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

Baoji Kano Phytochem Technology Co.,Ltd

Contact:86-917-3816534

Address:No.4 Huoju Road,High-Tech Development Zone
Luojiang Chenming Biological Products Co

Contact:+86 15000297032

Address:GROUP NO.4, HE SHENG VILLAGE, PANLONG TOWN,
Jurong Huaheng Natural Biological Products Factory

website:http://www.risebiochem.com

Contact:+86-13921007726

Address:Chuncheng town,Jurong city,Jiangsu province,China
Anyang Double Circle Auxiliary CO.,LTD

Contact:0086-134 6082 4403

Address:dongfeng road, anyang city, henan province,china
Hubei Jiutian Bio-medical Technology Co., Ltd

website:http://www.jiutian-bio.com

Contact:+86-027-88013699

Address:Room 03-6, 5th floor, building 1, international enterprise center phase iii, no. 1, guanggu avenue, east lake new technology development zone, wuhan city

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