In order to demonstrate the validity of the proposed degradation mechanism, p-nitrobenzaldehyde has been employed as a model of reaction of the nucleophylic attack of amino-opened structure of Azolam to an aldehyde to generate the first intermediate involved in Maillard reaction, a Schiff base.
Other names for this medication:
Alprazolam,
Aaram,
Alap,
Alark,
Albiz,
Aldep,
Aleez,
Alep,
Alfix,
Alfresh,
Allam,
Alltop,
Almee,
Alpam,
Alpram,
Alprax,
Alprose,
Altin,
Altrex,
Alzam,
Alzin,
Alzo,
Alzocum,
Alzolam,
Ambulax,
Ambutech,
Anax,
Anilam,
Anquil,
Anxicalm,
Anxit,
Anzi,
Anzilum,
Apna,
Atal,
Atam,
Azolam,
Azox,
Belfa,
Berest,
Bioclock,
Bliz,
Cardilax,
Cooltime,
Copax,
Dipra,
Endep,
Erazol,
Esteem,
Fluwel,
Lamad,
Loral,
Mandar,
Nitril,
Norex,
Nucalm,
Orten,
Poex,
Poize,
Prala,
Prazolam,
Procalm,
Prolam,
Pronext,
Quiet,
Reclam,
Resta,
Restam,
Resto,
Restyl,
Rian,
Rozin,
Secam,
Selam,
Serex,
Shant,
Shanti,
Silam,
Sinozol,
Solace,
Somnia,
Sowel,
Stresnil,
Tenan,
Tenolam,
Tenzo,
Texidep,
Tiox,
Tranax,
Trika,
Trustin,
Visram,
Xanti,
Xylonite,
Zenax,
Zepro,
Zocam,
Zoem,
Zola,
Zolam,
Zoldac,
Zolent,
Zolin,
Zoloid,
Zopax,
Zopral,
Zozo,
Xanax,
Niravam,
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Ramcet,
Celtium,
Talol,
Omec,
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