(+/-)-3-(2-(3-Fluoropyridin-2-yl)-6-methyl-3,4-dihydro-2H-chromen-7-yl)-6-methyl-4,6-dihydropyrido[4,3-d]pyrimidine-2,7(1H,3H)-dione

ID: ALA4102900

Chembl Id: CHEMBL4102900

PubChem CID: 137657582

Max Phase: Preclinical

Molecular Formula: C23H21FN4O3

Molecular Weight: 420.44

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cc2c(cc1N1Cc3cn(C)c(=O)cc3NC1=O)OC(c1ncccc1F)CC2

Standard InChI:  InChI=1S/C23H21FN4O3/c1-13-8-14-5-6-19(22-16(24)4-3-7-25-22)31-20(14)10-18(13)28-12-15-11-27(2)21(29)9-17(15)26-23(28)30/h3-4,7-11,19H,5-6,12H2,1-2H3,(H,26,30)

Standard InChI Key:  JEFODDXFNQEKAR-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4102900

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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: 420.44Molecular Weight (Monoisotopic): 420.1598AlogP: 3.85#Rotatable Bonds: 2
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: 1.29CX LogP: 2.06CX LogD: 2.06
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.68Np Likeness Score: -0.43

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