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| 目录号 | 产品名称 | 产品描述 |
| R10066 | Dapagliflozin; BMS512148 | Dapagliflozin (BMS-512148) 是一种用于治疗糖尿病 (DM) 的新型药物，是一种竞争性葡萄糖协同转运蛋白2 (SGLT2) 抑制剂，可导 |
| R10123 | Bosetan | Bosentan is an endothelin (ET) receptor antagonist for ET-A and ET-B with Ki of |
| R10132 | Canagliflozin | Canagliflozin is a highly potent and selective SGLT2 inhibitor for hSGLT2 with I |
| R10185 | Otenabant Hydrochloride (CP 945598 Hydrochloride) | Otenabant (CP945598)盐酸盐是CB1受体高亲和性拮抗剂，Ki为0.7 nM。 |
| R10186 | CP945598 free base | Otenabant 是一种有效的，选择性的 cannabinoid receptor CB1 拮抗剂，Ki 值为 0.7 nM，对其选择性是对 CB2 的 10 |
| R10242 | AMG073 | Cinacalcet HCl represents a new class of compounds for the treatment of hyperpar |
| R10260 | Sotagliflozin; LP802034; LX4211 | Sotagliflozin (LX-4211) 是SGLT1/2抑制剂，是抗糖尿病剂。 |
| R10406 | AMD3465 hexahydrobromide (GENZ-644494 hexahydrobromide) | AMD 3465 hexahydrobromide (GENZ-644494 hexahydrobromide) 是一种有效的 CXCR4 拮抗剂，在 SupT |
| R10436 | Ambrisentan; BSF208075; LU208075 | Ambrisentan 是一种选择性的ET A型受体 (ETAR) 拮抗剂。 |
| R10488 | Empagliflozin | Empagliflozin是一种选择性钠葡萄糖协同转运蛋白-2 (SGLT-2) 抑制剂，抑制人SGLT-2的IC50 为3.1 nM。 |
| R10489 | Canagliflozin hemihydrate | Canagliflozin 0.5 H2O(JNJ 28431754; TA 7284) is a highly potent and selective SG |
| R10491 | Ipragliflozin | Ipragliflozin (ASP1941) is a highly potent and selective SGLT2 inhibitor with IC |
| R10492 | Tofogliflozin | Tofogliflozin(CSG-452) hydrate is a potent and highly specific sodium/glucose co |
| R10543 | Plerixafor; AMD310 | Plerixafor (AMD3100) is a chemokine receptor antagonist for CXCR4 and CXCL12-med |
| R10609 | Reversine | Reversine 是一种ATP-竞争性的 Aurora kinase 抑制剂，作用于 Aurora A，Aurora B 和 Aurora C，IC50 分别 |
| R10725 | CYM5442 | CYM 5442 HCl is a potent and selective EDG-1 (S1P1) agonist in vitro (EC50 = 1.3 |
| R10794 | Capadenoson; BAY 68-4986 | Capadenoson (BAY 68-4986) is a new adenosine A1 receptor agonist. |
| R10848 | Ki16198 | Ki16198 is the methyl ester of Ki16425, which is a LPA antagonist and inhibits L |
| R10950 | ozanimod;RPC1063;RPC-1063 | Ozanimod 是一种有效的选择性 S1P1 和 S1P5 受体激动剂，在[35S]-GTPγS 结合实验中，EC50 分别为 410±160 pM 和 11 |
| R10953 | ABC294640 | ABC294640 is an orally bioavailable and selective sphingosine kinase-2 (SphK2) i |
| R11455 | Plerixafor octahydrochloride; AMD3100 octahydrochloride; JM3100 octahydrochloride; SID791 octahydrochloride | Plerixafor octahydrochloride (AMD3100 octahydrochloride) 是一种选择性的 CXCR4 |
| R11505 | SQ22536 | SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 μM. It can inhib |
