Products

Catalog No	Chemical Name	CAS Number	Purity
25194	VT-3989	2506273-81-8	≧98.0%
VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran
25166	Vepafestinib ( Synonyms: TAS0953 ; HM06)	2129515-96-2	≧98.0%
Vepafestinib, also known as HM06 and TAS0953, is a RET-selective inhibitor with enhan
25142	Vicadrostat	1868065-21-7	98% Min.
Vicadrostat is an aldosterone synthase inhibitor.
25047	Vimseltinib free base	1628606-05-2	98% Min.
Vimseltinib, also known as DCC-3014, is a potent and orally active inhibitor of the t
24159	VU-29	890764-36-0	98% Min.
VU 29 is a potent allosteric potentiator at the rat mGlu5 receptor (EC50 = 9 nM); bin
24154	VK-28	312611-92-0	98% Min.
VK-28, a brain-permeable iron chelator, inhibits both basal and Fe/ascorbate-induced
24110	VVD-130037 ( BAY-3605349 )	3034880-93-5	≧98.0%
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
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%
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