ID: ALA4578387

Max Phase: Preclinical

Molecular Formula: C12H14BrNO

Molecular Weight: 268.15

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C#CCN(C)Cc1ccc(Br)cc1OC

Standard InChI:  InChI=1S/C12H14BrNO/c1-4-7-14(2)9-10-5-6-11(13)8-12(10)15-3/h1,5-6,8H,7,9H2,2-3H3

Standard InChI Key:  LLPPVLYGJSFPJV-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: 268.15Molecular Weight (Monoisotopic): 267.0259AlogP: 2.52#Rotatable Bonds: 4
Polar Surface Area: 12.47Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.05CX LogP: 2.75CX LogD: 2.59
Aromatic Rings: 1Heavy Atoms: 15QED Weighted: 0.78Np Likeness Score: -1.11

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