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Cas Index 3

• 329932-55-0 | FM19G11 (Catalog# : 192211)FM19G11 is an inhibitor of Hypoxia Inducible Factors α (HIFα), reported to affect s
• 347174-05-4 | Ferrostatin-1 (Catalog# : 184210)Ferrostatin-1 (fe -1)是一种亲脂的抗氧化剂，有效地阻断了铁蛋白的形
• 38398-32-2 | Ganaxolone (Catalog# : 20630)Ganaxolone, also known as CCD 1042 and C1042, is a CNS-selective GABAA modulator that
• 3459-20-9 | Glymidine sodium (Catalog# : 20295)Glymidine sodium is a sulfonamide hypoglycemic agent which stimulates insulin secreti
• 306974-70-9 | GW1100 (Catalog# : 1811231)GW1100 is a a selective antagonist of GPR40.
• 317318-84-6 | GW0742 (Catalog# : 1791110)GW0742, also known as GW610742 and GW0742X is a PPARδ/β agonist. GW0742 Induces Ear
• 307983-31-9 | GRA Ex-25 (Catalog# : 17030701)GRA Ex-25 is an inhibitor of glucagon receptor. Inhibiting the interaction between gl
• 349085-82-1 | GSK137647A (Catalog# : 16123010)GSK137647A is an agonist of the free fatty acid receptor 4 (FFA4/GPR120) with pEC50s
• 328541-79-3 | GlyH-101 (Catalog# : 16123006)GlyH-101 is a CFTR inhibitor (cystic fibrosis transmembrane conductance regulator). G
• 317318-70-0 | GW501516 (Catalog# : 030905)Coming soon!
• 379270-37-8 | GS-7340 (Catalog# : 52611)GS-7340(Tenofovir alafenamide) is a prodrug of tenofovir (TFV) that more efficiently
• 3034479-99-4 | HC-5404-FU (Catalog# : 24112)HC-5404-FU is a novel, highly selective and potent PERK inhibitor.
• 34604-60-9 | 5-hydroxypyrazine-2-carboxylic acid (Catalog# : 17021403)5-hydroxypyrazine-2-carboxylic acid , a metabolite of anti-tuberculosis drug pyrazina
• 35354-74-6 | Honokiol (Catalog# : 161009024)Houpu has traditionally been used in Eastern medicine as analgesic and to treat anxie
• 338454-14-1 | 1H-Indazole-5-boronic acid (Catalog# : 032503)Coming soon!
• 388116-27-6 | indole-4-boronic acid pinacol ester (Catalog# : 21253)indole-4-boronic acid pinacol ester, CAS 388116-27-6, is an important intermeidate.
• 331862-41-0 | IMR-1A (Catalog# : 6111507)IMR-1A is the metabolite of IMR-1. IMR-1 is a novel class of Notch inhibitors targeti
• 371242-69-2 | IC-87114 (Catalog# : 160926004)It Inhibits p110, p110 and p110 only at much higher concentrations. It does not inhib
• 325715-02-4 | Indiplon (Catalog# : 102701)Indiplon is a pyrazolopyrimidine that acts as a high-affinity positive allosteric mod
• 313553-47-8 | INH1 (Catalog# : 102606)INH1 is a small molecule targeting the Hec1/Nek2 mitotic pathway suppresses tumor cel
• 336113-53-2 | Ispinesib (Catalog# : 52747)Ispinesib (SB-715992) is a potent, specific and reversible inhibitor of KSP (HsEg5) w
• 36945-98-9 | Icilin (Catalog# : 52561)Icilin(AG 3-5) is a synthetic super-agonist of TRPM8 ion channel.
• 309271-94-1 | Inauhzin (Catalog# : 52543)Inauhzin(INZ) is a novel small molecule that effectively reactivates p53 by inhibitin
• 314245-33-5 | IU1 (Catalog# : 51637)IU1 is a reversible and specific inhibitor of proteasome-associating Usp14. It does n
• 315705-75-0 | JNJ0966 (Catalog# : 193201)JNJ0966 is a highly selective allosteric inhibitor of matrix metalloproteinase-9 (MMP
• 383150-41-2 | JTE-013 (Catalog# : 184313)TE-013 is a potent, selective sphingosine-1-phosphate 2 (S1P2) receptor antagonist th
• 363571-83-9 | Kinesore (Catalog# : 193203)Kinesore is an activator of the function of kinesin-1 in controlling microtubule dyna
• 330676-02-3 | KH7 (Catalog# : 19362)KH7 is a novel Inhibitor of Soluble Adenylyl Cyclase (Sac).
• 342639-96-7 | KRIBB11 (Catalog# : 17031014)KRIBB11 abolishes the heat shock-induced luciferase activity with an IC50 of 1.2 M. I
• 355025-24-0 | Ki16425 (Catalog# : 61121)Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 wit