Molecule

Protoaculeine B

AlkaPlorer ID: AK311296

Synonym: None

IUPAC Name: 2-amino-3-[9-[3-[3-[3-[3-[3-[3-[3-[3-[3-[3-[3-[3-[3-(3-aminopropylamino)propylamino]propylamino]propylamino]propylamino]propylamino]propylamino]propylamino]propylamino]propylamino]propylamino]propylamino]propylamino]propylamino]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]propanoic acid

Structure

SMILES: NCCCNCCCNCCCNCCCNCCCNCCCNCCCNCCCNCCCNCCCNCCCNCCCNCCCNCCCNC1CCCN2C1=C(CC(N)C(=O)O)C1=CC=CC=C12

InChI: InChI=1S/C57H117N17O2/c58-21-4-22-60-23-5-24-61-25-6-26-62-27-7-28-63-29-8-30-64-31-9-32-65-33-10-34-66-35-11-36-67-37-12-38-68-39-13-40-69-41-14-42-70-43-15-44-71-45-16-46-72-47-17-48-73-54-19-3-49-74-55-20-2-1-18-51(55)52(56(54)74)50-53(59)57(75)76/h1-2,18,20,53-54,60-73H,3-17,19,21-50,58-59H2,(H,75,76)

InChIKey: YBSWAWNJIWVPIK-UHFFFAOYSA-N

Reference

Inhibitory activity of blasticidin A, a strong aflatoxin production inhibitor, on protein synthesis of yeast: selective inhibition of aflatoxin production by protein synthesis inhibitors

PubChem CID: 101548126

COCONUT: CNP0436036.1

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
None	Aculeata	Herpotrichiellaceae	Chaetothyriales	Eurotiomycetes	Ascomycota	Fungi	Eukaryota

Properties Information

Molecule Weight: 1072.679999999999

TPSA？: 262.69

MolLogP？: 1.105099999999973

Number of H-Donors: 17

Number of H-Acceptors: 18

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi