From Wikipedia, the free encyclopedia
Atropa belladonna, commonly known as
belladonna or deadly nightshade,
is a perennial herbaceous plant in the family Solanaceae, native to Europe, North Africa, and Western Asia. The foliage and berries are extremely toxic, containing tropane alkaloids.[1]
These toxins include scopolamine and hyoscyamine which cause a bizarre delirium and hallucinations.[2]
The drug atropine is
derived from the plant.
It has a long history of use as a medicine, cosmetic, and
poison. Before the Middle Ages, it was used as an anesthetic for surgery,
and it was used as a poison by early men, ancient Romans, including the wives of two
Emperors, and by Macbeth of Scotland before he
became a Scottish King.
The genus name "atropa" comes from Atropos, one of the three Fates in Greek mythology (the one who cuts the
thread of life), and the name "atropa bella donna" is derived from
an admonition in Italian and Greek meaning "do not betray a beautiful
lady".[3][4][5]
Description
Atropa belladonna is a branching herbaceous perennial,
often growing as a subshrub, from a fleshy rootstock. Plants grow
to 1.5 metres (4.9 ft) tall with 18 centimetres
(7.1 in) long ovate leaves. The bell-shaped flowers are dull purple with green tinges and
faintly scented. The fruits are
berries, which are green
ripening to a shiny black, and approximately 1 centimetre
(0.39 in) in diameter. The berries are sweet and are consumed
by animals that disperse the seeds
in their droppings, even though the seeds contain toxic alkaloids.[6] There
is a pale yellow flowering form called Atropa belladonna
var. lutea with pale yellow fruit.
Atropa belladona is rarely used in gardens, but when
grown it is usually for its large upright habit and showy
berries.[7] It is
naturalized in parts of North America,
where it is often found in shady, moist locations with limestone-rich soils. It is considered a weed species in parts of the
world,[8] where
it colonizes areas with disturbed soils.[9] Germination of the
small seeds is often difficult, due to hard seed coats that cause
seed dormancy. Germination
takes several weeks under alternating temperature conditions but
can be sped up with the use of gibberellic acid.[10] The
seedlings need sterile soil to prevent damping off and resent root disturbance
during transplanting.
Naming and
taxonomy
The first botanical description was by Linnaeus in Species
Plantarum in 1753.[11] It is
in the nightshade family
(Solanaceae),
which it shares with potatoes,
tomatoes, eggplants, jimsonweed, tobacco, wolfberry, and chili peppers. The common names for this
species include belladonna, deadly nightshade, divale, dwale,[3]
banewort, devil's cherries, naughty man's cherries, black cherry,
devil's herb, great morel, and dwayberry.[12]
The name Atropa is thought to be derived from that of the Greek
goddess Atropos, one of the
three Greek fates or destinies
who would determine the course of a man's life by the weaving of
threads that symbolized their birth, the events in their life and
finally their death; with Atropos cutting these threads to mark the
latter.[4][5]
The name "belladonna" comes from the Italian language, meaning "beautiful
lady";[3]
originating either from its usage as cosmetic for the face, or,
more probably, from its usage to increase the pupil size in
ladies.[4][5]
Toxicity
Belladonna is one of the most toxic plants found in the Western hemisphere. All parts of the plant
contain tropane alkaloids.[13]
The berries pose the greatest danger to children because they look
attractive and have a somewhat sweet taste.[12]
The consumption of two to five berries by children and ten to
twenty berries by adults can be lethal. The root of the plant is
generally the most toxic part, though this can vary from one
specimen to another. Ingestion of a single leaf of the plant can be
fatal to an adult.[13]
The active agents in Belladonna, atropine, hyoscine (scopolamine), and hyoscyamine, have anticholinergic
properties.[14][15]
Atropa belladonna has been mistaken for blueberries and ingestion
of six berries resulted in acute anticholinergic syndrome.[16] The
symptoms of belladonna poisoning include dilated pupils, sensitivity to light, blurred vision, tachycardia, loss of balance, staggering, headache, rash, flushing, dry mouth and throat,
slurred speech, urinary retention, constipation, confusion, hallucinations,
delirium, and convulsions.[14][17]
The plant's deadly symptoms are caused by atropine's disruption of
the parasympathetic nervous
system's ability to regulate non-volitional/subconscious
activities such as sweating, breathing, and heart rate. The antidote for belladonna
poisoning is physostigmine or pilocarpine, the same as for atropine.[18]
Atropa belladonna is also toxic to many domestic
animals, causing narcosis and paralysis.[19]
However, cattle and rabbits
seem to eat the plant without suffering harmful effects.[17]
Its anticholinergic properties will cause in humans the disruption
of cognitive capacities like memory and learning.[15]
Uses
Cosmetics
The common name belladonna originates from its historic
use by women - Bella Donna is Italian for beautiful lady.
Drops prepared from the belladonna plant were used to dilate women's pupils, an effect considered
attractive.[20][21] Today
it is known that the atropine in belladonna acts as an antimuscarinic, blocking receptors in the
muscles of the eye that constrict pupil size.[22]
Belladonna is currently rarely used cosmetically, as it carries the
adverse
effects of causing minor visual distortions, inability to focus
on near objects, and increased heart rate. Prolonged usage was
reputed to cause blindness.[23]
Medicine
There is currently insufficient scientific evidence to recommend
the use of A. belladonna in its natural form for any
condition,[14]
although some of its components, in particular l-atropine which was purified
from belladona in the 1830s, have accepted medical uses.[17]
Donnatal is a prescription pharmaceutical, approved in the United
States by the FDA, that combines natural belladonna
alkaloids in a specific, fixed ratio with phenobarbital to provide
peripheral anticholinergic/antispasmodic
action and mild sedation. According to its labeling, it is
possibly effective for use as adjunctive therapy in the treatment
of irritable bowel syndrome
(irritable colon, spastic colon, mucous colitis) and acute enterocolitis.[24]
Traditional and
alternative medicine
A. belladonna has been used in traditional treatments for
centuries for an assortment of conditions including headache,
menstrual symptoms, peptic ulcer disease, histaminic reaction,
inflammation, and motion sickness,[14]
with at least one 19th century eclectic medicine journal explaining
how to prepare a Belladona tincture for direct administration to
patients.[25]
Homeopathic
remedies prepared from the belladonna plant have been sold as
treatments for various conditions, although there is no scientific
evidence to support the efficacy of this use.[26][27]
Clinically and in research trials, the most common preparation is
diluted to the 30C level in homeopathic notation. This level of dilution
contains no molecules of the original plant,[27]
although preparations with lesser dilutions which statistically
contain trace amounts of the plant are advertised for sale.[28]
Recreational
drug
Atropa belladonna, along with related plants such as
jimson weed (Datura stramonium), have
occasionally been used as a recreational drug
because of the vivid hallucinations and delirium that it
produces. These hallucinations are most commonly described as very
unpleasant, however, and recreational use is considered extremely
dangerous because of the high risk of unintentional fatal overdose.[29][30][31] In
addition, the central nervous system effects of atropine include
memory disruption, which may lead to severe confusion.[32]
Poison
It was used by early men in poisonous arrows.[1]
In Ancient
Rome, it was used as a poison by Agrippina the Younger, wife of
Emperor Claudius, and Livia, who is rumored to have used
it to kill her husband Emperor Augustus.[1][33]
Macbeth of Scotland, when he was
still one of the lieutenants of King Duncan I
of Scotland, used it during a truce to poison the troops of the
invading Harold
Harefoot, King of England, to the point that the English troops
were unable to stand their ground and had to retreat to their
ships.[5]
Folklore
In the past, it was believed that witches used a mixture of
belladonna, opium
poppy, and other plants, typically poisonous (such as monkshood and poison hemlock) in
flying
ointment they applied to help them fly to gatherings with other
witches. Carlo
Ginzburg and others have argued that flying ointments were
preparations meant to encourage hallucinatory dreaming; a possible
explanation for the inclusion of belladonna and opium poppy in
flying ointments concerns the known antagonism between tropane
alkaloids of belladonna (specifically scopolamine) and opiate alkaloids in the
opium poppy, Papaver
somniferum (specifically morphine), which produces a
dream-like waking state. This antagonism was known in folk
medicine, discussed in eclectic (botanical) medicine
formularies[34], and
posited as the explanation of how flying ointments might have
actually worked in contemporary writing on witchcraft.[35] The
antagonism between opiates and tropanes is the original basis of
the Twilight Sleep that was provided to Queen Victoria to deaden pain as well as
consciousness during childbirth, and which was later modified so
that isolated alkaloids were used instead of plant materials. The
belladonna herb was also notable for its unpredictable effects from
toxicity.[36][37]
See also
Notes
References
- ^ a
b
c
Michael (1998). Alkaloids :
biochemistry, ecology, and medicinal applications. New
York: Plenum Press. pp. 20. ISBN 0306454653. http://books.google.com/books?id=bMCzyrAtrvYC&pg=PA20&dq=hallucinogenic++Atropa+belladonna&lr=&ei=Xe-ySYSOOY3qkQSU_Mm6Dg&client=firefox-a#PPA20,M1.
- ^ Wilson, Jeremy Foster Heather (2008). Buzzed : the
straight facts about the most used and abused drugs from alcohol to
ecstasy. New York City: W.W. Norton. pp. 107. ISBN 0393329852. http://books.google.com/books?id=0SjhNDtBerYC&pg=PA107&dq=hallucinogenic++Atropa+belladonna&ei=iOqySYryBZXSlQSkxcW5Dg&client=firefox-a#PPA107,M1.
- ^ a
b
c
Spiegl, Fritz (1996). Fritz Spiegl's Sick
Notes: An Alphabetical Browsing-Book of Derivatives, Abbreviations,
Mnemonics and Slang for Amusemen. Washington, DC: Taylor
& Francis. pp. 21–22. ISBN
1-85070-627-1. http://books.google.com/books?id=_CbA5a0u5E0C&pg=PA21&vq=belladonna&dq=fritz+Spiegl's+Sick+Notes:+An+Alphabetical+Browsing-Book+of+Derivatives,+Abbreviations,+Mnemonics+and+Slang+for+Amusemen&client=opera&hl=es&source=gbs_search_s&cad=0.
- ^ a
b
c
Edward Harris Ruddock (1867). The Homoeopathic Vade
Mecum of Modern Medicine and Surgery: For the Use of Junior
Practitioners, Students, Clergymen, Missionaries, Heads of
Families, Etc (2 ed.). Jarrold and Sons.
pp. 503–508. http://books.google.com/books?id=sxADAAAAQAAJ&pg=PA502&dq=belladonna+atropos+date:0-1900&lr=&as_brr=3&as_pt=ALLTYPES&hl=es.
- ^ a
b
c
d
R. Groombridge, ed (1839). The Naturalist:
Illustrative of the Animal, Vegetable, and Mineral
Kingdoms. p. 193. http://books.google.com/books?id=vfsWAAAAYAAJ&pg=PA193&dq=belladonna+atropos+date:0-1900&lr=&as_brr=3&as_pt=ALLTYPES&hl=es.
Notes: v.4-5
(1838-1839)
- ^
Kay QON (2008). Edible fruits in a
cool climate: the evolution and ecology of endozoochory in the
European flora. In: Fruit and Seed Production: Aspects of
Development, Environmental Physiology and Ecology (Society for
Experimental Biology Seminar Series) (Ed. by C. Marshall and J.
Grace). Cambridge, UK: Cambridge University Press.
pp. 240. ISBN
0-521-05045-6.
- ^
Stuart, David (2004). Dangerous
garden: the quest for plants to change our lives. Cambridge:
Harvard University Press. pp. 49. ISBN
0-674-01104-X.
- ^
"PLANTS Profile for Atropa
bella-donna (belladonna)". http://plants.usda.gov/java/profile?symbol=ATBE. Retrieved
2008-07-08.
- ^
Stepp JR (June 2004). "The role of
weeds as sources of pharmaceuticals". J Ethnopharmacol
92 (2-3): 163–6. doi:10.1016/j.jep.2004.03.002. PMID 15137997.
- ^
Genova E, Komitska G, Beeva Y
(1997). "Study on the germination of
Atropa Bella-Donna L. Seeds" (PDF). Bulgarian Journal of
Plant Physiology 23 (1-2): 61–66. http://www.bio21.bas.bg/ipp/gapbfiles/v-23/97_1-2_61-66.pdf. Retrieved
2008-07-08.
- ^
"Solanaceae Atropa belladonna
L.". Plant Name Details. IPNI. 2003-07-02. http://www.ipni.org/ipni/idPlantNameSearch.do?id=814358-1. Retrieved 2008-03-01.
"Solanaceae Atropa belladonna L. Species
Plantarum 2 1753 "Habitat in Austriae, Angliae montibus
sylvosis.""
- ^ a
b
Grieve, Margaret; Leyel C.F (1971). Modern Herbal.
Courier
Dover Publications. pp. 584. ISBN 0486227995. http://books.google.com/books?id=KgfHxvGFHAoC&pg=PA584&dq=The+berries+are+full+of+a+dark,+inky+juice&ei=Gvq9R6WgCIfCtAOE4L2eBQ&sig=4lGsladEfMUQwL5EFZHTxG1UFYo. Retrieved
2008-07-08.
- ^ a
b
"Committee for Veterinary
Medicinal Products, Atropa Belladonna, Summary Report" (pdf).
The European Agency for the Evaluation of Medicinal Products.
1998. http://www.emea.europa.eu/pdfs/vet/mrls/054098en.pdf. Retrieved
2008-07-08.
- ^ a
b
c
d
"Belladonna (Atropa
belladonna L. or its variety acuminata Royle ex Lindl)".
Medline Plus. 02/01/2008. http://mplus.nlm.nih.gov/medlineplus/druginfo/natural/patient-belladonna.html. Retrieved
2008-06-14.
- ^ a
b
Giancarlo Pepeu, Maria Grazia
Giovannini (2004). "Acetylcholine: I. Muscarinic
Receptors". in Gernot Riedel, Bettina Platt. From
messengers to molecules: memories are made of these
(illustrated ed.). Springer. ISBN 0306478625,
9780306478628. http://books.google.es/books?id=dCyscToVVJkC&pg=RA1-PA90&dq=belladonna+acetylcholine+anticholinergic.
- ^
Mateo Montoya A, Mavrakanas N,
Schutz JS (2009). "Acute anticholinergic syndrome from Atropa
belladonna mistaken for blueberries". Eur J Ophthalmol
19 (1): 170–2. PMID 19123171.
- ^ a
b
c
Lee MR (March 2007). "Solanaceae IV: Atropa
belladonna, deadly nightshade" (PDF). J R Coll Physicians
Edinb 37 (1): 77–84. PMID 17575737. http://www.rcpe.ac.uk/publications/articles/journal_37_1/R-lee.pdf.
- ^
Potter, Samuel O.L. (1893). A Handbook of Materia
Medica Pharmacy and Therapeutics. London: P. Blakiston's.
pp. 53. http://books.google.com/books?id=q2ku1dbnaLYC&pg=PA53&dq=the+antidote+for+belladonna+is+physostigmine+or+pilocarpine+the+same+as+for+atropine&ei=F5PAR6a0KofCtAPa_ty2CA.
- ^ North Carolina State University Department of
Plant Biology (2000). "Poisonous Vascular
Plants". NC State University. http://www.cals.ncsu.edu/plantbiology/ncsc/Poisonplants/Vascular_plants.htm. Retrieved
2008-07-07.
- ^
Hofmann, Albert; Schultes, Richard
Evans (1987). Plants of the Gods: Origins of Hallucinogenic
Use. New York: Van der Marck Editions. pp. 88. ISBN
0-912383-37-2.
- ^
Tombs S, Silverman I (2004).
"Pupillometry: A sexual selection approach". Evolution and
Human Behavior 25 (4): 211–228. doi:10.1016/j.evolhumbehav.2004.05.001.
- ^
"Atropine Eye Drops". http://www.netdoctor.co.uk/medicines/100002958.html. Retrieved
2008-07-08.
- ^
Wood, George Bacon (1867). A Treatise On
Therapeutics, And Pharmacology Or Materia Medica Vol1.
Philadelphia: J. B. Lippincott & Co. pp. 792–795. http://books.google.com/books?id=hw0DAAAAQAAJ&pg=PA792&lpg=PA792&dq=%22in+one,+producing+blindness+with+large+dilatation+of+the+pupil%22&source=web&ots=MtOqoVtaDu&sig=UoDTvni31htcPdpZEIZ2P8J3Qy0&hl=en&sa=X&oi=book_result&resnum=1&ct=result.
- ^
"Donnatal Extentabs
Prescribing Information". PBM Pharmaceuticals. 2009. http://www.donnatal.com/prescribing-info.aspx. Retrieved
2009-03-04.
- ^
Joseph R. Buchanan, R.S. Newton
(1854). Wm. Phillips and co.. ed. "Officinal preparations".
The Eclectic Medical Journal. http://books.google.com/books?id=Q3gBAAAAYAAJ&pg=PA24&vq=%22tincture+of+belladona%22+belladona+leaves&dq=belladona+tincture+date:0-1950&lr=&as_brr=0&as_pt=ALLTYPES&client=opera&hl=es&source=gbs_search_s&cad=0.
- ^ Vaughan, John Griffith; Patricia Ann Judd,
David Bellamy (2003). The Oxford Book of Health
Foods. Oxford University Press. pp. 59. ISBN 0198504594. http://books.google.com/books?id=mMl9vwVDxigC&pg=PA59&lpg=PA59&dq=%22deadly+nightshade%22+homeopathic&source=web&ots=xEccdnf4ox&sig=uQu-JUHbXaEd9Ru5vJAPS9hkk0Y.
- ^ a
b
Brien S, Lewith G, Bryant T
(November 2003). "Ultramolecular homeopathy
has no observable clinical effects. A randomized, double-blind,
placebo-controlled proving trial of Belladonna 30C". Br J
Clin Pharmacol 56 (5): 562–8. doi:10.1046/j.1365-2125.2003.01900.x. PMID 14651731. PMC 1884394. http://www3.interscience.wiley.com/cgi-bin/fulltext/118882565/PDFSTART.
- ^
example of website
selling different dilutions of belladonna
- ^
Dewitt MS, Swain R, Gibson LB
(1997). "The dangers of jimson weed and its abuse by teenagers in
the Kanawha Valley of West Virginia". West Virginia Medical
Journal 93 (4): 182–5. PMID 9274142.
- ^
Micke MM (October 1996). "The case
of hallucinogenic plants and the Internet". J Sch Health
66 (8): 277–80. doi:10.1111/j.1746-1561.1996.tb03397.x. PMID 8899584.
- ^
Cummins BM, Obetz SW, Wilson MR
(June 1968). "Belladonna poisoning as a facet of pschyodelia".
JAMA 204 (11): 1011. doi:10.1001/jama.204.11.1011. PMID 5694682.
- ^
Hardy TK, Wakely D (1962). "The
amnesic properties of hyoscine and atropine in pre-anæsthetic
medication". Anaesthesia 17: 331–336. doi:10.1111/j.1365-2044.1962.tb13473.x. PMID 13904669.
- ^ Timbrell, John (2005). The poison paradox :
chemicals as friends and foes. Oxford: Oxford Univ. Pr..
pp. 2. ISBN 0192804952. http://books.google.com/books?id=qYYOtQU37jcC&pg=PA2&lpg=PA2&dq=poisons+used+my+the+wife+of+Claudius&source=bl&ots=NgaDUDzm8y&sig=e00BxM5W5ApmPC3zHfeqjAg5Xgk&hl=en&ei=VNe6ScXHLIGCtwfn-LnkDw&sa=X&oi=book_result&resnum=5&ct=result.
- ^
"Belladonna.—Belladonna". http://www.henriettesherbal.com/eclectic/kings/atropa.html. Retrieved
2008-07-08.
- ^
Kuklin, Alexander (February 1999).
How Do Witches Fly?. DNA Press. ISBN
0966402707.
- ^
Kowalchik, Claire; Carr A Hylton W
(1987). Herb gardening.
Rodale. pp. 1 and 158. ISBN 087596964X. http://books.google.com/books?id=htGD3Y7WNxwC&printsec=frontcover&dq=Atropa+belladonna&lr=&source=gbs_summary_r#PPA1,M1.
- ^
Harner, Michael J. (1973).
Hallucinogens and Shamanism. Oxford [Oxfordshire]: Oxford
University Press. pp. 123–150. ISBN
0-19-501649-1.
Further
reading
| Hallucinogens |
|
Psychedelics
5-HT2AR Agonists |
Lysergamides: AL-LAD • ALD-52 • BU-LAD • CYP-LAD • DAM-57 • Diallyllysergamide • Ergometrine
(Ergonovine, Ergobasine) • ETH-LAD • LAE-32 • LSA (Ergine,
Lysergamide) • LSD • LSH • LPD-824 • LSM-775 • Lysergic Acid 2-Butyl
Amide|LSB • Lysergic Acid
2,4-Dimethylazetidide • Methylergometrine • Methylisopropyllysergamide •
Methysergide • MLD-41 • PARGY-LAD • PRO-LAD;
Phenethylamines: Aleph •
2C-B • 2C-B-FLY • 2CBFly-NBOMe • 2C-C • 2C-D • 2C-E • 2C-F • 2C-G • 2C-I • 2C-N • 2C-O • 2C-O-4 • 2C-P • 2C-T • 2C-T-2 • 2C-T-4 • 2C-T-7 • 2C-T-8 • 2C-T-9 • 2C-T-13 • 2C-T-15 • 2C-T-17 • 2C-T-21 • 2C-TFM • 2C-YN • 2CBCB-NBOMe • 25B-NBOMe • 25I-NBMD • 25I-NBOH • 25I-NBOMe • 3C-E • 3C-P • Br-DFLY • DESOXY • DMMDA-2 • DOB • DOC • DOEF • DOET • DOF • DOI
• DOM • DON • DOPR • DOTFM • Escaline • Ganesha • HOT-2 • HOT-7
• HOT-17 • Isoproscaline • Jimscaline • Lophophine • MDA •
MDEA • MDMA
• MMDA • MMDA-2 • MMDA-3a • MMDMA • Macromerine • Mescaline • Methallylescaline • Proscaline • TCB-2 • TFMFly • TMA;
Piperazines: pFPP •
TMFPP;
Tryptamines: 1-Methyl-5-methoxy-diisopropyltryptamine
• 2,N,N-TMT •
4,N,N-TMT • 4-HO-5-MeO-DMT •
4-Acetoxy-DET •
4-Acetoxy-DIPT
• 4-Acetoxy-DMT • 4-Acetoxy-DPT •
4-Acetoxy-MiPT • 4-HO-DPT
• 4-HO-MET •
4-Propionyloxy-DMT •
4-Hydroxy-N-Methyl-(a,N-trimethylene)tryptamine •
5-Me-MIPT • 5-N,N-TMT
• 5-AcO-DMT • 5-MeO-2,N,N-TMT •
5-MeO-4,N,N-TMT • 5-MeO-a,N,N-TMT • 5-MeO-a-ET • 5-MeO-a-MT • 5-MeO-DALT • 5-MeO-DET • 5-MeO-DIPT • 5-MeO-DMT • 5-MeO-DPT • 5-MeO-EiPT •
5-MeO-MET • 5-MeO-MIPT •
5-Methoxy-N-methyl-(a,N-trimethylene)tryptamine •
7,N,N-TMT • a,N,N-TMT • a-ET • a-MT • AL-37350A • Baeocystin • Bufotenin • DBT • DET • DIPT • DMT • DPT • EiPT • Ethocin • Ethocybin • Iprocin • MET
• Miprocin • MIPT
• Norbaeocystin
• PiPT • Psilocin • Psilocybin;
Others: AL-38022A • Ibogaine • Noribogaine • Voacangine
|
|
Dissociatives
NMDAR
Antagonists |
|
|
Deliriants
mAChR Antagonists |
|
|
Miscellaneous
Atypicals |
|
|
| Cholinergics |
|
Receptor
Ligands |
|
|
Agonists:
77-LH-28-1 • AC-42 • AC-260,584 • Aceclidine • Acetylcholine • AF30 • AF150(S) • AF267B
• AFDX-384 • Alvameline • AQRA-741 • Arecoline • Bethanechol • Butyrylcholine • Carbachol • CDD-0034 • CDD-0078 • CDD-0097 •
CDD-0098 • CDD-0102 • Cevimeline • cis-Dioxolane •
Ethoxysebacylcholine • LY-593,039 • L-689,660 • LY-2,033,298 •
McNA343 • Methacholine • Milameline • Muscarine • NGX-267 • Ocvimeline • Oxotremorine •
PD-151,832 • Pilocarpine • RS86 • Sabcomeline • SDZ 210-086 • Sebacylcholine
• Suberylcholine • Talsaclidine • Thiopilocarpine • Vedaclidine •
VU-0029767 • VU-0090157 • VU-0152099 • VU-0152100 • VU-0238429 •
WAY-132,983 • Xanomeline • YM-796
Antagonists: 3-Quinuclidinyl Benzilate •
4-DAMP • Atropine •
Atropine Methonitrate • Benactyzine • Benzatropine (Benztropine) • Benzydamine • BIBN 99 •
Biperiden • Bornaprine • CAR-226,086 • CAR-301,060 • CAR-302,196 •
CAR-302,282 • CAR-302,368 • CAR-302,537 • CAR-302,668 • CS-27349 •
Cyclobenzaprine • Cyclopentolate •
Darifenacin •
DAU-5884 • Dimethindene • Dexetimide • DIBD • Dicyclomine
(Dicycloverine) • Ditran • EA-3167 • EA-3443 • EA-3580 • EA-3834 • Elemicin • Etanautine • Etybenzatropine (Ethylbenztropine) • Flavoxate • Himbacine • HL-031,120 • Ipratropium • J-104,129
• Hyoscyamine • Mamba Toxin 3 • Mamba Toxin 7 • Mazaticol • Mebeverine • Methoctramine • Metixene • Myristicin • N-Ethyl-3-Piperidyl
Benzilate • N-Methyl-3-Piperidyl
Benzilate • Orphenadrine • Otenzepad • Oxybutynin • PBID •
PD-102,807 • Phenglutarimide • Phenyltoloxamine • Pirenzepine • Piroheptine • Procyclidine • Profenamine • RU-47,213
• SCH-57,790 • SCH-72,788 • SCH-217,443 • Scopolamine (Hyoscine) • Solifenacin • Telenzepine • Tiotropium • Tolterodine • Trihexyphenidyl
• Tripitamine • Tropatepine • Tropicamide • WIN-2299 • Zamifenacin;
Others: 1st
Generation Antihistamines ( Brompheniramine • Chlorpheniramine, Cyclizine, Cyproheptadine, Dimenhydrinate,
Diphenhydramine, Doxylamine, Hydroxyzine, Meclizine, Mepyramine/ Pyrilamine, Phenindamine, Pheniramine, Tripelennamine,
Triprolidine, etc)
• Tricyclic Antidepressants ( Amitriptyline, Doxepin, Trimipramine, etc) •
Tetracyclic Antidepressants
( Amoxapine, Maprotiline, etc) • Typical
Antipsychotics ( Chlorpromazine, Thioridazine, etc) • Atypical Antipsychotics ( Clozapine, Olanzapine, Quetiapine, etc)
|
|
|
|
Agonists: 5-HIAA • A-84,543 • A-366,833 • A-582,941 • A-867,744 • ABT-202 • ABT-418 • ABT-560 • ABT-894 • Acetylcholine • Altinicline • Anabasine • AR-R17779 • Butyrylcholine •
Carbachol • Cotinine • Cytisine • Decamethonium • Desformylflustrabromine • Dianicline • Dimethylphenylpiperazinium •
Epibatidine • Epiboxidine •
Ethoxysebacylcholine • EVP-4473 • EVP-6124 • Galantamine • GTS-21 • Ispronicline • Lobeline • MEM-63,908 (RG-3487) • Nicotine • NS-1738 • PHA-543,613 •
PHA-709,829 • PNU-120,596 • PNU-282,987 • Pozanicline • Rivanicline • Sazetidine A • Sebacylcholine • SIB-1508Y
• SIB-1553A • SSR-180,711 • Suberylcholine • TC-1698 • TC-1734 • TC-1827 •
TC-2216 • TC-5214 • TC-5619 • TC-6683 • Tebanicline • Tropisetron • UB-165 • Varenicline • XY-4083
Antagonists: 18-Methoxycoronaridine • α-Bungarotoxin • α-Conotoxin • Alcuronium • Anatruxonium • Atracurium • Bupropion (Amfebutamone) •
Chandonium • Chlorisondamine • Cisatracurium •
Coclaurine • Coronaridine • Dacuronium • Decamethonium • Dextromethorphan • Dextropropoxyphene • Dextrorphan • Diadonium
• DHβE • Dimethyltubocurarine (Metocurine) •
Dipyrandium • Dizocilpine (MK-801) • Doxacurium • Duador • Esketamine • Fazadinium • Gallamine • Hexafluronium • Hexamethonium (Benzohexonium) • Ibogaine • Ketamine • Kynurenic Acid •
Levacetylmethadol • Malouetine • Mecamylamine • Memantine • Methadone • Methorphan
(Racemethorphan) • Methyllycaconitine • Metocurine • Mivacurium • Morphanol (Racemorphanol) •
Neramexane • Pancuronium • Pempidine • Pentamine • Pentolinium • Phencyclidine • Pipecuronium • Radafaxine • Rapacuronium • Rocuronium • Surugatoxin • Suxamethonium
(Succinylcholine) • Toxiferine • Trimethaphan •
Tropeinium • Tubocurarine • Vecuronium
|
|
|
Reuptake
Inhibitors |
|
|
Enzyme
Inhibitors |
|
|
|
|
1-(-Benzoylethyl)pyridinium •
2-(α-Naphthoyl)ethyltrimethylammonium • 3-Chloro-4-stillbazole •
4-(1-Naphthylvinyl)pyridine • Acetylseco Hemicholinium-3 •
Acryloylcholine • AF64A • B115 • BETA • CM-54,903 •
N,N-Dimethylaminoethylacrylate •
N,N-Dimethylaminoethylchloroacetate
|
|
|
|
|
|
|
|
|
|
|
Many of the
acetylcholinesterase inhibitors listed above act as
butyrylcholinesterase inhibitors.
|
|
|
|
|
Others |
|
|