CAFFEIC ACID METHYL ESTER

COC(=O)\C=C\C1=CC=C(O)C(O)=C1

InChIKey=OCNYGKNIVPVPPX-HWKANZROSA-N

InChI=1S/C10H10O4/c1-14-10(13)5-3-7-2-4-8(11)9(12)6-7/h2-6,11-12H,1H3/b5-3+

Targets

Primary Target	Pharmacology	Potency
Sucrase-isomaltase 5 Target ID: CHEMBL3114 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20378981	Inhibitor 8504	1.5 mM [IC50]
Protein tyrosine kinase 1 Target ID: Protein tyrosine kinase Sources: https://www.ncbi.nlm.nih.gov/pubmed/1423745	Inhibitor 8504
Ornithine decarboxylase 15 Target ID: CHEMBL1869 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1423745	Inhibitor 8504

PubMed

Title	Date	PubMed
In vitro anticancer activity of methyl caffeate isolated from Solanum torvum Swartz. fruit.	2015-12-05	26415618
K20E, an oxidative-coupling compound of methyl caffeate, exhibits anti-angiogenic activities through down-regulations of VEGF and VEGF receptor-2.	2015-01-15	25481497
Activity of caffeic acid derivatives against Candida albicans biofilm.	2014-03-15	24582984
Inhibitory effects of caffeic acid phenethyl ester derivatives on replication of hepatitis C virus.	2013	24358168
Synthesis of trans-caffeate analogues and their bioactivities against HIV-1 integrase and cancer cell lines.	2008-12-15	18952420
Hydroxylated aromatic inhibitors of HIV-1 integrase.	1995-10-13	7473544

Patents

Name

Type

Language

METHYL CAFFEATE

Preferred Name

English

CAFFEIC ACID METHYL ESTER

Common Name

English

CINNAMIC ACID, 3,4-DIHYDROXY-, METHYL ESTER

Systematic Name

English

METHYL-3,4-DIHYDROXY CINNAMATE

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID401030290