Molecule

Araplysillin I; N20-(12ξ-Methyloctadecanoyl)

AlkaPlorer ID: AK289120

Synonym: Araplysillin V

IUPAC Name: 7,9-dibromo-N-[3-[2,6-dibromo-4-[2-(12-methyloctadecanoylamino)ethyl]phenoxy]propyl]-6-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,7,9-triene-3-carboxamide

Structure

SMILES: CCCCCCC(C)CCCCCCCCCCC(=O)NCCC1=CC(Br)=C(OCCCNC(=O)C2=NOC3(C=C(Br)C(OC)=C(Br)C3O)C2)C(Br)=C1

InChI: InChI=1S/C40H59Br4N3O6/c1-4-5-6-13-17-28(2)18-14-11-9-7-8-10-12-15-19-34(48)45-22-20-29-24-30(41)36(31(42)25-29)52-23-16-21-46-39(50)33-27-40(53-47-33)26-32(43)37(51-3)35(44)38(40)49/h24-26,28,38,49H,4-23,27H2,1-3H3,(H,45,48)(H,46,50)

InChIKey: GGMCHHYLYOWDEP-UHFFFAOYSA-N

Reference

A New Mode of Stereochemical Control Revealed by Analysis of the Biosynthesis of Dihydrogranaticin in Streptomyces violaceoruber Tü22

A Two-Step Mechanism for the Activation of Actinorhodin Export and Resistance in Streptomyces coelicolor

Unveiling Two Consecutive Hydroxylations: Mechanisms of Aromatic Hydroxylations Catalyzed by Flavin‐Dependent Monooxygenases for the Biosynthesis of Actinorhodin and Related Antibiotics

Chemical Characterisation of Disruptants of the Streptomyces coelicolor A3(2). ActVI Genes Involved in Actinorhodin Biosynthesis.

PubChem CID: 162876056

COCONUT: CNP0141232.2

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Suberea ianthelliformis	Suberea	Aplysinellidae	Verongiida	Demospongiae	Porifera	Metazoa	Eukaryota

Properties Information

Molecule Weight: 997.543

TPSA？: 118.48000000000002

MolLogP？: 10.684199999999992

Number of H-Donors: 3

Number of H-Acceptors: 7

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi