39063-89-3
39063-89-3
Chemical Structure
L-Proline-d7
- CAS No.: 39063-89-3
- Formula:C5H2D7NO2
- Molecular Weight:122.17
IUPAC Name: 3-(4-(5-fluoro-2-((1-((trifluoromethyl)sulfonyl)-1H-indol-5-yl)amino)pyrimidin-4-yl)-1H-pyrazol-1-yl)propanenitrile
InChIKey: ONIBWKKTOPOVIA-BFEYZEMLSA-N
SMILES: OC([C@]1([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])N1)=O
Biological Activity: L-Proline-d7 is the deuterium labeled L-Proline. L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins.
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L-Proline-d7 | 99.93% | L-Proline-d7 is the deuterium labeled L-Proline. L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | ||||||||||||||||||||
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L-Proline (Standard) | 99.67% | L-Proline (Standard) is the analytical standard of L-Proline. This product is intended for research and analytical applications. L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | ||||||||||||||||||||
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L-Proline-13C5,15N | 99.93% | L-Proline-13C5,1-15N is the 13C- and 15N-labeled L-Proline. L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | ||||||||||||||||||||
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L-Proline-13C5 | 99.93% | L-Proline-13C5 is the 13C-labeled L-Proline. L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | ||||||||||||||||||||
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L-Proline-15N | 99.97% | L-Proline-15N is the 15N-labeled L-Proline. L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | ||||||||||||||||||||
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L-Proline-d4 | L-Proline-d4 is the deuterium labeled L-Proline (HY-Y0252). L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | |||||||||||||||||||||
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L-Proline-d3 | 99.84% | L-Proline-d3 is the deuterium labeled L-Proline. L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | ||||||||||||||||||||
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L-Proline | 98.0% | L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | ||||||||||||||||||||
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N-Nitroso-DL-proline-d3 | N-Nitroso-DL-proline-d3 is the deuterium labeled N-Nitroso-DL-proline. | |||||||||||||||||||||
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L-Prolinamide-d3 | L-Prolinamide-d3 is the deuterium labeled L-Prolinamide. L-Prolinamide is a proline derivative. | |||||||||||||||||||||
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L-Hydroxyproline-d3 | 99.94% | L-Hydroxyproline-d3 is the deuterium labeled L-Hydroxyproline. L-Hydroxyproline, one of the hydroxyproline (Hyp) isomers, is a useful chiral building block in the production of many pharmaceuticals. | ||||||||||||||||||||
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(R)-pyrrolidine-2-carboxylic acid | 98.0% | (R)-pyrrolidine-2-carboxylic acid ((+)-(R)-Proline) is a proline isomer that exhibits high renal and hepatotoxicity in rats. (R)-pyrrolidine-2-carboxylic acid can be used to study amino acid metabolism and toxicity mechanisms. | ||||||||||||||||||||
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(R)-pyrrolidine-2-carboxylic acid (Standard) | ≥98% | (R)-pyrrolidine-2-carboxylic acid (Standard) is the analytical standard of (R)-pyrrolidine-2-carboxylic acid. This product is intended for research and analytical applications. (R)-pyrrolidine-2-carboxylic acid ((+)-(R)-Proline) is a proline isomer that exhibits high renal and hepatotoxicity in rats. (R)-pyrrolidine-2-carboxylic acid can be used to study amino acid metabolism and toxicity mechanisms. | ||||||||||||||||||||
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(R)-Pyrrolidine-2-carboxylic acid-d3 | (R)-Pyrrolidine-2-carboxylic acid-d3 is the deuterium labeled (R)-pyrrolidine-2-carboxylic acid. (R)-pyrrolidine-2-carboxylic acid is an endogenous metabolite. | |||||||||||||||||||||
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L-Pyroglutamic acid-d5 | 98.6% | L-Pyroglutamic acid-d5 is the deuterium labeled L-Pyroglutamic acid (HY-76082). L-Pyroglutamic acid is the levo-isomer of Pyroglutamic acid. L-Pyroglutamic acid is the biologically active enantiomer in humans. Pyroglutamic acid is an intermediate in glutathione metabolism. | ||||||||||||||||||||
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L-Pipecolic acid | 99.89% | L-Pipecolic acid (H-HoPro-OH) is an oral active metabolite of Lysine and can accumulate in the bodily fluids of infants with autosomal inherited diseases, such as Zellweger syndrome and neonatal adrenal insufficiency. L-Pipecolic acid can promote muscle cell health and growth by enhancing protein synthesis, and plays a role in promoting gut health. L-Pipecolic acid holds promise for research in the fields of metabolic disorders, muscle growth disorders, and intestinal diseases. | ||||||||||||||||||||
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DL-Pyroglutamic acid-d5 | 99.21% | DL-Pyroglutamic acid-d5 is the deuterium labeled DL-Pyroglutamic acid. | ||||||||||||||||||||
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DL-Proline | 98.0% | DL-Proline is a racemic mixture of D-Proline and L-Proline, belonging to cyclic imino acids with a five-membered ring structure. DL-Proline serves as a key structural unit in peptide synthesis. DL-Proline stabilizes β-turn conformations and affects the secondary structure of peptide segments. DL-Proline exhibits biological activities such as regulating peptide segment conformations and enhancing cyclic peptide stability. DL-Proline can be used in research on diseases related to peptide structure and function, including cancer and bacterial infections. | ||||||||||||||||||||
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DL-Proline-d7 | 98.0% | DL-Proline-d7 is the deuterated-labeled DL-Proline (HY-W012908). DL-Proline is a racemic mixture of D-Proline and L-Proline, belonging to cyclic imino acids with a five-membered ring structure. DL-Proline serves as a key structural unit in peptide synthesis. DL-Proline stabilizes β-turn conformations and affects the secondary structure of peptide segments. DL-Proline exhibits biological activities such as regulating peptide segment conformations and enhancing cyclic peptide stability. DL-Proline can be used in research on diseases related to peptide structure and function, including cancer and bacterial infections. | ||||||||||||||||||||
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DL-Proline-2-d1 | 98.0% | DL-Proline-2-d1 is the deuterated-labeled DL-Proline (HY-W012908). DL-Proline is a racemic mixture of D-Proline and L-Proline, belonging to cyclic imino acids with a five-membered ring structure. DL-Proline serves as a key structural unit in peptide synthesis. DL-Proline stabilizes β-turn conformations and affects the secondary structure of peptide segments. DL-Proline exhibits biological activities such as regulating peptide segment conformations and enhancing cyclic peptide stability. DL-Proline can be used in research on diseases related to peptide structure and function, including cancer and bacterial infections. | ||||||||||||||||||||
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DL-Proline-d3 | 99.67% | DL-Proline-d3 is the deuterated-labeled DL-Proline (HY-W012908). DL-Proline is a racemic mixture of D-Proline and L-Proline, belonging to cyclic imino acids with a five-membered ring structure. DL-Proline serves as a key structural unit in peptide synthesis. DL-Proline stabilizes β-turn conformations and affects the secondary structure of peptide segments. DL-Proline exhibits biological activities such as regulating peptide segment conformations and enhancing cyclic peptide stability. DL-Proline can be used in research on diseases related to peptide structure and function, including cancer and bacterial infections. | ||||||||||||||||||||
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1-Nitrosopyrrolidine-d8 | 99.89% | 1-Nitrosopyrrolidine-d8 is deuterium labeled 1-Nitrosopyrrolidine. | ||||||||||||||||||||
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L-Hydroxyproline-d4 | 99.85% | L-Hydroxyproline-d4 is deuterium labeled L-Hydroxyproline. L-Hydroxyproline, one of the hydroxyproline (Hyp) isomers, is a useful chiral building block in the production of many pharmaceuticals. | ||||||||||||||||||||
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L-Proline monohydrochloride | 97.00% | L-Proline monohydrochloride is a proline derivative. | ||||||||||||||||||||
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D-Pipecolinic acid | 97.0% | D-Pipecolinic acid is a D-form cyclic amino acid with a piperidine ring structure, which is used to enhance molecular rigidity and stability. | ||||||||||||||||||||
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D-Pipecolinic acid (Standard) | 98.91% | D-Pipecolinic acid is a normal human metabolite found in human biofluids. | ||||||||||||||||||||
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L-Proline-13C | 99.94% | L-Proline-13C is the 13C-labeled L-Proline. L-Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. | ||||||||||||||||||||
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Pipecolic acid | 99.92% | Pipecolic acid is an orally bioavailable, blood-brain barrier-permeable metabolite of lysine with antioxidant, inhibitor, and inducer activity. Pipecolic acid modulates the YAP-GPX4 signaling pathway, reduces retinal vascular tube formation, and mitigates ferroptosis. Pipecolic acid potentiates voltage-sensitive Ca2+ channel currents and induces neuronal apoptosis. Pipecolic acid can be used for the research of diabetic retinopathy. | ||||||||||||||||||||
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Pipecolic acid (Standard) | 98.97% | Pipecolic acid (Standard) is the analytical standard of Pipecolic acid. This product is intended for research and analytical applications. Pipecolic acid is a metabolite of lysine and an important precursor for many useful microbial secondary metabolites. Pipecolic acid slows ferroptosis in diabetic retinopathy by inhibiting the YAP-GPX4 signaling pathway. In addition, Pipecolic acid can be used as a diagnostic marker for pyridoxine-dependent epilepsy. | ||||||||||||||||||||
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Pipecolic acid-d9 | 99.9% | Pipecolic acid-d9 is the deuterium labeled Pipecolic acid. Pipecolic acid is a metabolite of lysine and an important precursor for many useful microbial secondary metabolites. Pipecolic acid slows ferroptosis in diabetic retinopathy by inhibiting the YAP-GPX4 signaling pathway. In addition, Pipecolic acid can be used as a diagnostic marker for pyridoxine-dependent epilepsy. | ||||||||||||||||||||
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Isonipecotic acid-d9 | 99.97% | Isonipecotic acid-d9 is the deuterium labeled Isonipecotic acid. Isonipecotic acid is a GABAA receptor partial agonist. | ||||||||||||||||||||
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