Cas Index 4

402957-28-2 | Telaprevir (Catalog# : 121423)Telaprevir is a potent, selective, peptidomimetic inhibitor of the hepatitis C virus
454713-13-4 | tert-butyl N-[(3R)-1-benzylpiperidin-3-yl]carbamate (Catalog# : 83118)Coming soon!
475272-55-0 | Tert-butyl (3S)-3-benzylpiperazine-1-carboxylate (Catalog# : 81904)Coming soon!
442908-10-3 | Vipadenant (Catalog# : 010436)Vipadenant is an adenosine A2a antagonist with Ki of 1.3 nM; less potent for A1(Ki=69
433967-28-3 | VU 0357121 (Catalog# : 122206)VU0357121 is a novel positive and highly selective allosteric modulator (PAM) of mGlu
443913-73-3 | Vandetanib (Catalog# : 52821)Vandetanib (ZD6474) is a potent inhibitor of VEGFR2 with IC50 of 40 nM.
440122-66-7 | WAY200070 (Catalog# : 12249)WAY200070 is a selective ERβ receptor agonist that displays 68-fold selectivity over
4506-66-5 | Y15 hydrochloride (Catalog# : 17030112)Y15 hydrochloride, also known as FAK Inhibitor 14, is a direct FAK autophosphorylatio
486443-73-6 | (3Z)-5-bromo-3-[(3-bromo-4,5-dihydroxyphenyl)methylidene]-1H-indol-2-one (Catalog# : 2071629)LC3-mHTT-IN-AN1 (Compound AN1) is amHTT-LC3linker compound, which interacts with both
49671-76-3 | ZLN005 (Catalog# : 16122852)ZLN005 is a PGC-1 Transcriptional Regulator, which shoed some beneficialfEffects on d
475110-96-4 | ZSTK474 (Catalog# : 160926006)Combination treatment using X-rays then ZSTK474 given orally for 8 days, starting 2

1898206-17-1 | Safusidenib (Catalog# : 25149)Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
2803470-63-3 | HC-7366 (Catalog# : 25076)HC-7366 is a potent and selective activator of the general control nonderepressible 2
2377000-84-3 | Dencatistat (Catalog# : 25177)Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
146426-40-6 | Flavopiridol ( Alvocidib ) (Catalog# : 237071)Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
2201056-66-6 | AG-270 (Catalog# : 25176)MAT2A Inhibitor AG-270 is an orally available small molecule inhibitor of methionine
618913-30-7 | AZD-5904 (Catalog# : 181121)AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590
2035010-37-6 | ALT-007 (Catalog# : 25157)ALT-007 is an orally bioavailable SPT inhibitor that is more potent than myriocin, sa
1633666-49-5 | Nizubaglustat ( Synonyms: AZ-3102 ) (Catalog# : 25175)Nizubaglustat (AZ-3102) is an oral small molecule which inhibits glucosylceramide syn
2736508-60-2 | Catadegbrutinib (Synonyms: BGB-16673; BTK-IN-29) (Catalog# : 25174)
209733-45-9 | Anatibant (Synonyms: LF 16-0687; XY-2405) (Catalog# : 25173)

Search By Initial