Scholarly article on 2β,3ξ,16α,20,25-pentahydroxy-10α-cucurbit-5-ene-11,22-dione 99529-81-4 from Journal of the American Chemical Society p. 710,713

DOI: 10.1021/ja01536a047

Source and publish data:

Journal of the American Chemical Society p. 710,713 (1958)

Update date:2022-08-04

Topics:

Authors:

Lavie Lavie

Willner Willner

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

Article abstract of DOI:10.1021/ja01536a047

Full text of DOI:10.1021/ja01536a047

Products guided by the article

Product name:2β,3ξ,16α,20,25-pentahydroxy-10α-cucurbit-5-ene-11,22-dione

Cas No:99529-81-4

R&D Labs maybe for 99529-81-4

Zhejiang Rongkai Chemical Technology Co.,Ltd.

Contact:+86-578-8185786

Address:Shangjiang Industrial Zone,Suichang
H&Y International Group Ltd

Contact:+86-571-86491666

Address:SHI XIANG ROAD
Changzhou Sunlight Pharmaceutical Co., Ltd.

Contact:+86-519-83131668;83139028;83138042;83137041

Address:JiuliStreet, Benniu Town Changzhou City, Jiangsu Province
Evershine Chemical CO Ltd

Contact:+86-571-87010026

Address:202, Zhenhua Road,
Onlychem (Jinan)Biotech Co.,Ltd

Contact:86-531-83175885

Address:No. 44, Honglou South Road, Jinan,China

Relevant to this article

Diversity-oriented synthesis of pyrazoles derivatives from flavones and isoflavones leads to the discovery of promising reversal agents of fluconazole resistance in Candida albicans

Doi:10.1016/j.bmcl.2018.03.066
(2018)
Interaction of deoxyhalosucrose derivatives with dextransucrase.

Doi:10.1016/0008-6215(85)85029-1
(1985)
Antibody-catalyzed decarboxylation and aldol reactions using a primary amine molecule as a functionalized small nonprotein component

Doi:10.1016/j.bmc.2013.09.015
(2013)
Regioselective synthesis and biological evaluation of: N -substituted 2-aminoquinazolin-4-ones

Doi:10.1039/c8ob00624e
(2018)
Doi:10.1021/ja01239a041
(1944)
Synthesis and biological evaluation of 4-hydroxy-5-oxo-2,5-dihydro-1: H -pyrrole-3-carboxamides and their zinc(II) complexes as candidate antidiabetic agents

Doi:10.1039/c7nj00970d
(2017)

Article Doi

DOI: 10.1021/ja01536a047