ID: ALA1162901

Max Phase: Preclinical

Molecular Formula: C16H12ClIN2

Molecular Weight: 267.74

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[n+]1c2ccccc2cc2[nH]c3cc(Cl)ccc3c21.[I-]

Standard InChI:  InChI=1S/C16H11ClN2.HI/c1-19-15-5-3-2-4-10(15)8-14-16(19)12-7-6-11(17)9-13(12)18-14;/h2-9H,1H3;1H

Standard InChI Key:  RSRRNMLJDLYUHQ-UHFFFAOYSA-N

Associated Targets(non-human)

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MAC15A 81 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 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: 267.74Molecular Weight (Monoisotopic): 267.0684AlogP: 3.95#Rotatable Bonds: 0
Polar Surface Area: 19.67Molecular Species: NEUTRALHBA: 0HBD: 1
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.81CX Basic pKa: CX LogP: -0.42CX LogD: -0.43
Aromatic Rings: 4Heavy Atoms: 19QED Weighted: 0.47Np Likeness Score: 0.30

References

1. Onyeibor O, Croft SL, Dodson HI, Feiz-Haddad M, Kendrick H, Millington NJ, Parapini S, Phillips RM, Seville S, Shnyder SD, Taramelli D, Wright CW..  (2005)  Synthesis of some cryptolepine analogues, assessment of their antimalarial and cytotoxic activities, and consideration of their antimalarial mode of action.,  48  (7): [PMID:15801861] [10.1021/jm040893w]

Source