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Cas Index 1

• 1027847-67-1 | AMG-009 (Catalog# : 17987)AMG 009 is an orally active, small molecule CRTH2 (chemoattractant receptor-homologou
• 1426136-04-0 | 5-amino-2-fluoro-4-methylbenzonitrile (Catalog# : 1781603)5-amino-2-fluoro-4-methylbenzonitrile 
• 1434141-67-9 | 2-azaspiro[3.5]nonan-7-ol hydrochloride (Catalog# : 1781602)2-azaspiro[3.5]nonan-7-ol hydrochloride
• 1609281-86-8 | AZD3264 (Catalog# : 178910)AZD3264 is a novel and small molecule IKK2 inhibitor.IKK2 serves as a protein subunit
• 1240308-45-5 | A-971432 (Catalog# : 178816)A‑971432 is highly selective for S1P5 and has excellent plasma and CNS exposure aft
• 1221443-94-2 | A-1165442 (Catalog# : 20178812)A-1165442 is a temperature-neutral transient receptor potential vanilloid-1 (TRPV1) a
• 1375466-18-4 | ACY-775 (Catalog# : 77821)ACY-775 is a potent and selective HDAC6 inhbiitor. ACY-775 inhibits HDAC6 with low na
• 1001404-83-6 | AAI-101 (Catalog# : 1773101)AAI101(AAI-101) is a novel extended-spectrum -lactamase inhibitor.The combination of
• 1196509-60-0 | AZD-7594 (Catalog# : 17022812)AZD-7594, also known as AZ13189620, is an inhaled selective glucocorticoid receptor (
• 1227163-56-5 | AZD3839 (Catalog# : 17022710)AZD3839 is a potent and selective BACE1 inhibitor. AZD3839 is clinical candidate for
• 1668553-26-1 | A-1210477 (Catalog# : 17022404)A-1210477 is a potent and selective MCL-1 inhibitor. A-1210477 induces the hallmarks
• 1383982-64-6 | AZD3293 (LY3314814) (Catalog# : 17021318)AZD3293, also known as LY3314814 is an oral beta-secretase 1 cleaving enzyme (BACE) 
• 1620576-64-8 | AZD-8835 (Catalog# : 102703)AZD8835 is a potent and selective inhibitor of PI3Kalpha and PI3Kdelata with excellen
• 1173900-37-2 | AZD6482 (S-isomer) (Catalog# : 17011901)AZD6482 is a potent, selective and ATP competitive PI3K inhibitor (IC(50) 0.01 μm).
• 1472624-85-3 | 7ACC2 (Catalog# : 17011302)7ACC2 is a potent MCT inhibitor. Monocarboxylate transporters (MCTs) catalyze the pro
• 1174043-16-3 | AZD-2461 (Catalog# : 16122863)AZD2461 is a novel and potent PARP inhibitor with lower affinity to P-glycoprotein. A
• 1557268-88-8 | Avitinib maleate (Catalog# : 16122862)Avitinib is an orally available, irreversible, epidermal growth factor receptor (EGFR
• 1192491-61-4 | Avibactam sodium (Catalog# : 16122861)Avibactam is a non--lactam -lactamase inhibitor antibiotic, which is a new drug appli
• 141396-28-3 | Argatroban (Catalog# : 16122858)Argatroban is an anticoagulant that is a direct thrombin inhibitor. Argatroban was ap
• 1442684-77-6 | AM-2394 (Catalog# : 16122855)AM-2394 is a potent and selective Glucokinase agonist (GKA), which catalyzes the phos
• 1047645-82-8 | Afuresertib HCl (Catalog# : 161227116)Afuresertib, also known as GSK2110183, is an orally bioavailable inhibitor of the ser
• 1375465-91-0 | ACY-738 (Catalog# : 161227114)ACY-738 is a potent and selective HDAC6 inhibitor with improved brain bioavailability
• 182167-02-8 | Acolbifene (Catalog# : 161227113)Acolbifene, also known as EM-652, or SCH-57068, is a selective estrogen receptor modu
• 1762-34-1 | Abametapir (Catalog# : 161227111)Abametapir is the active ingredient of Xeglyze Lotion. Abametapir inhibits metallopro
• 106566-58-9 | AS101 (Catalog# : 161227106)AS101, a potent in vitro and in vivo immunomodulator, is a novel inhibitor of IL-1bet
• 1420477-60-6 | ACP-196 (Catalog# : 16122783)Acalabrutinib is a selective second-generation Brutons tyrosine kinase (BTK) inhibito
• 1527503-11-2 | A-366 (Catalog# : 16122743)A-366 is a potent and selective G9a/GLP histone lysine methyltransferase inhibitor wi
• 1821428-35-6 | AZD0156 (Catalog# : 16122713)AZD0156 is a potent and selective inhibitors of ATM kinase, with potential chemo-/rad
• 1189904-01-5 | Acetazolamide D3 (Catalog# : 6111513)Acetazolamide D3 is deuterium labeled Acetazolamide, which is a potent carbonic anhyd
• 152918-26-8 | AB-MECA (Catalog# : 6111105)AB-MECA is a high affinity A3 adenosine receptor agonist, has high affinity for recom