ID: ALA1094568

Max Phase: Preclinical

Molecular Formula: C12H17F2N5O9P2S

Molecular Weight: 507.31

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CSc1nc(N)c2ncn([C@@H]3O[C@H](COP(=O)(O)C(F)(F)P(=O)(O)O)[C@@H](O)[C@H]3O)c2n1

Standard InChI:  InChI=1S/C12H17F2N5O9P2S/c1-31-11-17-8(15)5-9(18-11)19(3-16-5)10-7(21)6(20)4(28-10)2-27-30(25,26)12(13,14)29(22,23)24/h3-4,6-7,10,20-21H,2H2,1H3,(H,25,26)(H2,15,17,18)(H2,22,23,24)/t4-,6-,7-,10-/m1/s1

Standard InChI Key:  PLBBQVYTRYDROT-KQYNXXCUSA-N

Associated Targets(Human)

Ectonucleotide pyrophosphatase/phosphodiesterase family member 3 241 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 635 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ectonucleoside triphosphate diphosphohydrolase 8 96 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ectonucleoside triphosphate diphosphohydrolase 3 108 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ectonucleoside triphosphate diphosphohydrolase 2 116 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ectonucleoside triphosphate diphosphohydrolase 1 116 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Oryctolagus cuniculus 11301 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

P2Y purinoceptor 1 470 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: 507.31Molecular Weight (Monoisotopic): 507.0190AlogP: -0.32#Rotatable Bonds: 7
Polar Surface Area: 223.37Molecular Species: ACIDHBA: 12HBD: 6
#RO5 Violations: 3HBA (Lipinski): 14HBD (Lipinski): 7#RO5 Violations (Lipinski): 3
CX Acidic pKa: -0.27CX Basic pKa: 5.16CX LogP: -3.17CX LogD: -5.72
Aromatic Rings: 2Heavy Atoms: 31QED Weighted: 0.16Np Likeness Score: 0.31

References

1. Eliahu S, Martín-Gil A, Perez de Lara MJ, Pintor J, Camden J, Weisman GA, Lecka J, Sévigny J, Fischer B..  (2010)  2-MeS-beta,gamma-CCl2-ATP is a potent agent for reducing intraocular pressure.,  53  (8): [PMID:20337495] [10.1021/jm100030u]
2. Lecka J, Ben-David G, Simhaev L, Eliahu S, Oscar J, Luyindula P, Pelletier J, Fischer B, Senderowitz H, Sévigny J..  (2013)  Nonhydrolyzable ATP analogues as selective inhibitors of human NPP1: a combined computational/experimental study.,  56  (21): [PMID:24083941] [10.1021/jm400918s]

Source