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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
16122908Butylphthalide6066-49-598% 
Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of
16122907Buthionine Sulphoximine5072-26-498%
Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe
16122906Brivaracetam357336-20-098% 
Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra
16122905Brigatinib (AP-26113)1197953-54-098% 
Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL
16122904Brevianamide F38136-70-898% 
Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally o
16122903Bohemine189232-42-698% 
Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh
16122902BMS-6874531000998-59-398% 
BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR
16122901BML-210537034-17-698% 
BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition
16122868BIIB021848695-25-098% 
BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule
16122867BI605906960293-88-398% 
BI605906 is a IKK inhibitor. BI605906 inhibits TNF-dependent IB degradation and expre
16122866Benzbromarone3562-84-398% 
Benzbromarone is a uricosuric agent and non-competitive inhibitor of xanthine oxidase
16122805BAY-59-3074406205-74-198% 
BAY-59-3074 is a novel cannabinoid CB1/CB2 receptor partial agonist with analgesic pr
16122804Batimastat130370-60-498% 
Batimastat (also known as BB-94) is a synthetic matrix metalloproteinase inhibitor th
16122778BFH772890128-81-198% 
BFH772 is a novel potent oral VEGFR2 inhibitor, targeting VEGFR2 kinase with IC50 of
16122776BI-78D3883065-90-598% 
BI-78D3 is a competitive JNK inhibitor with IC50 of 280nM that displays > 100 fold
16122769BDA-3661909226-00-198% 
BDA-366 is a small-molecule Bcl2-BH4 domain antagonist and binds BH4 with high affini
16122742BI-72731883429-21-798% 
BI-7273 is a potent, selective, and cell-permeable BRD9 BD Inhibitor.
16122740BI-95641883429-22-898% 
BI-9564 is a selective inhibitor of BRD9 and BRD7 bromodomains with the IC50 of 75 nM
16122733BAW2881 (NVP-BAW2881)861875-60-798% 
BAW2881 (NVP-BAW2881) is a novel vascular endothelial growth factor (VEGF) receptor t
6111507BMS-9839701584713-87-098% 
BMS-983970 is an oral pan-Notch inhibitor for the treatment of cancer.
6111415BAY-61-3606648903-57-598% 
BAY-61-3606 is a potent and selective inhibitor of Syk kinase (Ki = 7.5 nM).
61402BH3I-1300817-68-998% 
BH3I-1 is an inhibitor of Bcl-xL with IC 50 of 293.95 M. BH3I-1 is a cell permeable B
61401Bax inhibitor peptide V5579492-81-298%
Bax inhibitor peptide V5 is a peptide inhibitor of Bax translocation to mitochondria.
61122BMS-9860201257213-50-598% 
BMS-986020 is a lysophosphatidic acid 1 receptor antagonist. BMS-986020 is in Phase 2
6111106(±)-Bisoprolol hemifumarate104344-23-298% 
Bisoprolol is a selective type 1 adrenergic receptor blocker.Bisoprolol, on beta 1-ad
6111023BNC105945771-74-498% 
BNC105 is a tubulin polymerization inhibitor with potent antiproliferative and tumor
61110026-bromo-[1,2,4]triazolo[1,5-a]pyridine356560-80-098% 
6-bromo-[1,2,4]triazolo[1,5-a]pyridine
611917Briciclib865783-99-998% 
Briciclib is a small molecule that suppresses cyclin D1 accumulation in cancer cells.
16812023-bromo-1-ethyl-1H-pyrrole-2,5-dione909397-54-298% 
3-bromo-1-ethyl-1H-pyrrole-2,5-dione,CAS#909397-54-2
1673102Bexagliflozin(EGT1442)1118567-05-798% by HNMR/HPLC 
EGT1442, a potent and selective SGLT2 inhibitor, attenuates blood glucose and HbA(1c)