Prunin
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Prunin
structure -
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CAS No:
529-55-5
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Formula:
C21H22O10
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Chemical Name:
Prunin
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Synonyms:
4H-1-Benzopyran-4-one,7-(β-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-,(2S)-;Prunin;4H-1-Benzopyran-4-one,7-(β-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-,(S)-;(2S)-7-(β-D-Glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;Naringenin 7-glucoside;(-)-Naringenin 7-β-D-glucoside;Naringenin 7-O-glucoside;Naringenin 7-O-β-D-glucoside;Naringenin 7-O-β-D-glucopyranoside;4′,5,7-Trihydroxyflavanone 7-O-β-D-glucopyranoside;NSC 135064;(2S)-Naringenin 7-O-β-D-glucopyranoside;30399-86-1;31049-13-5
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CAS No:
Description
Prunin is a potent inhibitor of human enterovirus A71 (HEVA71). Prunin shows strong inhibitory activity against protein tyrosine phosphatase 1B (PTP1B), with an IC50 of 5.5 µM[1][2].
Naringenin 7-O-beta-D-glucoside is a flavanone 7-O-beta-D-glucoside that is (S)-naringenin substituted by a beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. It has a role as a metabolite, a hypoglycemic agent, an antilipemic drug and an antibacterial agent. It is a flavanone 7-O-beta-D-glucoside, a dihydroxyflavanone, a monosaccharide derivative, a member of 4'-hydroxyflavanones and a (2S)-flavan-4-one. It derives from a (S)-naringenin.
Characteristics
166.14000
0.82
1.6±0.1 g/cm3
225 °C
802.4±65.0 °C at 760 mmHg
284.6±27.8 °C
1.691
-20°C
Computed Properties
Molecular Weight:434.4
XLogP3:0.6
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:4
Exact Mass:434.12129689
Monoisotopic Mass:434.12129689
Topological Polar Surface Area:166
Heavy Atom Count:31
Complexity:623
Defined Atom Stereocenter Count:6
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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