ID: ALA4638291

Max Phase: Preclinical

Molecular Formula: C18H18ClFN6O

Molecular Weight: 388.83

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1c2c(N)c(C(=O)NC3CN(c4ncc(Cl)cc4F)C3)ccc2nn1C

Standard InChI:  InChI=1S/C18H18ClFN6O/c1-9-15-14(24-25(9)2)4-3-12(16(15)21)18(27)23-11-7-26(8-11)17-13(20)5-10(19)6-22-17/h3-6,11H,7-8,21H2,1-2H3,(H,23,27)

Standard InChI Key:  KTLBBHAYTZNOAH-UHFFFAOYSA-N

Associated Targets(Human)

Muscarinic acetylcholine receptor M4 6041 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Muscarinic acetylcholine receptor M4 559 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: 388.83Molecular Weight (Monoisotopic): 388.1215AlogP: 2.27#Rotatable Bonds: 3
Polar Surface Area: 89.07Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.74CX LogP: 2.79CX LogD: 2.79
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.67Np Likeness Score: -1.67

References

1. Temple KJ, Long MF, Engers JL, Watson KJ, Chang S, Luscombe VB, Rodriguez AL, Niswender CM, Bridges TM, Conn PJ, Engers DW, Lindsley CW..  (2020)  Discovery of structurally distinct tricyclic M4 positive allosteric modulator (PAM) chemotypes.,  30  (4): [PMID:31787491] [10.1016/j.bmcl.2019.126811]

Source