ID: ALA4449105

Max Phase: Preclinical

Molecular Formula: C21H26N6O

Molecular Weight: 378.48

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccccc1-n1cc(-c2ccnc(NCCC3CCCN3C)n2)cn1

Standard InChI:  InChI=1S/C21H26N6O/c1-26-13-5-6-17(26)9-11-22-21-23-12-10-18(25-21)16-14-24-27(15-16)19-7-3-4-8-20(19)28-2/h3-4,7-8,10,12,14-15,17H,5-6,9,11,13H2,1-2H3,(H,22,23,25)

Standard InChI Key:  PCURNESJVHMDOH-UHFFFAOYSA-N

Associated Targets(Human)

Peptide N-myristoyltransferase 1 643 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Glycylpeptide N-tetradecanoyltransferase 109 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Dengue virus type 2 NS3 protein 2214 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 378.48Molecular Weight (Monoisotopic): 378.2168AlogP: 3.23#Rotatable Bonds: 7
Polar Surface Area: 68.10Molecular Species: BASEHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.23CX LogP: 2.71CX LogD: 0.88
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.68Np Likeness Score: -1.46

References

1. Kersten C, Fleischer E, Kehrein J, Borek C, Jaenicke E, Sotriffer C, Brenk R..  (2020)  How To Design Selective Ligands for Highly Conserved Binding Sites: A Case Study Using N-Myristoyltransferases as a Model System.,  63  (5): [PMID:31423787] [10.1021/acs.jmedchem.9b00586]

Source