N-(4-(5-(3-Morpholinopropyl)-2,3,4,5-tetrahydro-1H-benzo[b]-(1,4)diazepine-1-carbonyl)phenyl)-(1,1'-bipheny)-2-carboxamide

ID: ALA5207885

PubChem CID: 168294659

Max Phase: Preclinical

Molecular Formula: C36H38N4O3

Molecular Weight: 574.73

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccc(C(=O)N2CCCN(CCCN3CCOCC3)c3ccccc32)cc1)c1ccccc1-c1ccccc1

Standard InChI:  InChI=1S/C36H38N4O3/c41-35(32-13-5-4-12-31(32)28-10-2-1-3-11-28)37-30-18-16-29(17-19-30)36(42)40-23-9-22-39(33-14-6-7-15-34(33)40)21-8-20-38-24-26-43-27-25-38/h1-7,10-19H,8-9,20-27H2,(H,37,41)

Standard InChI Key:  CPMKYYVRVBLUEY-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA5207885

    ---

Associated Targets(Human)

AVPR2 Tclin Vasopressin V2 receptor (2912 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

Calculated Properties

Molecular Weight: 574.73Molecular Weight (Monoisotopic): 574.2944AlogP: 6.19#Rotatable Bonds: 8
Polar Surface Area: 65.12Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 7.11CX LogP: 5.52CX LogD: 5.35
Aromatic Rings: 4Heavy Atoms: 43QED Weighted: 0.27Np Likeness Score: -1.40

References

1. Cao X, Wang P, Yuan H, Zhang H, He Y, Fu K, Fang Q, Liu H, Su L, Yin L, Xu P, Xie Y, Xiong X, Wang J, Zhu X, Guo D..  (2022)  Benzodiazepine Derivatives as Potent Vasopressin V2 Receptor Antagonists for the Treatment of Autosomal Dominant Kidney Disease.,  65  (13.0): [PMID:35579344] [10.1021/acs.jmedchem.2c00567]

Source