4-Methoxy-N-(3-((3-nitrobenzyl)oxy)benzyl)-N-(pyridin-4-ylmethyl)benzamide

ID: ALA4175412

PubChem CID: 135187505

Max Phase: Preclinical

Molecular Formula: C28H25N3O5

Molecular Weight: 483.52

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc(C(=O)N(Cc2ccncc2)Cc2cccc(OCc3cccc([N+](=O)[O-])c3)c2)cc1

Standard InChI:  InChI=1S/C28H25N3O5/c1-35-26-10-8-24(9-11-26)28(32)30(18-21-12-14-29-15-13-21)19-22-4-3-7-27(17-22)36-20-23-5-2-6-25(16-23)31(33)34/h2-17H,18-20H2,1H3

Standard InChI Key:  CTIDVDPLXAFVRC-UHFFFAOYSA-N

Molfile:  

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M  CHG  2  34   1  36  -1
M  END

Alternative Forms

  1. Parent:

    ALA4175412

    ---

Associated Targets(Human)

KMS-11 (183 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC2A1 Tchem Glucose transporter (14755 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: 483.52Molecular Weight (Monoisotopic): 483.1794AlogP: 5.42#Rotatable Bonds: 10
Polar Surface Area: 94.80Molecular Species: NEUTRALHBA: 6HBD:
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 5.02CX LogP: 4.85CX LogD: 4.85
Aromatic Rings: 4Heavy Atoms: 36QED Weighted: 0.22Np Likeness Score: -1.44

References

1. Wei C, Bajpai R, Sharma H, Heitmeier M, Jain AD, Matulis SM, Nooka AK, Mishra RK, Hruz PW, Schiltz GE, Shanmugam M..  (2017)  Development of GLUT4-selective antagonists for multiple myeloma therapy.,  139  [PMID:28837922] [10.1016/j.ejmech.2017.08.029]

Source