ID: ALA584910

Max Phase: Preclinical

Molecular Formula: C26H50NO9P

Molecular Weight: 551.66

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)O[C@@H]1CN[C@@H](C(=O)O)C1

Standard InChI:  InChI=1S/C26H50NO9P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-25(29)34-20-22(28)21-35-37(32,33)36-23-18-24(26(30)31)27-19-23/h22-24,27-28H,2-21H2,1H3,(H,30,31)(H,32,33)/t22-,23+,24-/m1/s1

Standard InChI Key:  IQWNCAYPTZMTSA-TZRRMPRUSA-N

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: 551.66Molecular Weight (Monoisotopic): 551.3223AlogP: 5.10#Rotatable Bonds: 24
Polar Surface Area: 151.62Molecular Species: ZWITTERIONHBA: 8HBD: 4
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 1.20CX Basic pKa: 10.93CX LogP: 3.41CX LogD: 0.65
Aromatic Rings: 0Heavy Atoms: 37QED Weighted: 0.07Np Likeness Score: 0.84

References

1. Iwashita M, Makide K, Nonomura T, Misumi Y, Otani Y, Ishida M, Taguchi R, Tsujimoto M, Aoki J, Arai H, Ohwada T..  (2009)  Synthesis and evaluation of lysophosphatidylserine analogues as inducers of mast cell degranulation. Potent activities of lysophosphatidylthreonine and its 2-deoxy derivative.,  52  (19): [PMID:19743861] [10.1021/jm900598m]

Source