Weight | 178.143 g/mol |
---|---|
Formula | C9H6O4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
Esculetin (305-01-1)
aesculetin · 6,7-dihydroxycoumarin
Score:
#1833 in Biochemistry
,
#3976 in Biology
,
#5007 in Chemistry
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- Inhibition of cell cycle progression in human leukemia HL-60 cells by esculetin (Cancer Letters, 2002)
- Inhibitory effect of esculetin on 5-lipoxygenase and leukotriene biosynthesis (Biochimica et Biophysica Acta, 1983)
- Selective inhibition of platelet lipoxygenase by esculetin (Biochimica et Biophysica Acta, 1982)
- Evaluation of butylated hydroxyanisole, myo-inositol, curcumin, esculetin, resveratrol and lycopene as inhibitors of benzo[a]pyrene plus 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced lung tumorigenesis in A/J mice (Cancer Letters, 1999)
- Mushroom Tyrosinase Inhibitory Activity of Esculetin Isolated from Seeds of Euphorbia lathyris L. (Bioscience, Biotechnology, and Biochemistry, 2003)
- Inhibitory effect of esculetin on oxidative damage induced by t-butyl hydroperoxide in rat liver (Archives of Toxicology, 2000)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - aesculetin
- 6,7-dihydroxycoumarin
-
SMILESC1=CC(=O)OC2=CC(=C(C=C21)O)O
-
InChIKeyILEDWLMCKZNDJK-UHFFFAOYSA-N
- Pubchem - Esculetin
- Wikipedia - esculetin
Aesculetin (also known as esculetin, 6,7-dihydroxycoumarin and cichorigenin) is a derivative of coumarin. It is a natural lactone that derives from the intramolecular cyclization of a cinnamic acid derivative. It is present in chicory and in many toxic and medicinal plants, in form of glycosides and caffeic acid conjugates.
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