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Cas号索引 1

• 1040526-12-2 | LP-533401盐酸盐 (Catalog# : 1810262)LP-533401 HCl是色氨酸羟化酶-1 (Tph-1)的抑制剂，Tph-1是内脏衍生血清
• 1454808-95-7 | LP-922761 (Catalog# : 188101)LP-922761是一种强有力的和选择性AAK1抑制剂，在体外的IC50值为4.8±
• 1898283-02-7 | LY-3200882 (Catalog# : 186278)LY-3200882是一种口服TGFbeta抑制剂。LY3200882目标转化生长因子-beta (T
• 1610954-97-6 | LX2761 (Catalog# : 186275)LX2761是一种局部作用的SGLT1抑制剂，体外强效，延缓体内肠道葡萄
• 120408-07-3 | Lometrexol disodium (Catalog# : 186151)Lometrexol是一种具有抗肿瘤活性的叶酸模拟抗代谢产物。
• 1632032-53-1 | LB-100 (Catalog# : 185312)LB-100是一种蛋白磷酸酶2A(PP2A)抑制剂。
• 1292290-38-0 | LY2881835 (Catalog# : 185252)LY2881835是一种有效的选择性GPR40激动剂，可能用于治疗2型糖尿病。
• 1903008-80-9 | Lazertinib (Catalog# : 512194)Description：Lazertinib is a an orally available third-generation, selective inhibi
• 183499-57-2 | L-778123 (Catalog# : 1711249)L-778,123 is an inhibitor of FPTase and GGPTase-I.
• 1879887-96-3 | LTURM-34 (Catalog# : 1710138)LTURM-34是一种新的有效的和选择性的DNA-PK抑制剂，可减轻体外对多
• 1234015-54-3 | LY2606368 dihydrochloride (Catalog# : 1710137)Prexasertib (LY2606368)是一个与ATP竞争的CHK1抑制剂带Ki值0.9 nmol/L。对于
• 1361030-48-9 | LDC1267 (Catalog# : 179301)LDC1267显著降低小鼠乳腺癌和黑色素瘤转移依赖NK细胞。TAM酪氨酸激
• 125697-93-0 | N-(2,5-二羟基苄基)-5-氨基水杨酸 (Catalog# : 1791119)Lavendustin C，也被称为HDBA和NSC 666251，是一种有效的表皮生长因子（
• 1874276-76-2 | LXS-196 (Catalog# : 1781108)<span style="color:#34495E;font-family:"font-size:14px;background-color:
• 1453834-21-3 | LDC4297(LDC044297) (Catalog# : 178902)LDC4297也称为LCD044297,是一种有效、具有选择性的CDK7抑制剂。
• 1951483-29-6 | LY3214996 (Catalog# : 2017887)LY-3214996是一种有效且具有选择性的，可用于口服的细胞外信号的
• 1345407-05-7 | LTX-315 (Catalog# : 20178218)LTX-315是一种两性分子的阳离子肽可能用于治疗黑色素瘤、乳腺癌
• 186544-26-3 | LY 344864 (Catalog# : 20178212)LY344864是一种选择性5-HT1F受体激动剂，在最近克隆的5 - HT1F受体上
• 1217756-94-9 | 盐酸LY 344864 (Catalog# : 2017828)LY344864 hydrochloride is a potent and selective 5-HT1F receptor agonist. It has an E
• 1391426-24-6 | Lys05 trihydrochloride (Catalog# : 17030102)Lys05, 或Lys01三盐酸化物，是一种有效的水溶性溶酶体自噬抑制剂。
• 1421438-81-4 | LY3039478 ( Crenigacestat ) (Catalog# : 17021601)LY3039478 ( Crenigacestat ) 是一种选择性 NOTCH1 抑制剂，通过阻断 VEGFA/
• 1187020-80-9 | lumateperone(Tosylate) (Catalog# : 17012102)Lumateperone (ITI-722/ITI-007)是一种新型的双5HT2A受体拮抗剂/多巴胺磷蛋
• 1391426-22-4 | Lys05 (Catalog# : 16123043)Lys05 is a potent lysosomal autophagy inhibitor. Lys05 is a previously undescribed di
• 1627696-51-8 | LY-3177833 (Catalog# : 16123042)LY-3177833 is a potent and selective inhibitor of CDC7 (Cell Division Cycle 7-related
• 1454682-72-4 | LY3009120 (Catalog# : 16123041)LY3009120, also known as DP-4978, is potent and selective pan-RAF inhibitor with pote
• 187164-19-8 | Luliconazole (Catalog# : 16123038)Luliconazole is an azole antifungal drug. As a 1% topical cream, luliconazole is indi
• 1223403-58-4 | LOXO-101 (ARRY-470) (Catalog# : 16123036)Larotrectinib, also known as ARRY-470 and LOXO-101, is an orally bioavailable, potent
• 182431-12-5 | Lomitapide free base (Catalog# : 16123035)Lomitapide is a MTP inhibitor. Lomitapid is a novel agent for the treatment of homozy
• 106400-81-1 | Lometrexol disodium (Catalog# : 16123034)Lometrexol is a folate analog antimetabolite with antineoplastic activity. As the 6R
• 1243244-14-5 | LGK974 (WNT974) (Catalog# : 16123033)LGK974, aslo known as is a selective and orally bioavailable Porcupine (PORCN) inhibi