Synthesis of benzyl substituted naphthalenes from benzylidene tetralones.

about

Synthesis of benzyl substituted naphthalenes from benzylidene tetralones.

Item

http://www.wikidata.org/entity/Q36939001

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

Synthesis of benzyl substituted naphthalenes from benzylidene tetralones.

@en

type

Item

label

Synthesis of benzyl substituted naphthalenes from benzylidene tetralones.

@en

prefLabel

Synthesis of benzyl substituted naphthalenes from benzylidene tetralones.

@en

P1476

Synthesis of benzyl substituted naphthalenes from benzylidene tetralones.

@en

P2093

Alice Martinic

http://www.w3.org/2001/XMLSchema#string

Andrea Martinez

http://www.w3.org/2001/XMLSchema#string

David L Vander Jagt

http://www.w3.org/2001/XMLSchema#string

Lisa J Whalen

http://www.w3.org/2001/XMLSchema#string

Lorraine M Deck

http://www.w3.org/2001/XMLSchema#string

Quintino Mgani

http://www.w3.org/2001/XMLSchema#string

Robert E Royer

http://www.w3.org/2001/XMLSchema#string

P2860

Inhibition of lactate dehydrogenase A induces oxidative stress and inhibits tumor progression

Inhibition of human immunodeficiency virus type I replication by derivatives of gossypol

Selective inhibition of human immunodeficiency virus type 1 replication by the (-) but not the (+) enantiomer of gossypol

The effect of gossypol and 6-aminonicotinamide on tumor cell metabolism: a 31P-magnetic resonance spectroscopic study.

Apogossypol derivatives as antagonists of antiapoptotic Bcl-2 family proteins

Inhibitory action of gossypol on enzymes and growth of Trypanosoma cruzi.

Synthesis and evaluation of Apogossypol atropisomers as potential Bcl-xL antagonists

An overview of the clinical pharmacology and therapeutic potential of gossypol as a male contraceptive agent and in gynaecological disease.

Synthesis and CYP24A1 inhibitory activity of (E)-2-(2-substituted benzylidene)- and 2-(2-substituted benzyl)-6-methoxy-tetralones.

Structure-activity relationship study of tricyclic necroptosis inhibitors.

P304

373-376

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.TETLET.2011.11.065

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2012-01-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

241694930

http://www.w3.org/2001/XMLSchema#string

P698

23794758

http://www.w3.org/2001/XMLSchema#string

P932

3686124

http://www.w3.org/2001/XMLSchema#string