ID: ALA567937

Max Phase: Preclinical

Molecular Formula: C25H50NO8P

Molecular Weight: 523.65

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCCCCCCCCCCC(=O)OCCCOP(=O)(O)O[C@H](C)[C@H](N)C(=O)O

Standard InChI:  InChI=1S/C25H50NO8P/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-23(27)32-20-18-21-33-35(30,31)34-22(2)24(26)25(28)29/h22,24H,3-21,26H2,1-2H3,(H,28,29)(H,30,31)/t22-,24+/m1/s1

Standard InChI Key:  LTPPXTBEKMGKEX-VWNXMTODSA-N

Associated Targets(non-human)

Mus musculus 284745 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: 523.65Molecular Weight (Monoisotopic): 523.3274AlogP: 6.12#Rotatable Bonds: 25
Polar Surface Area: 145.38Molecular Species: ZWITTERIONHBA: 7HBD: 3
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 1.61CX Basic pKa: 9.45CX LogP: 4.71CX LogD: 1.59
Aromatic Rings: 0Heavy Atoms: 35QED Weighted: 0.07Np Likeness Score: 0.50

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