Saptomycin G; 14ξ,16ξ-Epoxide
AlkaPlorer ID: AK312927
Synonym: Saptomycin E
IUPAC Name: [4-(dimethylamino)-6-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-5-methyl-4,7,12-trioxonaphtho[2,3-h]chromen-10-yl]-2,4-dimethyloxan-3-yl] acetate
Structure
SMILES: CC(=O)OC1C(C)OC(C2=CC=C3C(=O)C4=CC(C)=C5C(=O)C=C(C6(C)OC6C)OC5=C4C(=O)C3=C2O)CC1(C)N(C)C
InChI: InChI=1S/C33H35NO9/c1-14-11-20-26(30-24(14)21(36)12-23(42-30)33(6)16(3)43-33)29(39)25-19(27(20)37)10-9-18(28(25)38)22-13-32(5,34(7)8)31(15(2)40-22)41-17(4)35/h9-12,15-16,22,31,38H,13H2,1-8H3
InChIKey: DLWNUUQBCVPEHS-UHFFFAOYSA-N
Reference
Novel antitumor antibiotics, saptomycins D and E.
PubChem CID: 3035678
CAS: 137714-92-2
LOTUS: LTS0263878
COCONUT: CNP0219640.3
{NPAtlas: NPA006909
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Streptomyces sp. | Streptomyces | Streptomycetaceae | Kitasatosporales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 589.6410000000002
TPSA？: 135.88
MolLogP？: 4.318220000000004
Number of H-Donors: 1
Number of H-Acceptors: 10
RingCount: 6
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|