Synthesis and hepatoprotective effects of soyasapogenol B derivatives

DOI: 10.1016/S0960-894X(96)00572-0

Source and publish data:

Bioorganic and Medicinal Chemistry Letters p. 85 - 88 (1997)

Update date:2022-08-03

Topics:

Authors:

Sasaki, Kazue

Minowa, Nobuto

Kuzuhara, Hiroyuki

Nishiyama, Shoji

Omoto, Shoji

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

Article abstract of DOI:10.1016/S0960-894X(96)00572-0

Derivatives of soyasapogenol B (1), which is the aglycon moiety of soyasaponins from soybean, were synthesized and evaluated for their hepatoprotective effects in vitro.

Full text of DOI:10.1016/S0960-894X(96)00572-0

Products guided by the article

Product name:C₄₀H₆₀O₅S

Cas No:195156-10-6

R&D Labs maybe for 195156-10-6

Hangzhou Pharma & Chem Co.,Ltd.

Contact:+86-571-87040515

Address:No,139Qingchun Rd
Wuhan Better Organic Technology Inc.

Contact:13307163183

Address:Wuhan Economic&Technology Development Zone, Hubei
Phantom-pharma

Contact:

Address:
Shaanxi King Stone Enterprise Company Limited

Contact:86-29-88353805,13609285751

Address:.209 Keji Road Hi-Tech industrial Develpment Zone .Xian China
GN chemicals co.,ltd

Contact:86 311 85902108 / 85902109

Address:room 1001-1005 ,huanghe Road ,shijiazhuang ,China

Relevant to this article

Doi:10.1021/jo01028a051
(1964)
SYNTHESIS OF PREGN-4-ENO(3,2-C)PYRAZOLES RELATED TO

Doi:10.1021/jm00333a023
(1964)
EFFECTS OF OXYGEN IN THE PHOTOLYSIS OF 2,6-DI-TERT-BUTYL-1,4-BENZOQUINONEDIAZIDE IN CCl4

Doi:10.1007/BF00962010
(1987)
Stereoselective synthesis of the LM ring moiety of ciguatoxin: Reagent control of asymmetric dihydroxylation

Doi:10.1246/cl.1997.845
(1997)
Doi:10.1021/jo01257a016
(1969)
Doi:10.1021/ja01008a600
(1968)

Article Doi