N-(4-((Benzylamino)methyl)benzyl)-4-methoxythieno[2,3-d]-pyrimidine-5-carboxamide

ID: ALA4580624

Chembl Id: CHEMBL4580624

PubChem CID: 155561261

Max Phase: Preclinical

Molecular Formula: C23H22N4O2S

Molecular Weight: 418.52

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ncnc2scc(C(=O)NCc3ccc(CNCc4ccccc4)cc3)c12

Standard InChI:  InChI=1S/C23H22N4O2S/c1-29-22-20-19(14-30-23(20)27-15-26-22)21(28)25-13-18-9-7-17(8-10-18)12-24-11-16-5-3-2-4-6-16/h2-10,14-15,24H,11-13H2,1H3,(H,25,28)

Standard InChI Key:  YAZAQLHNEIJYIG-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4580624

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Associated Targets(non-human)

trmD tRNA (guanine-N(1)-)-methyltransferase (63 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 418.52Molecular Weight (Monoisotopic): 418.1463AlogP: 3.92#Rotatable Bonds: 8
Polar Surface Area: 76.14Molecular Species: BASEHBA: 6HBD: 2
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 8.50CX LogP: 3.81CX LogD: 2.68
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.45Np Likeness Score: -1.44

References

1. Zhong W, Pasunooti KK, Balamkundu S, Wong YH, Nah Q, Gadi V, Gnanakalai S, Chionh YH, McBee ME, Gopal P, Lim SH, Olivier N, Buurman ET, Dick T, Liu CF, Lescar J, Dedon PC..  (2019)  Thienopyrimidinone Derivatives That Inhibit Bacterial tRNA (Guanine37-N1)-Methyltransferase (TrmD) by Restructuring the Active Site with a Tyrosine-Flipping Mechanism.,  62  (17): [PMID:31442049] [10.1021/acs.jmedchem.9b00582]

Source