ID: ALA4115156

Max Phase: Preclinical

Molecular Formula: C21H24F2N6O2S

Molecular Weight: 462.53

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1nn(C)c(C)c1NS(=O)(=O)c1cc(F)c(-c2ccnc(N3CCNCC3)c2)cc1F

Standard InChI:  InChI=1S/C21H24F2N6O2S/c1-13-21(14(2)28(3)26-13)27-32(30,31)19-12-17(22)16(11-18(19)23)15-4-5-25-20(10-15)29-8-6-24-7-9-29/h4-5,10-12,24,27H,6-9H2,1-3H3

Standard InChI Key:  RPRVKMUKWQSFNP-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 506 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Glycylpeptide N-tetradecanoyltransferase 27 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: 462.53Molecular Weight (Monoisotopic): 462.1650AlogP: 2.59#Rotatable Bonds: 5
Polar Surface Area: 92.15Molecular Species: BASEHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.53CX Basic pKa: 8.78CX LogP: 1.05CX LogD: 1.00
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.61Np Likeness Score: -1.97

References

1.  (2015)  N-myristoyl transferase inhibitors, 

Source

Source(1):