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This is a list of local anesthetic agents. Not all of these drugs are still used in clinical practice and in research. Some are primarily of historical interest.
Drug | Other common names | Image | First synthesis | Dates of clinical use | Chemical/structural class | Duration of effect | ||||
---|---|---|---|---|---|---|---|---|---|---|
amylocaine | Stovaine | 1904 (Ernest Fourneau) | ester- benzoic
|
|||||||
ambucaine | [1] | diester - aminosalicylic | ||||||||
articaine | Astracaine, Septanest, Septocaine, Ultracaine, Zorcaine | Amide | ||||||||
benzocaine | Anbesol, Orajel | Ester - Aminobenzoic | Short | |||||||
benzonatate | Tessalon | |||||||||
bupivacaine | Marcaine, Sensorcaine, Vivacaine | 1957 (Ekenstam) | 1963 (Widman and Telivuo) | Amide | Moderate | |||||
butacaine | ester- aminobenzoic | |||||||||
butanilicaine | Amide | |||||||||
chloroprocaine | Nesacaine | Ester - Aminobenzoic | ||||||||
cinchocaine (INN) | dibucaine (USAN), Cincain, Cinchocaine, Nupercainal, Nupercaine, Sovcaine | 1925 (Meischer) | 1930 (Uhlmann) | Ester - Aminobenzoic | ||||||
cocaine | 1855 (first isolation by Friedrich Gaedcke), 1898 (first synthesis by Richard Willstätter) | 1884 (Karl Koller, William Stewart Halsted) | Ester - Benzoic | |||||||
cyclomethycaine | [2] | Ester - hydroxybenzoic | ||||||||
dibucaine | [3] | Amide | ||||||||
diperodon | [4][5] | |||||||||
dimethocaine | larocaine | |||||||||
eucaine | α-Eucaine, β-eucaine |
|
1900. α[6] β[7][8] | |||||||
etidocaine | Duranest | 1971 (Takman) | 1972 (Lund) | |||||||
hexylcaine | Cyclaine, Osmocaine | |||||||||
fomocaine | [9] | ester - phenyl | ||||||||
fotocaine | [9] | |||||||||
hydroxyprocaine | [10] | ester - aminosalicylic | ||||||||
isobucaine | [11] | Ester - benzoic | ||||||||
levobupivacaine | Chirocaine | 1990s (Mather and Tucker) | 1995 | |||||||
lidocaine[12][13]
(lignocaine) |
Xylocaine | 1943 (Nils Löfgren and Bengt Lundqvist) | 1947 (Torsten Gordh) | |||||||
mepivacaine | Carbocaine, Polocaine | 1956 (Ekenstam and Egner) | 1957 (Dhuner) | |||||||
meprylcaine | Epirocain | |||||||||
metabutoxycaine | ||||||||||
nitracaine | Ester- Aminobenzoic | |||||||||
orthocaine | ||||||||||
oxetacaine (oxethazaine) | ||||||||||
oxybuprocaine | benoxinate, Novesine | |||||||||
Paraethoxycaine | [14] | |||||||||
phenacaine | Holocaine | |||||||||
piperocaine | metycaine | |||||||||
piridocaine | [15] | |||||||||
pramocaine | pramoxine | |||||||||
prilocaine | Citanest | 1959 (Nils Löfgren and Egner) | 1960 (Wielding) | |||||||
Primacaine | ||||||||||
procaine | Novocain, borocaine (procaine borate), ethocaine | 1904 (Alfred Einhorn) | 1905 (Heinrich Braun) | |||||||
procainamide | ||||||||||
proparacaine | proxymetacaine | |||||||||
propoxycaine[16] | ||||||||||
Pyrrocaine | [17] | |||||||||
quinisocaine (INN) | dimethisoquin (USAN) | [18] | ||||||||
ropivacaine | Naropin | 1957 (Ekenstam) | 1997 | |||||||
trimecaine | Mesdicain, Mesocain, Mesokain | |||||||||
tetracaine | amethocaine, Dicaine, Pontocaine | 1928 (O. Eisleb) | 1931 | |||||||
Tolycaine | [19] | |||||||||
Tropacocaine[20] |
See also
edit- 4-Aminobenzoic acid
- Amino amide
- Amino esters
- Anesthesia
- Anesthetic
- Brachial plexus block
- Cocaine analogues: local anesthetics
- Dental anesthesia
- Dibucaine number
- Epidural
- Intravenous regional anesthesia
- Local anesthesia
- Local anesthetic with vasoconstrictor
- Local anesthetic toxicity
- Methemoglobin
- Sodium channel blocker
- Spinal anesthesia
- Topical anesthesia
- Veterinary anesthesia
References
edit- ^ Büchi, J; Stünzi, E; Flury, M; Hirt, R; Labhart, P; Ragaz, L (1951). "Über lokalanästhetisch wirksame basische Ester und Amide verschiedener Alkoxy-amino-benzoesäuren". Helvetica Chimica Acta. 34 (4): 1002–1013. doi:10.1002/hlca.19510340404.
- ^ S. M. McElvain and T. P. Carney, J. Amer. Chem. Soc, 68, 2592 (1946).
- ^ K. Miescher, Helv. Chim. Acta, 15, 163 (1932).
- ^ 44. T. H. Rider, J. Amer. Chem. Soc, 52, 2115 (1930).
- ^ M. S. Raasch and W. R. Brode, J. Amer. Chem. Soc, 64, 1112 (1942).
- ^ Harries, C. (1903). "Ueber ein neues p-Menthadiën aus Dihydrocarvylamin". Justus Liebig's Annalen der Chemie. 328 (3): 322–326. doi:10.1002/jlac.19033280303.
- ^ G. Meiling, Chem. Ber., 6, 173 (1896).
- ^ H. King, J. Chem. Soc, 125, 41 (1924).
- ^ a b Schoenberger, Matthias; Damijonaitis, Arunas; Zhang, Zinan; Nagel, Daniel; Trauner, Dirk (2014). "Development of a New Photochromic Ion Channel Blocker via Azologization of Fomocaine". ACS Chemical Neuroscience. 5 (7): 514–518. doi:10.1021/cn500070w. ISSN 1948-7193. PMC 4102962. PMID 24856540.
- ^ W. Grimme and H. Schmitz, Chem. Ber., 84, 734 (1917).
- ^ J. R. Reasenberg and S. D. Goldberg, J. Amer. Chem. Soc, 67, 933 (1945).
- ^ "Lignocaine - C14H22N2O". ChemSpider. Retrieved 2015-10-13.
- ^ "Lidocaine". The Merck Index Online. Retrieved 2015-10-13.
- ^ W. G. Christiansen and S. E. Harris, U. S. Patent 2,404,691 (1946).
- ^ L. A. Walter and R. J. Fosbinder, J. Amer. Chem. Soc, 61, 1713 (1939).
- ^ Clinton, R. O.; Salvador, U. J.; Laskowski, S. C.; Wilson, Mary (February 1952). "Derivatives of 4-Amino-2-hydroxybenzoic Acid. II". Journal of the American Chemical Society. 74 (3): 592–598. doi:10.1021/ja01123a005.
- ^ N. Lofgren, C. Tegner, and B. Takman, Acta Chem. Scand., 11, 1724 (1957).
- ^ T. H. Rider, J. Amer. Chem. Soc, 52, 2115 (1930).
- ^ R. Hiltmann, F. Mietzsch, and W. Wirth, U.S. patent 2,921,077 (1960).
- ^ Jowett, Hooper Albert Dickinson; Pyman, Frank Lee (1909). "CXVI.—Relation between chemical constitution and physiological action in the tropeines. Part II". J. Chem. Soc., Trans. 95: 1020–1032. doi:10.1039/CT9099501020.