Medermycin; 4a,10a-Epoxide
AlkaPlorer ID: AK305400
Synonym: Lactoquinomycin B
IUPAC Name: 5-[4-(dimethylamino)-5-hydroxy-6-methyloxan-2-yl]-4-hydroxy-17-methyl-12,16,18-trioxapentacyclo[8.7.1.01,10.03,8.011,15]octadeca-3(8),4,6-triene-2,9,13-trione
Structure
SMILES: CC1OC(C2=CC=C3C(=O)C45OC4(C(=O)C3=C2O)C(C)OC2CC(=O)OC25)CC(N(C)C)C1O
InChI: InChI=1S/C24H27NO9/c1-9-18(27)13(25(3)4)7-14(31-9)11-5-6-12-17(19(11)28)21(30)23-10(2)32-15-8-16(26)33-22(15)24(23,34-23)20(12)29/h5-6,9-10,13-15,18,22,27-28H,7-8H2,1-4H3
InChIKey: UKGUMAYTBDAONQ-UHFFFAOYSA-N
Reference
Lactoquinomycin B, a novel antibiotic.
PubChem CID: 130509
CAS: 101342-94-3
LOTUS: LTS0076497
COCONUT: CNP0144273.1
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Streptomyces tanashiensis | Streptomyces | Streptomycetaceae | Kitasatosporales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 473.4780000000002
TPSA？: 135.13
MolLogP？: 0.5227999999999999
Number of H-Donors: 2
Number of H-Acceptors: 10
RingCount: 6
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|