Antitumor agents. II. Tulipinolide, a new germacranolide sesquiterpene, and constunolide. Two cytotoxic substances from Liriodendron tulipifera L.

DOI: 10.1002/jps.2600580720

Source and publish data:

Journal of Pharmaceutical Sciences p. 877 - 880 (1969)

Update date:2022-07-30

Topics:

Authors:

Doskotch

el-Feraly

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

Article abstract of DOI:10.1002/jps.2600580720

Full text of DOI:10.1002/jps.2600580720

Products guided by the article

Product name:Dihydrocostunolid

Cas No:13822-36-1

R&D Labs maybe for 13822-36-1

guide(suzhou) fine materials co. ltd

Contact:0512-80972173

Address:21st Building, No.369 Lushan Rd, New District Suzhou China 215129
Quzhou Aokai Chemical Co., Ltd.

Contact:86-570-3032832

Address:NO.16 , Laodong Road,Quzhou City, Zhejiang Province,China
Hubei Lansun Biochemical Pharmaceutical Co., Ltd

Contact:714-6395977

Address:No. 81 Pengcheng Avenue, economic and technological development zone, Huangshi City, Hubei Province,China
Hangzhou JINLAN Pharm-Drugs Technology Co., Ltd

website:http://www.jlpharms.com

Contact:86-571-86982636

Address:Rm A606, Fuyi Center, jianqiao street
Shanghai Korey Pharm Co.,Ltd.(expird)

Contact:021-61840961 021-61840962

Address:No.157,Zhuguang Rd, Qingpu, Shanghai, China

Relevant to this article

Selective reduction of alkynes by the reagent Sml₂ - Transition metal catalysts - proton donors

Doi:10.1016/0040-4039(91)80083-I
(1991)
Design of crystal packings of styrylheterocycles and [2+2] photocycloaddition reactions in their single crystals 7.* Crystal structures of 4-styrylpyridine hydroperchlorates and solid-state [2+2] autophotocycloaddition reactions of these compounds

Doi:10.1007/s11172-011-0259-8
(2011)
N-Substituted-2′-O,3′-N-carbonimidoyl bridged macrolides: Novel anti-inflammatory macrolides without antimicrobial activity

Doi:10.1021/jm300356u
(2012)
Highly Chemo- and Regioselective Vinylation of N-Heteroarenes with Vinylsulfonium Salts

Doi:10.1021/acs.joc.8b00682
(2018)
Oxidative Generation of N-Acyliminium Ions from N-1-(Tributylstannyl)alkyl Carboxamides and Carbamates and Their Reactions with Carbon Nucleophiles

Doi:10.1246/bcsj.66.3456
(1993)
Structure-guided modification of isoxazole-type FXR agonists: Identification of a potent and orally bioavailable FXR modulator

Doi:10.1016/j.ejmech.2020.112910
(2021)

Article Doi