3-benzyl 5-(2-methoxyethyl) 2,6-dimethyl-4-(1-methyl-1H-indazol-5-yl)-1,4-dihydropyridine-3,5-dicarboxylate

ID: ALA5199616

Chembl Id: CHEMBL5199616

PubChem CID: 168292067

Max Phase: Preclinical

Molecular Formula: C27H29N3O5

Molecular Weight: 475.55

Associated Items:

Names and Identifiers

Canonical SMILES:  COCCOC(=O)C1=C(C)NC(C)=C(C(=O)OCc2ccccc2)C1c1ccc2c(cnn2C)c1

Standard InChI:  InChI=1S/C27H29N3O5/c1-17-23(26(31)34-13-12-33-4)25(20-10-11-22-21(14-20)15-28-30(22)3)24(18(2)29-17)27(32)35-16-19-8-6-5-7-9-19/h5-11,14-15,25,29H,12-13,16H2,1-4H3

Standard InChI Key:  XTKHITZLGMPCPE-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5199616

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Associated Targets(Human)

PDE1C Tclin Phosphodiesterase 1C (228 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: 475.55Molecular Weight (Monoisotopic): 475.2107AlogP: 3.74#Rotatable Bonds: 8
Polar Surface Area: 91.68Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 1.21CX LogP: 3.00CX LogD: 3.00
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.39Np Likeness Score: -0.87

References

1. Huang MX, Tian YJ, Han C, Liu RD, Xie X, Yuan Y, Yang YY, Li Z, Chen J, Luo HB, Wu Y..  (2022)  Structural Modifications of Nimodipine Lead to Novel PDE1 Inhibitors with Anti-pulmonary Fibrosis Effects.,  65  (12.0): [PMID:35666471] [10.1021/acs.jmedchem.2c00458]

Source