ID: ALA5202045

Max Phase: Preclinical

Molecular Formula: C27H28N2O6

Molecular Weight: 476.53

Associated Items:

Representations

Canonical SMILES:  O=C(N[C@@H](c1ccccc1)c1cccc(OCc2cc(C(=O)O)co2)c1)O[C@H]1CN2CCC1CC2

Standard InChI:  InChI=1S/C27H28N2O6/c30-26(31)21-14-23(33-16-21)17-34-22-8-4-7-20(13-22)25(19-5-2-1-3-6-19)28-27(32)35-24-15-29-11-9-18(24)10-12-29/h1-8,13-14,16,18,24-25H,9-12,15,17H2,(H,28,32)(H,30,31)/t24-,25-/m0/s1

Standard InChI Key:  GEAWITYNOXRHRJ-DQEYMECFSA-N

Associated Targets(Human)

Muscarinic acetylcholine receptor M3 7750 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 476.53Molecular Weight (Monoisotopic): 476.1947AlogP: 4.47#Rotatable Bonds: 8
Polar Surface Area: 101.24Molecular Species: ZWITTERIONHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.30CX Basic pKa: 9.01CX LogP: 1.25CX LogD: 1.25
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.49Np Likeness Score: -0.26

References

1. Carzaniga L, Linney ID, Rizzi A, Delcanale M, Schmidt W, Knight CK, Pastore F, Miglietta D, Carnini C, Cesari N, Riccardi B, Mileo V, Venturi L, Moretti E, Blackaby WP, Patacchini R, Accetta A, Biagetti M, Bassani F, Tondelli M, Murgo A, Battipaglia L, Villetti G, Puccini P, Catinella S, Civelli M, Rancati F..  (2022)  Discovery of Clinical Candidate CHF-6366: A Novel Super-soft Dual Pharmacology Muscarinic Antagonist and β2 Agonist (MABA) for the Inhaled Treatment of Respiratory Diseases.,  65  (15.0): [PMID:35901125] [10.1021/acs.jmedchem.2c00609]

Source