2005
DOI: 10.1080/13880200590951711
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Two New Compounds from the Galls of Quercus infectoria. with Nitric Oxide and Superoxide Inhibiting Ability

Abstract: Two compounds isolated from the ethanol extract of the galls of Quercus infectoria. Olivier exhibited nitric oxide (NO) and superoxide [Formula: see text] inhibiting activity. Their structures were established as ellagic acid-4-O.-[β.-D-glucopyranosyl]-10-O.-[β.-D-glucopyranosyl]-(4 → 1)-β.-D-rhamnopyranoside (1) and 2-methyl-3-hydroxymethylene-4,5,6,7,8-pentahydroxynaphthalene (2) on the basis of spectroscopic and chemical evidence.

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Cited by 25 publications
(19 citation statements)
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“…Water-methanolic extract of Quercus galls has a large amount of tannins. Regarding the role of microbes and the oxidative inflammatory process in induction of colitis, the first thing that comes to mind is to relate the benefit of Quercus to its antibacterial [ 29 – 34 ], antioxidant [ 35 , 36 ], and anti-inflammatory properties [ 24 ].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Water-methanolic extract of Quercus galls has a large amount of tannins. Regarding the role of microbes and the oxidative inflammatory process in induction of colitis, the first thing that comes to mind is to relate the benefit of Quercus to its antibacterial [ 29 – 34 ], antioxidant [ 35 , 36 ], and anti-inflammatory properties [ 24 ].…”
Section: Discussionmentioning
confidence: 99%
“…Quercus brantii galls (locally called ‘mazoo’) are famous in traditional Iranian medicine for treating chronic diarrhea and many diseases, with or without inflammatory pathogenesis [ 26 ]. Regarding its great medicinal value, Quercus galls have been reported to have the following pharmacological actions: astringent, anti-pyretic, anti-parkinsonism [ 25 ], anti-tremorine, local anesthetic, central nervous system (CNS) depressant, analgesic [ 25 , 27 ], anti-diabetic [ 25 , 28 ], anti-bacterial [ 29 – 34 ], anti-oxidant [ 35 , 36 ] and anti-inflammatory [ 25 ].…”
Section: Introductionmentioning
confidence: 99%
“…The 13 C NMR spectrum exhibited aglycone ester carbonyl carbon at δ C 170.51 (C-7), aromatic carbons at δ C   1-6 146.49, 139.69, 123.48, 110.43, 118.37, and 122.06, one anomeric sugar carbon at δ C 90.31 (C-1′) and other sugar carbons at δ C 90.31– 64.51. The methyl carbon (CH 3 ) give signals at δ C 13.18, 15.07, and 17.38 23 . The compound shows a typical fragmentation pattern with molecular ions and a few fragment ions.…”
Section: Discussionmentioning
confidence: 99%
“…Opposite to other dimers (like proanthocyanidin B 3 , prodelphinidin C) this compound did not exhibit any duplicate signals in its 1 H NMR spectrum. It seems that the concurrent presence of two bulky substituents at C-3 (glucose) and C-4 (catechin) forces them to assume spatial positions as far as possible, preventing rotation around the interflavanyl bond and enhancing thus one rotameric form in both methanol-d 4 and acetone-d 6 The 1 H NMR spectrum displayed signals belonging to two flavan-3-ol skeletons and a sugar moiety. Accordingly, the ESI-MS spectrum (positive ion mode) exhibited a fragment at m/z 275.0, characteristic of the presence of afzelechin, while a peak at 419.0 [M-290] suggested the loss of catechin and gave evidence of the linkage between afzelechin and a methylpentose.…”
Section: Introductionmentioning
confidence: 98%