Benzoylgomisin Q and benzoylgomisin P, two new lignans from Schisandra sphenanthera Rehd. et Wils.

DOI: 10.1248/cpb.38.1408

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1408 - 1411 (1990)

Update date:2022-08-05

Topics:

Authors:

Ikeya Ikeya

Miki Miki

Okada Okada

Mitsuhashi

Chai Chai

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

Article abstract of DOI:10.1248/cpb.38.1408

Full text of DOI:10.1248/cpb.38.1408

NII-Electronic Library Service

Products guided by the article

Product name:Benzoic acid (5S,6S,7S)-6,10,11-trihydroxy-1,2,3,12-tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydro-dibenzo[a,c]cycloocten-5-yl ester

Cas No:130783-35-6

R&D Labs maybe for 130783-35-6

Zhejiang Golden-Shell Pharmaceutical Co.,Ltd.

Contact:+86-576-87501888 / 87501988

Address:No.89 Zhongxing Road. Li'ao, Yuhuan, Zhejiang, China
qingdao goldenchem imp and exp co.,ltd.

Contact:532-55579246

Address:no.62 ,haier road laoshan distirct
Shanghai Egoal Chemical Co.,Ltd

Contact:+86-21-50333091

Address:Yangming Garden Square 3,YangGao North Road 1188, Pudong New District, Shanghai
Yingkou Sanzheng Organic Chemical Co. Ltd.

Contact:+86-417-3638818

Address:25 Gengxinli Village, Daqing Road, Yingkou, Liaoning, China
GN chemicals co.,ltd

Contact:86 311 85902108 / 85902109

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

Relevant to this article

Triphenylene-fused porphyrins

Doi:10.1021/ol200853g
(2011)
Catalytic asymmetric vinylogous Mannich-type (AVM) reaction of nonactivated α-angelica lactone

Doi:10.1021/ol200939t
(2011)
Nano polypropylenimine dendrimer (DAB-PPI-G₁): As a novel nano basic-polymer catalyst for one-pot synthesis of 2-amino-2-chromene derivatives

Doi:10.1039/c5ra04458h
(2015)
Synthesis of 2,3-dihydro-4(1H)-quinolones and the corresponding 4(1H)-quinolones via low-temperature fries rearrangement of N-arylazetidin-2- ones

Doi:10.1071/CH10465
(2011)
Synthesis and cyclizations of 1-azapolyene derivatives

Doi:10.1016/j.tet.2011.03.058
(2011)
Discovery of highly potent human deoxyuridine triphosphatase inhibitors based on the conformation restriction strategy

Doi:10.1021/jm300416h
(2012)

Article Doi