Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 1710161 | AZD-5153 HNT salt | 1869912-40-2 | >98% |  |
| AZD-5153 HNT salt, is a 6-hydroxy-2-naphthoic acid salt of AZD-5153.AZD5153 is highly | ||||
| 1710131 | ABT-100 | 450839-40-4 | >98% |  |
| ABT-100 is an orally bioavailable farnesyltransferase inhibitor. | ||||
| 179159 | Acebilustat | 943764-99-6 | 98.0% |  |
| Acebilustat, also known as ZK322, is a potent and selective leukotriene A4 hydrolase | ||||
| 179158 | AR-7 | 80306-38-3 | 98.0% |  |
| AR-7, also known as Atypical retinoid 7 , is a potent and selective enhancer of the c | ||||
| 179151 | Adelmidrol | 1675-66-7 | 98.0% |  |
| Adelmidrol is the semisynthetic diethanolamide derivative of azelaic acid, and has a | ||||
| 179136 | AZD7545 | 252017-04-2 | 98.0% |  |
| AZD7545 is an inhibitor of pyruvate dehydrogenase kinase 2 (PDHK2) (IC50 value of 6.4 | ||||
| 179117 | AMG-9810 | 545395-94-6 | 98.0% |  |
| AMG 9810 is a competitive antagonist of capsaicin activation of the vanilloid recepto | ||||
| 179832 | AS-2444697 HCl | 1287665-60-4 | 98.0% |  |
| AS-2444697 is a RAK-4 inhibitor. Six weeks' repeated administration of AS2444697 (0.3 | ||||
| 179829 | Acecainide HCl | 34118-92-8 | 98.0% |  |
| Acecainide, also known as N-acetylprocainamide and ASL 601, is the N-acetylated metab | ||||
| 179816 | ASC-J9 | 52328-98-0 | 98.0% |  |
| <span style="color:#34495E;font-family:"font-size:14px;background-color: | ||||
| 17987 | AMG-009 | 1027847-67-1 | 98.0% |  |
| AMG 009 is an orally active, small molecule CRTH2 (chemoattractant receptor-homologou | ||||
| 1781603 | 5-amino-2-fluoro-4-methylbenzonitrile | 1426136-04-0 | 98.0% |  |
| 5-amino-2-fluoro-4-methylbenzonitrile | ||||
| 1781602 | 2-azaspiro[3.5]nonan-7-ol hydrochloride | 1434141-67-9 | 96.0% |  |
| 2-azaspiro[3.5]nonan-7-ol hydrochloride | ||||
| 178910 | AZD3264 | 1609281-86-8 | 98.0% |  |
| AZD3264 is a novel and small molecule IKK2 inhibitor.IKK2 serves as a protein subunit | ||||
| 178816 | A-971432 | 1240308-45-5 | 98.0% |  |
| A‑971432 is highly selective for S1P5 and has excellent plasma and CNS exposure aft | ||||
| 20178812 | A-1165442 | 1221443-94-2 | 98.0% |  |
| A-1165442 is a temperature-neutral transient receptor potential vanilloid-1 (TRPV1) a | ||||
| 20178710 | AZD4205 | 2091134-35-7 | 98.0% |  |
| AZD4205 is a highly potent JAK1-selective kinase inhibitor with excellent preclinical | ||||
| 77821 | ACY-775 | 1375466-18-4 | 98.0% by HPLC |  |
| ACY-775 is a potent and selective HDAC6 inhbiitor. ACY-775 inhibits HDAC6 with low na | ||||
| 1773101 | AAI-101 | 1001404-83-6 | 98.0% |  |
| AAI101(AAI-101) is a novel extended-spectrum -lactamase inhibitor.The combination of | ||||
| 17030105 | AV-412 Tosylate | 451493-31-5 | 98% |  |
| AV-412, also known as MP-412, is a second-generation, orally bioavailable dual kinase | ||||
| 17022812 | AZD-7594 | 1196509-60-0 | 98% |  |
| AZD-7594, also known as AZ13189620, is an inhaled selective glucocorticoid receptor ( | ||||
| 17022710 | AZD3839 | 1227163-56-5 | 98% |  |
| AZD3839 is a potent and selective BACE1 inhibitor. AZD3839 is clinical candidate for | ||||
| 17022404 | A-1210477 | 1668553-26-1 | 98% | |
| A-1210477 is a potent and selective MCL-1 inhibitor. A-1210477 induces the hallmarks | ||||
| 17022301 | Apatinib | 811803-05-1 | 98% |  |
| Apatinib is an orally bioavailable, selective VEGFR2 inhibitor with IC50 of 1 nM. | ||||
| 17021407 | Amikacin sulfate | 39831-55-5 | 98% |  |
| Amikacin sulfate(BAY416651 sulfate) is a semi-synthetic aminoglycoside antibiotic der | ||||
| 17021406 | AFN-1252 | 620175-39-5 | 98% |  |
| AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (F | ||||
| 17021318 | AZD3293 (LY3314814) | 1383982-64-6 | 98% | |
| AZD3293, also known as LY3314814 is an oral beta-secretase 1 cleaving enzyme (BACE) | ||||
| 17021316 | APR-246 (PRIMA-1MET) | 5291-32-7 | 98% | -cas-5291-32-7.png) |
| APR-246, also known as PRIMA-1MET, is a small organic molecule that has been shown to | ||||
| 102703 | AZD-8835 | 1620576-64-8 | ≧98.0% |  |
| AZD8835 is a potent and selective inhibitor of PI3Kalpha and PI3Kdelata with excellen | ||||
| 17011901 | AZD6482 (S-isomer) | 1173900-37-2 | 98% | -cas-1173900-37-2.png) |
| AZD6482 is a potent, selective and ATP competitive PI3K inhibitor (IC(50) 0.01 μm). | ||||