ID: ALA2323434

Max Phase: Preclinical

Molecular Formula: C16H28Cl2N4

Molecular Weight: 276.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[n+]1ccn(CCCCCCCCn2cc[n+](C)c2)c1.[Cl-].[Cl-]

Standard InChI:  InChI=1S/C16H28N4.2ClH/c1-17-11-13-19(15-17)9-7-5-3-4-6-8-10-20-14-12-18(2)16-20;;/h11-16H,3-10H2,1-2H3;2*1H/q+2;;/p-2

Standard InChI Key:  OLSDEZQOJHMNLQ-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: 276.43Molecular Weight (Monoisotopic): 276.2303AlogP: 1.98#Rotatable Bonds: 9
Polar Surface Area: 17.62Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: -4.76CX LogD: -4.76
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.49Np Likeness Score: -0.18

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