ID: ALA4439932

Max Phase: Preclinical

Molecular Formula: C10H15FN5O13P3

Molecular Weight: 525.17

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Nc1nc(O)c2ncn([C@@H]3O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](F)[C@H]3O)c2n1

Standard InChI:  InChI=1S/C10H15FN5O13P3/c11-4-3(1-26-31(22,23)29-32(24,25)28-30(19,20)21)27-9(6(4)17)16-2-13-5-7(16)14-10(12)15-8(5)18/h2-4,6,9,17H,1H2,(H,22,23)(H,24,25)(H2,19,20,21)(H3,12,14,15,18)/t3-,4-,6-,9-/m1/s1

Standard InChI Key:  JLJLWXVCGGANRA-DXTOWSMRSA-N

Associated Targets(Human)

Cyclic GMP-AMP synthase 693 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Cyclic GMP-AMP synthase 121 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 525.17Molecular Weight (Monoisotopic): 524.9863AlogP: -0.95#Rotatable Bonds: 8
Polar Surface Area: 279.13Molecular Species: ACIDHBA: 14HBD: 7
#RO5 Violations: 3HBA (Lipinski): 18HBD (Lipinski): 8#RO5 Violations (Lipinski): 3
CX Acidic pKa: 0.90CX Basic pKa: 0.62CX LogP: -2.40CX LogD: -9.20
Aromatic Rings: 2Heavy Atoms: 32QED Weighted: 0.20Np Likeness Score: 0.84

References

1. Novotná B, Vaneková L, Zavřel M, Buděšínský M, Dejmek M, Smola M, Gutten O, Tehrani ZA, Pimková Polidarová M, Brázdová A, Liboska R, Štěpánek I, Vavřina Z, Jandušík T, Nencka R, Rulíšek L, Bouřa E, Brynda J, Páv O, Birkuš G..  (2019)  Enzymatic Preparation of 2'-5',3'-5'-Cyclic Dinucleotides, Their Binding Properties to Stimulator of Interferon Genes Adaptor Protein, and Structure/Activity Correlations.,  62  (23): [PMID:31715099] [10.1021/acs.jmedchem.9b01062]

Source