Microbial metabolism. Part 13. Metabolites of hesperetin.Bioorg Med Chem Lett. 2011 Oct 01; 21(19):5784-6.BM
Abstract
The fungal culture, Mucor ramannianus (ATCC 2628) transformed hesperitin (1) to four metabolites: 4'-methoxy-5,7,8,3'-tetrahydroxyflavanone (8-hydroxyhesperetin) (2), 5,7,3',4'-tetrahydroxyflavanone (eriodictyol) (3), 4'-methoxy-5,3'-dihydroxyflavanone 7-sulfate (hesperetin 7-sulfate) (4) and 5,7,3'-trihydroxyflavanone 4'-O-α-quinovopyranoside (eriodictyol 4'-O-α-quinovopyranoside) (5). The structures were established by spectroscopic methods.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Language
eng
PubMed ID
21873058
Citation
Herath, Wimal, and Ikhlas Ahmad Khan. "Microbial Metabolism. Part 13. Metabolites of Hesperetin." Bioorganic & Medicinal Chemistry Letters, vol. 21, no. 19, 2011, pp. 5784-6.
Herath W, Khan IA. Microbial metabolism. Part 13. Metabolites of hesperetin. Bioorg Med Chem Lett. 2011;21(19):5784-6.
Herath, W., & Khan, I. A. (2011). Microbial metabolism. Part 13. Metabolites of hesperetin. Bioorganic & Medicinal Chemistry Letters, 21(19), 5784-6. https://doi.org/10.1016/j.bmcl.2011.08.004
Herath W, Khan IA. Microbial Metabolism. Part 13. Metabolites of Hesperetin. Bioorg Med Chem Lett. 2011 Oct 1;21(19):5784-6. PubMed PMID: 21873058.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Microbial metabolism. Part 13. Metabolites of hesperetin.
AU - Herath,Wimal,
AU - Khan,Ikhlas Ahmad,
Y1 - 2011/08/09/
PY - 2011/06/02/received
PY - 2011/07/29/revised
PY - 2011/08/01/accepted
PY - 2011/8/30/entrez
PY - 2011/8/30/pubmed
PY - 2012/4/17/medline
SP - 5784
EP - 6
JF - Bioorganic & medicinal chemistry letters
JO - Bioorg Med Chem Lett
VL - 21
IS - 19
N2 - The fungal culture, Mucor ramannianus (ATCC 2628) transformed hesperitin (1) to four metabolites: 4'-methoxy-5,7,8,3'-tetrahydroxyflavanone (8-hydroxyhesperetin) (2), 5,7,3',4'-tetrahydroxyflavanone (eriodictyol) (3), 4'-methoxy-5,3'-dihydroxyflavanone 7-sulfate (hesperetin 7-sulfate) (4) and 5,7,3'-trihydroxyflavanone 4'-O-α-quinovopyranoside (eriodictyol 4'-O-α-quinovopyranoside) (5). The structures were established by spectroscopic methods.
SN - 1464-3405
UR - https://www.unboundmedicine.com/medline/citation/21873058/Microbial_metabolism__Part_13__Metabolites_of_hesperetin_
L2 - https://linkinghub.elsevier.com/retrieve/pii/S0960-894X(11)01075-4
DB - PRIME
DP - Unbound Medicine
ER -