Key details
| Part number | RXSOL-60-6604-645 |
|---|---|
| Standard packing | 25.00 Kg.Liq |
| Supply locations | GLYCINE AR manufacturers, suppliers, exporters in Mumbai, Gandhidham, Kolkata, Varanasi, Visakhapatnam, Chennai, Fujairah, Dubai, Canada BC, Barka, Sohar, Muscat, Oman. Lab chemicals manufacturers, suppliers, exporters in India, UAE Middle East, Barka, Sohar, Muscat, Oman, Canada. GLYCINE AR is available in small packing as well as in bulk. Buy premium quality GLYCINE AR and other lab chemicals from one of the most trusted brands. |
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<strong><em><span style="font-family:georgia,serif;"><span style="font-size:14px;">Glycine is used for treating schizophrenia, stroke, benign prostatic hyperplasia (BPH), and some rare inherited metabolic disorders. It is also used to protect kidneys from the harmful side effects of certain drugs used after organ transplantation as well as the liver from harmful effects of alcohol.</span></span></em></strong></p>
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<strong><em><span style="font-family:georgia,serif;"><span style="font-size:14px;">Glycine, like arginine, is a conditional amino acid, so your body may need more of it from time to time. This amino acid quickly penetrates deep into the inner layers of the skin barrier—down to the dermis, which contains the skin-strengthening protein collagen. Once there, glycine helps stimulate collagen production.</span></span></em></strong></p>
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<span style="color:#000;"><strong><em><span style="font-family:georgia,serif;"><span style="font-size:12px;"><span style="background-color:#fff;">Glycine (symbol Gly or G;</span></span></span></em></strong></span><strong><em><span style="font-family:georgia,serif;"><span style="font-size:12px;"><a href="https://en.wikipedia.org/wiki/Glycine#cite_note-6"><span style="color:#000;"><span style="background-color:#fff;">[6]</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> </span></span><a href="https://en.wikipedia.org/wiki/Help:IPA/English" title="Help:IPA/English"><span style="color:#000;"><span style="background-color:#fff;">/ˈɡlaɪsiːn/</span></span></a><span style="color:#000;"><span style="background-color:#fff;">)</span></span><a href="https://en.wikipedia.org/wiki/Glycine#cite_note-7"><span style="color:#000;"><span style="background-color:#fff;">[7]</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> is an </span></span><a href="https://en.wikipedia.org/wiki/Amino_acid" title="Amino acid"><span style="color:#000;"><span style="background-color:#fff;">amino acid</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> that has a single </span></span><a href="https://en.wikipedia.org/wiki/Hydrogen" title="Hydrogen"><span style="color:#000;"><span style="background-color:#fff;">hydrogen</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> atom as its </span></span><a href="https://en.wikipedia.org/wiki/Side_chain" title="Side chain"><span style="color:#000;"><span style="background-color:#fff;">side chain</span></span></a><span style="color:#000;"><span style="background-color:#fff;">. It is the simplest stable amino acid (</span></span><a href="https://en.wikipedia.org/wiki/Carbamic_acid" title="Carbamic acid"><span style="color:#000;"><span style="background-color:#fff;">carbamic acid</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> is unstable), with the </span></span><a href="https://en.wikipedia.org/wiki/Chemical_formula" title="Chemical formula"><span style="color:#000;"><span style="background-color:#fff;">chemical formula</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> </span></span><a href="https://en.wikipedia.org/wiki/Amine" title="Amine"><span style="color:#000;"><span style="background-color:#fff;">NH2</span></span></a><span style="color:#000;"><span style="background-color:#fff;">‐</span></span><a href="https://en.wikipedia.org/wiki/Methylene_group" title="Methylene group"><span style="color:#000;"><span style="background-color:#fff;">CH2</span></span></a><span style="color:#000;"><span style="background-color:#fff;">‐</span></span><a href="https://en.wikipedia.org/wiki/Carboxylic_acid" title="Carboxylic acid"><span style="color:#000;"><span style="background-color:#fff;">COOH</span></span></a><span style="color:#000;"><span style="background-color:#fff;">. Glycine is one of the </span></span><a href="https://en.wikipedia.org/wiki/Proteinogenic_amino_acid" title="Proteinogenic amino acid"><span style="color:#000;"><span style="background-color:#fff;">proteinogenic amino acids</span></span></a><span style="color:#000;"><span style="background-color:#fff;">. It is </span></span><a href="https://en.wikipedia.org/wiki/Genetic_code" title="Genetic code"><span style="color:#000;"><span style="background-color:#fff;">encoded</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> by all the </span></span><a href="https://en.wikipedia.org/wiki/Codon" title="Codon"><span style="color:#000;"><span style="background-color:#fff;">codons</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> starting with GG (GGU, GGC, GGA, GGG). Glycine is integral to the formation of </span></span><a href="https://en.wikipedia.org/wiki/Alpha_helix" title="Alpha helix"><span style="color:#000;"><span style="background-color:#fff;">alpha-helices</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> in </span></span><a href="https://en.wikipedia.org/wiki/Secondary_protein_structure" title="Secondary protein structure"><span style="color:#000;"><span style="background-color:#fff;">secondary protein structure</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> due to its compact form. For the same reason, it is the most abundant amino acid in </span></span><a href="https://en.wikipedia.org/wiki/Collagen" title="Collagen"><span style="color:#000;"><span style="background-color:#fff;">collagen</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> triple-helices. Glycine is also an inhibitory </span></span><a href="https://en.wikipedia.org/wiki/Neurotransmitter" title="Neurotransmitter"><span style="color:#000;"><span style="background-color:#fff;">neurotransmitter</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> – interference with its release within the spinal cord (such as during a </span></span><a href="https://en.wikipedia.org/wiki/Clostridium_tetani" title="Clostridium tetani"><span style="color:#000;"><span style="background-color:#fff;">Clostridium tetani</span></span></a><span style="color:#000;"><span style="background-color:#fff;"> infection) can cause </span></span><a href="https://en.wikipedia.org/wiki/Spasticity" title="Spasticity"><span style="color:#000;"><span style="background-color:#fff;">spastic</span></span></a></span></span></em></strong><span style="color:#000;"><strong><em><span style="font-family:georgia,serif;"><span style="font-size:12px;"><span style="background-color:#fff;"> paralysis due to uninhibited muscle contraction.</span></span></span></em></strong></span></p>
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