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  2. Huperzine A - Wikipedia

    en.wikipedia.org/wiki/Huperzine_A

    Huperzine A, in spite of the possible cholinergic side effects, seems to have a wide margin of safety. Toxicology studies show huperzine A to be non-toxic even when administered at 50-100 times the human therapeutic dose. The extract is active for 6 hours at a dose of 2 μg/kg with no remarkable side effects.

  3. Acetylcholinesterase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Acetylcholinesterase_inhibitor

    Acetylcholine Acetylcholinesterase Acetylcholinesterase inhibition. Acetylcholinesterase inhibitors (AChEIs) also often called cholinesterase inhibitors, [1] inhibit the enzyme acetylcholinesterase from breaking down the neurotransmitter acetylcholine into choline and acetate, [2] thereby increasing both the level and duration of action of acetylcholine in the central nervous system, autonomic ...

  4. If Your Dog Has Stomach Issues, These Vet-Recommended ... - AOL

    www.aol.com/dog-stomach-issues-vet-recommended...

    Proviable-DC Capsules Digestive Supplement for Cats & Dogs. The Nutramax Proviable-DC Capsules are unique in that they can be fed in capsule form or split open to be sprinkled on as a powder. It's ...

  5. C15H18N2O - Wikipedia

    en.wikipedia.org/wiki/C15H18N2O

    Huperzine A; Ro60-0213 This page was last edited on 30 March 2023, at 15:13 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...

  6. 30 of the Best Brain Supplements for Adults - AOL

    www.aol.com/entertainment/30-best-brain...

    Related: 30 Best Weight Loss Supplements for Men This is branded content. Us Weekly is not endorsing the websites or products set forth below. The use of THC in any capacity may lead to health ...

  7. Huprine X - Wikipedia

    en.wikipedia.org/wiki/Huprine_X

    Huprine X is a synthetic cholinergic compound developed as a hybrid between the natural product Huperzine A and the synthetic drug tacrine.It is one of the most potent reversible inhibitors of acetylcholinesterase known, with a binding affinity of 0.026nM, [1] as well as showing direct agonist activity at both nicotinic and muscarinic acetylcholine receptors.