heminigerone (Q27290019)

Rubrofusarin B (English)

14 October 2016

chemical formula

C₁₆H₁₄O₅

1 reference

Rubrofusarin B (English)

14 October 2016

canonical SMILES

CC1=CC(=O)C2=C(O1)C=C3C=C(C=C(C3=C2O)OC)OC

1 reference

Effect of selected phytotoxins from Guanomyces polythrix on the calmodulin-dependent activity of the enzymes cAMP phosphodiesterase and NAD-kinase

Rubrofusarin B (English)

14 October 2016

7 references

Phytotoxic compounds from the new coprophilous fungus guanomyces polythrix

Phytotoxic compounds from the new coprophilous fungus guanomyces polythrix

Phytotoxic compounds from the new coprophilous fungus guanomyces polythrix

Phytotoxic compounds from the new coprophilous fungus guanomyces polythrix

Phytotoxic naphthopyranone derivatives from the coprophilous fungus Guanomyces polythrix.

Phytotoxic compounds from the new coprophilous fungus guanomyces polythrix

Aspergillus niger

3 references

Asnipyrones A and B, Two Novel Metabolites from Aspergillus niger

Structural elucidation of the nigerones, four new naphthopyrones from cultures of Aspergillus niger

TMC-256A1 and C1, new inhibitors of IL-4 signal transduction produced by Aspergillus niger var niger TC 1629

Aspergillus tubingensis

7 references

Isolation, Structure elucidation, and antimycobacterial properties of dimeric naphtho-gamma-pyrones from the marine-derived fungus Aspergillus carbonarius

Three Dimeric Naphtho-γ-Pyrones from the Mangrove Endophytic FungusAspergillus tubingensisIsolated fromPongamia pinnata

Asperpyrone D and other metabolites of the plant-associated fungal strain Aspergillus tubingensis

Three Dimeric Naphtho-γ-Pyrones from the Mangrove Endophytic FungusAspergillus tubingensisIsolated fromPongamia pinnata

Asperpyrone D and other metabolites of the plant-associated fungal strain Aspergillus tubingensis

Cytotoxic Naphtho-γ-pyrones from the Mangrove Endophytic Fungus Aspergillus tubingensis (GX1-5E)

A new pyrone derivative from an endophytic Aspergillus tubingensis of Lycium ruthenicum.

Cladosporium herbarum

1 reference

Structural revision of aspernigrin A, reisolated from Cladosporium herbarum IFB-E002.

Aspergillus fonsecaeus

1 reference

Two novel metabolites ofAspergillus fonsecaeus

Alternaria alternata

1 reference

Seven naphtho-γ-pyrones from the marine-derived fungus Alternaria alternata: structure elucidation and biological properties

Pongamia pinnata

1 reference

Three Dimeric Naphtho-γ-Pyrones from the Mangrove Endophytic FungusAspergillus tubingensisIsolated fromPongamia pinnata

Identifiers

InChI

InChI=1S/C16H14O5/c1-8-4-11(17)15-13(21-8)6-9-5-10(19-2)7-12(20-3)14(9)16(15)18/h4-7,18H,1-3H3

1 reference

Rubrofusarin B (English)

14 October 2016

2 references

Rubrofusarin B (English)

14 October 2016

ChEBI release 2020-09-01

CAS Registry Number

17276-15-2

2 references

Global Substance Registration System

UNII

TLJ90R747F

heminigerone (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=17276-15-2

10 April 2021

1 reference

5-Hydroxy-6,8-dimethoxy-2-methyl-4H-benzo[g]chromen-4-one (English)

14 October 2016

2 references

Rubrofusarin B (English)

14 October 2016

ChEBI ID

133805

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C16H14O5/c1-8-4-11(17)15-13(21-8)6-9-5-10(19-2)7-12(20-3)14(9)16(15)18/h4-7,18H,1-3H3

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

RUBROFUSARIN B (English)

14 October 2016

1 reference

2 references

DSSTOX compound identifier

0 references

2 references

inferred from InChIKey

UNII

TLJ90R747F

2 references

Global Substance Registration System

UNII

TLJ90R747F

heminigerone (English)

14 October 2016