Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 18831 | TW-37 | 877877-35-5 | >98% |  |
| TW-37 is a small-molecule inhibitor of Bcl-2 family proteins, inhibited cell growth a | ||||
| 187202 | TAK-715 | 303162-79-0 | >98% |  |
| TAK-715 is a potent p38 MAPK inhibitor. which displays potent inhibitory activity and | ||||
| 18762 | TAK-960 | 1137868-52-0 | >98% |  |
| TAK-960 is an orally available PLK1 inhibitor with potential antineoplastic activity. | ||||
| 186235 | Theliatinib | 1353644-70-8 | >98% |  |
| Theliatinib, also known as HMPL-309, is a novel small molecule, epidermal growth fact | ||||
| 186233 | Tucidinostat | 1616493-44-7 | >98% |  |
| Tucidinostat is a benzamide type inhibitor of histone deacetylase (HDAC) isoenzymes 1 | ||||
| 18672 | Takinib | 1111556-37-6 | >98% |  |
| Takinib is a selective TAK1 inhibitor that induces apoptosis following TNF-α stimula | ||||
| 185254 | TMP269 | 1314890-29-3 | >98% |  |
| TMP269 is a highly potent, selective and cell-permeable class IIa HDAC inhibitor with | ||||
| 185235 | Trilaciclib (G1T28) | 1374743-00-6 | >98% |  |
| TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A | ||||
| 185181 | TAPI-1 | 171235-71-5 | >98% |  |
| TAPI-1 is and inhibitor of TACE. It inhibits the cleavage of TNF-a, TNFRI (p60), and | ||||
| 185175 | TG100572 HCl | 867331-64-4 | >98% |  |
| TG-100572 is a potent and selective VEGFR2/Src kinase inhibitor. | ||||
| 18594 | TLN-232 | 158899-10-6 | >98% |  |
| TLN-232, also known as CAP-232, is a synthetic cyclic heptapeptide with potential ant | ||||
| 18593 | TRC051384 | 867164-40-7 | >98% |  |
| TRC051384 is a inducer of heat shock protein Hsp70. | ||||
| 18592 | Triptorelin Acetate | 140194-24-7 | >98% |  |
| Triptorelin is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the ac | ||||
| 18591 | Tropifexor | 1383816-29-2 | >98% |  |
| Tropifexor, also known as LJN452, is a farnesoid X receptor agonist for the Treatment | ||||
| 184172 | THZ531 | 1702809-17-3 | >98% |  |
| THZ531 is a covalent CDK12 and CDK13 covalent inhibitor. Cyclin-dependent kinases 12 | ||||
| 184311 | Tofogliflozin | 903565-83-3 | >98% |  |
| Tofogliflozin, also known as CSG 452, is a potent and high selective SGLT2 inhibitor | ||||
| 18423 | TPX-0005 | 1802220-02-5 | >98% |  |
| TPX-0005 is a Src/FAK/Janus kinase 2 (JAK2) inhibitor. TPX-0005 plus EGFR TKI suppres | ||||
| 183214 | tert-butyl ((1H-benzo[d][1,2,3]triazol-1-yl)methyl)carbamate | 305860-41-7 | >96% | methyl)carbamate_305860-41-7.png) |
| tert-butyl (1H-benzo[d][1,2,3]triazol-1-yl)methylcarbamate是一种药物中间体。 | ||||
| 1712152 | Timapiprant | 851723-84-7 | >98% |  |
| Timapiprant，又名OC000459，是一种强效、选择性和口服的CRTH2拮抗剂。 | ||||
| 1791519 | TUG-770 | 1402601-82-4 | 98.0% |  |
| TUG-770 is a Highly Potent Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist for Treatm | ||||
| 179157 | TH-2120 | 81686-22-8 | 98.0% |  |
| TH-2120, also known as Sodium ionophore III, is a ionophore. Ionophore is suitable fo | ||||
| 1791113 | Thiomyristoyl | 1429749-41-6 | 98.0% |  |
| Thiomyristoyl is a potent and specific SIRT2 inhibitor with an IC50 of 28 nM. IC50 & | ||||
| 179828 | TC-O9311 | 444932-31-4 | 98.0% |  |
| TC-O9311 is a potent GPR139 agonist (EC50 = 39 nM in CHO-K1 cells expressing human GP | ||||
| 179811 | Trelagliptin succinate | 1029877-94-8 | 98.0% |  |
| Trelagliptin, also known as SYR-472, is a long acting dipeptidyl peptidase-4 (DPP-4) | ||||
| 1783014 | TUG-891 | 1374516-07-0 | 98.0% |  |
| TUG-891 is a potent and selective agonist of the free fatty acid receptor 4 (FFA4/GPR | ||||
| 178303 | TP-3654 | 1361951-15-6 | 98.0% | |
| TP-3654 is a Pim-1 and Pim-3 kinase inhibitor potentially for the treatment of prosta | ||||
| 1791412 | TAK1 INHIBITOR | 1326712-16-6 | >98% |  |
| TAK1 inhibitor is discontinued. | ||||
| 17031308 | TPCA-1 | 507475-17-4 | 98% |  |
| TPCA-1 is a potent IKK-2 inhibitor. TPCA-1 is also an effective inhibitor of STAT3 ph | ||||
| 17031306 | Trichostatin A | 58880-19-6 | 98% |  |
| Trichostatin A, also known as TSA, is a HDAC inhibitor. TSA inhibits the eukaryotic c | ||||
| 17031304 | Thiotepa | 52-24-4 | 98% |  |
| Thiotepa is a polyfunctional, organophosphorus alkylating agent and a stable derivati | ||||