ID: ALA5275704

Max Phase: Preclinical

Molecular Formula: C20H21N7

Molecular Weight: 359.44

Associated Items:

Representations

Canonical SMILES:  N#Cc1c2n(c3c(N4CCN(c5ccccn5)CC4)ncnc13)CCCC2

Standard InChI:  InChI=1S/C20H21N7/c21-13-15-16-5-2-4-8-27(16)19-18(15)23-14-24-20(19)26-11-9-25(10-12-26)17-6-1-3-7-22-17/h1,3,6-7,14H,2,4-5,8-12H2

Standard InChI Key:  HOKJHROTLIWDND-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: 359.44Molecular Weight (Monoisotopic): 359.1858AlogP: 2.36#Rotatable Bonds: 2
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: 6.42CX LogP: 3.12CX LogD: 3.08
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.70Np Likeness Score: -1.86

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