NEW PRODUCTS
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 2091501 | AB-680 | 2105904-82-1 | 98% Min. |  |
| AB-680 is highly potent, reversible and selective CD73 inhibitor. AB680 to be a rever | ||||
| 185235 | Trilaciclib (G1T28) | 1374743-00-6 | >98% |  |
| TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A | ||||
| 52023 | DCC-2036(Rebastinib) | 1020172-07-9 | 98% | _1020172-07-9.png) |
| Rebastinib(DCC-2036;DCC2036) is an inhibitor of tyrosine kinases TIE2 and ABL1.Rebast | ||||
| 20103003 | ML380 | 1627138-52-6 | ≧98.0% |  |
| ML380 is a highly potent and the first CNS penetrant M5 positive allosteric modulator | ||||
| 187122 | Gefapixant | 1015787-98-0 | 98% |  |
| Gefapixant, also known as AF-219 or MK-7264, is a P2X3 receptor antagonist. Gefapixan | ||||
| 1810164 | Pemigatinib (INCB054828) | 1513857-77-6 | 98% |  |
| Pemigatinib (INCB054828) is an orally active, selectiveFGFRinhibitor withIC50s of 0.4 | ||||
| 122524 | GW2580 | 870483-87-7 | 98% |  |
| GW2580 is an orally bioavailable inhibitor of c-FMS kinase; completely inhibited huma | ||||
| 203071 | CC-90009 | 1860875-51-9 | 98% |  |
| CC-90009 is a modulator of cereblon (CRBN), which is part of the cullin 4-RING E3 ubi | ||||
| 17011802 | EX-527 S-enantiomer | 848193-68-0 | 98% |  |
| EX-527 S-enantiomer is a potent and selective SIRT1 inhibitor with IC50 of 123 nM; no | ||||
| 120103 | AGI-5198 | 1355326-35-0 | 98% |  |
| AGI-5198 is a novel R132H-IDH1 inhibitor, identified through a high-throughput screen | ||||
| 17031018 | Etrasimod | 1206123-37-6 | 99.73% |  |
| Etrasimod ( APD334 ) is a potent, once-daily, oral, highly selective sphingosine 1-ph | ||||
| 2073107 | Trilaciclib hydrochloride (G1T28 hydrochloride) | 1977495-97-8 | 98% Min. | .png) |
| TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A | ||||