ID: ALA2312447

Max Phase: Preclinical

Molecular Formula: C21H21NO3S

Molecular Weight: 367.47

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(OCc1ccccc1)c1sc2ccccc2c1OC1CCNCC1

Standard InChI:  InChI=1S/C21H21NO3S/c23-21(24-14-15-6-2-1-3-7-15)20-19(25-16-10-12-22-13-11-16)17-8-4-5-9-18(17)26-20/h1-9,16,22H,10-14H2

Standard InChI Key:  KYSZDGRYJADZAK-UHFFFAOYSA-N

Associated Targets(Human)

Peptide N-myristoyltransferase 2 44 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Peptide N-myristoyltransferase 1 643 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Glycylpeptide N-tetradecanoyltransferase 128 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: 367.47Molecular Weight (Monoisotopic): 367.1242AlogP: 4.39#Rotatable Bonds: 5
Polar Surface Area: 47.56Molecular Species: BASEHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.82CX LogP: 4.20CX LogD: 1.83
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.68Np Likeness Score: -0.53

References

1. Rackham MD, Brannigan JA, Moss DK, Yu Z, Wilkinson AJ, Holder AA, Tate EW, Leatherbarrow RJ..  (2013)  Discovery of novel and ligand-efficient inhibitors of Plasmodium falciparum and Plasmodium vivax N-myristoyltransferase.,  56  (1): [PMID:23170970] [10.1021/jm301474t]

Source