Araplysillin I; N20-(10ξ-Methylhexadecanoyl)
AlkaPlorer ID: AK289119
Synonym: Araplysillin IV
IUPAC Name: 7,9-dibromo-N-[3-[2,6-dibromo-4-[2-(10-methylhexadecanoylamino)ethyl]phenoxy]propyl]-6-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,7,9-triene-3-carboxamide
Structure
SMILES: CCCCCCC(C)CCCCCCCCC(=O)NCCC1=CC(Br)=C(OCCCNC(=O)C2=NOC3(C=C(Br)C(OC)=C(Br)C3O)C2)C(Br)=C1
InChI: InChI=1S/C38H55Br4N3O6/c1-4-5-6-11-15-26(2)16-12-9-7-8-10-13-17-32(46)43-20-18-27-22-28(39)34(29(40)23-27)50-21-14-19-44-37(48)31-25-38(51-45-31)24-30(41)35(49-3)33(42)36(38)47/h22-24,26,36,47H,4-21,25H2,1-3H3,(H,43,46)(H,44,48)
InChIKey: OZRCQUDHJHHCTQ-UHFFFAOYSA-N
Reference
A Peptidyl‐Transesterifying Type I Thioesterase in Salinamide Biosynthesis
PubChem CID: 162903575
COCONUT: CNP0171847.2
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Suberea ianthelliformis | Suberea | Aplysinellidae | Verongiida | Demospongiae | Porifera | Metazoa | Eukaryota |
Properties Information
Molecule Weight: 969.489
TPSA？: 118.48000000000002
MolLogP？: 9.903999999999998
Number of H-Donors: 3
Number of H-Acceptors: 7
RingCount: 3
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|