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

ID: ALA4555970

Chembl Id: CHEMBL4555970

PubChem CID: 155556816

Max Phase: Preclinical

Molecular Formula: C18H24N8OS

Molecular Weight: 400.51

Molecule Type: Unknown

Associated Items:

Names and Identifiers

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

Standard InChI:  InChI=1S/C18H24N8OS/c1-2-3-26-7-14(23-24-26)10-28-9-13-6-25(8-15(13)27)5-12-4-20-17-16(12)21-11-22-18(17)19/h2,4,7,11,13,15,20,27H,1,3,5-6,8-10H2,(H2,19,21,22)/t13-,15+/m1/s1

Standard InChI Key:  ROJBUFVFGMELNB-HIFRSBDPSA-N

Alternative Forms

  1. Parent:

    ALA4555970

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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: 400.51Molecular Weight (Monoisotopic): 400.1794AlogP: 1.04#Rotatable Bonds: 8
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: 8.28CX LogP: 0.71CX LogD: -0.22
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.48Np Likeness Score: -1.07

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