : 1710165, Cas# : 1420071-30-2)Bioymifi is an DR5 activator (Kd = 1.2 µM; IC50 = 2 µM). Bioymifi induces apoptosis
• BLU-554 (Catalog# : 1710162, Cas# : 1707289-21-1)BLU-554 is a fibroblast growth factor receptor 4 (FGFR4) inhibitor potentially for th
• BX-517 (Catalog# : 1791314, Cas# : 850717-64-5)BX-517, also known as PDK1 inhibitor2, is a potent and selective PDK1 inhibitor.
• BBT-594 (Catalog# : 179133, Cas# : 882405-89-2)BBT594, also known as NVP-BBT594, is potent and selective RET and JAK2 inhibitor. NVP
• BAY41-4109 racemic (Catalog# : 1791117, Cas# : 298708-79-9)BAY41-4109 racemic is a mixture of R-isomer of BAY41-4109 and S-isomer of BAY41-4109.
• BAR-501 (Catalog# : 179821, Cas# : 1632118-69-4)BAR-501 is a selective GPBAR1 agonist devoid of any FXR agonistic activity. BAR501 ef
• Batefenterol(free base) (Catalog# : 179820, Cas# : 743461-65-6)Batefenterol, also known as GSK961081 and TD-5959, is a Muscarinic Antagonist and β2
• BI-847325 (Catalog# : 83101, Cas# : 1207293-36-4)BI-847325 is an orally bioavailable, and selective dual MEK/Aurora kinase inhibitor w
• BAY-598 (Catalog# : 17982, Cas# : 1906919-67-2)BAY-598 is a potent, peptide-competitive chemical probe for SMYD2. BAY-598 has a uniq
• BAY-598 R-isomer (Catalog# : 17981, Cas# : 1906920-28-2)BAY-598 R-isomer is the R-isomer of BAY589. BAY-598 R-isomer may be used as a referen
• Brasofensine (Catalog# : 17916, Cas# : 171655-91-7)Brasofensine is a monoamine reuptake blocker is a phenyltropane that had been under d
• B02 (Catalog# : 1783013, Cas# : 1290541-46-6)B02, also known as RAD51-IN-02, is a RAD51 inhibitor. B02 can enhance DOX sensitivity
• BLU-285 (Catalog# : 1781003, Cas# : 1703793-34-3)BLU-285 is a potent and selective inhibitor of PDGFR D842V and KIT Exon 17 mutants an
• BAY-1895344 (Catalog# : 1781002, Cas# : 1876467-74-1)BAY-1895344 is developed for the treatment of patients with advanced solid tumors and
• BIBR1532 (Catalog# : 178813, Cas# : 321674-73-1)BIBR1132 is highly selective for inhibition of telomerase, resulting in delayed growt
• BMS-932481 (Catalog# : 2017877, Cas# : 1263871-36-8)BMS-932481 modulates A Peptides in the Plasma and Cerebrospinal Fluid of Healthy Volu
• B-1613 (Catalog# : 20178216, Cas# : 214066-78-1)(2S,4S)-1-tert-butyl 2-Methyl 4-(aMinoMethyl)pyrrolidine-1,2-dicarboxylate 
• Balamapimod (Catalog# : 2017822, Cas# : 863029-99-6)Balamapimod, also known as MKI-822, is a Ras/Raf/MEK inhibitor. Balamapimod, may be p
• BP-1-102 (Catalog# : 17030606, Cas# : 1334493-07-0)BP-1-102 is a potent, orally bioavailable and selective STAT3 inhibitor. BP-1-102 bin
• BAY-876 (Catalog# : 17030604, Cas# : 1799753-84-6)BAY-876 is a potent and Selective GLUT1 Inhibitor. BAY-876 showed good metabolic stab
• BRD-7552 (Catalog# : 17030312, Cas# : 1137359-47-7)BRD-7552 is a PDX1 transcription factor inducer. It up regulates PDX1 expression in b
• BDA-366 (Catalog# : 17030305, Cas# : 1821496-27-8)BDA-366 is a BCL2-BH4 antagonist. BDA-366 suppresses human myeloma growth. BDA-366 in
• Bimiralisib (Catalog# : 17030116, Cas# : 1225037-39-7)Bimiralisib, also known as PQR309, is an orally bioavailable pan inhibitor of phospho
• BEC HCl (Catalog# : 17030110, Cas# : 222638-67-7)BEC, also known as S-(2-boronoethyl)-L-cysteine, is an a slow-binding and competitive
• BGP-15 (Catalog# : 17109003, Cas# : 66611-37-8)BGP-15, is a nicotinic amidoxime derivative with PARP inhibitory activity. It has bee