Paromomycin; 3'-Deoxy
AlkaPlorer ID: AK309416
Synonym: Lividomycin B, Quintomycin D, SF 767D, Antibiotic SF 767D
IUPAC Name: 5-amino-2-(aminomethyl)-6-[5-[3,5-diamino-2-[3-amino-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxycyclohexyl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxyoxane-3,4-diol
Structure
SMILES: NCC1OC(OC2C(CO)OC(OC3C(O)C(N)CC(N)C3OC3OC(CO)C(O)CC3N)C2O)C(N)C(O)C1O
InChI: InChI=1S/C23H45N5O13/c24-3-10-15(33)16(34)13(28)22(36-10)40-19-12(5-30)38-23(17(19)35)41-20-14(32)6(25)1-7(26)18(20)39-21-8(27)2-9(31)11(4-29)37-21/h6-23,29-35H,1-5,24-28H2
InChIKey: BRSBFYLXCMGALM-UHFFFAOYSA-N
Reference
STUDIES ON NEW ANTIBIOTIC LIVIDOMYCINS
PubChem CID: 216713
CAS: 37636-51-4
LOTUS: LTS0032960
COCONUT: CNP0319915.4
{NPAtlas: NPA021203
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Streptomyces lividus | Streptomyces | Streptomycetaceae | Kitasatosporales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 599.6350000000003
TPSA？: 327.09000000000003
MolLogP？: -7.832500000000013
Number of H-Donors: 12
Number of H-Acceptors: 18
RingCount: 4
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|