3-(((3R,4R)-3-Hydroxy-4-(hydroxymethyl)pyrrolidin-1-yl)methyl)-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one

ID: ALA4569556

Chembl Id: CHEMBL4569556

PubChem CID: 155550712

Max Phase: Preclinical

Molecular Formula: C13H17N3O3

Molecular Weight: 263.30

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  O=c1[nH]ccc2c(CN3C[C@H](CO)[C@@H](O)C3)c[nH]c12

Standard InChI:  InChI=1S/C13H17N3O3/c17-7-9-5-16(6-11(9)18)4-8-3-15-12-10(8)1-2-14-13(12)19/h1-3,9,11,15,17-18H,4-7H2,(H,14,19)/t9-,11+/m1/s1

Standard InChI Key:  WQAUMEFUWUJWAK-KOLCDFICSA-N

Alternative Forms

  1. Parent:

    ALA4569556

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Associated Targets(Human)

MTAP Tchem S-methyl-5-thioadenosine phosphorylase (233 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: 263.30Molecular Weight (Monoisotopic): 263.1270AlogP: -0.36#Rotatable Bonds: 3
Polar Surface Area: 92.35Molecular Species: NEUTRALHBA: 4HBD: 4
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: 12.32CX Basic pKa: 7.95CX LogP: -1.17CX LogD: -1.83
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.61Np Likeness Score: 0.11

References

1. Harijan RK, Hoff O, Ducati RG, Firestone RS, Hirsch BM, Evans GB, Schramm VL, Tyler PC..  (2019)  Selective Inhibitors of Helicobacter pylori Methylthioadenosine Nucleosidase and Human Methylthioadenosine Phosphorylase.,  62  (7): [PMID:30860833] [10.1021/acs.jmedchem.8b01642]

Source