ID: ALA4214786

Max Phase: Preclinical

Molecular Formula: C36H72N4O11

Molecular Weight: 736.99

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCCOC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O[C@H]3O[C@H](CN)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](N)C[C@H]2N)[C@H](O)[C@@H](N)[C@@H]1OCCCCCCCCC

Standard InChI:  InChI=1S/C36H72N4O11/c1-3-5-7-9-11-13-15-17-46-21-25-34(47-18-16-14-12-10-8-6-4-2)26(40)28(42)35(49-25)50-32-22(38)19-23(39)33(31(32)45)51-36-30(44)29(43)27(41)24(20-37)48-36/h22-36,41-45H,3-21,37-40H2,1-2H3/t22-,23+,24-,25-,26-,27-,28-,29+,30-,31-,32+,33-,34-,35+,36-/m1/s1

Standard InChI Key:  SVRLLXRKEPURDL-DSNJFVELSA-N

Associated Targets(Human)

Gap junction beta-2 protein 74 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HeLa 62764 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 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: 736.99Molecular Weight (Monoisotopic): 736.5198AlogP: 0.26#Rotatable Bonds: 24
Polar Surface Area: 260.61Molecular Species: BASEHBA: 15HBD: 9
#RO5 Violations: 3HBA (Lipinski): 15HBD (Lipinski): 13#RO5 Violations (Lipinski): 3
CX Acidic pKa: 12.07CX Basic pKa: 9.50CX LogP: 1.32CX LogD: -4.00
Aromatic Rings: 0Heavy Atoms: 51QED Weighted: 0.06Np Likeness Score: 0.97

References

1. AlFindee MN, Subedi YP, Fiori MC, Krishnan S, Kjellgren A, Altenberg GA, Chang CT..  (2018)  Inhibition of Connexin Hemichannels by New Amphiphilic Aminoglycosides without Antibiotic Activity.,  (7): [PMID:30034603] [10.1021/acsmedchemlett.8b00158]

Source