ID: ALA5268990

Max Phase: Preclinical

Molecular Formula: C23H27N7

Molecular Weight: 401.52

Associated Items:

Representations

Canonical SMILES:  N#Cc1c2n(c3c(N4CCN(CCc5ccncc5)CC4)ncnc13)CCCCC2

Standard InChI:  InChI=1S/C23H27N7/c24-16-19-20-4-2-1-3-10-30(20)22-21(19)26-17-27-23(22)29-14-12-28(13-15-29)11-7-18-5-8-25-9-6-18/h5-6,8-9,17H,1-4,7,10-15H2

Standard InChI Key:  UNGRUSULKAQDEF-UHFFFAOYSA-N

Associated Targets(Human)

Multidrug resistance-associated protein 1 2587 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

P-glycoprotein 1 14716 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: 401.52Molecular Weight (Monoisotopic): 401.2328AlogP: 2.79#Rotatable Bonds: 4
Polar Surface Area: 73.87Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.74CX LogP: 3.10CX LogD: 2.59
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.67Np Likeness Score: -1.48

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