70788-28-2,MFCD00209841
Catalog No.:AA0064DB

70788-28-2 | Flurofamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
2mg
95%
1 week  
$93.00   $65.00
- +
5mg
95%
1 week  
$118.00   $83.00
- +
10mg
92%
1 week  
$225.00   $158.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0064DB
Chemical Name:
Flurofamide
CAS Number:
70788-28-2
Molecular Formula:
C7H9FN3O2P
Molecular Weight:
217.1374
MDL Number:
MFCD00209841
SMILES:
O=C(c1ccc(cc1)F)NP(=O)(N)N
Properties
Properties
 
Form:
Solid  
MP:
>215°C (sub.)  
Storage:
-20 ℃;Keep in dry area;  

Computed Properties
 
Complexity:
260  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.6  

Literature

Title: Urea, fluorofamide, and omeprazole treatments alter helicobacter colonization in the mouse gastric mucosa.

Journal: Helicobacter 20061001

Title: Selection and properties of Streptococcus thermophilus mutants deficient in urease.

Journal: Journal of dairy science 20040601

Title: Effect of the metabolism of urea on the acidifying activity of Streptococcus thermophilus.

Journal: Journal of dairy science 20040301

Title: Suppression of Helicobacter pylori-induced gastritis by urease inhibitors in Mongolian gerbils.

Journal: Gan to kagaku ryoho. Cancer & chemotherapy 20020201

Title: Marked reduction of Helicobacter pylori-induced gastritis by urease inhibitors, acetohydroxamic acid and flurofamide, in Mongolian gerbils.

Journal: Biochemical and biophysical research communications 20010720

Title: Millner OE Jr, et al. Flurofamide: a potent inhibitor of bacterial urease with potential clinical utility in the treatment of infection induced urinary stones. J Urol. 1982 Feb;127(2):346-50.

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Tags:70788-28-2 Molecular Formula|70788-28-2 MDL|70788-28-2 SMILES|70788-28-2 Flurofamide
Catalog No.: AA0064DB
70788-28-2,MFCD00209841
70788-28-2 | Flurofamide
Pack Size: 2mg
Purity: 95%
1 week
$93.00 $65.00
Pack Size: 5mg
Purity: 95%
1 week
$118.00 $83.00
Pack Size: 10mg
Purity: 92%
1 week
$225.00 $158.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA0064DB
Chemical Name: Flurofamide
CAS Number: 70788-28-2
Molecular Formula: C7H9FN3O2P
Molecular Weight: 217.1374
MDL Number: MFCD00209841
SMILES: O=C(c1ccc(cc1)F)NP(=O)(N)N
Properties
Form: Solid  
MP: >215°C (sub.)  
Storage: -20 ℃;Keep in dry area;  
Complexity: 260  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.6  
Literature fold

Title: Urea, fluorofamide, and omeprazole treatments alter helicobacter colonization in the mouse gastric mucosa.

Journal: Helicobacter20061001

Title: Selection and properties of Streptococcus thermophilus mutants deficient in urease.

Journal: Journal of dairy science20040601

Title: Effect of the metabolism of urea on the acidifying activity of Streptococcus thermophilus.

Journal: Journal of dairy science20040301

Title: Suppression of Helicobacter pylori-induced gastritis by urease inhibitors in Mongolian gerbils.

Journal: Gan to kagaku ryoho. Cancer & chemotherapy20020201

Title: Marked reduction of Helicobacter pylori-induced gastritis by urease inhibitors, acetohydroxamic acid and flurofamide, in Mongolian gerbils.

Journal: Biochemical and biophysical research communications20010720

Title: Millner OE Jr, et al. Flurofamide: a potent inhibitor of bacterial urease with potential clinical utility in the treatment of infection induced urinary stones. J Urol. 1982 Feb;127(2):346-50.

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