Molecule

N-acetyl-S-(8-methoxy-4H-thiazolo[5,4-b]indol-2-yl)-L-cysteine

AlkaPlorer ID: AK327806

Synonym: None

IUPAC Name: (2R)-2-acetamido-3-[(8-methoxy-4H-[1,3]thiazolo[5,4-b]indol-2-yl)sulfanyl]propanoic acid

Structure

SMILES: COC1=CC=CC2=C1C1=C(N2)SC(SC[C@H](NC(C)=O)C(=O)O)=N1

InChI: InChI=1S/C15H15N3O4S2/c1-7(19)16-9(14(20)21)6-23-15-18-12-11-8(17-13(12)24-15)4-3-5-10(11)22-2/h3-5,9,17H,6H2,1-2H3,(H,16,19)(H,20,21)/t9-/m0/s1

InChIKey: CCYURQHTZWFINX-VIFPVBQESA-N

Reference

Unveiling fungal detoxification pathways of the cruciferous phytoalexin rapalexin A: Sequential L-cysteine conjugation, acetylation and oxidative cyclization mediated by Colletotrichum spp.

PubChem CID: 156582604

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NPAtlas: NPA031865

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Colletotrichum higginsianum	Colletotrichum	Glomerellaceae	Glomerellales	Sordariomycetes	Ascomycota	Fungi	Eukaryota

Properties Information

Molecule Weight: 365.4360000000001

TPSA？: 104.31

MolLogP？: 2.4676

Number of H-Donors: 3

Number of H-Acceptors: 6

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi