ID: ALA5287272

Max Phase: Preclinical

Molecular Formula: C22H25N7

Molecular Weight: 387.49

Associated Items:

Representations

Canonical SMILES:  N#Cc1c2n(c3c(N4CCN(CCc5ccncc5)CC4)ncnc13)CCCC2

Standard InChI:  InChI=1S/C22H25N7/c23-15-18-19-3-1-2-9-29(19)21-20(18)25-16-26-22(21)28-13-11-27(12-14-28)10-6-17-4-7-24-8-5-17/h4-5,7-8,16H,1-3,6,9-14H2

Standard InChI Key:  LWWJUPLADHFZFX-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: 387.49Molecular Weight (Monoisotopic): 387.2171AlogP: 2.40#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: 2.65CX LogD: 2.15
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.68Np Likeness Score: -1.52

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