(3R,4S)-4-((3-(1-allyl-1H-1,2,3-triazol-4-yl)propylthio)methyl)-1-((4-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)methyl)pyrrolidin-3-ol

ID: ALA4469234

Chembl Id: CHEMBL4469234

PubChem CID: 155533746

Max Phase: Preclinical

Molecular Formula: C20H28N8OS

Molecular Weight: 428.57

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  C=CCn1cc(CCCSC[C@H]2CN(Cc3c[nH]c4c(N)ncnc34)C[C@@H]2O)nn1

Standard InChI:  InChI=1S/C20H28N8OS/c1-2-5-28-10-16(25-26-28)4-3-6-30-12-15-9-27(11-17(15)29)8-14-7-22-19-18(14)23-13-24-20(19)21/h2,7,10,13,15,17,22,29H,1,3-6,8-9,11-12H2,(H2,21,23,24)/t15-,17+/m1/s1

Standard InChI Key:  JUOWXLBMLKBSGG-WBVHZDCISA-N

Alternative Forms

  1. Parent:

    ALA4469234

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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: 428.57Molecular Weight (Monoisotopic): 428.2107AlogP: 1.48#Rotatable Bonds: 10
Polar Surface Area: 121.77Molecular Species: NEUTRALHBA: 9HBD: 3
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: 13.47CX Basic pKa: 8.37CX LogP: 1.45CX LogD: 0.43
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.33Np Likeness Score: -1.00

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