Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 1812282 | TP0463518 | 1558021-37-0 | >98% | |
| TP0463518 is a novel, highly potent HIF prolyl hydroxylase (PHD) inhibitor. TP0463518 | ||||
| 1812133 | Thiamet G | 1009816-48-1 | >98% |  |
| Thiamet G is a potent and selective inhibitor of O-GlcNAcase. | ||||
| 181252 | Talmapimod HCl | 309915-12-6 | >98% |  |
| Talmapimod, also known as SCIO-469, is an orally bioavailable, small-molecule, p38 mi | ||||
| 181232 | TG4-155 | 1164462-05-8 | >98% |  |
| TG4-155 is a brain penetrant EP2 antagonist (KB = 2.4 nM) that is over 1000-fold less | ||||
| 181231 | Tebanicline HCl | 203564-54-9 | >98% |  |
| Tebanicline, also known as ABT-594 and Ebanicline, a potent synthetic nicotinic (non- | ||||
| 1811212 | Topotecan | 123948-87-8 | >98% |  |
| Topocecan is a semisynthetic derivative of camptothecin with antineoplastic activity. | ||||
| 1811191 | TAS-120 | 1448169-71-8 | >98% |  |
| TAS-120 is an orally bioavailable inhibitor of the fibroblast growth factor receptor | ||||
| 1811161 | Tulrampator ( CX-1632 ) | 1038984-31-4 | ≧98.0% | _1038984-31-4.png) |
| Tulrampator, also known as S-47445 and CX-1632, is a positive allosteric modulator (P | ||||
| 1811122 | Thiazovivin | 1226056-71-8 | >98% |  |
| Thiazovivin is a selective, cell-permeable small molecule that inhibits ROCK activity | ||||
| 1811021 | TH 1217 | 1862212-48-3 | >98% |  |
| TH 1217 is a potent dCTP pyrophosphatase 1 inhibitor. | ||||
| 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 | ||||