N,N-Dimethyl-N-(3-(tetradecylamino)propyl)-vancomycin Carboxamide hydrochloride salt

Product Name N,N-Dimethyl-N-(3-(tetradecylamino)propyl)-vancomycin Carboxamide hydrochloride salt
Alternate Names Vancomycin Impurities, Impurities of Vancomycin
CAT No. CS-O-32815
CAS No. 1428645-19-5(Freebase)
Category Impurities
Stock IN-Stock
Mol. Wt. 1766.25 g/mol
Mol. For. C85H116Cl3N11O23
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Vancomycin
Therapeutic Antibiotics
Smileys C[N+](CCCCCCCCCCCCCC)(CCCNC([C@]1(NC([C@@]2([C@@H](C3=CC=C(OC4=CC([C@]([H])(C(N[C@]([H])(C5=CC(C6=C1C=C(C=C6O)O)=C(C=C5)O)C(N2)=O)=O)NC([C@H](CC(N)=O)NC7=O)=O)=CC(OC8=CC=C(C=C8Cl)[C@@H](O)[C@H]7NC([C@@H](CC(C)C)NC)=O)=C4O[C@@H]([C@@H]9O[C@@]([H])(C[C@]%10(C)N)O[C@H]([C@H]%10O)C)O[C@@H]([C@H]([C@@H]9O)O)CO)C(Cl)=C3)O)[H])=O)[H])=O)C.[Cl-]
Controlled No
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N,N-Dimethyl-N-(3-(tetradecylamino)propyl)-vancomycin Carboxamide hydrochloride salt, also known as TDV, is a modified form of the antibiotic vancomycin. It is designed to be more effective against Gram-negative bacteria, which are often resistant to traditional antibiotics. TDV works by binding to the bacterial cell wall, interfering with its synthesis and ultimately causing the cell to rupture. The addition of the tetradecylamino group enhances the molecule’s ability to penetrate the outer membrane of Gram-negative bacteria, allowing it to reach its target more effectively. In addition to its antibacterial properties, TDV has been shown to have anti-inflammatory effects. It has been studied for potential use in the treatment of infections caused by multidrug-resistant bacteria, as well as for the treatment of inflammatory bowel disease. Chemically, TDV is a complex molecule with a molecular weight of approximately 2,500 Daltons. It is a hydrochloride salt, meaning that it is a compound formed by the reaction of TDV with hydrochloric acid, resulting in a charged molecule that is more soluble in water. Overall, TDV represents a promising development in the fight against antibiotic-resistant bacteria and inflammatory diseases, and further research is needed to explore its potential clinical applications.

Related Compounds

Vancomycin Impurity-G | N,N-Dimethyl-N-(3-(octylamino)propyl)-vancomycin Carboxamide hydrochloride salt | Vancomycin B | Vancomycin RS-1- Impurity | Vancomycin Hexapeptide | alfa-Avoparcin | epi-26-Vancomycin B | Vancomycin EP Impurity D | Desmethylleucyl Vancomycin | Vancomycin EP Impurity H | N-Methylleucyl Vancomycin | Vancomycin EP Impurity C | Vancomycin EP Impurity J | Vancomycin Impurity-L | Vancomycin EP Impurity B | Vancomycin EP Impurity I | Vancomycin EP Impurity A | Vancomycin RS-3- Impurity | Vancomycin Impurity B2 | beta-Avoparcin | Vancomycin EP Impurity G HCl | Vancomycin EP Impurity E | Vancomycin EP Impurity K | Vancomycin RS-2- Impurity | Vancomycin CDP-1 | Vancomycin Didechloro Impurity | Vancomycin Impurity-F | N-desmethyl Vancomycin |

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