Structure-activity relationship studies of 4-methylcoumarin derivatives as anticancer agents.

about

Design, Synthesis, and Evaluation of the Kinase Inhibition Potential of Pyridylpyrimidinylaminophenyl Derivatives.Fruits as Prospective Reserves of bioactive Compounds: A Review

P2860

Q48106257-747F73A0-393D-4806-946D-85A2523A6097 Q58805328-2FC9BB66-DB9E-416E-B190-A01C3813FCBF

P2860

Structure-activity relationship studies of 4-methylcoumarin derivatives as anticancer agents.

Item

http://www.wikidata.org/entity/Q49171571

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

Structure-activity relationshi ...... ivatives as anticancer agents.

@en

Structure-activity relationshi ...... ivatives as anticancer agents.

@nl

type

Item

label

Structure-activity relationshi ...... ivatives as anticancer agents.

@en

Structure-activity relationshi ...... ivatives as anticancer agents.

@nl

prefLabel

Structure-activity relationshi ...... ivatives as anticancer agents.

@en

Structure-activity relationshi ...... ivatives as anticancer agents.

@nl

P1476

Structure-activity relationshi ...... ivatives as anticancer agents.

@en

P2093

Ashok K Prasad

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

Badri Parshad

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

Divya Mathur

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

Fatemeh Khakdan

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

Luciano Saso

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

Marc E Bracke

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

Maryam Nejati

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

Sunil K Sharma

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

Virinder S Parmar

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

P2860

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

Growth inhibition and apoptosis induced by osthole, a natural coumarin, in hepatocellular carcinoma

Quantification of coumarin in cinnamon and woodruff beverages using DIP-APCI-MS and LC-MS.

Structure-activity relationship of dihydroxy-4-methylcoumarins as powerful antioxidants: correlation between experimental & theoretical data and synergistic effect.

Review on natural coumarin lead compounds for their pharmacological activity

Esculetin suppresses proliferation of human colon cancer cells by directly targeting β-catenin.

Dentatin Induces Apoptosis in Prostate Cancer Cells via Bcl-2, Bcl-xL, Survivin Downregulation, Caspase-9, -3/7 Activation, and NF-κB Inhibition.

Coumarin-based inhibitors of Bacillus anthracis and Staphylococcus aureus replicative DNA helicase: chemical optimization, biological evaluation, and antibacterial activities

A coumarin derivative (RKS262) inhibits cell-cycle progression, causes pro-apoptotic signaling and cytotoxicity in ovarian cancer cells.

Synthesis, characterization, cytotoxicity of mixed ligand complexes of palladium(II) with dipyrido[3,2-d:2',3'-f]quinoxaline/dipyrido[3,2-a:2',3'-c](6,7,8,9-tetrahydro)phenazine and 4-toluensulfonyl-L-amino acid dianion.

P304

105-110

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

P31

scholarly article

P356

10.3109/13880209.2015.1016183

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

P433

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

P478

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

P50

Omidreza Firuzi

Ramin Miri

P577

2015-05-27T00:00:00Z

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

P5875

277335787

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

P698

26017566

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

Structure-activity relationship studies of 4-methylcoumarin derivatives as anticancer agents.

about

P2860

P2860

Structure-activity relationship studies of 4-methylcoumarin derivatives as anticancer agents.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698