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Merck

D3821

Sigma-Aldrich

地伐西匹

≥98% (HPLC), powder

别名:

(S)-N-(2,3-二氢-1-甲基-2-氧代-5-苯基-1H-1,4-苯并二氮杂-3-基)吲哚-2-甲酰胺, L-364,718, MK 329

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About This Item

经验公式(希尔记法):
C25H20N4O2
分子量:
408.45
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

儲存條件

desiccated

顏色

white to off-white

溶解度

DMSO: >5 mg/mL

起源

Merck & Co., Inc., Kenilworth, NJ, U.S.

儲存溫度

2-8°C

SMILES 字串

CN1C(=O)[C@@H](NC(=O)c2cc3ccccc3[nH]2)N=C(c4ccccc4)c5ccccc15

InChI

1S/C25H20N4O2/c1-29-21-14-8-6-12-18(21)22(16-9-3-2-4-10-16)27-23(25(29)31)28-24(30)20-15-17-11-5-7-13-19(17)26-20/h2-15,23,26H,1H3,(H,28,30)/t23-/m1/s1

InChI 密鑰

NFHRQQKPEBFUJK-HSZRJFAPSA-N

一般說明

地伐西匹通过化学修饰而衍生自阿斯匹林,具有苯并二氮杂骨架。

應用

地伐西匹在人胚胎肾293T细胞和人胰腺切片中已被用作胆囊收缩素受体1(CCK1R)拮抗剂。

生化/生理作用

地伐西匹是一种CCK1(CCK-A)受体拮抗剂和CCK8拮抗剂。
地伐西匹是一种胆囊收缩素受体1(CCK1R)拮抗剂。它可抑制CCK与外周型受体(CCK-A)的结合。地伐西匹可逆转胆囊收缩素八肽(CCK-8)对吗啡的拮抗作用。

特點和優勢

该化合物是由Merck & Co., Inc., Kenilworth, NJ, U.S.开发的。想要浏览其他由制药公司开发的化合物以及已批准药物/候选药物清单, 请单击此处

象形圖

Skull and crossbones

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 1 Oral

儲存類別代碼

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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