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Cas号索引 1

• 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
• 1256388-51-8 | Ledipasvir (GS5885) (Catalog# : 16122765)Ledipasvir (GS5885) is a HCV NS5A polymerase inhibitor, used for the treatment of hep
• 1793053-37-8 | LLY-507 (Catalog# : 16122739)LLY-507 is a cell-active, potent, and selective inhibitor of protein-lysine Methyltra
• 1621862-70-1 | Lirametostat ( CPI-1205 ) (Catalog# : 16122736)Lirametostat ( CPI-1205 ) 是一种有效的、选择性的、辅助因子竞争性的
• 159182-43-1 | L755507 (Catalog# : 16122732)L-755,507 is characterized as a potent and selective 3 adrenergic receptor partial ag
• 169939-93-9 | LY333531 (Catalog# : 16122722)LY333531 is a -specific protein kinase C inhibitor. It competitively and reversibly i
• 1243329-97-6 | Lenalidomide hydrochloride (Catalog# : 6111410)Lenalidomide (Revlimid, CC-5013) is a TNF- secretion inhibitor with IC50 of 13 nM
• 1223405-08-0 | LOXO-101 (Catalog# : 61123)LOXO-101 is an oral potent and selective ATP-competitive inhibitor of tropomyosin rec
• 1017606-66-4 | LPA2 antagonist 1 (Catalog# : 61120)LPA2 antagonist 1 is a selective inhibitor of LPA2 activity in with IC50 17 nM in vit