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naphtho-gamma-pyrone

Any naphthopyran whose skeleton consists of a naphathalene ring system ortho-fused to a gamma-pyrone.

ChEBI ID: 64542

Members (7)

MemberDefinitionRole
adefovirA dimeric naphthopyran with formula C32H26O10, originally isolated from Aspergillus niger.aurasperone A
alpha-naphthoflavoneAn extended flavonoid resulting from the formal fusion of a benzene ring with the h side of flavone. A synthetic compound, it is an inhibitor of aromatase (EC 1.14.14.14).alpha-naphthoflavone
beta-naphthoflavoneAn extended flavonoid resulting from the formal fusion of a benzene ring with the f side of flavone.beta-naphthoflavone
flavasperoneA naphtho-gamma-pyrone that is 4H-naphtho[1,2-b]pyran-4-one carrying a methyl substituent at position2, a hydroxy substituent at position 5 and two methoxy substotuents at positions 8 and 10. Originally isolated from Aspergillus niger.flavasperone
fonsecinA naphtho-gamma-pyrone that is 2,3-dihydro-4H-benzo[g]chromen-4-one bearing a methyl substituent at position 2, a methoxy substituent at position 6 and three hydroxy substituents at positions 2, 5 and 8.fonsecin
fonsecinone aA dimeric naphthopyran with formula C32H26O10, originally isolated from Aspergillus niger.fonsecinone A
rubrofusarin BA benzochromenone that is rubrofusarin in which the hydroxy group at position 6 has been converted to the corresponding methyl ether.rubrofusarin B

Research

Studies (1,739)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-1990490 (28.18)18.7374
1990's516 (29.67)18.2507
2000's406 (23.35)29.6817
2010's268 (15.41)24.3611
2020's59 (3.39)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials1 (0.05%)5.53%
Reviews20 (1.03%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other1,912 (98.91%)84.16%