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| 中文名称 | Indisulam |
|---|---|
| 中文别名 | N-(3-氯-1H-吲哚-7-基)-1,4-苯二磺酰胺;2-[N-(2-氰乙基)-4-[(2,6-二氯-4-硝基苯基)偶氮]苯胺基]乙酸乙酯 |
| 英文名称 | E7070; E 7070; E-7070; ER35744; ER 35744; ER-35744; D04522 |
| 英文别名 | Indisulam;N-(3-Chloro-1H-indol-7-yl)-1,4-benzenedisulfonamide;4-N-(3-chloro-1H-indol-7-yl)benzene-1,4-disulfonamide;1,4-Benzenedisulfonamide,N-(3-chloro-1H-indol-7-yl);E7070;Indisulam (IND);N-(3-chloro-1H-indol-7-yl)benzene-1,4-disulfonamide;N-(3-chloro-1H-indol-7-yl)-4-sulfamoylbenzenesulfonamide;N1-(3-Chloro-1H-indol-7-yl)-1,4-benzenedisulfonamide;E-7070;ER-35744;IndisulaM (E7070);IndisulaM (E7070) (ER-35744);N1-(3-Chloro-1H-indol-7-yl)benzene-1,4-disulfonamide;1,4-Benzenedisulfonamide, N-(3-chloro-1H-indol-7-yl)-;E 7070;WJ98J3NM90;N-(3-Chloro-1H-indol-7-yl)benzene-1,4disulfonamide;Indisulam (USAN/INN);N-(3-chl;INDISULAM;CS-0007710;FT-0740093;A904802;EF6;UNII-WJ98J3NM90;INDISULAM [WHO-DD];SB16544;indisulam (e7070);1-N-(3-chloro-1H-indol-7-yl)benzene-1,4-disulfonamide;indisulamum;INDISULAM [INN];Indisulam [USAN:INN:BAN];C14H12ClN3O4S2;HY-13650;1,4-BENZENEDISULFONAMIDE, N-(3-CHLORO-1H-INDOL-7-YL);165668-41-7;N(1)-(3-chloro-1H-indol-7-yl)benzene-1,4-disulfonamide;INDISULAM [USAN];C73201;Z2724205552;DB06370;1,4-Benzenedisulfonamide, N1-(3-chloro-1H-indol-7-yl)-;NS00068354;s9742;EN300-7378250;CHEMBL77517;N1-(3-chloro-1H-indol-7-yl)benzene-1,4-disulfonamide;GTPL7046;AKOS022181456;D04522;BCP06110;AS-69532;BDBM10890;CHEBI:145431;SCHEMBL91389;Q27078056;Indisulam, >=98% (HPLC);DTXSID50168008;n-(3-chloro-1h-indol-7-yl)-4-sulfamoylbenzenesulfonamide;INDISULAM [MI];AC-36646;N~1~-(3-chloro-1H-indol-7-yl)benzene-1,4-disulfonamide;N-(3-chloro-7-indolyl)-1,4-benzenedisulphonamide |
| CAS号 | 165668-41-7 |
| 分子式 | C14H12ClN3O4S2 |
| 分子量 | 385.85 |
| 产品描述 | Indisulam (E 7070) 是一种碳酸酐酶抑制剂，具有抗癌活性。Indisulam (E 7070) 是细胞周期 G1 期的靶向化合物。Indisulam (E 7070) 通过抑制 CDK2 和周期蛋白 E 的激活，引起 G1/S 转化被阻滞。Indisulam (E 7070) 通过募集 DCAF15 诱导 RBM39 降解来靶向剪接。 |
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