Blasticidin H
AlkaPlorer ID: AK020220
Synonym: None
IUPAC Name: (2S,3S,5R,6S)-3-[[(3S)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-5-hydroxyoxane-2-carboxylic acid
Structure
SMILES: CN(CC[C@H](N)CC(O)=N[C@H]1C[C@@H](O)[C@@H](N2C=CC(=N)N=C2O)O[C@@H]1C(=O)O)C(=N)N
InChI: InChI=1S/C17H28N8O6/c1-24(16(20)21)4-2-8(18)6-12(27)22-9-7-10(26)14(31-13(9)15(28)29)25-5-3-11(19)23-17(25)30/h3,5,8-10,13-14,26H,2,4,6-7,18H2,1H3,(H3,20,21)(H,22,27)(H,28,29)(H2,19,23,30)/t8-,9-,10+,13-,14-/m0/s1
InChIKey: DBZWUKQWLUXEEQ-XXBVRILMSA-N
Reference
Studies on the biosynthesis of blasticidin S. VI. The isolation and structure of blasticidin H.
PubChem CID: 139589145
LOTUS: LTS0019727
{NPAtlas: NPA021111
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Streptomyces griseochromogenes | Streptomyces | Streptomycetaceae | Kitasatosporales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 440.4610000000002
TPSA？: 240.38
MolLogP？: -1.940959999999997
Number of H-Donors: 8
Number of H-Acceptors: 10
RingCount: 2
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|