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Name Index A

• AR-7 (Catalog# : 179158, Cas# : 80306-38-3)AR-7, also known as Atypical retinoid 7 , is a potent and selective enhancer of the c
• Adelmidrol (Catalog# : 179151, Cas# : 1675-66-7)Adelmidrol is the semisynthetic diethanolamide derivative of azelaic acid, and has a
• AZD7545 (Catalog# : 179136, Cas# : 252017-04-2)AZD7545 is an inhibitor of pyruvate dehydrogenase kinase 2 (PDHK2) (IC50 value of 6.4
• AMG-9810 (Catalog# : 179117, Cas# : 545395-94-6)AMG 9810 is a competitive antagonist of capsaicin activation of the vanilloid recepto
• AS-2444697 HCl (Catalog# : 179832, Cas# : 1287665-60-4)AS-2444697 is a RAK-4 inhibitor. Six weeks' repeated administration of AS2444697 (0.3
• Acecainide HCl (Catalog# : 179829, Cas# : 34118-92-8)Acecainide, also known as N-acetylprocainamide and ASL 601, is the N-acetylated metab
• ASC-J9 (Catalog# : 179816, Cas# : 52328-98-0)<span style="color:#34495E;font-family:"font-size:14px;background-color:
• AMG-009 (Catalog# : 17987, Cas# : 1027847-67-1)AMG 009 is an orally active, small molecule CRTH2 (chemoattractant receptor-homologou
• 5-amino-2-fluoro-4-methylbenzonitrile (Catalog# : 1781603, Cas# : 1426136-04-0)5-amino-2-fluoro-4-methylbenzonitrile 
• 2-azaspiro[3.5]nonan-7-ol hydrochloride (Catalog# : 1781602, Cas# : 1434141-67-9)2-azaspiro[3.5]nonan-7-ol hydrochloride
• AZD3264 (Catalog# : 178910, Cas# : 1609281-86-8)AZD3264 is a novel and small molecule IKK2 inhibitor.IKK2 serves as a protein subunit
• A-971432 (Catalog# : 178816, Cas# : 1240308-45-5)A‑971432 is highly selective for S1P5 and has excellent plasma and CNS exposure aft
• A-1165442 (Catalog# : 20178812, Cas# : 1221443-94-2)A-1165442 is a temperature-neutral transient receptor potential vanilloid-1 (TRPV1) a
• AZD4205 (Catalog# : 20178710, Cas# : 2091134-35-7)AZD4205 is a highly potent JAK1-selective kinase inhibitor with excellent preclinical
• ACY-775 (Catalog# : 77821, Cas# : 1375466-18-4)ACY-775 is a potent and selective HDAC6 inhbiitor. ACY-775 inhibits HDAC6 with low na
• AAI-101 (Catalog# : 1773101, Cas# : 1001404-83-6)AAI101(AAI-101) is a novel extended-spectrum -lactamase inhibitor.The combination of
• AV-412 Tosylate (Catalog# : 17030105, Cas# : 451493-31-5)AV-412, also known as MP-412, is a second-generation, orally bioavailable dual kinase
• AZD-7594 (Catalog# : 17022812, Cas# : 1196509-60-0)AZD-7594, also known as AZ13189620, is an inhaled selective glucocorticoid receptor (
• AZD3839 (Catalog# : 17022710, Cas# : 1227163-56-5)AZD3839 is a potent and selective BACE1 inhibitor. AZD3839 is clinical candidate for
• A-1210477 (Catalog# : 17022404, Cas# : 1668553-26-1)A-1210477 is a potent and selective MCL-1 inhibitor. A-1210477 induces the hallmarks
• Apatinib (Catalog# : 17022301, Cas# : 811803-05-1)Apatinib is an orally bioavailable, selective VEGFR2 inhibitor with IC50 of 1 nM.
• Amikacin sulfate (Catalog# : 17021407, Cas# : 39831-55-5)Amikacin sulfate(BAY416651 sulfate) is a semi-synthetic aminoglycoside antibiotic der
• AFN-1252 (Catalog# : 17021406, Cas# : 620175-39-5)AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (F
• AZD3293 (LY3314814) (Catalog# : 17021318, Cas# : 1383982-64-6)AZD3293, also known as LY3314814 is an oral beta-secretase 1 cleaving enzyme (BACE) 
• APR-246 (PRIMA-1MET) (Catalog# : 17021316, Cas# : 5291-32-7)APR-246, also known as PRIMA-1MET, is a small organic molecule that has been shown to
• AZD-8835 (Catalog# : 102703, Cas# : 1620576-64-8)AZD8835 is a potent and selective inhibitor of PI3Kalpha and PI3Kdelata with excellen
• AZD6482 (S-isomer) (Catalog# : 17011901, Cas# : 1173900-37-2)AZD6482 is a potent, selective and ATP competitive PI3K inhibitor (IC(50) 0.01 μm).
• 7ACC2 (Catalog# : 17011302, Cas# : 1472624-85-3)7ACC2 is a potent MCT inhibitor. Monocarboxylate transporters (MCTs) catalyze the pro
• AZD-5597 (Catalog# : 16122865, Cas# : 924641-59-8)AZD-5597 is potent CDK inhibitor with in vitro anti-proliferative effects against a r
• AZD-5069 (Catalog# : 16122864, Cas# : 878385-84-3)AZD-5069 is a potent and selective CXCR2 antagonist with the potential to inhibit neu