ID: ALA4283734

Max Phase: Preclinical

Molecular Formula: C26H52N4O11

Molecular Weight: 596.72

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCO[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](N)C[C@H](N)[C@H]1O[C@H]1O[C@H](CN)[C@@H](O)[C@H](O)[C@H]1N

Standard InChI:  InChI=1S/C26H52N4O11/c1-2-3-4-5-6-7-8-37-24-22(40-25-16(30)19(34)17(32)14(10-27)38-25)12(28)9-13(29)23(24)41-26-21(36)20(35)18(33)15(11-31)39-26/h12-26,31-36H,2-11,27-30H2,1H3/t12-,13+,14+,15+,16+,17+,18+,19+,20-,21+,22+,23-,24-,25+,26+/m0/s1

Standard InChI Key:  OHFBPVVVXICADV-NVUPSPOHSA-N

Associated Targets(non-human)

Fusarium graminearum 1554 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 596.72Molecular Weight (Monoisotopic): 596.3633AlogP: -3.91#Rotatable Bonds: 14
Polar Surface Area: 271.61Molecular Species: BASEHBA: 15HBD: 10
#RO5 Violations: 3HBA (Lipinski): 15HBD (Lipinski): 14#RO5 Violations (Lipinski): 3
CX Acidic pKa: 12.14CX Basic pKa: 9.64CX LogP: -3.32CX LogD: -8.31
Aromatic Rings: 0Heavy Atoms: 41QED Weighted: 0.09Np Likeness Score: 1.29

References

1. Subedi YP, AlFindee MN, Takemoto JY, Chang CT..  (2018)  Antifungal amphiphilic kanamycins: new life for an old drug.,  (6): [PMID:30108980] [10.1039/C8MD00155C]

Source