(Q27135298)

inferred from InChI

chemical formula

C₂₂H₁₂Cl₄N₂O₄

1 reference

Marinopyrrole A (English)

7 October 2016

canonical SMILES

C1=CC=C(C(=C1)C(=O)C2=CC(=C(N2C3=C(NC(=C3Cl)Cl)C(=O)C4=CC=CC=C4O)Cl)Cl)O

1 reference

The marinopyrroles, antibiotics of an unprecedented structure class from a marine Streptomyces sp.

Marinopyrrole A (English)

7 October 2016

1 reference

Identifiers

InChI

InChI=1S/C22H12Cl4N2O4/c23-12-9-13(19(31)10-5-1-3-7-14(10)29)28(22(12)26)18-16(24)21(25)27-17(18)20(32)11-6-2-4-8-15(11)30/h1-9,27,29-30H

1 reference

Marinopyrrole A (English)

7 October 2016

2 references

Marinopyrrole A (English)

7 October 2016

stated in

ChEBI release 2020-09-01

1 reference

marinopyrrole A (English)

7 October 2016

2 references

Marinopyrrole A (English)

7 October 2016

Reaxys registry number

11303256

1 reference

(-)-marinopyrrole A (English)

7 October 2016

ChEBI ID

66678

mapping relation type

2 references

(-)-marinopyrrole A (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C22H12Cl4N2O4/c23-12-9-13(19(31)10-5-1-3-7-14(10)29)28(22(12)26)18-16(24)21(25)27-17(18)20(32)11-6-2-4-8-15(11)30/h1-9,27,29-30H

1 reference

Human Metabolome Database ID

CHEMBL3393621 (English)

7 October 2016

1 reference

HMDB0242215

2 references

inferred from InChIKey

KNApSAcK ID

C00048770

2 references

inferred from InChIKey

Natural Product Atlas ID

NPA003314

2 references

inferred from InChIKey