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产品目录

编号化学名称Cas号纯度化学结构
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
20617Adrixetinib2394874-66-798% 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
205631,1'-Azobis(formamide)123-77-398% Min.
1,1'-Azobis(formamide) has been shown to have the ability to induce asthma and sk
20552Adaptaquin385786-48-198% Min.
Adaptaquin is a hydroxyquinoline inhibitor of HIF-PHD enzymes. Adaptaquin reduces neu
20540Atrasentan173937-91-298% Min.
Atrasentan, also known as ABT-627, is a orally available ETA receptor antagonist with
20535Arazasetron2025360-90-998% Min.
Arazasetron is an antiemetic which acts as a 5-HT3 receptor antagonist, pKi = 9.27.
20532AZD474798% Min.
AZD4747 is a Potent and Selective Inhibitor of Mutant GTPase KRASG12C with Demonstrab
205153-氨基-3-(4-氯苯基)丙酸19947-39-898% Min.
20508AZD59912143061-81-6≧98.0%
AZD-5991 是一种有效的选择性 Mcl-1 抑制剂。
20507ASLAN0031035688-66-498% Min.
ASLAN003 is an orally active and potent inhibitor of DHODH (Human Dihydroorotate Dehy
237072AZD00952750001-23-9≧98.0%
AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
20502Alentemol HBr112892-51-098% Min.
Alentemol, also known as U-66444B and alentamol, is a selective dopamine autoreceptor
20501Alfacalcidol41294-56-898% Min.
Alfacalcidol is an active metabolite of Vitamin D, which performs important functions
20490AG-7404343565-99-198% Min.
AG-7404 is a potent protease inhibitor with Anti-poliovirus activity. AG-7404 was act
20476AZD57182041075-86-798% Min.
AZD5718 is a novel Inhibitor of 5-Lipoxygenase Activating Protein(FLAP) for Treatment
20450ALZ-8011034190-08-398% Min.
ALZ-801 is an oral, small-molecule inhibitor of beta amyloid (Aβ) oligomer formation
20440AZD-2207866598-45-098% Min.
AZD-2207 is a cannabinoid receptor CB1 antagonist and highly lipophilic compound for
20439AZD6703851845-37-998% Min.
AZD6703 is a potent, selective and reversible orally bioavailable inhibitor of p38 mi
20429Afizagabar1398496-82-698% Min.
Afizagabar, also known as S44819 and Egis 13529, is a GABA receptor antagonist.
20427N'-(1H-苯并咪唑-2-甲基)-N'-((S)-5,6,7,8-四氢喹啉-8-基)丁烷-1,4-二胺558447-26-098% Min.
1714531-(6-氨基吡啶-2-基)乙-1-酮1060801-23-1≧98.0%
1-(6-氨基吡啶-2-基)乙-1-酮, CAS 1060801-23-1.
171553Anle138b882697-00-9≧98.0%
Anle138b 是一种口服的、可透过血脑屏障的蛋白质抑制剂。在 α-突
204252-吗啉基-3-溴-5-氨基吡啶1215932-56-198% Min.
204242-氨基-5-溴-3-氰基-4-甲氧基吡啶951884-75-698% Min.
204214-氨基-6-碘嘧啶53557-69-098% Min.