ID: ALA4745697

Max Phase: Preclinical

Molecular Formula: C28H32NO10P

Molecular Weight: 573.54

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[C@H](COP(=O)(O)OC[C@H](N)C(=O)O)OC(=O)CCc1ccccc1OCc1cccc(Oc2ccccc2)c1

Standard InChI:  InChI=1S/C28H32NO10P/c1-20(17-36-40(33,34)37-19-25(29)28(31)32)38-27(30)15-14-22-9-5-6-13-26(22)35-18-21-8-7-12-24(16-21)39-23-10-3-2-4-11-23/h2-13,16,20,25H,14-15,17-19,29H2,1H3,(H,31,32)(H,33,34)/t20-,25+/m1/s1

Standard InChI Key:  WTQTXPXOHUNDIF-NLFFAJNJSA-N

Associated Targets(non-human)

G protein-coupled receptor 34 411 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Putative P2Y purinoceptor 10 276 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: 573.54Molecular Weight (Monoisotopic): 573.1764AlogP: 4.47#Rotatable Bonds: 16
Polar Surface Area: 163.84Molecular Species: ZWITTERIONHBA: 9HBD: 3
#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 1.57CX Basic pKa: 9.38CX LogP: 2.58CX LogD: -0.49
Aromatic Rings: 3Heavy Atoms: 40QED Weighted: 0.16Np Likeness Score: 0.01

References

1. Nakamura S,Sayama M,Uwamizu A,Jung S,Ikubo M,Otani Y,Kano K,Omi J,Inoue A,Aoki J,Ohwada T.  (2020)  Non-naturally Occurring Regio Isomer of Lysophosphatidylserine Exhibits Potent Agonistic Activity toward G Protein-Coupled Receptors.,  63  (17): [PMID:32787112] [10.1021/acs.jmedchem.0c01126]

Source