N-((1-benzyl-3-(benzylamino)piperidin-3-yl)methyl)-2-guanidinoacetamide

ID: ALA3361417

PubChem CID: 118724978

Max Phase: Preclinical

Molecular Formula: C23H32N6O

Molecular Weight: 408.55

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  N=C(N)NCC(=O)NCC1(NCc2ccccc2)CCCN(Cc2ccccc2)C1

Standard InChI:  InChI=1S/C23H32N6O/c24-22(25)26-15-21(30)27-17-23(28-14-19-8-3-1-4-9-19)12-7-13-29(18-23)16-20-10-5-2-6-11-20/h1-6,8-11,28H,7,12-18H2,(H,27,30)(H4,24,25,26)

Standard InChI Key:  KTOXXPQPJXGXPZ-UHFFFAOYSA-N

Molfile:  

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    5.9746  -11.9273    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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    7.2121  -11.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9746  -10.4983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.8620  -12.6417    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

Alternative Forms

  1. Parent:

    ALA3361417

    ---

Associated Targets(Human)

NPFFR2 Tchem Neuropeptide FF receptor 2 (533 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NPFFR1 Tchem Neuropeptide FF receptor 1 (514 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: 408.55Molecular Weight (Monoisotopic): 408.2638AlogP: 1.41#Rotatable Bonds: 9
Polar Surface Area: 106.27Molecular Species: BASEHBA: 4HBD: 5
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 11.09CX LogP: 1.43CX LogD: -2.20
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.32Np Likeness Score: -0.75

References

1. Journigan VB, Mésangeau C, Vyas N, Eans SO, Cutler SJ, McLaughlin JP, Mollereau C, McCurdy CR..  (2014)  Nonpeptide small molecule agonist and antagonist original leads for neuropeptide FF1 and FF2 receptors.,  57  (21): [PMID:25268943] [10.1021/jm500989n]

Source