Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 20656 | IK-930 | 2563892-44-2 | ≧98.0% |  |
| IK-930 is a novel, selective, small molecule inhibitor of TEAD that prevents palmitat | ||||
| 20649 | Iptacopan hydrochloride hydrate | 2447007-60-3 | 98% Min. |  |
| Iptacopan hydrochloride hydrate is a highly potent and highly selective factor B inhi | ||||
| 20623 | Itruvone | 21321-89-1 | 98% Min. |  |
| Itruvone is an antidepressant. | ||||
| 20591 | ITK inhibitor 6 | 2404604-06-2 | 98% Min. |  |
| 20475 | Imlunestrant | 2408840-26-4 | 98% Min. |  |
| Imlunestrant is a biochemical | ||||
| 20406 | 1-ISOPROPOXYBENZENE | 2741-16-4 | 98% Min. |  |
| 822221 | IACS-13909 | 2160546-07-4 | ≧98.0% |  |
| IACS-13909 is a specific and potent allosteric inhibitor of SHP2, that suppresses sig | ||||
| L20336 | IMM-H007 | 1221412-23-2 | 98% Min. |  |
| IMM-H007 is a novel lipid-lowering agent, increasing abca1 protein expression | ||||
| L20330 | Indirubin-3’-oxime | 160807-49-8 | 98% Min. |  |
| Indirubin-3’-oxime is a potent inhibitor of glycogen synthase kinase 3β (GSK3β; I | ||||
| 20326 | Imatinib free base | 152459-95-5 (free base) | 98% Min. | |
| Imatinib is a tyrosine kinase inhibitor with antineoplastic activity. Imatinib binds | ||||
| 20288 | Ispronicline | 252870-53-4(free base) | 98% Min. |  |
| Ispronicline, also known as AZD3480; TC 1734; TC-0173, and RJR 1734, is a alpha4beta2 | ||||
| 21253 | indole-4-boronic acid pinacol ester | 388116-27-6 | ≧95.0% |  |
| indole-4-boronic acid pinacol ester, CAS 388116-27-6, is an important intermeidate. | ||||
| 20122401 | IOX4 | 1154097-71-8 | 98% Min. |  |
| 2091905 | 9-ING-41 | 1034895-42-5 | 98% Min. |  |
| 9-ING-41 is a glycogen synthase kinase-3 (GSK-3) inhibitor. | ||||
| 20911 | IACS-9439 | 2231259-57-5 | 98% Min. |  |
| IACS-9439 is a potent, highly selective and orally bioavailable CSF1R inhibitor. IACS | ||||
| 2071519 | IITZ-01 | 1807988-47-1 | 98% Min. |  |
| IITZ-01 (Autophagy inhibitor IITZ-01) is a novel potent lysosomotropic autophagy inhi | ||||
| 2062023 | 4-iodo-2-isopropyl-1-Methyl-1H-iMidazole | 851870-24-1 | 96% Min. |  |
| 2062008 | 1-iodo-2-methoxy-4-methylbenzene | 186583-59-5 | 98% Min. | |
| 2051507 | IUN76750 | 1690176-75-0 | 98% Min. |  |
| IUN76750 is a PAR-2 signaling pathway inhibitor. IUN76750 has CAS#1690176-75-0, has n | ||||
| 204306 | ICEC0942 mesylate | 98% Min. |  | |
| ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective | ||||
| 204305 | ICEC0942 HCl | 1805789-54-1 (HCl) | 98% Min. | .gif) |
| ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective | ||||
| 204304 | ICEC0942 free base | 1805833-75-3 (free base) | 98% Min. | .gif) |
| ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective | ||||
| 54192 | ITI-214 | 1160521-50-5 | >98% |  |
| ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic | ||||
| 512193 | ITI-214(phosphate) | 1642303-38-5 | 98% Min. |  |
| ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic | ||||
| 19319 | IDH889 | 1429179-07-6 | >98% |  |
| IDH889 is a potent and selective inhibitors of IDH1. IDH899 shows IDH (R132H) IC50 = | ||||
| 191143 | INCB3284 mesylate | 887401-93-6 | >98% |  |
| INCB3284 is a potent, selective, and orally bioavailable hCCR2 Antagonist. | ||||
| 1812131 | Indeglitazar | 835619-41-5 | >98% |  |
| Indeglitazar, also known as PPM-204 and PLX-204, is an orally available peroxisome pr | ||||
| 181025 | IU1-47 | 670270-31-2 | >98% |  |
| IU1-47 is a potent and selective inhibitor of USP14. | ||||
| 186277 | Inarigivir soproxil | 942123-43-5 | >98% |  |
| Inarigivir soproxil, also known as SB 9200, is an antiviral agent. | ||||
| 186276 | IT-901 | 1584121-99-2 | >98% |  |
| IT-901 is a c-Rel Inhibitor That Mediates Anticancer Properties in Hematologic Malign | ||||