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产品目录

编号化学名称Cas号纯度化学结构
25071AT-0072170729-29-898% Min.
AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
25033Azeliragon603148-36-3≧98.0%
Azeliragon (TTP488) 是一种口服生物可利用的 AGE (RAGE) 受体小分子抑制
24152AKOS0376522562171065-77-198% Min.
AKOS037652256 can be used as a TRPML modulator for the treatment of diseases associat
24135AF-615122510-61-698% Min.
AF-615 is a novel Inhibitor of CDT1/Geminin Protein Complex, promoting DNA Damage and
24134AkaLumine HCl2558205-28-898% Min.
AkaLumine is a luciferin analogue. The bioluminescence produced by AkaLumine in react
24122Azenosertib2376146-48-298% Min.
Azenosertib, also known as ZN-c3, is a highly selective Wee1 inhibitor (ICV50 = 3.8 n
24114Arimoclomol citrate368860-21-398% Min.
Arimoclomol citrate is a heat shock protein amplifier potentially useful for the trea
24088ART-4462984543-29-398% Min.
24083AF-710B1235733-73-998% Min.
AF-710B is an agonist of sigma and M1 muscarinic receptors; AF710B is an enantiomer o
24070AZD-1656919783-22-598% Min.
AZD-1656 is a glucokinase (GK) activator potentially for the treatment of type 2 diab
24068Acoramidis hydrochloride2242751-53-5≧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
24063ABX-0022156649-32-898% Min.
24015ASX-1732748800-08-8≧98.0%
ASX-173 是一种抑制天冬酰胺合成酶 (ASNS) 活性的化合物。
24051Aldoxorubicin hydrochloride1361563-03-298% Min.
Aldoxorubicin (INNO-206) hydrochloride is an albumin-binding proagent of Doxorubicin
24043AZD-54622787501-83-9≧98.0%
AZD5462 是 RXFP1 松弛素受体的小分子激动剂。
24041ASN-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
24036Aticaprant1174130-61-098% Min.
Aticaprant (CERC-501) is a potent and centrally-penetrantkappa opioidreceptor antagon
24026AMXT-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
20679AOH11602089314-57-698% Min.
AOH1160 is a potent oral small molecule proliferating cell nuclear antigen (PCNA) inh
20669AG-09/1356776-32-498% Min.
AG-09/1 is a specific formyl peptide receptor 1 (FPR1) agonist.
24018AM-97472691869-82-4≧98.0%
AM-9747 是一种 MTA 协同 PRMT5 抑制剂。 AM-9747 选择性抑制 HCT116 MTAP 缺
24017AMG-1932790567-82-598.62%; 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
20664ADT-0071945941-09-298% Min.
ADT-007 is a potent and orally active pan-RAS inhibitor with strong anticancer effect
24009Asengeprast (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
20648AZD79861802148-05-598% Min.
Brensocatib, also known as AZD7986, INS 1007, is an oral reversible inhibitor of dipe
20638ATH434 mesylate2387898-69-1≧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
20617Adrixetinib ( Q-702 )2394874-66-798% Min.
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag
20616Alpibectir2285440-39-198% Min.
Alpibectir is an antibacterial agent.
20609ARV-4712229711-68-498% Min.
20574ABI-2311332881-26-1(free base)98% Min.
ABI-231 is a potent, orally bioavailable tubulin inhibitor that interacts with the co