Stilbene glycosides are natural product inhibitors of FGF-2-induced angiogenesis

BMC Cell Biology

Volumn 10, Issue , 2009, Pages

  Hussain, Sajjad ^a   Slevin, Mark ^b   Ahmed, Nessar ^b   West, David ^c   Choudhary, Muhammad Iqbal ^d   Naz, Humera ^d   Gaffney, John ^b  

^a MAYO CLINIC   (United States)

^b MANCHESTER METROPOLITAN UNIVERSITY   (United Kingdom)

^c UNIVERSITY OF LIVERPOOL   (United Kingdom)

^d UNIVERSITY OF KARACHI   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

4',5' DIHYDROXY 3 METHOXYSTILBENE 5 O [ALPHA LEVO RHAMNOPYRANOSYL(1-2) ALPHA LEVO RHAMNOPYRANOSYL(1-6)] BETA DEXTRO GLUCOPYRANOSIDE; 4',5' DIHYDROXY 3 METHOXYSTILBENE 5 O [ALPHA LEVO RHAMNOPYRANOSYL(1-6)] BETA DEXTRO GLUCOPYRANOSIDE; EPIDERMAL GROWTH FACTOR; FIBROBLAST GROWTH FACTOR 2; FIBROBLAST GROWTH FACTOR RECEPTOR 1; FIBROBLAST GROWTH FACTOR RECEPTOR 2; GLYCOSIDE; MITOGEN ACTIVATED PROTEIN KINASE 1; UNCLASSIFIED DRUG; VASCULOTROPIN; ANGIOGENESIS INHIBITOR; GLUCOSIDE; MITOGEN ACTIVATED PROTEIN KINASE 3; STILBENE DERIVATIVE; TRANS 4',5' DIHYDROXY 3 METHOXYSTILBENE 5 O (ALPHA L RHAMNOPYRANOSYL (1 2) (ALPHA L RHAMNOPYRANOSYL (1 6)) BETA D GLUCOPYRANOSIDE); TRANS-4',5'-DIHYDROXY-3-METHOXYSTILBENE-5-O-(ALPHA-L-RHAMNOPYRANOSYL-(1-2)-(ALPHA-L-RHAMNOPYRANOSYL-(1-6))-BETA-D-GLUCOPYRANOSIDE);

ANTIANGIOGENIC ACTIVITY; ARTICLE; CELL PROLIFERATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; DOWN REGULATION; DRUG STRUCTURE; ENDOTHELIUM CELL; ENZYME PHOSPHORYLATION; HUMAN; HUMAN CELL; IC 50; PROTEIN BINDING; TOXICITY TESTING; WOUND HEALING; ANIMAL; BURSERACEAE; CATTLE; CELL LINE; CELL MOTION; CHEMISTRY; DRUG ANTAGONISM; ISOLATION AND PURIFICATION; METABOLISM;

BOSWELLIA;

ANGIOGENESIS INHIBITORS; ANIMALS; BURSERACEAE; CATTLE; CELL LINE; CELL MOVEMENT; DOWN-REGULATION; FIBROBLAST GROWTH FACTOR 2; GLUCOSIDES; GLYCOSIDES; HUMANS; INHIBITORY CONCENTRATION 50; MITOGEN-ACTIVATED PROTEIN KINASE 3; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 1; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; STILBENES;

EID: 65649152029     PISSN: None     EISSN: 14712121     Source Type: Journal    
DOI: 10.1186/1471-2121-10-30     Document Type: Article

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