AN APIOSE-CONTAINING COUMARIN GLYCOSIDE FROM GMELINA ARBOREA ROOT

DOI: 10.1016/S0031-9422(00)82575-3

Source and publish data:

Phytochemistry p. 1862 - 1863 (1985)

Update date:2022-08-29

Topics:

Authors:

Satyanarayana, P.

Subrahmanyam, P.

Kasai, R.

Tanaka, O.

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

Article abstract of DOI:10.1016/S0031-9422(00)82575-3

Umbelliferone 7-apiosylglucoside has been characterized from the root of Gmelina arborea. Key Word Index - Gmelina arborea; Verbenaceae; root; coumarin; β-apiofuranosyl-(1->6)-β-D-glucopyranosyl-umbelliferone.

Full text of DOI:10.1016/S0031-9422(00)82575-3

Products guided by the article

Product name:7-Hydroxycoumarin

Cas No:93-35-6

R&D Labs maybe for 93-35-6

Shanghai Zhihua ChemTech Co., Ltd.

Contact:+86-13774313779

Address:Room 817 Suite B 3333 Shenjiang Road
MS( MAOSHENG )Chemical CO.,LTD

Contact:+86-519-82726678.82726378

Address:TAOXI INDUSTRY ZONE JINTAN
SHANDONG AONA CHEMICAL CO.,LTD.

Contact:86-532-85762926

Address:LIUYUAN TOWN, ZAOZHUANG CITY, SHANGDONG PROVINCE.
SuZhou Hua-Emy Chemical Import and Export Co., LTD.

Contact:+86-512-88804994; +86-512-88804550;

Address:710, Building B, International Trade Center, 12 Huanghelu, Changshu, Jiangsu,China
Hebei Think-Do Environment Co., Ltd

website:http://www.thinkdo-environment.com

Contact:0311-86510809-

Address:No 6, Shilian Middle Street, Circular Chemical Industry Park

Relevant to this article

Synthesis of new melatonin analogues from dimers of azaindole and indole by use of Suzuki homocoupling

Doi:10.3987/COM-02-9695
(2003)
Isoflavone glucosides exist as their 6''-O-malonyl esters in Pueraria lobata and its cell suspension cultures

Doi:10.1248/cpb.40.1978
(1992)
Phase equilibria in the SrS-Ga₂S₃ system

Doi:10.1134/S0036023610080231
(2010)
Rh(I)-catalyzed enantioselective hydrogenation of (E)- and (Z)-beta-(acylamino)acrylates using 1,4-bisphosphine ligands under mild conditions.

Doi:10.1021/ol0261884
(2002)
Synthesis of new combretastatin A-4 analogues and study of their anti-inflammatory activity

Doi:10.1134/S1068162015010033
(2015)
Directed evolution to investigate steric control of enzymatic oxidosqualene cyclization. An isoleucine-to-valine mutation in cycloartenol synthase allows lanosterol and parkeol biosynthesis [9]

Doi:10.1021/ja992589b
(1999)

Article Doi