ID: ALA3216135

Max Phase: Preclinical

Molecular Formula: C24H44Cl2N4

Molecular Weight: 386.63

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cl.Cl.c1cn(CCCCCCCCCCCCCCCCCCn2ccnc2)cn1

Standard InChI:  InChI=1S/C24H42N4.2ClH/c1(3-5-7-9-11-13-15-19-27-21-17-25-23-27)2-4-6-8-10-12-14-16-20-28-22-18-26-24-28;;/h17-18,21-24H,1-16,19-20H2;2*1H

Standard InChI Key:  RLCVJIZLDJFWAN-UHFFFAOYSA-N

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: 386.63Molecular Weight (Monoisotopic): 386.3409AlogP: 7.02#Rotatable Bonds: 19
Polar Surface Area: 35.64Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 6.84CX LogP: 6.79CX LogD: 6.71
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.24Np Likeness Score: -0.56

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. Crandall IE, Zhao B, Vlahakis JZ, Szarek WA..  (2013)  The interaction of imidazole-, imidazolium-, and tetrazolium-containing compounds with DNA.,  23  (5): [PMID:23375791] [10.1016/j.bmcl.2012.11.106]

Source