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Filtered Search Results
eMolecules 9-Decenoic acid | 14436-32-9 | MFCD00036663 | 25g
Oakwood Chemical | 9-Decenoic acid | 25g | 537663845 | 002775 | | 14436-32-9 | MFCD00036663 | 170.252 | C10H18O2
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Medchemexpress LLC 6-Methylheptanoic ac 500mg
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6-Methylheptanoic acid is an ester product
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Selleck Chemical LLC 2-Methylhexanoic acid
2-Methylhexanoic acid is a flavouring ingredient
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Apexbio Technology LLC (6-)ε-Aminocaproic acid 60-32-2 10mM (in 1mL DMSO)
6-epsilon-Aminocaproic acid is a small-molecule inhibitor targeting plasminogen activators It is designed to competitively inhibit the conversion of plasminogen to plasmin thereby regulating the fibrinolytic pathway and hemostatic processes 6-epsilon-Aminocaproic acid exerts its biological activity primarily through antifibrinolytic inhibition by blocking plasmin-mediated fibrin degradation Based on these pharmacological properties 6-epsilon-Aminocaproic acid holds research potential in coagulation studies thrombosis bleeding disorders and the investigation of pathological fibrinolysis mechanisms
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Medchemexpress LLC 10-Undecenoic acid (Undecylenic acid) | 112-38-9 | 100.0% | 50 G
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10-Undecenoic acid (Undecylenic acid) is an antifungal agent with neuroprotective and anticancer effects. It works by inhibiting Aβ oligomerization, scavenging Reactive Oxygen Species (ROS), and inhibiting μ-calpain activity. This compound has shown efficacy against *C. albicans* biofilm formation and MRSA infection, and can also inhibit quorum sensing signals in *Bacillus subtilis* and *Pseudomonas aeruginosa*.
- Induces apoptosis in various tumor cells
- Stimulates osteoblast differentiation
- Offers neuroprotection against cell death induced by glutamate, H2O2, and Aβ1-42
- Inhibits *C. albicans* biofilm formation and MRSA infection
- Scavenges reactive oxygen species
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Medchemexpress LLC 10-Undecenoic acid | 112-38-9 | 99.99% | 5 G
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10-Undecenoic acid (Undecylenic acid) is an antifungal agent. It inhibits Aβ oligomerization, scavenges reactive oxygen species (ROS), and inhibits μ-calpain activity. It exhibits neuroprotective and anticancer effects on various tumors. Additionally, it inhibits *C. albicans* biofilm formation and MRSA infection, and suppresses quorum sensing signals of *Bacillus subtilis* and *Pseudomonas aeruginosa*.
- Exhibits dose-dependent cytotoxicity against human tumor cell lines HeLa, A549, Jurkat, and U937.
- Reduces *C. albicans* biofilm viability and thickness, while increasing *C. glabrata* cell count and metabolic activity.
- Provides neuroprotection against glutamate, H₂O₂, and Aβ1-42 induced cell death in SH-SY5Y cells.
- Reduces cell death induced by H₂O₂ and partially attenuates Staurosporine and Doxorubicin-induced cell death in SH-SY5Y cells.
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Medchemexpress LLC N-propargylglycine | 58160-95-5 | MFCD11168312 | 99.7% | 113.11 | C5H7NO2 | 5 MG
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N-propargylglycine is an orally active, irreversible inhibitor of proline dehydrogenase (PRODH) used in research on mitochondrial metabolism and neurodegenerative diseases. It has reported antitumor activity and is supplied as an off-white to light-yellow solid for laboratory research.
- Orally active, irreversible PRODH inhibitor.
- Applicable to studies of mitochondrial metabolism and neurodegeneration.
- Reported antitumor activity supports cancer research use.
- High purity (99.7%) for reproducible experimental results.
- Solid form facilitates storage and handling in the laboratory.
- Available in small package sizes suitable for screening and pilot studies.
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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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C(O)=O | 5g | 536856753](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000473063.jpg-250.jpg)
eMolecules 16338-48-0 | L-Allylglycine | ChemScene | MFCD00002627 | 115.132 | C5H9NO2 | 97.000 | N[C@@H](CC=C)C(O)=O | 5g | 536856753
L-Allylglycine | ChemScene | 16338-48-0 | MFCD00002627 | 115.132 | C5H9NO2 | 97.000 | N[C@@H](CC=C)C(O)=O | 5g | 536856753
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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 | 5g | 455888856
L-Allylglycine | Accela ChemBio (ASD) | 16338-48-0 | MFCD00002627 | 115.132 | C5H9NO2 | 98.000 | N[C@@H](CC=C)C(O)=O | 5g | 455888856
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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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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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Medchemexpress LLC Itaconic acid | 97-65-4 | MFCD00004260 | 100.0% | 130.10 g·mol-1 | C5H6O4 | 10mg
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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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C(O)=O | 1g | 525107437](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502425564.JPG-250.jpg)
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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C(O)=O | 10g | 455888854](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000473589.jpg-250.jpg)
eMolecules 16338-48-0 | L-Allylglycine | Accela ChemBio (ASD) | MFCD00002627 | 115.132 | C5H9NO2 | 98.000 | N[C@@H](CC=C)C(O)=O | 10g | 455888854
L-Allylglycine | Accela ChemBio (ASD) | 16338-48-0 | MFCD00002627 | 115.132 | C5H9NO2 | 98.000 | N[C@@H](CC=C)C(O)=O | 10g | 455888854
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