ID: ALA2392530

Max Phase: Preclinical

Molecular Formula: C17H18ClIN2O3

Molecular Weight: 460.70

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=c1cc(CCl)oc(CN2CCN(c3ccc(I)cc3)CC2)c1O

Standard InChI:  InChI=1S/C17H18ClIN2O3/c18-10-14-9-15(22)17(23)16(24-14)11-20-5-7-21(8-6-20)13-3-1-12(19)2-4-13/h1-4,9,23H,5-8,10-11H2

Standard InChI Key:  DSBSXWLYJZSZFB-UHFFFAOYSA-N

Associated Targets(Human)

HeLa 62764 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MRC5 9203 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Epidermophyton floccosum 561 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nannizzia gypsea 2039 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: 460.70Molecular Weight (Monoisotopic): 460.0051AlogP: 3.01#Rotatable Bonds: 4
Polar Surface Area: 56.92Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.95CX Basic pKa: 5.50CX LogP: 3.39CX LogD: 3.37
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.56Np Likeness Score: -0.96

References

1. Aytemir MD, Ozçelik B, Karakaya G..  (2013)  Evaluation of bioactivities of chlorokojic acid derivatives against dermatophytes couplet with cytotoxicity.,  23  (12): [PMID:23664872] [10.1016/j.bmcl.2013.03.098]

Source