Fatty acid conjugates
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Filtered Search Results
eMolecules 198561-07-8 | Fmoc-L-propargylglycine | Combi-Blocks | MFCD01075095 | 335.359 | C20H17NO4 | 98.000 | OC(=O)[C@H](CC#C)NC(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 117537505
Fmoc-L-propargylglycine | Combi-Blocks | 198561-07-8 | MFCD01075095 | 335.359 | C20H17NO4 | 98.000 | OC(=O)[C@H](CC#C)NC(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 117537505
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eMolecules 198561-07-8 | Fmoc-L-Propargylglycine | AA Blocks LLC | MFCD01075095 | 335.359 | C20H17NO4 | 0.000 | OC(=O)[C@H](CC#C)NC(=O)OCC1c2ccccc2-c2ccccc12 | 25g | 410158435
Fmoc-L-Propargylglycine | AA Blocks LLC | 198561-07-8 | MFCD01075095 | 335.359 | C20H17NO4 | 0.000 | OC(=O)[C@H](CC#C)NC(=O)OCC1c2ccccc2-c2ccccc12 | 25g | 410158435
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Medchemexpress LLC 4-pentenoic acid, 2-amino-, (2S)- | 16338-48-0 | ≥98.0% | 115.13 | 5 G
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L-Allylglycine is an amino acid derivative that functions as an inhibitor for glutamate decarboxylase (GAD), thereby reducing GABA biosynthesis in the brain. It is known to exhibit convulsant activity.
- Amino acid derivative
- Inhibitor for glutamate decarboxylase (GAD)
- Reduces GABA biosynthesis in the brain
- Exhibits convulsant activity
- Purity: ≥98.0%
- For research use only
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eMolecules 16338-48-0 | (S)-2-Allylglycine | Acrotein ChemBio Inc. | MFCD00002627 | 115.132 | C5H9NO2 | 97.000 | N[C@@H](CC=C)C(O)=O | 100g | 851114426
(S)-2-Allylglycine | Acrotein ChemBio Inc. | 16338-48-0 | MFCD00002627 | 115.132 | C5H9NO2 | 97.000 | N[C@@H](CC=C)C(O)=O | 100g | 851114426
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Medchemexpress LLC N-Propargylglycine | 58160-95-5 | 99.70% | C5H7NO2 | 100 MG
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N-Propargylglycine is a brain-penetrant and orally active PRODH inhibitor. It functions by inhibiting proline and 4-hydroxyproline catabolism, enhancing mitochondrial proteostasis, and stimulating neural processes. This compound is used in research for various neurodegenerative disorders, breast cancer, and primary hyperoxaluria type 2.
- Brain-penetrant and orally active PRODH inhibitor
- Inhibits proline and 4-hydroxyproline catabolism
- Enhances mitochondrial proteostasis
- Stimulates neural processes
- Useful in research for neurodegenerative disorders and breast cancer
- Reduces hyperoxaluria and prevents calcium oxalate stone formation
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Medchemexpress LLC Itaconic acid | 97-65-4 | MFCD00004260 | 100.0% | 130.10 g/mol | C5H6O4 | 25mg
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Itaconic acid (Standard) is the analytical standard of Itaconic acid This product is intended for research and analytical applications 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 Itaconic acid has anti-inflammatory anti-microbial and immunomodulatory effect[1][2][4][5]
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Chemscene CHEMSCENE
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5000578154 L-ALLYLGLYCINE 100G
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eMolecules 6600-40-4 | H-Nva-OH | Ambeed | MFCD00064421 | 117.148 | C5H11NO2 | 97.000 | CCC[C@H](N)C(O)=O | 1g | 525107437
H-Nva-OH | Ambeed | 6600-40-4 | MFCD00064421 | 117.148 | C5H11NO2 | 97.000 | CCC[C@H](N)C(O)=O | 1g | 525107437
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000741565 TERT-BUTYL 6-AMINOH 10G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000740826 TERT-BUTYL 6-AMINOH 1G
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Medchemexpress LLC Chitopentaose (pentahydrochloride) | 117467-64-8 | 10 MG
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Chitopentaose pentahydrochloride is a chitosan oligosaccharide that exhibits an anti-inflammatory effect. It also serves as a substrate for the gene encoding chitinase B (FjchiB).
- Chitosan oligosaccharide
- Substrate of gene encoding chitinase B (FjchiB)
- Purity: 99.94%
- Appearance: Solid, white to off-white
- Molecular weight: 1006.10
- Formula: C30H62Cl5N5O21
- CAS number: 117467-64-8
- Initial source: Microorganisms (Bacillus amyloliquefaciens)
- Soluble in H2O at 250 mg/mL (248.48 mM; requires ultrasonic)
- Anti-inflammatory effect
- Promotes heart rehabilitation in a rat myocarditis model by improving antioxidant, anti-inflammatory, and antiapoptotic properties
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Medchemexpress LLC Itaconic acid | 97-65-4 | MFCD00004260 | 100.0% | 130.10 g/mol | C5H6O4 | 50mg
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Itaconic acid (Standard) is the analytical standard of Itaconic acid This product is intended for research and analytical applications 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 Itaconic acid has anti-inflammatory anti-microbial and immunomodulatory effect[1][2][4][5]
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eMolecules 57718-07-7 | Ethyl itaconate | Combi-Blocks | MFCD00059138 | 158.153 | C7H10O4 | 95.000 | CCOC(=O)CC(=C)C(O)=O | 1g | 342864706
Ethyl itaconate | Combi-Blocks | 57718-07-7 | MFCD00059138 | 158.153 | C7H10O4 | 95.000 | CCOC(=O)CC(=C)C(O)=O | 1g | 342864706
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eMolecules 69954-66-1 | 4-Dimethylaminobutyric acid hydrochloride | Combi-Blocks | MFCD00012613 | 167.630 | C6H14ClNO2 | 98.000 | Cl.CN(C)CCCC(O)=O | 5g | 267176129
4-Dimethylaminobutyric acid hydrochloride | Combi-Blocks | 69954-66-1 | MFCD00012613 | 167.630 | C6H14ClNO2 | 98.000 | Cl.CN(C)CCCC(O)=O | 5g | 267176129
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eMolecules 69954-66-1 | 4-Dimethylaminobutyric acid hydrochloride | Combi-Blocks | MFCD00012613 | 167.630 | C6H14ClNO2 | 98.000 | Cl.CN(C)CCCC(O)=O | 100g | 296392476
4-Dimethylaminobutyric acid hydrochloride | Combi-Blocks | 69954-66-1 | MFCD00012613 | 167.630 | C6H14ClNO2 | 98.000 | Cl.CN(C)CCCC(O)=O | 100g | 296392476
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