ID: ALA4746113

Max Phase: Preclinical

Molecular Formula: C18H28NO5P

Molecular Weight: 369.40

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C/C(=C\CCP(=O)(N[C@@H](C)C(=O)OC(C)C)Oc1ccccc1)CO

Standard InChI:  InChI=1S/C18H28NO5P/c1-14(2)23-18(21)16(4)19-25(22,12-8-9-15(3)13-20)24-17-10-6-5-7-11-17/h5-7,9-11,14,16,20H,8,12-13H2,1-4H3,(H,19,22)/b15-9+/t16-,25?/m0/s1

Standard InChI Key:  MRVPZKQGAYTXHJ-WESGCFAHSA-N

Associated Targets(Human)

Butyrophilin subfamily 3 member A1 291 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: 369.40Molecular Weight (Monoisotopic): 369.1705AlogP: 3.52#Rotatable Bonds: 10
Polar Surface Area: 84.86Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.64CX Basic pKa: CX LogP: 2.18CX LogD: 2.18
Aromatic Rings: 1Heavy Atoms: 25QED Weighted: 0.37Np Likeness Score: 0.58

References

1. Kadri H,Taher TE,Xu Q,Sharif M,Ashby E,Bryan RT,Willcox BE,Mehellou Y.  (2020)  Aryloxy Diester Phosphonamidate Prodrugs of Phosphoantigens (ProPAgens) as Potent Activators of Vγ9/Vδ2 T-Cell Immune Responses.,  63  (19.0): [PMID:32930595] [10.1021/acs.jmedchem.0c01232]

Source