编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
24014 | Zelasudil | 2365193-22-0 | ≧98.0% | |
Zelasudil 是一种有效的、高选择性的口服活性抑制剂,针对 Rho 相关 | ||||
24013 | Ziftomenib ( KO-539 ) | 2134675-36-6 | ≧98.0% | |
Ziftomenib 是一种口服、有效、选择性的小分子抑制剂,针对 menin 和 | ||||
24012 | Zunsemetinib | 1640282-42-3 | ≧98.0% | |
Zunsemetinib是一种在研口服丝裂原活化蛋白激酶活化蛋白激酶2(MK2 | ||||
24011 | Zongertinib ( BI 1810631 ) | 2728667-27-2 | ≧98.0% | |
Zongertinib [BI 1810631] 是一种人表皮生长因子受体 2 (HER2) 抑制剂。 | ||||
24010 | Zasocitinib | 2272904-53-5 | ≧98.0% | |
Zasocitinib是一种作用于非受体酪氨酸蛋白激酶 (TYK2)靶点的抑制 | ||||
20657 | Zilurgisertib | 2173389-57-4 | ≧98.0% | |
Zilurgisertib(之前称为 INCB 00928)是一种激活素受体样激酶 2(ALK2, | ||||
20651 | Zatolmilast | 1606974-33-7 | 98% Min. | |
Zatolmilast is a phosphodiesterase IV inhibitor. | ||||
20628 | Zagociguat | 2201048-82-8 | 98% Min. | |
Zagociguat is a guanylate cyclase activator. | ||||
20610 | Zavondemstat | 1851412-93-5 | ≧98.0% | |
Zavondemstat 是一种 KDM4 抑制剂,具有抗肿瘤药物的潜力。 | ||||
20567 | 1Z105 | 1438280-73-9 | 98% Min. | |
1Z105 is a TLR4/MD2 ligand, significantly reducing the IL-6 secretion by subsequent c | ||||
20524 | Zidesamtinib ( NVL-520 ) | 2739829-00-4 | ≧98.0% | |
Zidesamtinib ( NVL-520 ) 是一种新型脑渗透性 ROS1 选择性酪氨酸激酶抑 | ||||
20513 | ZINC40099027 (ZN27) | 1211825-25-0 | ≧98.0% | |
ZINC40099027 (ZN27) 是一种特异性粘着斑激酶 (FAK) 激活剂,可促进缺血 | ||||
20446 | Zagociguat | 2201048-82-8 | 98% Min. | |
Zagociguat is a guanylate cyclase activator. | ||||
20416 | N-苄氧羰基-L-丙氨酸 N-羟基琥珀酰亚胺酯 | 3401-36-3 | 98% Min. | |
20318 | Zotizalkib ( TPX-0131 ) | 2648641-36-3 | ≧98.0% | |
TPX-0131是下一代 ALK 抑制剂候选药物,目前正在我们针对 ALK+ 晚期 | ||||
20317 | Zipalertinib | 1661854-97-2 | 98% Min. | |
Zipalertinib, also known as TAS6417, CLN-081, is a Novel EGFR Inhibitor Targeting Exo | ||||
20301 | ZZW-115 | 801991-87-7 | 98% Min. | |
ZZW-115is a potent NUPR1 inhibitor. ZZW-115 induces ferroptosis in a mitochondria-dep | ||||
2071629 | (3Z)-5-bromo-3-[(3-bromo-4,5-dihydroxyphenyl)methylidene]-1H-indol-2-one | 486443-73-6 | 98% Min. | |
LC3-mHTT-IN-AN1 (Compound AN1) is amHTT-LC3linker compound, which interacts with both | ||||
2071513 | ZK824859 | 2254001-81-3 | 98% Min. | |
ZK824859 is a potent uPA inhibitor as a potential treatment for multiple sclerosis. Z | ||||
193281 | ZL0454 | 2229042-77-5 | >98% | |
ZL0454是一种有效的选择性BRD4抑制剂。ZL0454减少气道炎症,抑制TLR3- | ||||
19352 | ZM223 | 2031177-48-5 | >98% | |
ZM223是一种新型非磺胺NEDD8激活酶抑制剂,对HCT116结肠癌细胞具有 | ||||
181233 | Z944 | 1199236-64-0 | >98% | |
Z944是一种T型钙通道拮抗剂,有望用于疼痛的治疗。Z944对癫痫大鼠 | ||||
189271 | Zamicastat | 1080028-80-3 | >98% | |
Zamicastat是一个强有力的和选择性的多巴胺β-mono-oxygenase抑制剂。 | ||||
185186 | 扎达维林 | 101975-10-4 | >98% | |
扎达维林是一种磷酸二酯酶3/4抑制剂。 | ||||
18577 | Zanubrutinib | 1691249-45-2 | >98% | |
Zanubrutinib,也称为BGB-3111, 是一种有效且高选择性的小分子BTK抑制 | ||||
183213 | methyl 2-(4-(hydroxymethyl)phenyl)acetate | 155380-11-3 | >96% | |
Methyl 2-(4-(hydroxymethyl)phenyl)acetate is a drug Intermediate. | ||||
183212 | 2-(4-(Hydroxymethyl)phenyl)acetic acid | 73401-74-8 | >96% | |
2-(4-(Hydroxymethyl)phenyl)acetic acid is a drug Intermediate. | ||||
183211 | 4-(Bromomethyl)phenylacetic acid | 13737-36-5 | >96% | |
4-(Bromomethyl)phenylacetic acid is a drug Intermediate. | ||||
1712151 | GBR-12935 free base | 76778-22-8 | >98% | |
GBR-12935 is a piperazine derivative which is a potent and selective dopamine reuptak | ||||
1712142 | Etifoxine HCl | 56776-32-0 | >98% | |
Etifoxine, also known as HOE 36801 and etafenoxine, is an anxiolytic and anticonvulsa |