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Name Index B

• 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
• Butylphthalide (Catalog# : 16122908, Cas# : 6066-49-5)Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of
• Buthionine Sulphoximine (Catalog# : 16122907, Cas# : 5072-26-4)Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe
• Brivaracetam (Catalog# : 16122906, Cas# : 357336-20-0)Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra
• Brigatinib (AP-26113) (Catalog# : 16122905, Cas# : 1197953-54-0)Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL
• Brevianamide F (Catalog# : 16122904, Cas# : 38136-70-8)Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally o
• Bohemine (Catalog# : 16122903, Cas# : 189232-42-6)Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh
• BMS-687453 (Catalog# : 16122902, Cas# : 1000998-59-3)BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR
• BML-210 (Catalog# : 16122901, Cas# : 537034-17-6)BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition
• BIIB021 (Catalog# : 16122868, Cas# : 848695-25-0)BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule
• BI605906 (Catalog# : 16122867, Cas# : 960293-88-3)BI605906 is a IKK inhibitor. BI605906 inhibits TNF-dependent IB degradation and expre
• Benzbromarone (Catalog# : 16122866, Cas# : 3562-84-3)Benzbromarone is a uricosuric agent and non-competitive inhibitor of xanthine oxidase
• BAY-59-3074 (Catalog# : 16122805, Cas# : 406205-74-1)BAY-59-3074 is a novel cannabinoid CB1/CB2 receptor partial agonist with analgesic pr
• Batimastat (Catalog# : 16122804, Cas# : 130370-60-4)Batimastat (also known as BB-94) is a synthetic matrix metalloproteinase inhibitor th
• BFH772 (Catalog# : 16122778, Cas# : 890128-81-1)BFH772 is a novel potent oral VEGFR2 inhibitor, targeting VEGFR2 kinase with IC50 of
• BI-78D3 (Catalog# : 16122776, Cas# : 883065-90-5)BI-78D3 is a competitive JNK inhibitor with IC50 of 280nM that displays > 100 fold
• BDA-366 (Catalog# : 16122769, Cas# : 1909226-00-1)BDA-366 is a small-molecule Bcl2-BH4 domain antagonist and binds BH4 with high affini
• BI-7273 (Catalog# : 16122742, Cas# : 1883429-21-7)BI-7273 is a potent, selective, and cell-permeable BRD9 BD Inhibitor.
• BI-9564 (Catalog# : 16122740, Cas# : 1883429-22-8)BI-9564 is a selective inhibitor of BRD9 and BRD7 bromodomains with the IC50 of 75 nM
• BAW2881 (NVP-BAW2881) (Catalog# : 16122733, Cas# : 861875-60-7)BAW2881 (NVP-BAW2881) is a novel vascular endothelial growth factor (VEGF) receptor t
• BMS-983970 (Catalog# : 6111507, Cas# : 1584713-87-0)BMS-983970 is an oral pan-Notch inhibitor for the treatment of cancer.
• BAY-61-3606 (Catalog# : 6111415, Cas# : 648903-57-5)BAY-61-3606 is a potent and selective inhibitor of Syk kinase (Ki = 7.5 nM).
• BH3I-1 (Catalog# : 61402, Cas# : 300817-68-9)BH3I-1 is an inhibitor of Bcl-xL with IC 50 of 293.95 M. BH3I-1 is a cell permeable B
• Bax inhibitor peptide V5 (Catalog# : 61401, Cas# : 579492-81-2)Bax inhibitor peptide V5 is a peptide inhibitor of Bax translocation to mitochondria.