ID: ALA4566548

Max Phase: Preclinical

Molecular Formula: C6H9O12P3

Molecular Weight: 366.05

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=P(O)(O)Oc1cccc(OP(=O)(O)O)c1OP(=O)(O)O

Standard InChI:  InChI=1S/C6H9O12P3/c7-19(8,9)16-4-2-1-3-5(17-20(10,11)12)6(4)18-21(13,14)15/h1-3H,(H2,7,8,9)(H2,10,11,12)(H2,13,14,15)

Standard InChI Key:  ALWMWBDJLPREOH-UHFFFAOYSA-N

Associated Targets(Human)

Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 180 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Inositol 1,4,5-trisphosphate 5-phosphatase 11 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Type I inositol-1,4,5-trisphosphate 5-phosphatase 17 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: 366.05Molecular Weight (Monoisotopic): 365.9307AlogP: 0.10#Rotatable Bonds: 6
Polar Surface Area: 200.28Molecular Species: ACIDHBA: 6HBD: 6
#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 6#RO5 Violations (Lipinski): 2
CX Acidic pKa: 1.21CX Basic pKa: CX LogP: -0.90CX LogD: -10.42
Aromatic Rings: 1Heavy Atoms: 21QED Weighted: 0.37Np Likeness Score: 0.59

References

1. White G, Prior C, Mills SJ, Baker K, Whitfield H, Riley AM, Oganesyan VS, Potter BVL, Brearley CA..  (2020)  Regioisomeric Family of Novel Fluorescent Substrates for SHIP2.,  11  (3): [PMID:32184962] [10.1021/acsmedchemlett.9b00368]

Source