ID: ALA3298108

Max Phase: Preclinical

Molecular Formula: C18H13I2NO2

Molecular Weight: 529.12

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1c(I)cc(I)cc1C(=O)Nc1ccc2ccccc2c1

Standard InChI:  InChI=1S/C18H13I2NO2/c1-23-17-15(9-13(19)10-16(17)20)18(22)21-14-7-6-11-4-2-3-5-12(11)8-14/h2-10H,1H3,(H,21,22)

Standard InChI Key:  LSZPGMLJSBNNPG-UHFFFAOYSA-N

Associated Targets(Human)

HEK-293T 167025 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Caenorhabditis elegans 1055 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Onchocerca volvulus 56 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Chitinase 71 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: 529.12Molecular Weight (Monoisotopic): 528.9036AlogP: 5.31#Rotatable Bonds: 3
Polar Surface Area: 38.33Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 2HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 5.75CX LogD: 5.75
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.47Np Likeness Score: -1.17

References

1. Gooyit M, Tricoche N, Lustigman S, Janda KD..  (2014)  Dual protonophore-chitinase inhibitors dramatically affect O. volvulus molting.,  57  (13): [PMID:24918716] [10.1021/jm5006435]

Source