ID: ALA4848032

Max Phase: Preclinical

Molecular Formula: C30H32ClF3N6O4

Molecular Weight: 633.07

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cn1c(=O)[nH]c2c(Cl)cc3c(c21)CN(CC(F)(F)F)C(=O)[C@H](CC(=O)N1CCC(N2CCc4ccccc4NC2=O)CC1)C3

Standard InChI:  InChI=1S/C30H32ClF3N6O4/c1-37-26-21-15-39(16-30(32,33)34)27(42)19(12-18(21)13-22(31)25(26)36-28(37)43)14-24(41)38-9-7-20(8-10-38)40-11-6-17-4-2-3-5-23(17)35-29(40)44/h2-5,13,19-20H,6-12,14-16H2,1H3,(H,35,44)(H,36,43)/t19-/m0/s1

Standard InChI Key:  JXGSAMHWEISJEV-IBGZPJMESA-N

Associated Targets(Human)

Calcitonin gene-related peptide type 1 receptor 1509 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytochrome P450 3A4 53859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Callithrix jacchus 111 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: 633.07Molecular Weight (Monoisotopic): 632.2126AlogP: 4.05#Rotatable Bonds: 4
Polar Surface Area: 110.75Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.20CX Basic pKa: CX LogP: 2.73CX LogD: 2.73
Aromatic Rings: 3Heavy Atoms: 44QED Weighted: 0.45Np Likeness Score: -0.52

References

1. Luo G, Jiang XJ, Chen L, Conway CM, Gulianello M, Kostich W, Keavy D, Signor LJ, Chen P, Davis C, Whiterock VJ, Schartman R, Widmann KA, Macor JE, Dubowchik GM..  (2021)  Calcitonin gene-related peptide (CGRP) receptor antagonists: Heterocyclic modification of a novel azepinone lead.,  43  [PMID:33932522] [10.1016/j.bmcl.2021.128077]

Source