1-(4,5-dimethyl-6-(thiophen-2-yl)pyrimidin-2-yl)-3-(3-(pyrrolidin-1-yl)propyl)guanidine

ID: ALA5221050

PubChem CID: 168298770

Max Phase: Preclinical

Molecular Formula: C18H26N6S

Molecular Weight: 358.52

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1nc(NC(=N)NCCCN2CCCC2)nc(-c2cccs2)c1C

Standard InChI:  InChI=1S/C18H26N6S/c1-13-14(2)21-18(22-16(13)15-7-5-12-25-15)23-17(19)20-8-6-11-24-9-3-4-10-24/h5,7,12H,3-4,6,8-11H2,1-2H3,(H3,19,20,21,22,23)

Standard InChI Key:  XACXGLVMKBOOEW-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

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M  END

Alternative Forms

  1. Parent:

    ALA5221050

    ---

Associated Targets(Human)

Premature termination codon (106 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 358.52Molecular Weight (Monoisotopic): 358.1940AlogP: 3.24#Rotatable Bonds: 6
Polar Surface Area: 76.93Molecular Species: BASEHBA: 5HBD: 3
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 9.50CX LogP: 2.92CX LogD: 0.36
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.42Np Likeness Score: -1.67

References

1. Morrill C, Friesen WJ, Babu S, Baiazitov RY, Du W, Karloff DB, Lee CS, Moon YC, Ren H, Sierra J, Tomizawa Y, Vazirani P, Welch EM, Xue X, Zhuo J..  (2022)  Guanidino quinazolines and pyrimidines promote readthrough of premature termination codons in cells with native nonsense mutations.,  76  [PMID:36150638] [10.1016/j.bmcl.2022.128989]

Source