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Filtered Search Results
Medchemexpress LLC 2-amino-4-pentynoic acid | 50428-03-0 | MFCD00056728 | 98.0% | 113.11 g·mol⁻¹ | C5H7NO2 | 100 MG
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DL-Propargylglycine (2-amino-4-pentynoic acid, CAS 50428-03-0) is an alkyne-containing glycine derivative used as a click-chemistry reagent and research building block. It supports bioconjugation and small-molecule synthesis, and is supplied as a solid suitable for laboratory use.
- Contains a terminal alkyne for copper-catalyzed azide-alkyne cycloaddition (CuAAC).
- Useful as a small-molecule probe or building block in organic synthesis and bioconjugation.
- Supplied as a solid for accurate weighing and convenient storage.
- High purity suitable for research applications (98.0%).
- Molecular formula C5H7NO2; molecular weight 113.11 g·mol⁻¹.
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AdipoGen Hyperforin DCHA
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Chemical. CAS 238074-03-8. Formula C35H51O4 . C12H24N. MW 535.8 . 182.3. Isolated from St. Johns wort Hypericum perforatum. Key constituent of St. Johns wort. Shows properties of potential pharmacological interest, including antibacterial, anti-malarial, anti-inflammatory, anti-cancer and anti-angiogenic effects. Anti-depressant and anxiolytic compound. Specific activator of TRPC6 channels. Inhibits the re-uptake of neurotransmitters in synapses serotonin, norepinephrine, dopamine, GABA, glutamate. Activator of the pregnane X receptor PXR. Regulates expression of the cytochrome P450 CYP3A4 and CYP2C9 and hepatic drugs metabolism. Potential anti-Alzheimer compound. Potent SIRT1 sirtuin 1 and SIRT2 sirtuin 2 inhibitor.
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Medchemexpress LLC N-Propargylglycine | 58160-95-5 | 99.7% | C5H7NO2 | 10MM/1ML
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N-Propargylglycine is a brain-penetrant, orally active PRODH inhibitor. It irreversibly inhibits proline and 4-hydroxyproline catabolism by covalently modifying enzyme-bound FAD and active site lysine. This compound induces UPRmt, upregulates mitochondrial chaperones, and enhances mitochondrial proteostasis. It also stimulates neural processes, increases brain proline levels, and normalizes Huntington's disease transcriptomes. Additionally, N-Propargylglycine reduces hyperoxaluria and prevents calcium oxalate stone formation.
- Brain-penetrant and orally active PRODH inhibitor
- Irreversible inhibition of proline catabolism
- Enhances mitochondrial proteostasis
- Stimulates neural processes; increases brain proline
- Normalizes Huntington's disease transcriptomes
- Reduces hyperoxaluria; prevents calcium oxalate stones
- Research applications include breast cancer and neurodegenerative disorders
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eMolecules 50428-03-0 | 2-Aminopent-4-ynoic acid | AA Blocks LLC | MFCD00056728 | 113.116 | C5H7NO2 | 0.000 | NC(CC#C)C(O)=O | 1g | 448662355
2-Aminopent-4-ynoic acid | AA Blocks LLC | 50428-03-0 | MFCD00056728 | 113.116 | C5H7NO2 | 0.000 | NC(CC#C)C(O)=O | 1g | 448662355
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eMolecules 16338-48-0 | L-Allylglycine | Accela ChemBio (ASD) | MFCD00002627 | 115.132 | C5H9NO2 | 98.000 | N[C@@H](CC=C)C(O)=O | 1g | 455888855
L-Allylglycine | Accela ChemBio (ASD) | 16338-48-0 | MFCD00002627 | 115.132 | C5H9NO2 | 98.000 | N[C@@H](CC=C)C(O)=O | 1g | 455888855
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eMolecules 16338-48-0 | L-Allylglycine | Accela ChemBio (ASD) | MFCD00002627 | 115.132 | C5H9NO2 | 98.000 | N[C@@H](CC=C)C(O)=O | 0.25g | 455889008
L-Allylglycine | Accela ChemBio (ASD) | 16338-48-0 | MFCD00002627 | 115.132 | C5H9NO2 | 98.000 | N[C@@H](CC=C)C(O)=O | 0.25g | 455889008
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eMolecules 23235-01-0 | L-PROPARGYLGLYCINE | AstaTech | MFCD00077855 | 113.116 | C5H7NO2 | 95.000 | N[C@@H](CC#C)C(O)=O | 10g | 256637057
L-PROPARGYLGLYCINE | AstaTech | 23235-01-0 | MFCD00077855 | 113.116 | C5H7NO2 | 95.000 | N[C@@H](CC#C)C(O)=O | 10g | 256637057
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Medchemexpress LLC L-propargylglycine | 23235-01-0 | 113.11 | 5 G
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L-Propargylglycine, also known as (S)-2-Aminopent-4-ynoic acid, is a synthetic amino acid. It can be utilized in the synthesis of folate-conjugates and corresponding metal-chelate complexes. As a click chemistry reagent, it contains an Alkyne group and is capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Synthetic amino acid
- Useful in synthesis of folate-conjugates
- Enables synthesis of metal-chelate complexes
- Functions as a click chemistry reagent
- Contains an alkyne group
- Capable of copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Supports bioorthogonal chemistry
- Offers rapid and selective reactions
- Does not interfere with biological processes under physiological conditions
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Chem-Impex International, Inc. Boc-5-aminovaleric acid | 27219-07-4 | MFCD00076903 | 1G
Boc-5-aminovaleric acid, 27219-07-4, MFCD00076903, 1G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000772180 DL-PROPARGYLGLYCINE 10G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000772313 DL-PROPARGYLGLYCINE 100MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000772978 DL-PROPARGYLGLYCINE 5G
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Medchemexpress LLC Itaconic acid-13C5 | 2095777-38-9 | 97.0% | 135.06 | 13C5H6O4 | 50ug
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Itaconic acid-13C5 is the 13C labeled Itaconic acid Itaconic acid a precursor of polymers chemicals and fuels can be synthesized by many fungi Itaconic acid also is a macrophage-specific metabolite Itaconic acid mediates crosstalk between macrophage metabolism and peritoneal tumors[1][2]
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eMolecules 446276-15-9 | 3-[Cyclohexyl(methyl)amino]-1,1,1-trifluoro-2-propanol | Combi-Blocks, Inc. | MFCD03001225 | 225.255 | C10H18F3NO | 95.000 | CN(CC(O)C(F)(F)F)C1CCCCC1 | 250mg | 603151730
3-[Cyclohexyl(methyl)amino]-1,1,1-trifluoro-2-propanol | Combi-Blocks, Inc. | 446276-15-9 | MFCD03001225 | 225.255 | C10H18F3NO | 95.000 | CN(CC(O)C(F)(F)F)C1CCCCC1 | 250mg | 603151730
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Chem-Impex International, Inc. Boc-5-aminovaleric acid | 27219-07-4 | MFCD00076903 | 5G
Boc-5-aminovaleric acid, 27219-07-4, MFCD00076903, 5G
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