ID: ALA2386133

Max Phase: Preclinical

Molecular Formula: C12H16ClN3O3

Molecular Weight: 285.73

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(Nc1ccnc(Cl)c1)OCCN1CCOCC1

Standard InChI:  InChI=1S/C12H16ClN3O3/c13-11-9-10(1-2-14-11)15-12(17)19-8-5-16-3-6-18-7-4-16/h1-2,9H,3-8H2,(H,14,15,17)

Standard InChI Key:  HUEKDASCTSZWES-UHFFFAOYSA-N

Associated Targets(non-human)

Sterol 14-alpha demethylase 857 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

L6 7924 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Leishmania donovani 89745 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypanosoma cruzi 99888 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypanosoma brucei rhodesiense 7991 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: 285.73Molecular Weight (Monoisotopic): 285.0880AlogP: 1.62#Rotatable Bonds: 4
Polar Surface Area: 63.69Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.64CX Basic pKa: 6.12CX LogP: 1.24CX LogD: 1.21
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.85Np Likeness Score: -2.01

References

1. Friggeri L, Scipione L, Costi R, Kaiser M, Moraca F, Zamperini C, Botta B, Di Santo R, De Vita D, Brun R, Tortorella S..  (2013)  New Promising Compounds with in Vitro Nanomolar Activity against Trypanosoma cruzi.,  (6): [PMID:24900706] [10.1021/ml400039r]

Source