ID: ALA5286733

Max Phase: Preclinical

Molecular Formula: C24H27N7

Molecular Weight: 413.53

Associated Items:

Representations

Canonical SMILES:  CCCn1cc(C#N)c2ncnc(N3CCN(CCc4c[nH]c5ccccc45)CC3)c21

Standard InChI:  InChI=1S/C24H27N7/c1-2-8-31-16-19(14-25)22-23(31)24(28-17-27-22)30-12-10-29(11-13-30)9-7-18-15-26-21-6-4-3-5-20(18)21/h3-6,15-17,26H,2,7-13H2,1H3

Standard InChI Key:  GKBREYOSDUWPNK-UHFFFAOYSA-N

Associated Targets(Human)

Multidrug resistance-associated protein 1 2587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

P-glycoprotein 1 14716 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

ATP-binding cassette sub-family G member 2 4927 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

Properties

Molecular Weight: 413.53Molecular Weight (Monoisotopic): 413.2328AlogP: 3.56#Rotatable Bonds: 6
Polar Surface Area: 76.77Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.30CX LogP: 4.15CX LogD: 3.21
Aromatic Rings: 4Heavy Atoms: 31QED Weighted: 0.52Np Likeness Score: -1.36

References

1. Stefan K, Schmitt SM, Wiese M..  (2017)  9-Deazapurines as Broad-Spectrum Inhibitors of the ABC Transport Proteins P-Glycoprotein, Multidrug Resistance-Associated Protein 1, and Breast Cancer Resistance Protein.,  60  (21): [PMID:29016119] [10.1021/acs.jmedchem.7b00788]

Source