ID: ALA4080219

Max Phase: Preclinical

Molecular Formula: C26H23ClN2O11P2

Molecular Weight: 636.87

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(COc1ccc2cc(C(=O)Nc3ccc(Cl)cc3)ccc2c1)NCc1ccc(OP(=O)(O)O)c(OP(=O)(O)O)c1

Standard InChI:  InChI=1S/C26H23ClN2O11P2/c27-20-5-7-21(8-6-20)29-26(31)19-3-2-18-13-22(9-4-17(18)12-19)38-15-25(30)28-14-16-1-10-23(39-41(32,33)34)24(11-16)40-42(35,36)37/h1-13H,14-15H2,(H,28,30)(H,29,31)(H2,32,33,34)(H2,35,36,37)

Standard InChI Key:  SPIZHJIUMWIWJF-UHFFFAOYSA-N

Associated Targets(Human)

Signal transducer and activator of transcription 5A 227 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Signal transducer and activator of transcription 5B 90 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: 636.87Molecular Weight (Monoisotopic): 636.0466AlogP: 4.38#Rotatable Bonds: 11
Polar Surface Area: 200.95Molecular Species: ACIDHBA: 7HBD: 6
#RO5 Violations: 2HBA (Lipinski): 13HBD (Lipinski): 6#RO5 Violations (Lipinski): 3
CX Acidic pKa: 1.41CX Basic pKa: CX LogP: 3.21CX LogD: -3.10
Aromatic Rings: 4Heavy Atoms: 42QED Weighted: 0.13Np Likeness Score: -0.79

References

1. Elumalai N, Natarajan K, Berg T..  (2017)  Halogen-substituted catechol bisphosphates are potent and selective inhibitors of the transcription factor STAT5b.,  25  (14): [PMID:28559059] [10.1016/j.bmc.2017.05.039]

Source