| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 122947 | Bafetinib | 859212-16-1 | 98% | ![]() |
| Bafetinib is a potent and selective dual Bcr-Abl/Lyn inhibitor with IC50 of 5.8 nM/19 | ||||
| 122946 | BMN 673 | 1207456-01-6 | 98% | ![]() |
| BMN 673 is a novel PARP1/2 inhibitor with IC50 of 0.58 nM(PARP1); does not inhibit PA | ||||
| 122920 | BMS-564929 | 627530-84-1 | 98% | ![]() |
| BMS-564929 is a novel, highly potent, orally active, nonsteroidal tissue selective an | ||||
| 122918 | Beloranib | 251111-30-5 | 98% | ![]() |
| Beloranib is a fumagillin analogue and inhibitor of methionine aminopeptidase 2 (META | ||||
| 122914 | BI-D1870 | 501437-28-1 | 98% | ![]() |
| BI-D1870 is an ATP-competitive inhibitor of S6 ribosome for RSK1/2/3/4 with IC50 of 3 | ||||
| 122840 | BRAF inhibitor | 918505-61-0 | 98% | ![]() |
| BRAF inhibitor is a potent BRAF inhibitor. | ||||
| 122834 | (-)-Blebbistatin | 856925-71-8 | 98% | ![]() |
| (-)-Blebbistatin is a selective inhibitor of myosin II ATPase activity with IC50 of 0 | ||||
| 122826 | BQCA | 338747-41-4 | 98% | ![]() |
| Coming soon! | ||||
| 122805 | Balipodect ( TAK-063 ) | 1238697-26-1 | 98% | ![]() |
| Balipodect (TAK 063 )is a novel PDE10A inhibitor. It has shown high inhibitory activi | ||||
| 122520 | BD-1047 dihydrobromide | 138356-21-5 | 98% | ![]() |
| BD-1047 dihydrobromide is a selective functional antagonist of sigma receptors, shows | ||||
| 122517 | BIX 01294 Trihydrochloride | 1392399-03-9 | 98% | ![]() |
| BIX01294 is a potent chemical inhibitor of G9a methyltransferase that catalyzes the m | ||||
| 122514 | Bleomycin sulfate | 9041-93-4 | 98% | ![]() |
| Bleomycin is a glycopeptide antibiotic; used as an anticancer agent; Bleomycin acts b | ||||
| 122507 | Bicalutamide | 90357-06-5 | 98% | ![]() |
| Bicalutamide is an oral non-steroidal anti-androgen for prostate cancer; binds to the | ||||
| 122205 | BIX02188 | 334949-59-6 | 98% | ![]() |
| BIX02188 is a selective inhibitor of MEK5 with IC50 of 4.3 nM, also inhibits ERK5 cat | ||||
| 121807 | Bilastine | 202189-78-4 | 98% | ![]() |
| Bilastine is a selective histamine H1 receptor antagonist used for treatment of aller | ||||
| 121417 | BMS-777607 | 1025720-94-8 | 98% | ![]() |
| BMS 777607 是一种 Met-related 抑制剂,能够抑制 c-Met,Axl,Ron 和 Tyro3 | ||||
| 121411 | Benzyl Dichlorophosphite | 76101-29-6 | 98% | ![]() |
| Coming soon! | ||||
| 121403 | BPTES | 314045-39-1 | 98% | ![]() |
| BPTES is a potent and selective allosteric inhibitor of kidney-type glutaminase (GLS) | ||||
| 121401 | Belotecan hydrochloride | 213819-48-8 | 98% | ![]() |
| Belotecan Hydrochloride is the hydrochloride salt of the semi-synthetic camptothecin | ||||
| 120702 | Belinostat acid | 866323-87-7 | 98% | ![]() |
| Coming soon! | ||||
| 120405 | Benazepril | 86541-75-5 | 98% | ![]() |
| Coming soon! | ||||
| 120108 | BX471 | 217645-70-0 | 98% | ![]() |
| BX471 is a potent, selective non-peptide CCR1 antagonist (Ki = 1 nM for human CCR1); | ||||
| 120107 | BMH-21 | 896705-16-1 | 98% | ![]() |
| BMH-21 is a small molecule DNA intercalator that binds ribosomal DNA and inhibits RNA | ||||
| 111912 | BIX 02189 | 1265916-41-3 | 98% | ![]() |
| BIX 02189 is a selective MEK5/ERK5 inhibitor with an IC50 of 59 nM, which was reporte | ||||
| 111907 | BAZ2-ICR | 1665195-94-7 | 98% | ![]() |
| BAZ2-ICR is a small molecule inhibitor of BAZ2A (Kd = 109 nM; IC50 = 130 nM) and BAZ2 | ||||
| 111903 | BMS-863233 HCl | 1169562-71-3 | 98% | ![]() |
| BMS-863233, also known as XL-413, is an orally bioavailable cell division cycle 7 hom | ||||
| 111902 | BAY 57-1293 | 348086-71-5 | 98% | ![]() |
| BAY 57-1293 is a potent helicase primase inhibitor. BAY 57-1293 inhibits replication | ||||
| 111001 | BIX02188 | 1094614-84-2 | 98% | ![]() |
| BIX02188 is a MEK5-selective inhibitor with an IC50 of 0.8 1.0 M, which inhibited ca | ||||
| 110908 | BMS-754807 | 1001350-96-4 | 98% | ![]() |
| BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR with IC50 of 1.8 nM/1. | ||||
| 110227 | BRD4770 | 1374601-40-7 | 98% | ![]() |
| BRD4770 is a novel G9a(EHMT2) inhibitor with EC50 of 5 uM (trimethylated H3K9 in PANC | ||||
