ID: ALA3604541

Max Phase: Preclinical

Molecular Formula: C12H32N9O12P3S

Molecular Weight: 551.30

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[n+]1cn([C@@H]2O[C@H](CO[P@@](=O)(S)OP(=O)([O-])CP(=O)(O)O)[C@@H](O)[C@H]2O)c2nc(N)nc(O)c21.N.N.N.N

Standard InChI:  InChI=1S/C12H20N5O12P3S.4H3N/c1-16-3-17(9-6(16)10(20)15-12(13)14-9)11-8(19)7(18)5(28-11)2-27-32(26,33)29-31(24,25)4-30(21,22)23;;;;/h3,5,7-8,11,18-19H,2,4H2,1H3,(H6-,13,14,15,20,21,22,23,24,25,26,33);4*1H3/t5-,7-,8-,11-,32-;;;;/m1..../s1

Standard InChI Key:  QZXONQZSODVTLZ-QMTFSUPWSA-N

Associated Targets(Human)

Eukaryotic translation initation factor 600 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Scavenger mRNA-decapping enzyme DcpS 115 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Serum 96 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Eukaryotic translation initiation factor 4E 100 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: 551.30Molecular Weight (Monoisotopic): 551.0042AlogP: -2.08#Rotatable Bonds: 8
Polar Surface Area: 263.72Molecular Species: ACIDHBA: 14HBD: 7
#RO5 Violations: 3HBA (Lipinski): 17HBD (Lipinski): 7#RO5 Violations (Lipinski): 3
CX Acidic pKa: 0.78CX Basic pKa: 2.07CX LogP: -7.86CX LogD: -11.42
Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.11Np Likeness Score: 0.83

References

1. Ziemniak M, Kowalska J, Lukaszewicz M, Zuberek J, Wnek K, Darzynkiewicz E, Jemielity J..  (2015)  Phosphate-modified analogues of m(7)GTP and m(7)Gppppm(7)G-Synthesis and biochemical properties.,  23  (17): [PMID:26264844] [10.1016/j.bmc.2015.07.052]

Source