(Q27137130)

CHEMBL1673300 (English)

7 October 2016

chemical formula

C₁₅H₁₂O₈

1 reference

CHEMBL1673300 (English)

7 October 2016

canonical SMILES

CC1=CC2=C(C(O1)OC)C(=O)C3=C(C(=C(C=C3O2)O)O)C(=O)O

1 reference

Inducing secondary metabolite production by the endophytic fungus Chaetomium sp. through fungal–bacterial co-culture and epigenetic modification

CHEMBL1673300 (English)

7 October 2016

1 reference

Identifiers

InChI

InChI=1S/C15H12O8/c1-5-3-7-10(15(21-2)22-5)13(18)9-8(23-7)4-6(16)12(17)11(9)14(19)20/h3-4,15-17H,1-2H3,(H,19,20)

1 reference

CHEMBL1673300 (English)

CBEPLTZXYMLBAP-UHFFFAOYSA-N

7 October 2016

InChIKey

2 references

CHEMBL1673300 (English)

7 October 2016

stated in

ChEBI release 2020-09-01

1 reference

7,8-Dihydroxy-1-methoxy-3-methyl-10-oxo-1H,10H-pyrano[4,3-b]chromene-9-carboxylic acid (English)

7 October 2016

2 references

CHEMBL1673300 (English)

matched by identifier from

7 October 2016

InChIKey

CBEPLTZXYMLBAP-UHFFFAOYSA-N

Reaxys registry number

9580812

1 reference

7,8-dihydroxy-1-methoxy-3-methyl-10-oxo-1H,10H-pyrano[4,3-b]chromene-9-carboxylic acid (English)

7 October 2016

ChEBI ID

68710

mapping relation type

2 references

7,8-dihydroxy-1-methoxy-3-methyl-10-oxo-1H,10H-pyrano[4,3-b]chromene-9-carboxylic acid (English)

matched by identifier from

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H12O8/c1-5-3-7-10(15(21-2)22-5)13(18)9-8(23-7)4-6(16)12(17)11(9)14(19)20/h3-4,15-17H,1-2H3,(H,19,20)

1 reference