Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H10O4 |
Molecular Weight | 194.184 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)\C=C\C1=CC(O)=C(O)C=C1
InChI
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+
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3114 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20378981 |
1.5 mM [IC50] | ||
Target ID: Protein tyrosine kinase Sources: https://www.ncbi.nlm.nih.gov/pubmed/1423745 |
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Target ID: CHEMBL1869 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1423745 |
PubMed
Title | Date | PubMed |
---|---|---|
Hydroxylated aromatic inhibitors of HIV-1 integrase. | 1995 Oct 13 |
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In vitro anticancer activity of methyl caffeate isolated from Solanum torvum Swartz. fruit. | 2015 Dec 5 |
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K20E, an oxidative-coupling compound of methyl caffeate, exhibits anti-angiogenic activities through down-regulations of VEGF and VEGF receptor-2. | 2015 Jan 15 |
Patents
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DTXSID401030290
Created by
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6856
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3843-74-1
Created by
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METHYL CAFFEATE
Created by
admin on Fri Dec 15 17:50:48 GMT 2023 , Edited by admin on Fri Dec 15 17:50:48 GMT 2023
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N79173B9HF
Created by
admin on Fri Dec 15 17:50:48 GMT 2023 , Edited by admin on Fri Dec 15 17:50:48 GMT 2023
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689075
Created by
admin on Fri Dec 15 17:50:48 GMT 2023 , Edited by admin on Fri Dec 15 17:50:48 GMT 2023
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SUBSTANCE RECORD