Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C18H32N2O11P2 |
| Molecular Weight | 514.401 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCOP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1OP(O)(=O)OCCCC)N2C=C(C)C(=O)NC2=O
InChI
InChIKey=ZXQBUNYVGNOEBQ-ARFHVFGLSA-N
InChI=1S/C18H32N2O11P2/c1-4-6-8-27-32(23,24)29-12-15-14(31-33(25,26)28-9-7-5-2)10-16(30-15)20-11-13(3)17(21)19-18(20)22/h11,14-16H,4-10,12H2,1-3H3,(H,23,24)(H,25,26)(H,19,21,22)/t14-,15+,16+/m0/s1
| Molecular Formula | C18H32N2O11P2 |
| Molecular Weight | 514.401 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
1-(3,5-BIS-O-(BUTOXYHYDROXYPHOSPHINYL)-2-DEOXY-D-ERYTHRO-PENTOFURANOSYL)-5-METHYL-2,4(1H,3H)-PYRIMIDINEDIONE (Nu-3), a Bisphosphocins, is being developed by Lakewood-Amedex (formerly Nu Pharmas), for the treatment of diabetic foot ulcer, lung infections, stomatitis. Nu-3, a novel synthetic broad-spectrum antimicrobial proven to be effective in killing a wide range of Gram-positive, Gram-negative and antibiotic-resistant bacteria, recently completed a Phase 1/2a clinical trial in patients, showing no treatment-related adverse events and a trend toward efficacy. Patients treated with 2% Nu-3 for seven days had a 65.5% reduction in ulcer area versus a 29.9% reduction in the placebo arm, as measured 14 days after treatment began. In addition, 62.5% of patients treated with 2% Nu-3 saw a reduction in the microbiological load, versus 20% in the placebo. Three additional Phase 2a adaptive arm clinical trials providing robust clinical data in areas of urgent medical need are expected to be completed by 2020.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://lakewoodamedex.com/pipeline/nu-3-dfu/
Patients treated with 2% Nu-3 for seven days had a 65.5% reduction in ulcer area versus a 29.9% reduction in the placebo arm, as measured 14 days after treatment began. In addition, 62.5% of patients treated with 2% Nu-3 saw a reduction in the microbiological load, versus 20% in the placebo.
Route of Administration:
Topical
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21232163
Minimum inhibitory concentrations of Nu-3 against Staphylococcus aureus cvcc 2248 is 4.4 mg/ml.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:44:43 GMT 2025
by
admin
on
Mon Mar 31 20:44:43 GMT 2025
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| Record UNII |
8BK3483OW5
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| Record Status |
Validated (UNII)
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1630942-91-4
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8BK3483OW5
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admin on Mon Mar 31 20:44:43 GMT 2025 , Edited by admin on Mon Mar 31 20:44:43 GMT 2025
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ACTIVE MOIETY |
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