Other grades of this product :
| Nafcillin sodium salt monohydrate Basic information |
| Product Name: | Nafcillin sodium salt monohydrate | | Synonyms: | Nafcillin monohydrate sodium salt;D00928;Nafcillin sodium (usp);Nafcillin sodium monohydrate;Unipen (tn);Nafcillin sodium salt monohydrate,6-(2-Ethoxy-1-naphthamido)penicillin;Nafcillin Sodium (200 mg);Nafcillin sodiuM salt Monohydr | | CAS: | 7177-50-6 | | MF: | C21H23N2NaO6S | | MW: | 454.47 | | EINECS: | 628-594-2 | | Product Categories: | | Mol File: | 7177-50-6.mol |
| Nafcillin sodium salt monohydrate Chemical Properties |
| Nafcillin sodium salt monohydrate Usage And Synthesis |
| Originator | Unipen,Wyeth,US,1964 | | Uses | Sodium Nafcillin Monohydrate is used as an antibiotic, used in the treatment, used in the treatment of gram-positive bacteria. | | Uses | Antibacterial;Bacterial transpeptidase inhibitor
| | Uses | Nafcillin sodium salt monohydrate is an antibiotic resistant to beta-lactamase.
| | Manufacturing Process | A stirred suspension of 12.6 grams 6-aminopenicillanic acid in 130 ml dry
alcohol-free chloroform was treated with 16 ml triethylamine and then with
13.8 grams of a solution of 2-ethoxy-1-naphthoyl chloride in 95 ml
chloroform. After being washed successively with 58 ml each of 1 N and then
0.1 N hydrochloric acid the chloroform solution was extracted with N aqueous
sodium bicarbonate (58 ml + 6 ml). The combined bicarbonate extracts were
washed with 20 ml ether and then evaporated at low temperature and
pressure to give the crude sodium salt of 2-ethoxy-1-naphthylpenicillin [also
called sodium 6-(2-ethoxy-1-naphthamido)penicillinate] as a yellow powder
(20.3 grams). This was dissolved in 20 ml water at 30°C and diluted with 180
ml n-butanol, also at 30°C, with stirring. Slow cooling to 0°C gave colorless
needles of the product. | | Brand name | Nallpen (GlaxoSmithKline). | | Therapeutic Function | Antibacterial | | Clinical Use | Nafcillin sodium, 6-(2-ethoxy-1-naphthyl)penicillin sodium(Unipen), is another semisynthetic penicillin that resultedfrom the search for penicillinase-resistant compounds. Likemethicillin, nafcillin has substituents in positions ortho tothe point of attachment of the aromatic ring to the carboxamidegroup of penicillin. No doubt, the ethoxy group andthe second ring of the naphthalene group play steric roles instabilizing nafcillin against penicillinase. Very similar structureshave been reported to produce similar results in somesubstituted 2-biphenylpenicillins. Unlike methicillin, nafcillin is stable enough in acid topermit its use by oral administration. When it is givenorally, its absorption is somewhat slow and incomplete,but satisfactory plasma levels may be achieved in about1 hour. Relatively small amounts are excreted throughthe kidneys; most is excreted in the bile. Even thoughsome cyclic reabsorption from the gut may occur, nafcillingiven orally should be readministered every 4 to 6 hours.This salt is readily soluble in water and may be administeredintramuscularly or intravenously to obtain highplasma concentrations quickly for the treatment of seriousinfections.Nafcillin sodium may be used in infections causedsolely by penicillin G-resistant staphylococci or whenstreptococci are present also. Although it is recommendedthat it be used exclusively for such resistant infections, nafcillin is also effective against pneumococci and groupA -hemolytic streptococci. Because, like other penicillins,it may cause allergic side effects, it should be administeredwith care. |
| Nafcillin sodium salt monohydrate Preparation Products And Raw materials |
|
日本语
한국어
Français
Deutsch
España
Türkiye