3-(N-Hydroxy-N-methylcarbamoyl)-2-phenyl-propylphosphonic acid

ID: ALA3422247

Chembl Id: CHEMBL3422247

PubChem CID: 118735472

Max Phase: Preclinical

Molecular Formula: C11H16NO5P

Molecular Weight: 273.23

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CN(O)C(=O)CC(CP(=O)(O)O)c1ccccc1

Standard InChI:  InChI=1S/C11H16NO5P/c1-12(14)11(13)7-10(8-18(15,16)17)9-5-3-2-4-6-9/h2-6,10,14H,7-8H2,1H3,(H2,15,16,17)

Standard InChI Key:  RGWBBKVQKPJVGW-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA3422247

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Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 273.23

Molecular Weight (Monoisotopic): 273.0766

AlogP: 1.19

#Rotatable Bonds: 5

Polar Surface Area: 98.07

Molecular Species: ACID

HBA: 3

HBD: 3

#RO5 Violations: 0

HBA (Lipinski): 6

HBD (Lipinski): 3

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 1.80

CX Basic pKa:

CX LogP: -0.34

CX LogD: -2.73

Aromatic Rings: 1

Heavy Atoms: 18

QED Weighted: 0.42

Np Likeness Score: 0.03

References

1. Chofor R, Sooriyaarachchi S, Risseeuw MD, Bergfors T, Pouyez J, Johny C, Haymond A, Everaert A, Dowd CS, Maes L, Coenye T, Alex A, Couch RD, Jones TA, Wouters J, Mowbray SL, Van Calenbergh S..  (2015)  Synthesis and bioactivity of β-substituted fosmidomycin analogues targeting 1-deoxy-D-xylulose-5-phosphate reductoisomerase.,  58  (7): [PMID:25781377] [10.1021/jm5014264]

Source

Source(1):

• Scientific Literature