cyclopropyl(4-((1-(3-methylbenzyl)-1H-benzo[d]imidazol-2-yl)methyl)piperazin-1-yl)methanone

ID: ALA4871242

PubChem CID: 164618634

Max Phase: Preclinical

Molecular Formula: C24H28N4O

Molecular Weight: 388.52

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  Cc1cccc(Cn2c(CN3CCN(C(=O)C4CC4)CC3)nc3ccccc32)c1

Standard InChI:  InChI=1S/C24H28N4O/c1-18-5-4-6-19(15-18)16-28-22-8-3-2-7-21(22)25-23(28)17-26-11-13-27(14-12-26)24(29)20-9-10-20/h2-8,15,20H,9-14,16-17H2,1H3

Standard InChI Key:  UUGHMMOWDDXPKH-UHFFFAOYSA-N

Molfile:  

 
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   21.6230  -12.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   23.6849  -11.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4460  -10.7465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   24.3945  -11.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

Alternative Forms

  1. Parent:

    ALA4871242

    ---

Associated Targets(Human)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A2 Tchem Retinal dehydrogenase 2 (226 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A3 Tchem Aldehyde dehydrogenase 1A3 (336 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH2 Tclin Aldehyde dehydrogenase (509 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH3A1 Tchem Aldehyde dehydrogenase dimeric NADP-preferring (307 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 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

Calculated Properties

Molecular Weight: 388.52Molecular Weight (Monoisotopic): 388.2263AlogP: 3.45#Rotatable Bonds: 5
Polar Surface Area: 41.37Molecular Species: NEUTRALHBA: 4HBD:
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 5.36CX LogP: 3.59CX LogD: 3.59
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.67Np Likeness Score: -1.96

References

1. Ma Z, Jiang L, Li B, Liang D, Feng Y, Liu L, Jiang C..  (2021)  Discovery of benzimidazole derivatives as potent and selective aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitors with glucose consumption improving activity.,  46  [PMID:34403955] [10.1016/j.bmc.2021.116352]

Source