Aminoacids and derivatives
Amino acids are compounds with a structure based on an amino group (-NH₂) and a carboxyl group (-COOH), both attached to a central carbon atom. This structure makes them essential for the synthesis of proteins and other biomolecules. Their derivatives can have regulatory properties over metabolic processes and biological systems, with applications in nutrition, health, and regenerative medicine.
At CymitQuimica, we offer a wide range of amino acids and their derivatives, ideal for research and the formulation of bioactive products.
Found 12270 products of "Aminoacids and derivatives"
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N,N-Dimethyl-4,4′-azodianiline
CAS:Formula:C14H16N4Purity:95.0%Color and Shape:SolidMolecular weight:240.311-Methyl-4-(4-methylpiperidin-4-yl)piperazine trihydrochloride
CAS:Purity:95+%Molecular weight:306.700012207031251,1-Dimethyl-2-piperidin-1-yl-ethylamine
CAS:Formula:C9H20N2Purity:95.0%Color and Shape:LiquidMolecular weight:156.273Tert-Butyl (6S,8aR)-6-(hydroxymethyl)hexahydropyrrolo[1,2-a]pyrazine-2(1H)-carboxylate
CAS:Purity:97%Molecular weight:256.34600830078125N,N'-(pentane-1,5-diyl)bis(5-(dimethylamino)naphthalene-1-sulfonamide)
CAS:Purity:98%Molecular weight:568.75Tert-Butyl (1S,6S)-3,7-diazabicyclo[4.2.0]octane-7-carboxylate
CAS:Purity:98%Molecular weight:212.29299926757812Glycine 6-Ethylchenodeoxycholate-d5
CAS:Controlled Product<p>Applications Glycine 6-Ethylchenodeoxycholate-d5 is the labelled version of Glycine 6-Ethylchenodeoxycholate (G625250) which can be used as reactant/reagent in synthetic preparation of bile acid analogs as FXR/TGR5 agonists.<br>References Or, Y., et al.: PCT Int. Appl., WO 2016073767 A1 20160512 (2016)<br></p>Formula:C28H42D5NO5Color and Shape:White SolidMolecular weight:482.71Tert-butyl 4-phenyl-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine-1-carboxylate
CAS:Purity:95.0%Molecular weight:324.424011230468754-[4-(dimethylamino)benzoyl]-8-ethyl-1-oxa-4,8-diazaspiro[4.5]decane-3-carboxylic acid
CAS:Purity:95.0%Molecular weight:361.4419860839844L-Homocysteine Thiolactone Hydrochloride
CAS:Controlled Product<p>Applications L-Homocysteine Thiolactone Hydrochloride is used to prepare substituted homocysteine analogs as inhibitors of peptidylglycine α-amidating monooxygenase. It is also used to synthesize (mercaptoacyl)alanylprolines as metalloprotease inhibitors.<br>References Erion, M., et al.: J. Med. Chem., 37, 4430 (1994); Slusarchyk, W., et al.: Bioorg. Med. Chem. Lett., 5, 753 (1995)<br></p>Formula:C4H8ClNOSColor and Shape:NeatMolecular weight:153.63Tert-Butyl 1',2'-dihydrospiro[azetidine-3,3'-pyrrolo[3,2-b]pyridine]-1-carboxylate
CAS:Purity:95.0%Molecular weight:261.325012207031251',4'-dihydro-3'H-spiro[piperidine-4,2'-quinoxalin]-3'-one hydrochloride
CAS:Purity:95.0%Molecular weight:253.729995727539063-(3-Methyl-piperidin-1-yl)-propylamine
CAS:Formula:C9H20N2Purity:95.0%Color and Shape:LiquidMolecular weight:156.273N4-(3-Ethynylphenyl)-7-methoxyquinazoline-4,6-diamine
CAS:Purity:95.0%Molecular weight:290.32598876953125
![Tert-Butyl (6S,8aR)-6-(hydroxymethyl)hexahydropyrrolo[1,2-a]pyrazine-2(1H)-carboxylate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF601856.webp&w=3840&q=75)
![Tert-Butyl (1S,6S)-3,7-diazabicyclo[4.2.0]octane-7-carboxylate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF620603.webp&w=3840&q=75)
![4-[4-(dimethylamino)benzoyl]-8-ethyl-1-oxa-4,8-diazaspiro[4.5]decane-3-carboxylic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF525710.webp&w=3840&q=75)
![Tert-Butyl 1',2'-dihydrospiro[azetidine-3,3'-pyrrolo[3,2-b]pyridine]-1-carboxylate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF464234.webp&w=3840&q=75)
![1',4'-dihydro-3'H-spiro[piperidine-4,2'-quinoxalin]-3'-one hydrochloride](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF402050.webp&w=3840&q=75)
