Details
Stereochemistry | ACHIRAL |
Molecular Formula | C15H12O5 |
Molecular Weight | 272.2528 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(C(=O)\C=C\C2=CC=C(O)C(O)=C2)C(O)=C1
InChI
InChIKey=AYMYWHCQALZEGT-ORCRQEGFSA-N
InChI=1S/C15H12O5/c16-10-3-4-11(14(19)8-10)12(17)5-1-9-2-6-13(18)15(20)7-9/h1-8,16,18-20H/b5-1+
Butein, a plant polyphenol, has been reported to exhibit several important pharmacological effects, such as anti-inflammatory, anti-cancer, anti-oxidant and anti-angiogenic. It was first found in Toxicodendronvernicifluum, a tree widely used as a local food additive and therapeutic supplement in South East Asia. It can also be isolated from the heartwood of Dalbergiaodorifera, the seed of Cyclopiasubternata and the stems of Semecarpusanacardium, as well as many other plants. Butein was shown to be a specific protein tyrosine kinase inhibitor. This compound inhibited tyrosine-specific protein kinase activities of EGF receptor and p60(c-Src). In preclinical settings, it was shown to improve the treatment outcome of several chronic diseases including inflammation, neurological disorders, neoplasms, atherosclerosis, as well as infectious diseases, and most of these actions were accomplished by the inhibition of the transcription factor NF-κB and its downstream targets.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL267 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9571170 |
65.0 µM [IC50] | ||
Target ID: CHEMBL2363049 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9571170 |
16.0 µM [IC50] | ||
Target ID: Glutathione S-transferase (rat) Sources: https://www.ncbi.nlm.nih.gov/pubmed/8010991 |
9.0 µM [IC50] | ||
Target ID: GO:0034440 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9630680 |
3.3 µM [IC50] | ||
Target ID: map04064 Sources: https://www.ncbi.nlm.nih.gov/pubmed/28586006 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
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Geometrically and conformationally restrained cinnamoyl compounds as inhibitors of HIV-1 integrase: synthesis, biological evaluation, and molecular modeling. | 1998 Oct 8 |
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Inhibitory activity of flavonoids and tannins against HIV-1 protease. | 2000 Sep |
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The small polyphenolic molecule kaempferol increases cellular energy expenditure and thyroid hormone activation. | 2007 Mar |
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Butein suppresses the expression of nuclear factor-kappa B-mediated matrix metalloproteinase-9 and vascular endothelial growth factor in prostate cancer cells. | 2010 Oct |
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Butein protects human dental pulp cells from hydrogen peroxide-induced oxidative toxicity via Nrf2 pathway-dependent heme oxygenase-1 expressions. | 2013 Mar |
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The depletion of securin enhances butein-induced apoptosis and tumor inhibition in human colorectal cancer. | 2014 Sep 5 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26694191
Mice: 1, 3 or 10 mg/kg was administered every day from 3 days before tumor cell injection to 21 days after tumor cell injection.
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9571170
Butein up to 500 uM scarcely inhibited protein kinase C and cAMP-dependent protein kinase activities in HepG2 cells.
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NCI_THESAURUS |
C1967
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487-52-5
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C1028
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BUTEIN
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3237
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ACTIVE MOIETY
PARENT (METABOLITE)