ID: ALA4105007

Max Phase: Preclinical

Molecular Formula: C13H20N4O2

Molecular Weight: 264.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)c1nccn1CCN1C(=O)NC(C)(C)C1=O

Standard InChI:  InChI=1S/C13H20N4O2/c1-9(2)10-14-5-6-16(10)7-8-17-11(18)13(3,4)15-12(17)19/h5-6,9H,7-8H2,1-4H3,(H,15,19)

Standard InChI Key:  LBJHQZFVJKJOEI-UHFFFAOYSA-N

Associated Targets(Human)

Protein-arginine deiminase type-1 130 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Protein-arginine deiminase type-4 309 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Protein-arginine deiminase type-2 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: 264.33Molecular Weight (Monoisotopic): 264.1586AlogP: 1.34#Rotatable Bonds: 4
Polar Surface Area: 67.23Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.73CX Basic pKa: 7.09CX LogP: 1.05CX LogD: 0.89
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.83Np Likeness Score: -1.55

References

1. Sarswat A, Wasilewski E, Chakka SK, Bello AM, Caprariello AV, Muthuramu CM, Stys PK, Dunn SE, Kotra LP..  (2017)  Inhibitors of protein arginine deiminases and their efficacy in animal models of multiple sclerosis.,  25  (9): [PMID:28341402] [10.1016/j.bmc.2017.03.006]

Source