Attempted inhibition of histidine decarboxylase with β aklyl analogues of histidine

DOI: 10.1021/jm00215a021

Source and publish data:

Journal of Medicinal Chemistry p. 721 - 723 (1977)

Update date:2022-07-29

Topics:

Authors:

Kelley Kelley

Miller Miller

McLean McLean

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/jm00215a021

The synthesis of β-methyl-(10b),β-ethyl-(10c), and β-n-hexylhistidine in five steps from 4-(N-triphenyl-methyl) imidazolecarboxaldehyde is described. Neither of the amino acids nor the methyl esters of 10b or 10c were inhibitors of the histidine decarboxylase from rat stomach.

Full text of DOI:10.1021/jm00215a021

Products guided by the article

Product name:1H-Imidazole-4-methanol, a-hexyl-1-(triphenylmethyl)-

Cas No:62256-52-4

R&D Labs maybe for 62256-52-4

Nanjing lanbai chemical Co.,Ltd.

Contact:+86-25-85499326

Address:Room 908, 9F Taiyue Building,No.285 Heyan Road
Guangzhou Chemical Reagent Factory

Contact:+86-20-8435 9820 or 8435 7345

Address:Southern Guangzhou, Guangdong, China
Hangzhou Eastbiopharm Co.,Ltd.

Contact:+86-571-88931780

Address:Hangzhou,China
Neworld Chemical Co., Ltd Shanghai(expird)

Contact:+86-21-62202658

Address:11F, Blvd 2, No. 1969 PuXing Rd, Shanghai
Zhengzhou Xinlian Chemical Tech Co. ,Ltd

Contact:0371-65771781 021-52042910

Address:H Part, Building I, No. 700 Gonglu Road, Pudong New Area, Shanghai

Relevant to this article

Doi:10.1007/BF00920897
()
Total synthesis of (+)-geldanamycin and (-)-o-quinogeldanamycin: Asymmetric glycolate aldol reactions and biological evaluation

Doi:10.1021/jo034870l
(2003)
Doi:10.1039/jr9510000734
(1951)
A new water-compatible dehydrating agent DPTF

Doi:10.1016/0040-4039(96)01712-1
(1996)
Doi:10.1021/jo01351a027
(1961)
Doi:10.1021/jo00437a038
(1977)

Article Doi