ID: ALA4475507

Max Phase: Preclinical

Molecular Formula: C11H16BrN

Molecular Weight: 242.16

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCN(C)Cc1ccc(Br)cc1

Standard InChI:  InChI=1S/C11H16BrN/c1-3-8-13(2)9-10-4-6-11(12)7-5-10/h4-7H,3,8-9H2,1-2H3

Standard InChI Key:  CHUVVHJIKQOWLZ-UHFFFAOYSA-N

Associated Targets(Human)

Pyrroline-5-carboxylate reductase 1, mitochondrial 71 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: 242.16Molecular Weight (Monoisotopic): 241.0466AlogP: 3.29#Rotatable Bonds: 4
Polar Surface Area: 3.24Molecular Species: BASEHBA: 1HBD: 0
#RO5 Violations: 0HBA (Lipinski): 1HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.25CX LogP: 3.56CX LogD: 1.72
Aromatic Rings: 1Heavy Atoms: 13QED Weighted: 0.78Np Likeness Score: -1.63

References

1. Milne K, Sun J, Zaal EA, Mowat J, Celie PHN, Fish A, Berkers CR, Forlani G, Loayza-Puch F, Jamieson C, Agami R..  (2019)  A fragment-like approach to PYCR1 inhibition.,  29  (18): [PMID:31362921] [10.1016/j.bmcl.2019.07.047]

Source