6-(cyclopentylmethyl)aminopurine

ID: ALA4240562

Chembl Id: CHEMBL4240562

PubChem CID: 43317478

Max Phase: Preclinical

Molecular Formula: C11H15N5

Molecular Weight: 217.28

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  c1nc(NCC2CCCC2)c2nc[nH]c2n1

Standard InChI:  InChI=1S/C11H15N5/c1-2-4-8(3-1)5-12-10-9-11(14-6-13-9)16-7-15-10/h6-8H,1-5H2,(H2,12,13,14,15,16)

Standard InChI Key:  GZGJCGSYSBOIMS-UHFFFAOYSA-N

Alternative Forms

Associated Targets(non-human)

Nicotiana tabacum (382 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Amaranthus caudatus (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Triticum aestivum (1582 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 217.28Molecular Weight (Monoisotopic): 217.1327AlogP: 1.96#Rotatable Bonds: 3
Polar Surface Area: 66.49Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.87CX Basic pKa: 4.07CX LogP: 1.44CX LogD: 1.44
Aromatic Rings: 2Heavy Atoms: 16QED Weighted: 0.82Np Likeness Score: -0.68

References

1. Hönig M, Plíhalová L, Spíchal L, Grúz J, Kadlecová A, Voller J, Svobodová AR, Vostálová J, Ulrichová J, Doležal K, Strnad M..  (2018)  New cytokinin derivatives possess UVA and UVB photoprotective effect on human skin cells and prevent oxidative stress.,  150  [PMID:29604584] [10.1016/j.ejmech.2018.03.043]

Source