ID: ALA604223

Max Phase: Preclinical

Molecular Formula: C16H25N5O5

Molecular Weight: 367.41

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)CCCOc1nc(N)c2ncn(C3O[C@@H](CO)[C@H](O)[C@@H]3O)c2n1

Standard InChI:  InChI=1S/C16H25N5O5/c1-8(2)4-3-5-25-16-19-13(17)10-14(20-16)21(7-18-10)15-12(24)11(23)9(6-22)26-15/h7-9,11-12,15,22-24H,3-6H2,1-2H3,(H2,17,19,20)/t9-,11-,12-,15?/m0/s1

Standard InChI Key:  FFVMJGITPVUYTE-PHOHYCPASA-N

Associated Targets(Human)

Adenosine A2 receptor 1064 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Adenosine receptors; A1 & A2 188 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Adenosine A1 receptor 540 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

Properties

Molecular Weight: 367.41Molecular Weight (Monoisotopic): 367.1856AlogP: -0.17#Rotatable Bonds: 7
Polar Surface Area: 148.77Molecular Species: NEUTRALHBA: 10HBD: 4
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.45CX Basic pKa: 4.22CX LogP: 0.49CX LogD: 0.49
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.49Np Likeness Score: 0.94

References

1. Ueeda M, Thompson RD, Arroyo LH, Olsson RA..  (1991)  2-Alkoxyadenosines: potent and selective agonists at the coronary artery A2 adenosine receptor.,  34  (4): [PMID:2016707] [10.1021/jm00108a014]

Source