[(3-Nitro-phenylamino)-phosphono-methyl]-phosphonic acid

ID: ALA450938

PubChem CID: 5277490

Max Phase: Preclinical

Molecular Formula: C7H10N2O8P2

Molecular Weight: 312.11

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  O=[N+]([O-])c1cccc(NC(P(=O)(O)O)P(=O)(O)O)c1

Standard InChI:  InChI=1S/C7H10N2O8P2/c10-9(11)6-3-1-2-5(4-6)8-7(18(12,13)14)19(15,16)17/h1-4,7-8H,(H2,12,13,14)(H2,15,16,17)

Standard InChI Key:  VPXZTOOBAWPNGR-UHFFFAOYSA-N

Molfile:  

     RDKit          2D

 19 19  0  0  0  0  0  0  0  0999 V2000
    3.1917   -1.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9042   -0.7042    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    3.1917   -1.9417    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3750   -0.7167    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4792   -0.7042    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3375   -1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0500   -0.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3833    0.1083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9042    0.1208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6042   -2.5250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0958   -1.1292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7667   -1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3167   -1.4167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7292   -0.7042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0167   -1.9417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4042   -2.7375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3375   -1.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0500   -2.3667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7667   -1.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  3  1  1  0
  4  6  1  0
  5  1  1  0
  6  7  1  0
  7 12  2  0
  8  4  1  0
  9  2  2  0
 10  3  2  0
 11  4  2  0
 12  5  1  0
 13  2  1  0
 14  2  1  0
 15  3  1  0
 16  3  1  0
 17 18  1  0
 18 19  2  0
 19 12  1  0
  6 17  2  0
M  CHG  2   4   1   8  -1
M  END

Alternative Forms

1. Parent:

   

   ALA450938

   (3-NITROPHENYLAMINO)METHYLENEDIPHOSPHONIC ACID

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: 312.11

Molecular Weight (Monoisotopic): 311.9912

AlogP: 0.65

#Rotatable Bonds: 5

Polar Surface Area: 170.23

Molecular Species: ACID

HBA: 5

HBD: 5

#RO5 Violations: ┄

HBA (Lipinski): 10

HBD (Lipinski): 5

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 0.95

CX Basic pKa: ┄

CX LogP: 0.02

CX LogD: -4.80

Aromatic Rings: 1

Heavy Atoms: 19

QED Weighted: 0.30

Np Likeness Score: -0.96

References

1. Kotsikorou E, Song Y, Chan JM, Faelens S, Tovian Z, Broderick E, Bakalara N, Docampo R, Oldfield E..  (2005)  Bisphosphonate inhibition of the exopolyphosphatase activity of the Trypanosoma brucei soluble vacuolar pyrophosphatase.,  48  (19): [PMID:16162013] [10.1021/jm058220g]

2. Hudock MP, Sanz-Rodríguez CE, Song Y, Chan JM, Zhang Y, Odeh S, Kosztowski T, Leon-Rossell A, Concepción JL, Yardley V, Croft SL, Urbina JA, Oldfield E..  (2006)  Inhibition of Trypanosoma cruzi hexokinase by bisphosphonates.,  49  (1): [PMID:16392806] [10.1021/jm0582625]

3. Sanz-Rodríguez CE, Concepción JL, Pekerar S, Oldfield E, Urbina JA..  (2007)  Bisphosphonates as inhibitors of Trypanosoma cruzi hexokinase: kinetic and metabolic studies.,  282  (17): [PMID:17329254] [10.1074/jbc.m607286200]

4. Forlani G, Giberti S, Berlicki L, Petrollino D, Kafarski P..  (2007)  Plant P5C reductase as a new target for aminomethylenebisphosphonates.,  55  (11): [PMID:17474756] [10.1021/jf0701032]

5. Obojska A, Berlicki L, Kafarski P, Lejczak B, Chicca M, Forlani G..  (2004)  Herbicidal pyridyl derivatives of aminomethylene-bisphosphonic acid inhibit plant glutamine synthetase.,  52  (11): [PMID:15161194] [10.1021/jf049843q]

6. Tauro M, Laghezza A, Loiodice F, Agamennone M, Campestre C, Tortorella P..  (2013)  Arylamino methylene bisphosphonate derivatives as bone seeking matrix metalloproteinase inhibitors.,  21  (21): [PMID:24071448] [10.1016/j.bmc.2013.08.054]

7. Tauro M, Loiodice F, Ceruso M, Supuran CT, Tortorella P..  (2014)  Arylamino bisphosphonates: potent and selective inhibitors of the tumor-associated carbonic anhydrase XII.,  24  (8): [PMID:24650641] [10.1016/j.bmcl.2014.03.001]

Source

Source(1):

• Scientific Literature