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Cas Index 1

• 1909226-00-1 | BDA-366 (Catalog# : 16122769)BDA-366 is a small-molecule Bcl2-BH4 domain antagonist and binds BH4 with high affini
• 1883429-21-7 | BI-7273 (Catalog# : 16122742)BI-7273 is a potent, selective, and cell-permeable BRD9 BD Inhibitor.
• 1883429-22-8 | BI-9564 (Catalog# : 16122740)BI-9564 is a selective inhibitor of BRD9 and BRD7 bromodomains with the IC50 of 75 nM
• 1584713-87-0 | BMS-983970 (Catalog# : 6111507)BMS-983970 is an oral pan-Notch inhibitor for the treatment of cancer.
• 1257213-50-5 | BMS-986020 (Catalog# : 61122)BMS-986020 is a lysophosphatidic acid 1 receptor antagonist. BMS-986020 is in Phase 2
• 104344-23-2 | (±)-Bisoprolol hemifumarate (Catalog# : 6111106)Bisoprolol is a selective type 1 adrenergic receptor blocker.Bisoprolol, on beta 1-ad
• 1118567-05-7 | Bexagliflozin(EGT1442) (Catalog# : 1673102)EGT1442, a potent and selective SGLT2 inhibitor, attenuates blood glucose and HbA(1c)
• 1104546-89-5 | BYK204165 (Catalog# : 16071031)BYK204165 is a potent and selective poly(ADP-ribose) polymerase (PARP)-1 inhibitor (p
• 1338247-30-5 | BMS-3 (Catalog# : 16071026)BMS-3 is a LIM kinase 1 (LIMK1) inhibitor. LIMK inhibition with 1 M BMS-3 damaged MTO
• 1619994-69-2 | Bromosporine (Catalog# : 16070108)Bromosporine is a broad spectrum inhibitor for bromodomains and as such will be very
• 1554458-53-5 | BAY1217389 (Catalog# : 16060801)BAY1217389 is an orally bioavailable, selective inhibitor of the serine/threonine kin
• 1059630-07-7 | 6-bromo-2,3,4,4a(S),5,9b(R)-hexahydropyrido[4,3-b]indole (Catalog# : 633001)6-bromo-2,3,4,4a(S),5,9b(R)-hexahydropyrido[4,3-b]indole;CAS#1059630-07-7 provide cus
• 1059734-66-5 | BMS-833923 (Catalog# : 032512)Coming soon!
• 133085-33-3 | Bibs-39 (Catalog# : 031004)Coming soon!
• 1505453-59-7 | BET bromodomain inhibitor (Catalog# : 030301)Coming soon!
• 1191448-17-5 | Burixafor (Catalog# : 012003)Burixafor is an orally bioavailable inhibitor of CXC chemokine receptor 4 (CXCR4) wit
• 1227158-85-1 | BAY 87-2243 (Catalog# : 011920)BAY 87-2243 is a highly potent and selective inhibitor of hypoxia-induced gene activa
• 130641-38-2 | Bindarit (Catalog# : 011116)Bindarit, a CCL2, CCL7 and CCL8 inhibitor, is an anti-inflammatory agent.
• 1271022-90-2 | BMS-911543 (Catalog# : 010817)BMS-911543 is a potent and selective small-molecule inhibitor of JAK2; displayes pote
• 1338247-35-0 | BMS 5 (Catalog# : 010611)This product is for custom synthesis.
• 1207456-01-6 | BMN 673 (Catalog# : 122946)BMN 673 is a novel PARP1/2 inhibitor with IC50 of 0.58 nM(PARP1); does not inhibit PA
• 1238697-26-1 | Balipodect ( TAK-063 ) (Catalog# : 122805)Balipodect (TAK 063 ) is a novel PDE10A inhibitor. It has shown high inhibitory activ
• 138356-21-5 | BD-1047 dihydrobromide (Catalog# : 122520)BD-1047 dihydrobromide is a selective functional antagonist of sigma receptors, shows
• 1392399-03-9 | BIX 01294 Trihydrochloride (Catalog# : 122517)BIX01294 is a potent chemical inhibitor of G9a methyltransferase that catalyzes the m
• 1025720-94-8 | BMS-777607 (Catalog# : 121417)BMS-777607 is an inhibitor of MET tyrosine kinase with potential antineoplastic activ
• 1265916-41-3 | BIX 02189 (Catalog# : 111912)BIX 02189 is a selective MEK5/ERK5 inhibitor with an IC50 of 59 nM, which was reporte
• 1665195-94-7 | BAZ2-ICR (Catalog# : 111907)BAZ2-ICR is a small molecule inhibitor of BAZ2A (Kd = 109 nM; IC50 = 130 nM) and BAZ2
• 1169562-71-3 | BMS-863233 HCl (Catalog# : 111903)BMS-863233, also known as XL-413, is an orally bioavailable cell division cycle 7 hom
• 1094614-84-2 | BIX02188 (Catalog# : 111001)BIX02188 is a MEK5-selective inhibitor with an IC50 of 0.8 1.0 M, which inhibited ca
• 1001350-96-4 | BMS-754807 (Catalog# : 110908)BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR with IC50 of 1.8 nM/1.