muscarine
[muhs-ker-in, -kuh-reen]
- a poisonous compound, C8H19NO3, found in certain mushrooms, especially fly agaric, and in decaying fish.
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Origin of muscarine
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Based on the Random House Unabridged Dictionary, © Random House, Inc. 2018
Examples from the Web for muscarine
Historical Examples of muscarine
An example of this kind of myosis is the action of muscarine.
Poisons: Their Effects and DetectionAlexander Wynter Blyth
It is not very toxic, but on uniting with oxygen it passes over to muscarine.
Studies of American Fungi. Mushrooms, Edible, Poisonous, etc.George Francis Atkinson
Neurin is almost identical in its physiological effects with muscarine, which is described below.
Studies of American Fungi. Mushrooms, Edible, Poisonous, etc.George Francis Atkinson
This alkaloid, like ordinary atropin, neutralizes to a greater or less extent the muscarine.
Studies of American Fungi. Mushrooms, Edible, Poisonous, etc.George Francis Atkinson
The symptoms of poisoning with muscarine are not at once evident, as is the case with several of the less virulent poisons.
Studies of American Fungi. Mushrooms, Edible, Poisonous, etc.George Francis Atkinson
muscarine
- a poisonous alkaloid occurring in certain mushrooms. Formula: C 9 H 21 NO 3
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Word Origin for muscarine
C19: from Latin muscārius of flies, from musca fly
Collins English Dictionary - Complete & Unabridged 2012 Digital Edition
© William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins
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muscarine
(mŭs′kə-rēn′)- A highly toxic alkaloid related to the cholines and having neurologic effects, isolated from certain mushrooms, especially Amanita muscaria.
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The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
muscarine
[mŭs′kə-rēn′]
- A highly toxic, hallucinogenic alkaloid related to the cholines, derived from the red form of the mushroom Amanita muscaria and other mushrooms and found in decaying animal tissue. Chemical formula: C9H20NO2.
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The American Heritage® Science Dictionary
Copyright © 2011. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.