编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
25071 | AT-007 | 2170729-29-8 | 98% Min. | ![]() |
AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in | ||||
25033 | Azeliragon | 603148-36-3 | ≧98.0% | ![]() |
Azeliragon (TTP488) 是一种口服生物可利用的 AGE (RAGE) 受体小分子抑制 | ||||
24152 | AKOS037652256 | 2171065-77-1 | 98% Min. | ![]() |
AKOS037652256 can be used as a TRPML modulator for the treatment of diseases associat | ||||
24135 | AF-615 | 122510-61-6 | 98% Min. | ![]() |
AF-615 is a novel Inhibitor of CDT1/Geminin Protein Complex, promoting DNA Damage and | ||||
24134 | AkaLumine HCl | 2558205-28-8 | 98% Min. | ![]() |
AkaLumine is a luciferin analogue. The bioluminescence produced by AkaLumine in react | ||||
24122 | Azenosertib | 2376146-48-2 | 98% Min. | ![]() |
Azenosertib, also known as ZN-c3, is a highly selective Wee1 inhibitor (ICV50 = 3.8 n | ||||
24114 | Arimoclomol citrate | 368860-21-3 | 98% Min. | ![]() |
Arimoclomol citrate is a heat shock protein amplifier potentially useful for the trea | ||||
24088 | ART-446 | 2984543-29-3 | 98% Min. | ![]() |
24083 | AF-710B | 1235733-73-9 | 98% Min. | ![]() |
AF-710B is an agonist of sigma and M1 muscarinic receptors; AF710B is an enantiomer o | ||||
24070 | AZD-1656 | 919783-22-5 | 98% Min. | ![]() |
AZD-1656 is a glucokinase (GK) activator potentially for the treatment of type 2 diab | ||||
24068 | Acoramidis hydrochloride | 2242751-53-5 | ≧98.0% | ![]() |
Acoramidis是一种口服、强效、高选择性小分子转甲状腺素蛋白(TTR | ||||
24063 | ABX-002 | 2156649-32-8 | 98% Min. | ![]() |
24015 | ASX-173 | 2748800-08-8 | ≧98.0% | ![]() |
ASX-173 是一种抑制天冬酰胺合成酶 (ASNS) 活性的化合物。 | ||||
24051 | Aldoxorubicin hydrochloride | 1361563-03-2 | 98% Min. | ![]() |
Aldoxorubicin (INNO-206) hydrochloride is an albumin-binding proagent of Doxorubicin | ||||
24043 | AZD-5462 | 2787501-83-9 | ≧98.0% | ![]() |
AZD5462 是 RXFP1 松弛素受体的小分子激动剂。 | ||||
24041 | ASN-90 ( ASN-120290, FNP-223 ) | 2129093-74-7 | ≧98.0% | ![]() |
ASN-90 (ASN-120290、FNP-223) 是一种口服、脑渗透性 O-GlcNAcase 酶小分子 | ||||
24036 | Aticaprant | 1174130-61-0 | 98% Min. | ![]() |
Aticaprant (CERC-501) is a potent and centrally-penetrantkappa opioidreceptor antagon | ||||
24026 | AMXT-1501 ( AMX-513 ) | 441022-64-6 | ≧98.0% | ![]() |
AMXT-1501 ( AMX-513 )是一种新型多胺转运系统抑制剂。 AMXT1501 可以阻 | ||||
20679 | AOH1160 | 2089314-57-6 | 98% Min. | ![]() |
AOH1160 is a potent oral small molecule proliferating cell nuclear antigen (PCNA) inh | ||||
20669 | AG-09/1 | 356776-32-4 | 98% Min. | |
AG-09/1 is a specific formyl peptide receptor 1 (FPR1) agonist. | ||||
24018 | AM-9747 | 2691869-82-4 | ≧98.0% | ![]() |
AM-9747 是一种 MTA 协同 PRMT5 抑制剂。 AM-9747 选择性抑制 HCT116 MTAP 缺 | ||||
24017 | AMG-193 | 2790567-82-5 | 98.62%; EE 98.28% | ![]() |
AMG-193是安进公司开发的一种口服小分子甲硫腺苷协同PRMT5酶抑制剂 | ||||
20664 | ADT-007 | 1945941-09-2 | 98% Min. | |
ADT-007 is a potent and orally active pan-RAS inhibitor with strong anticancer effect | ||||
24009 | Asengeprast (FT011) | 1001288-58-9 | ≧98.0% | ![]() |
Asengeprast (FT011) 是一种抗纤维化剂,降低胶原蛋白 I 和 III 的 mRNA | ||||
20648 | AZD7986 | 1802148-05-5 | 98% Min. | ![]() |
Brensocatib, also known as AZD7986, INS 1007, is an oral reversible inhibitor of dipe | ||||
20638 | ATH434 mesylate | 2387898-69-1 | ≧98.0% | ![]() |
ATH434 是一种口服药物,旨在抑制与神经变性有关的病理蛋白的聚 | ||||
20617 | Adrixetinib ( Q-702 ) | 2394874-66-7 | 98% Min. | ![]() |
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag | ||||
20616 | Alpibectir | 2285440-39-1 | 98% Min. | ![]() |
Alpibectir is an antibacterial agent. | ||||
20609 | ARV-471 | 2229711-68-4 | 98% Min. | ![]() |
20574 | ABI-231 | 1332881-26-1(free base) | 98% Min. | ![]() |
ABI-231 is a potent, orally bioavailable tubulin inhibitor that interacts with the co |