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产品目录

编号化学名称Cas号纯度化学结构
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
611936Bendamustine D498% 
Bendamustine D4 is the deuterium labeled Bendamustine(SDX-105), which is an alkylatin
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)
16071105BCX-1777209799-67-798% by HPLC 
BCX-1777
16071031BYK2041651104546-89-598% by HPLC 
BYK204165 is a potent and selective poly(ADP-ribose) polymerase (PARP)-1 inhibitor (p
16071026BMS-31338247-30-598% by HPLC 
BMS-3 is a LIM kinase 1 (LIMK1) inhibitor. LIMK inhibition with 1 M BMS-3 damaged MTO
16071006BAM 7331244-89-498% by HPLC 
BAM 7 is a Bax activator (EC50 = 3.3 M). BCL-2 family proteins are key regulators of
16071005BTZ043957217-65-198% by HPLC 
BTZ043 racemate is adecaprenylphosphoryl--D-ribose 2'-epimerase (DprE1)inhibitor acti
16070108Bromosporine1619994-69-298% by HPLC 
Bromosporine is a broad spectrum inhibitor for bromodomains and as such will be very
16062903BMS-582949623152-17-098% by HPLC 
BMS-582949 is a potent and selective P38 mitogen-activated protein kinase (P38 MAPK)
16060801BAY12173891554458-53-598% by HPLC 
BAY1217389 is an orally bioavailable, selective inhibitor of the serine/threonine kin
6330016-bromo-2,3,4,4a(S),5,9b(R)-hexahydropyrido[4,3-b]indole1059630-07-798% by HPLC;EE>98% By chiral HPLC 
6-bromo-2,3,4,4a(S),5,9b(R)-hexahydropyrido[4,3-b]indole;CAS#1059630-07-7 provide cus
032512BMS-8339231059734-66-598% 
Coming soon!
0325101-benzyl-4-bromobenzene2116-36-198% 
Coming soon!
0325073-Bromo-2-iodopyridine408502-43-298% 
Coming soon!