ID: ALA2323425

Max Phase: Preclinical

Molecular Formula: C24H44Cl2N4

Molecular Weight: 388.64

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[n+]1ccn(CCCCCCCCCCCCCCCCn2cc[n+](C)c2)c1.[Cl-].[Cl-]

Standard InChI:  InChI=1S/C24H44N4.2ClH/c1-25-19-21-27(23-25)17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-28-22-20-26(2)24-28;;/h19-24H,3-18H2,1-2H3;2*1H/q+2;;/p-2

Standard InChI Key:  NSDFJZGMBYSIQS-UHFFFAOYSA-L

Associated Targets(Human)

Beta-1,3-galactosyltransferase 5 26 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Beta-1,4-galactosyltransferase 1 37 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: 388.64Molecular Weight (Monoisotopic): 388.3555AlogP: 5.10#Rotatable Bonds: 17
Polar Surface Area: 17.62Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: -1.20CX LogD: -1.20
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.26Np Likeness Score: -0.13

References

1. Gao Y, Vlahakis JZ, Szarek WA, Brockhausen I..  (2013)  Selective inhibition of glycosyltransferases by bivalent imidazolium salts.,  21  (5): [PMID:23375091] [10.1016/j.bmc.2012.12.034]
2. Kocev A, Melamed J, Wang S, Kong X, Vlahakis JZ, Xu Y, Szarek WA, Brockhausen I..  (2020)  Inhibition of bacterial growth and galactosyltransferase activity of WbwC by α, ω-bis(3-alkyl-1H-imidazolium)alkane salts: Effect of varying carbon content.,  28  (11): [PMID:32312486] [10.1016/j.bmc.2020.115494]

Source