rel-(1S,2R)-2-amino-1-hydroxy-3-phenylpropylphosphonic acid

ID: ALA2287554

Chembl Id: CHEMBL2287554

PubChem CID: 76327382

Max Phase: Preclinical

Molecular Formula: C9H14NO4P

Molecular Weight: 231.19

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  N[C@H](Cc1ccccc1)[C@@H](O)P(=O)(O)O

Standard InChI:  InChI=1S/C9H14NO4P/c10-8(9(11)15(12,13)14)6-7-4-2-1-3-5-7/h1-5,8-9,11H,6,10H2,(H2,12,13,14)/t8-,9+/m1/s1

Standard InChI Key:  IPVUODADXZPVCG-BDAKNGLRSA-N

Associated Targets(non-human)

Cucumis sativus (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lepidium sativum (398 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

Calculated Properties

Molecular Weight: 231.19Molecular Weight (Monoisotopic): 231.0660AlogP: 0.05#Rotatable Bonds: 4
Polar Surface Area: 103.78Molecular Species: ZWITTERIONHBA: 3HBD: 4
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 1.00CX Basic pKa: 9.74CX LogP: -1.40CX LogD: -1.60
Aromatic Rings: 1Heavy Atoms: 15QED Weighted: 0.55Np Likeness Score: 0.30

References

1. Zygmunt J, Gancarz R, Lejczak B, Wieczorek P, Kafarski P.  (1996)  Stereoselective synthesis of 2-amino-1-hydroxy-3-phenylpropylphosphonic acid,  (24): [10.1016/S0960-894X(96)00545-8]

Source