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 12278 products of "Aminoacids and derivatives"
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tert-Butyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate
CAS:Purity:97%Molecular weight:226.324-Piperidineacetic acid, α-amino-1-[(1,1-dimethylethoxy)carbonyl]-
CAS:Purity:98%Molecular weight:258.318Sulfo-Cy3 diacid NHS ester
CAS:<p>Cy 3 (Non-Sulfonated) is a CY3-derived dye. CY3 is an amine-reactive cyanine orange dye for fluorescent labelling of proteins and nucleic acids.</p>Formula:C43H50N4O14S2Purity:98%Color and Shape:SolidMolecular weight:911.01Nordalbergin
CAS:<p>Nordalbergin, a coumarin isolated from the bark of Dalbergia sissoo, can significantly induce the differentiation of HL-60 cells.</p>Formula:C15H10O4Purity:99.84% - 99.86%Color and Shape:SolidMolecular weight:254.24L-Histidine Monohydrochloride Monohydrate
CAS:Controlled Product<p>Applications L-Histidine Monohydrochloride Monohydrate is a histamine precursor via histidine decarboxylase. Also, they are grown as crystals which possesses anti-bacterial activity.<br>References Chandra, J. S., et al.: World J. Pharm. Res., 4, 1408-1429 (2015)<br></p>Formula:C6H9N3O2·ClH·H2OColor and Shape:NeatMolecular weight:209.63(S)-(-)-Carbidopa
CAS:Controlled Product<p>Stability Unstable in Solution<br>Applications (S)-(-)-Carbidopa is a peripheral decarboxylase inhibitor that is commonly used in combination with L-DOPA (D533751) for treatment of Parkinsonism. S(-)-Carbidopa ( has also been shown to prolong the elimination half-life of L-DOPA from blood plasma and skeletal muscle.<br>References Henry, G.M. et al.: Psychosom. Med., 38, 95 (1976); Leguire, L.E. et al.: Invest. Ophthalmol. Vis. Sci. 34, 3090 (1993); Deleu, D. et al.: Naun. Schmied. Arch. Pharmacol. 348: 576 (1993);<br></p>Formula:C10H14N2O4Color and Shape:NeatMolecular weight:226.23N-(3S)-1-Azabicyclo[2.2.2]oct-3-yl-5,6-dihydro-1-Naphthalenecarboxamide
CAS:Controlled Product<p>Applications N-(3S)-1-Azabicyclo[2.2.2]oct-3-yl-5,6-dihydro-1-Naphthalenecarboxamide is an impurity of Palonosetron (P165800), a serotonin 5-HT3 receptor antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV). Antiemetic.<br>References Clark, R.D., et al.: J. Med. Chem., 36, 2645 (1993), Wong, E.H.F., et al.: Br. J. Pharmacol., 114, 851 (1995), Grunberg, S.M., et al.: Expert. Opin. Pharmacother., 4, 2297 (2003), Eisenberg, P., et al.: Ann. Oncol., 15, 330 (2004), Siddiqui, M.A.A., et al.: Drugs, 64, 1125 (2004),<br></p>Formula:C18H22N2OColor and Shape:NeatMolecular weight:282.38Isopropyl 6-Aminohexanoate
CAS:Controlled ProductFormula:C9H19NO2Color and Shape:NeatMolecular weight:173.253-(4-Chlorophenyl)glutaramic Acid
CAS:Controlled ProductFormula:C11H12ClNO3Color and Shape:NeatMolecular weight:241.67Glycine-d2
CAS:Controlled Product<p>Applications Glycine-d2, is the labeled analogue of Glycine (G615990), a non-essential amino acid for human development. Glycine is an inhibitory neurotransmitter in spinal cord, allosteric regulator of NMDA receptors.<br>References Scott, D., et al.: J. Neurosci., 21, 3063 (2001); Laube, B., et al.: Neuropharmacology, 47, 994 (2004); Papadakis, M., et al.: J. Biol. Chem., 279, 14703 (2004), Chen, P., et al.: Mol. Pharmacol., 67, 1470 (2005), Wolosker, H., et al.: Mol. Neurobiol., 36, 152 (2007);<br></p>Formula:C22H2H3NO2Color and Shape:NeatMolecular weight:77.083S-Hydroxy-N6,N6,N6-trimethyl-L-lysine Inner Salt (~90%)
CAS:Controlled ProductFormula:C9H20N2O3Purity:~90%Color and Shape:NeatMolecular weight:204.27
![tert-Butyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF792012.webp&w=3840&q=75)
![4-Piperidineacetic acid, α-amino-1-[(1,1-dimethylethoxy)carbonyl]-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF980082.webp&w=3840&q=75)
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