6-furfurylamino-9-(tetrahydrofuran-2-yl)purin

ID: ALA4250095

Chembl Id: CHEMBL4250095

PubChem CID: 53237485

Max Phase: Preclinical

Molecular Formula: C14H15N5O2

Molecular Weight: 285.31

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  c1coc(CNc2ncnc3c2ncn3C2CCCO2)c1

Standard InChI:  InChI=1S/C14H15N5O2/c1-3-10(20-5-1)7-15-13-12-14(17-8-16-13)19(9-18-12)11-4-2-6-21-11/h1,3,5,8-9,11H,2,4,6-7H2,(H,15,16,17)

Standard InChI Key:  JOYIPGMQUYRXNO-UHFFFAOYSA-N

Alternative Forms

Associated Targets(Human)

NHDF (1164 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

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
Caenorhabditis elegans (1055 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: 285.31Molecular Weight (Monoisotopic): 285.1226AlogP: 2.34#Rotatable Bonds: 4
Polar Surface Area: 78.00Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.72CX LogP: 1.24CX LogD: 1.23
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.79Np Likeness Score: -0.84

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