Molecule

Alldimycin A

AlkaPlorer ID: AK021463

Synonym: None

IUPAC Name: (7S,9R,10R)-7-[(2R,4S,5R,6R)-4-(dimethylamino)-5-hydroxy-6-methyloxan-2-yl]oxy-9-ethyl-1,4,9,10,11-pentahydroxy-8,10-dihydro-7H-tetracene-5,12-dione

Structure

SMILES: CC[C@@]1(O)C[C@H](O[C@H]2C[C@H](N(C)C)[C@@H](O)[C@@H](C)O2)C2=CC3=C(C(=O)C4=C(O)C=CC(O)=C4C3=O)C(O)=C2[C@H]1O

InChI: InChI=1S/C28H33NO10/c1-5-28(37)10-17(39-18-9-14(29(3)4)23(32)11(2)38-18)12-8-13-19(25(34)20(12)27(28)36)26(35)22-16(31)7-6-15(30)21(22)24(13)33/h6-8,11,14,17-18,23,27,30-32,34,36-37H,5,9-10H2,1-4H3/t11-,14+,17+,18+,23+,27-,28-/m1/s1

InChIKey: KPUUTJSVCSKVTL-FSBDOOBYSA-N

Reference

Anthracycline metabolites from Streptomyces violaceus A262. I. Isolation of antibiotic-blocked mutants from Streptomyces violaceus A262.

PubChem CID: 139589235

LOTUS: LTS0032004

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NPAtlas: NPA021279

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Streptomyces violaceus	Streptomyces	Streptomycetaceae	Kitasatosporales	Actinomycetes	Actinomycetota	None	Bacteria

Properties Information

Molecule Weight: 543.5690000000004

TPSA？: 177.22

MolLogP？: 1.6407

Number of H-Donors: 6

Number of H-Acceptors: 11

RingCount: 5

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi