(Z)-1-((3-hydroxynaphthalen-2-yl)methyl)-3-(2-oxo-1-propylindolin-3-ylidene)thiocarbamide

ID: ALA4171024

Chembl Id: CHEMBL4171024

PubChem CID: 145952431

Max Phase: Preclinical

Molecular Formula: C23H21N3O2S

Molecular Weight: 403.51

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCN1C(=O)/C(=N\C(=S)NCc2cc3ccccc3cc2O)c2ccccc21

Standard InChI:  InChI=1S/C23H21N3O2S/c1-2-11-26-19-10-6-5-9-18(19)21(22(26)28)25-23(29)24-14-17-12-15-7-3-4-8-16(15)13-20(17)27/h3-10,12-13,27H,2,11,14H2,1H3,(H,24,29)/b25-21-

Standard InChI Key:  GRBBZVKJQNEWDO-DAFNUICNSA-N

Alternative Forms

  1. Parent:

    ALA4171024

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Associated Targets(Human)

ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 403.51Molecular Weight (Monoisotopic): 403.1354AlogP: 4.17#Rotatable Bonds: 4
Polar Surface Area: 64.93Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 9.00CX Basic pKa: CX LogP: 4.43CX LogD: 4.42
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.64Np Likeness Score: -0.89

References

1. Manikandan A, Moharil P, Sathishkumar M, Muñoz-Garay C, Sivakumar A..  (2017)  Therapeutic investigations of novel indoxyl-based indolines: A drug target validation and Structure-Activity Relationship of angiotensin-converting enzyme inhibitors with cardiovascular regulation and thrombolytic potential.,  141  [PMID:29032034] [10.1016/j.ejmech.2017.09.076]

Source