ID: ALA4299199

Max Phase: Preclinical

Molecular Formula: C12H33BN9O12P3

Molecular Weight: 531.06

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  B[P@@](=O)(OC[C@H]1O[C@@H](n2c[n+](C)c3c(O)nc(N)nc32)[C@H](O)[C@@H]1O)OP(=O)([O-])CP(=O)(O)O.N.N.N.N

Standard InChI:  InChI=1S/C12H21BN5O12P3.4H3N/c1-17-3-18(9-6(17)10(21)16-12(14)15-9)11-8(20)7(19)5(29-11)2-28-33(13,27)30-32(25,26)4-31(22,23)24;;;;/h3,5,7-8,11,19-20H,2,4,13H2,1H3,(H5-,14,15,16,21,22,23,24,25,26);4*1H3/t5-,7-,8-,11-,33-;;;;/m1..../s1

Standard InChI Key:  CJXPNKWMDYCPOV-PKCZVLDDSA-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)

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: 531.06Molecular Weight (Monoisotopic): 531.0493AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

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