6-Benzyl-3-(3-(pyridin-2-ylmethoxy)phenyl)-4,6-dihydropyrido[4,3-d]pyrimidine-2,7(1H,3H)-dione

ID: ALA4070179

Chembl Id: CHEMBL4070179

PubChem CID: 137638168

Max Phase: Preclinical

Molecular Formula: C26H22N4O3

Molecular Weight: 438.49

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C1Nc2cc(=O)n(Cc3ccccc3)cc2CN1c1cccc(OCc2ccccn2)c1

Standard InChI:  InChI=1S/C26H22N4O3/c31-25-14-24-20(16-29(25)15-19-7-2-1-3-8-19)17-30(26(32)28-24)22-10-6-11-23(13-22)33-18-21-9-4-5-12-27-21/h1-14,16H,15,17-18H2,(H,28,32)

Standard InChI Key:  NZYWZQVSAMCCCA-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4070179

    ---

Associated Targets(Human)

SNRNP200 Tchem U5 small nuclear ribonucleoprotein 200 kDa helicase (313 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: 438.49Molecular Weight (Monoisotopic): 438.1692AlogP: 4.42#Rotatable Bonds: 6
Polar Surface Area: 76.46Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 11.96CX Basic pKa: 3.78CX LogP: 2.43CX LogD: 2.43
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.48Np Likeness Score: -1.45

References

1. Iwatani-Yoshihara M, Ito M, Klein MG, Yamamoto T, Yonemori K, Tanaka T, Miwa M, Morishita D, Endo S, Tjhen R, Qin L, Nakanishi A, Maezaki H, Kawamoto T..  (2017)  Discovery of Allosteric Inhibitors Targeting the Spliceosomal RNA Helicase Brr2.,  60  (13): [PMID:28586220] [10.1021/acs.jmedchem.7b00461]

Source