6-(2-thiophen-2-ylethyl)aminopurine

ID: ALA4250669

Chembl Id: CHEMBL4250669

Cas Number: 143355-22-0

PubChem CID: 29037167

Max Phase: Preclinical

Molecular Formula: C11H11N5S

Molecular Weight: 245.31

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  c1csc(CCNc2ncnc3[nH]cnc23)c1

Standard InChI:  InChI=1S/C11H11N5S/c1-2-8(17-5-1)3-4-12-10-9-11(14-6-13-9)16-7-15-10/h1-2,5-7H,3-4H2,(H2,12,13,14,15,16)

Standard InChI Key:  YIZWRPPLSSLNNX-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: 245.31Molecular Weight (Monoisotopic): 245.0735AlogP: 2.07#Rotatable Bonds: 4
Polar Surface Area: 66.49Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.87CX Basic pKa: 4.07CX LogP: 1.70CX LogD: 1.69
Aromatic Rings: 3Heavy Atoms: 17QED Weighted: 0.74Np Likeness Score: -1.92

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