产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 6111523 | K145 | 1309444-75-4 | 98% |  |
| K145 is a selective SphK2 inhibitor with an IC50 of 4.300.06 M , while no inhibition | ||||
| 6111510 | KS176 | 1253452-78-6 | 98% |  |
| KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BC | ||||
| 6111416 | KYA1797K | 1956356-56-1 | 98% | |
| KYA1797K is a highly potent and selective Wnt/-catenin inhibitor with IC50 of 0.75 M | ||||
| 6111406 | KJ Pyr 9 | 581073-80-5 | 98% | |
| KJ Pyr 9 is a novel small-molecule inhibitor of MYC, KJ-Pyr-9, from a Kr?hnke pyridin | ||||
| 61121 | Ki16425 | 355025-24-0 | 98% |  |
| Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 wit | ||||
| 611942 | Kif15-IN-2 | 672926-33-9 | 98% | |
| Kif15-IN-2 is a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in tu | ||||
| 611941 | Kif15-IN-1 | 672926-32-8 | 98% | |
| Kif15-IN-1 is a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in tu | ||||
| 611922 | KH-CB19 | 1354037-26-5 | 98% | |
| KH-CB19 is a potent and highly specific inhibitor of the CDC2-like kinase isoforms 1 | ||||
| 611921 | K03861 | 853299-07-7 | 98% |  |
| K03861 is a type II CDK2 inhibitor with Kd of 8.2 nM.K03861 inhibits CDK2 activity by | ||||
| 160926003 | KU 57788 | 503468-95-9 | 98% by HPLC |  |
| Potent and selective DNA-PK inhibitor (IC50= 14 nM). Selective for DNA-PK over a rang | ||||
| 16071012 | KW-2449 | 1000669-72-6 | 98% by HPLC |  |
| KW-2449 is a novel multikinase inhibitor, which suppresses the growth of leukemia cel | ||||
| 122525 | Ketoconazole | 65277-42-1 | 98% |  |
| Ketoconazole is an imidazole anti-fungal agent, a CYP3A4 inhibitor. | ||||
| 121431 | KW-2478 | 819812-04-9 | 98% |  |
| KW-2478 是一种针对人类热休克蛋白 90 (Hsp90) 的药物，具有潜在的抗 | ||||
| 121424 | Ku-0063794 | 938440-64-3 | 98% |  |
| KU-0063794 is a selective inhibitor of mammalian target of rapamycin (mTOR) (IC50 ~10 | ||||
| 111908 | Ko 143 | 461054-93-3 | 98% |  |
| Ko 143 is a potent and selective breast cancer resistance protein multidrug transport | ||||
| 111002 | Kevetrin HCl | 66592-89-0 | 98% |  |
| Kevetrin hydrochloride is a small molecule and activator of the tumor suppressor prot | ||||
| 52728 | K02288 | 1431985-92-0 | 98% | |
| K02288 is a novel small molecule inhibitor of ALK1/2/3/6 with IC50s of 1.8/1.1/34.4/6 | ||||
| 52576 | KU-60019 | 925701-49-1 | 98% |  |
| KU-60019 is an improved analogue of KU-55933, with IC50 of 6.3 nM for ATM | ||||
| 52568 | kb NB 142-70 | 1233533-04-4 | 98% |  |
| kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28.3, 5 | ||||
| 52212 | KY02111 | 1118807-13-8 | 98% |  |
| KY02111 is a small molecule which can promote differentiation of hPSCs to cardiomyocy | ||||
| 52215 | Kartogenin | 4727-31-5 | 98% |  |
| Kartogenin(KGN) is a small molecule stimulator of chondrogenesis; promotes chondrocyt | ||||
| 52237 | Kobe0065 | 436133-68-5 | 98% |  |
| Kobe0065 is a novel and effective small-molecule compound inhibiting RasCRaf interact | ||||
| 52245 | KX1-004 | 518058-84-9 | 98% |  |
| KX1-004 is a potent small molecule inhibitor of Src-PTK as a potential protective dru | ||||
| 51502 | kb-NB77-78 | 1350622-33-1 | 98% |  |
| kb-NB77-78 is an analog of CID797718, which is a by-product of the synthesis of the p | ||||
| 52401 | kobe2602 | 454453-49-7 | 98% |  |
| kobe2602 is a novel and effective small-molecule compound inhibiting RasCRaf interact | ||||
| 51611 | KU-55933 | 587871-26-9 | 98% |  |
| KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor withIC50/Kiof | ||||
| 52002 | K-7174 dihydrochloride | 191089-60-8 | 98% |  |
| K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of | ||||
| 51912 | KRN 633 | 286370-15-8 | 98% |  |
| KRN 633 is an ATP-competitive inhibitor ofVEGFR1/2/3withIC50of 170 nM/160 nM/125 nM, | ||||