Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 20631 | Vorasidenib | 1644545-52-7 | 98% Min. |  |
| Vorasidenib, also known as AG-881, is a potent and selective orally available inhibit | ||||
| 20612 | Valemetostat tosylayte | 1809336-93-3 | 98% Min. |  |
| Valemetostat, also known as DS-3201 is a potent, selective and orally active EZH1/2 i | ||||
| 20566 | 1V209 | 1062444-54-5 | 98% Min. |  |
| 1V209, also known as TLR7 agonist T7, is a novel Toll-like receptor 7 (TLR7) agonist, | ||||
| 20547 | Venglustat malate | 1629063-78-0 | 98% Min. |  |
| Venglustat, also known as Ibiglustat, GZ402671, GZ-452; Genz-682452 and SAR402671, is | ||||
| 20536 | VV116 | 2647442-33-7 | 98% Min. |  |
| VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SA | ||||
| 20525 | VX-548 | 2649467-58-1 | 98% Min. |  |
| 20435 | Vacquinol-1 | 5428-80-8 | 98% Min. |  |
| Vacquinol-1, also known as NSC 13316, is an activator of MKK4-dependent macropinocyto | ||||
| 171423 | Visomitin (Synonyms: SKQ1) | 934826-68-3 | ≧98.0% | _934826-68-3.png) |
| Visomitin (Synonyms: SKQ1) is mitochondria-targeted antioxidant. | ||||
| G20377 | VTX-27 | 1321924-70-2 | 98% Min. |  |
| VTX-27 is a novel potent and selective PKCθ inhibitor. | ||||
| 822223 | Venglustat ( ibiglustat ) | 1401090-53-6 | ≧98.0% |  |
| Venglustat(ibiglustat)is an oral inhibitor of an enzyme called glucosylceramide synth | ||||
| 20302 | VAS3947 | 869853-70-3 | ≧98.0% |  |
| VAS3947 is a selective inhibitor of NADPH oxidase activity in low micromolar concentr | ||||
| 20299 | Venadaparib | 1681017-83-3 | 98% Min. |  |
| Venadaparib, also known as IDX-1197, is a potent, selective and orally active PARP in | ||||
| 20284 | Vatiquinone | 1213269-98-7 | 98% Min. |  |
| Vatiquinone, also known as EPI 743, is an orally bioavailable para-benzoquinone being | ||||
| 20112601 | Val-Cit-PAB-MMAE | 644981-35-1 | 98% Min. |  |
| Val-Cit-PAB-MMAE is a MMAE derivative with a cleavable linker, which is useful to mak | ||||
| 20111202 | VTP-50469 | 2169916-18-9 | 98% Min. |  |
| VTP-50469 is a novel, potent, selective, orally-available MeninMLL1 inhibitor, being | ||||
| 2071627 | VU0238441 | 85511-68-8 | 98% Min. | |
| 2071548 | VU0238429 | 1160247-92-6 | 98% Min. |  |
| VU0238429 is a selective positive allosteric modulator of M5 receptors (EC50 values a | ||||
| 2071547 | VU0119498 | 79183-37-2 | 98% Min. |  |
| VU0119498 is a M1 muscarinic receptor agonist (EC50 = 3.1 μM) and pan mAChR M3, M5 p | ||||
| 2071543 | Vonafexor | 1192171-69-9 | 98% Min. |  |
| Vonafexor, also known as EYP001, is a farnesoid X receptor agonist. | ||||
| 2071534 | VUN34002 | 2173134-00-2 | 98% Min. |  |
| VUN34002, also known as Vanin-1-IN-1 is an inhibitor of vanin-1 enzyme which is a cel | ||||
| 112091 | VAL-083 | 23261-20-3 | 98% Min. |  |
| VAL-083 is a bi-functional alkylating agent, with potential antineoplastic activity. | ||||
| 19529 | Vesatolimod(GS-9620) | 1228585-88-3 | 98% Min. |  |
| DescriptionGS-9620 is a potent and selective orally active small molecule agonist ofT | ||||
| 193114 | Valecobulin | 1188371-47-2 | >98% |  |
| Valecobulin is an anti-neoplastic beta-tubulin polymerization inhibitor. Tubulin poly | ||||
| 192154 | Vecabrutinib | 1510829-06-7 | >98% |  |
| Vecabrutinib, also known as SNS-062; FP-182, BSK-4841 and BIIB-062; is a potent, nonc | ||||
| 192141 | Valemetostat | 1809336-39-7 | >98% |  |
| Valemetostat is an antineoplastic drug candidate. | ||||
| 1812285 | Verdiperstat | 890655-80-8 | >98% |  |
| erdiperstat, also known as AZD-3241, is a selective and irreversible inhibitor of mye | ||||
| 181253 | Vaborbactam | 1360457-46-0 | >98% |  |
| Vaborbactam, also known as RPX7009, is a potent and selective beta-lactamase inhibito | ||||
| 1810151 | VU0463271 | 1391737-01-1 | >98% |  |
| VU0463271 inhibits co-transporter KCC2. | ||||
| 18891 | Vafidemstat | 1357362-02-7 | >98% |  |
| Vafidemstat, also known as ORY 2001, is a lysine-specific histone demethylase (LSD1) | ||||
| 187201 | Verteporfin | 129497-78-5 | >98% |  |
| Verteporfin, also known as Benzoporphyrin derivative monoacid ring A or BPD-MA, is a | ||||