| Verifiedrevid: | 414278352 |
| Iupac Name: | 3-(1-benzyl-1H-indazol-3-yloxy)-N,N-dimethylpropan-1-amine |
| Tradename: | Maxtra Gargle, Difflam, Tantum |
| Pregnancy Au: | B2 |
| Legal Br: | C1 |
| Legal Br Comment: | [1] |
| Legal Uk: | GSL |
| Legal Eu: | OTC |
| Routes Of Administration: | Oral, topical |
| Protein Bound: | <20% |
| Elimination Half-Life: | 13 hours |
| Excretion: | Kidney |
| Cas Number: | 642-72-8 |
| Atc Prefix: | A01 |
| Atc Suffix: | AD02 |
| Atc Supplemental: | |
| Pubchem: | 12555 |
| Chemspiderid: | 12036 |
| Chebi: | 94563 |
| Unii: | 4O21U048EF |
| Kegg: | D07516 |
| Chembl: | 12610 |
| C: | 19 |
| H: | 23 |
| N: | 3 |
| O: | 1 |
| Smiles: | n2c(OCCCN(C)C)c1ccccc1n2Cc3ccccc3 |
| Stdinchi: | 1S/C19H23N3O/c1-21(2)13-8-14-23-19-17-11-6-7-12-18(17)22(20-19)15-16-9-4-3-5-10-16/h3-7,9-12H,8,13-15H2,1-2H3 |
| Stdinchikey: | CNBGNNVCVSKAQZ-UHFFFAOYSA-N |
Benzydamine (also known as Tantum Verde and branded in some countries as Maxtra Gargle, Difflam and Septabene), available as the hydrochloride salt, is a locally acting nonsteroidal anti-inflammatory drug (NSAID) with local anaesthetic and analgesic properties for pain relief and anti-inflammatory treatment of inflammatory conditions of the mouth and throat.[2] It falls under class of chemicals known as indazole.
It was synthesized in Italy in 1964 and marketed in 1966.[3]
It may be used alone or as an adjunct to other therapy giving the possibility of increased therapeutic effect with little risk of interaction.
In some markets, the drug is supplied as an over-the-counter cream (Lonol in Mexico from Boehringer Ingelheim) used for topical treatment of musculoskeletal system disorders: sprains, strains, bursitis, tendinitis, synovitis, myalgia, periarthritis.
Benzydamine has been used recreationally. In overdosages it acts as a deliriant and CNS stimulant. Such use, particularly among teenagers, has been reported in Brazil,[4] [5] Poland, Romania, and Turkey.
There are no contraindications to the use of benzydamine except for known hypersensitivity.
Benzydamine is well tolerated. Occasionally oral tissue numbness or stinging sensations may occur, as well as itching, a skin rash, skin swelling or redness, difficulty breathing and wheezing.
It selectively binds to inflamed tissues (Prostaglandin synthetase inhibitor) and is normally free of adverse systemic effects.Unlike other NSAIDs, it does not inhibit cyclooxygenase or lipooxygenase, and is not ulcerogenic.[6] [7] It has powerful reinforcing effect and has cross sensitization with drugs of abuse such as heroin and cocaine in animals. It is hypothesized that it has cannabinoid agonistic activity.
Benzydamine is poorly absorbed through skin[8] and vagina.[9]
Synthesis starts with the reaction of the N-benzyl derivative from methyl anthranilate with nitrous acid to give the N-nitroso derivative. Reduction by means of sodium thiosulfate leads to the transient hydrazine (3), which undergoes spontaneous internal hydrazide formation. Treatment of the enolate of this amide with 3-chloro-1-dimethylamino propane gives benzydamine (5). Please note there is an error in this section: US3318905 states that the nitroso derivative is reduced with sodium hydrosulfite (sodium dithionite) and not with sodium hyposulfite (sodium thiosulfate), as shown in the above scheme and stated in text. An interesting alternative synthesis of this substance starts by sequential reaction of N-benzylaniline with phosgene, and then with sodium azide to product the corresponding carbonyl azide. On heating, nitrogen is evolved and a separatable mixture of nitrene insertion product and the desired ketoindazole # results. The latter reaction appears to be a Curtius rearrangement type product to produce an N-isocyanate #, which then cyclizes. Alkylation of the enol with sodium methoxide and 3-dimethylaminopropyl chloride gives benzydamine.
Alternatively, use of chloroacetamide in the alkylation step followed by acid hydrolysis produces bendazac instead.
Studies indicate that benzydamine has notable in vitro antibacterial activity and also shows synergism in combination with other antibiotics, especially tetracyclines, against antibiotic-resistant strains of Staphylococcus aureus and Pseudomonas aeruginosa.[10] [11]
It also has some cannabinoid activity in rats but has not been tested in humans.[12] It is also hypothesized to act on 5-HT2A receptors due to its structural similarity with serotonin.