N-arylhydroxamic acid N,O-acyltransferase. Positional requirements for the substrate hydroxyl group

DOI: 10.1021/jm00366a026

Source and publish data:

Journal of Medicinal Chemistry p. 1780 - 1784 (1983)

Update date:2022-08-05

Topics:

Authors:

Banks Banks

Smith Smith

Hanna Hanna

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

Article abstract of DOI:10.1021/jm00366a026

N-Arylhydroxamic acid N,O-acyltransferase (AHAT) is a cytosolic enzyme system that is capable of converting toxic and carcinogenic N-arylhydroxamic acids into electrophilic reactants and of catalyzing the transacetylation of acrylamines. The role of the N

Full text of DOI:10.1021/jm00366a026

Products guided by the article

Product name:trans-4-glycolamidostilbene

Cas No:87711-65-7

R&D Labs maybe for 87711-65-7

NINGBO YINLIANG FOREIGN TRADE CO., LTD.

Contact:+86-574-87834016 / 87898057

Address:23F NO.666JINYU ROAD,YINGZHOU DISTRICT,NINGBO.CHINA
NOVASYNCS CO., LTD

Contact:0512-63006287

Address:no.88.YISHENG Road,etdz-WUJIANG,SUZHOU,CHINA
Shanghai Mio Chemical Co., Ltd

Contact:0086 21- 64401188-622

Address:16 Floor NO.2 Jiefang Building, No. 4855 Dushi Road, 201100 Shanghai, P.R.China
Suzhou HeChuang Chemical Co.,Ltd.

Contact:+86-512-88800520

Address:No.9 Guanchao Rd,Changshu Advanced Materials Industy Park
QINGDAO HONG JIN CHEMICAL CO.,LTD.

website:http://www.hongjinchem.com

Contact:+86-532-83657313

Address:2ND Building, 8 Shangqing Road, Qingdao, Shandong Province, China.

Relevant to this article

HETEROARYLTIN COMPOUNDS. THE CHEMISTRY AND 119Sn MOESSBAUER SPECTROSCOPY OF SOME 3-THIENYLTIN HALIDES, AND A COMPARISON WITH 2-THIENYL AND 2-FURYL ANALOGUES

Doi:10.1016/0022-328X(83)80242-3
(1983)
14-Membered cyclodepsipeptides with alternating β-hydroxy and α-amino acids by cyclodimerization

Doi:10.1016/j.tet.2005.11.002
(2006)
A fluoroacetamidine-based inactivator of protein arginine deiminase 4: Design, synthesis, and in vitro and in vivo evaluation

Doi:10.1021/ja0576233
(2006)
Ansa-chromocene complexes. 2. Isocyanide derivatives of Cr(II) and Cr(III), their syntheses, X-ray crystal structures, and physical properties

Doi:10.1021/om050710j
(2006)
NK₁ antagonists based on seven membered lactam scaffolds

Doi:10.1016/j.bmcl.2006.02.080
(2006)
Design and synthesis of phenolic hydrazide hydrazones as potent poly(ADP-ribose) glycohydrolase (PARG) inhibitors

Doi:10.1016/j.bmcl.2014.06.065
(2014)

Article Doi