3',8-Dihydroxy-4',6,7-trimethoxyisoflavone

3',8-Dihydroxy-4',6,7-trimethoxyisoflavone

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3',8-Dihydroxy-4',6,7-trimethoxyisoflavone
Category Enzyme inhibitors
Catalog number BBF-01151
CAS 57800-11-0
Molecular Weight 344.32
Molecular Formula C18H16O7

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Description

It is produced by the strain of Streptomyces sp. It is a catechole-O-methyltransferase inhibitor (IC50 is 0.2 g/mL).

Specification

Synonyms 6,7-Dimethoxy-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran; 4H-1-Benzopyran, 6,7-dimethoxy-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-
IUPAC Name 8-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-6,7-dimethoxychromen-4-one
Canonical SMILES COC1=C(C=C(C=C1)C2=COC3=C(C(=C(C=C3C2=O)OC)OC)O)O
InChI InChI=1S/C18H16O7/c1-22-13-5-4-9(6-12(13)19)11-8-25-17-10(15(11)20)7-14(23-2)18(24-3)16(17)21/h4-8,19,21H,1-3H3
InChI Key CFAKQDITHIYGEK-UHFFFAOYSA-N

Properties

Boiling Point 587.0 °C at 760 mmHg
Density 1.387 g/cm3
Solubility Soluble in Ethanol

Reference Reading

1. New isoflavones, inhibiting catechol-O-methyltransferase, produced by Streptomyces
H Chimura, T Sawa, Y Kumada, H Naganawa, M Matsuzaki J Antibiot (Tokyo). 1975 Sep;28(9):619-26. doi: 10.7164/antibiotics.28.619.
In the screening of catechol-O-methyltransferase inhibitors in streptomyces culture filtrates, three new isoflavones were isolated. Their structures were shown to be 3',5,7-trihydroxy-4',6-dimethoxyisoflavone (I), 3',5,7-trihydroxy-4',8-dimethoxyisoflavone (II), 3',8-dihydroxy-4',6,7-trimethoxyisoflavone (III). I and II inhibited both catechol-O-methyltransferase and dopa decarboxylase, and showed hypotensive action. III was a specific inhibitor of catechol-O-methyltransferase, and showed no hypotensive action.

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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