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产品目录

编号化学名称Cas号纯度化学结构
20631Vorasidenib1644545-52-798% Min.
Vorasidenib, also known as AG-881, is a potent and selective orally available inhibit
20612Valemetostat tosylayte1809336-93-398% Min.
Valemetostat, also known as DS-3201 is a potent, selective and orally active EZH1/2 i
205661V2091062444-54-598% Min.
1V209, also known as TLR7 agonist T7, is a novel Toll-like receptor 7 (TLR7) agonist,
20547Venglustat malate1629063-78-098% Min.
Venglustat, also known as Ibiglustat, GZ402671, GZ-452; Genz-682452 and SAR402671, is
20536VV1162647442-33-798% Min.
VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SA
20525VX-5482649467-58-198% Min.
20435Vacquinol-15428-80-898% Min.
Vacquinol-1, also known as NSC 13316, is an activator of MKK4-dependent macropinocyto
171423Visomitin (Synonyms: SKQ1)934826-68-3≧98.0%
Visomitin(别名:SKQ1)是一种线粒体靶向抗氧化剂。
G20377VTX-271321924-70-298% Min.
VTX-27 is a novel potent and selective PKCθ inhibitor.
822223Venglustat ( ibiglustat ) 1401090-53-6≧98.0%
Ibiglustat (Venglustat) 是一种具有口服活性的,可透过血脑屏障的葡萄
20302VAS3947869853-70-3≧98.0%
VAS3947 is a selective inhibitor of NADPH oxidase activity in low micromolar concentr
20299Venadaparib1681017-83-398% Min.
Venadaparib, also known as IDX-1197, is a potent, selective and orally active PARP in
20284Vatiquinone1213269-98-798% Min.
Vatiquinone, also known as EPI 743, is an orally bioavailable para-benzoquinone being
20112601Val-Cit-PAB-MMAE644981-35-198% Min.
Val-Cit-PAB-MMAE is a MMAE derivative with a cleavable linker, which is useful to mak
20111202VTP-504692169916-18-998% Min.
VTP-50469 is a novel, potent, selective, orally-available MeninMLL1 inhibitor, being
2071627 VU023844185511-68-898% Min.
2071548 VU02384291160247-92-698% Min.
VU0238429 is a selective positive allosteric modulator of M5 receptors (EC50 values a
2071547 VU011949879183-37-298% Min.
VU0119498 is a M1 muscarinic receptor agonist (EC50 = 3.1 μM) and pan mAChR M3, M5 p
2071543 Vonafexor1192171-69-998% Min.
Vonafexor, also known as EYP001, is a farnesoid X receptor agonist.
2071534VUN340022173134-00-298% Min.
VUN34002, also known as Vanin-1-IN-1 is an inhibitor of vanin-1 enzyme which is a cel
112091VAL-08323261-20-398% Min.
VAL-083 is a bi-functional alkylating agent, with potential antineoplastic activity.
19529Vesatolimod(GS-9620)1228585-88-398% Min.
DescriptionGS-9620 is a potent and selective orally active small molecule agonist ofT
193114Valecobulin1188371-47-2>98%
Valecobulin是一种抗肿瘤的β-微管蛋白聚合抑制剂。微管蛋白聚合抑
192154Vecabrutinib1510829-06-7>98%
Vecabrutinib,又名SNS-062;FP-182, BSK-4841, BIIB-062;是一种有效的,非共价
192141Valemetostat1809336-39-7>98%
Valemetostat是一种抗肿瘤药物。
1812285Verdiperstat890655-80-8>98%
Verdiperstat,又称AZD-3241,是一种选择性和不可逆的髓过氧化物酶抑
181253Vaborbactam 1360457-46-0>98%
Vaborbactam,也称为RPX7009, 是一种有效且具有选择性的β-内酰胺酶抑
1810151VU04632711391737-01-1>98%
VU0463271抑制协同转运蛋白KCC2。
18891Vafidemstat1357362-02-7>98%
Vafidemstat又称ORY 2001,是一种赖氨酸特异性组蛋白去甲基化酶(LSD1)
187201Verteporfin129497-78-5>98%
Verteporfin,也被称为苯卟啉衍生物A或BPD-MA,是一种苯卟啉衍生物,