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文件

C6022

Sigma-Aldrich

赛庚啶 盐酸盐 倍半水合物

≥98% (TLC), solid

同義詞:

水合哌啶4-(5H-二苯并[a,d]环庚基-5-亚烷基)-1-甲基-盐酸盐 (2:3)

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About This Item

經驗公式(希爾表示法):
C21H21N·HCl·1.5H2O
CAS號碼:
分子量::
350.88
EC號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (TLC)

形狀

solid

顏色

white to slightly yellow

溶解度

ethanol: soluble
methanol: soluble

起源

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

SMILES 字串

Cl.CN1CCC(\CC1)=C2/c3ccccc3C=Cc4ccccc24

InChI

1S/2C21H21N.2ClH.3H2O/c2*1-22-14-12-18(13-15-22)21-19-8-4-2-6-16(19)10-11-17-7-3-5-9-20(17)21;;;;;/h2*2-11H,12-15H2,1H3;2*1H;3*1H2

InChI 密鑰

ZEAUHIZSRUAMQG-UHFFFAOYSA-N

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應用

盐酸赛庚啶倍半水合物已被用于:
  • 检测5-羟色胺受体(5-HT)诱导的炎症中的抗炎活性
  • 螃蟹中体内体外生物检测中5-HT的抑制
  • 胚胎生理性实验中5-HT的抑制

降钙素基因相关肽(CGRP)的抑制

生化/生理作用

赛庚啶盐酸盐倍半水合物是一种血清素受体(5-HT2 / 5-HT1C)拮抗剂、H1组胺受体拮抗剂和止痒剂。赛庚啶对5-HT的抑制作用可改善精神分裂症的认知功能。赛庚啶对治疗功能性胃肠道疾病(FGID)有效。食品药品监督管理局(FDA)批准的赛庚啶具有抗抑郁和抗血小板功能。它可有效地治疗血栓栓塞性疾病。赛庚啶能够抑制赖氨酸甲基转移酶7/9(Set7/9),导致乳腺癌细胞中雌激素受体(ERα)的表达减少和生长停滞。

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

危險分類

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 3

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


分析證明 (COA)

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E O Okoro
The Journal of pharmacy and pharmacology, 51(8), 953-957 (1999-09-30)
We have previously shown that elimination of buffer Ca2+ markedly reduced maximum 5-HT-induced contractions. We have now investigated the effect of L-type Ca2+-channel blockers and 5-HT2 receptor antagonists on 5-HT- and K+-induced contractions in rat aorta to explore the possibility
H W Suh et al.
Neuropeptides, 33(2), 121-129 (2000-02-05)
The present study was designed to investigate the modulatory effects of blockade of spinal histamine receptors on antinociception induced by supraspinally administered mu-epsilon-, delta-, and kappa-opioid receptor agonists. The effects of intrathecal (i.t.) injections with cyproheptadine [a histamine-1 (H1) receptor
Cyproheptadine: a potentially effective treatment for functional gastrointestinal disorders in children
Krasaelap A and Madani S
Pediatric Annals, 46(3), e120-e125 (2017)
Identification of cyproheptadine as an inhibitor of SET domain containing lysine methyltransferase 7/9 (Set7/9) that regulates estrogen-dependent transcription
Takemoto Y, et al.
Journal of Medicinal Chemistry, 59(8), 3650-3660 (2016)
Anti-inflammatory activity of bartogenic acid containing fraction of fruits of Barringtonia racemosa Roxb. in acute and chronic animal models of inflammation
Patil KR and Patil CR
Journal of traditional and complementary medicine, 7(1), 86-93 (2017)

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