Lipids and Lipid Derivatives
Cayman Chemical 5-HexynoIc AcId 10g
A protein labeling compound; has been used to label proteins at acylation sites in a fatty acid synthase-dependent manner; can be further conjugated to fluorescent probes or biotin via click chemistry for protein identification
Medchemexpress LLC p-Hydroxyphenethyl trans-ferulate | 84873-15-4 | 5 MG
p-Hydroxyphenethyl trans-ferulate is a compound known for its diverse biological activities. It exhibits anti-hyperglycemic, antioxidant, and anti-inflammatory properties, alongside inhibitory anticancer and serotonergic activities.
- Exhibits anti-hyperglycemic activity against yeast α-glucosidase (IC50=19.24 ± 1.73 μM)
- Possesses antioxidant properties
- Demonstrates anti-inflammatory activities
- Shows inhibitory anticancer activity against various human cell lines
- Exhibits serotonergic activity by displacing [3H]LSD from human recombinant 5HT7 receptor
- Has anticomplement activity in sheep and rabbit erythrocytes
- High purity of 99.68%
Medchemexpress LLC Undecanoic acid | 112-37-8 | 2730 | 186.29 | 100 G
Undecanoic acid is a monocarboxylic acid with antifungal properties. It inhibits the production of exocellular keratinase and lipase, and the biosynthesis of several phospholipids in T. rubrum. It also demonstrates strong antifungal activity by disrupting crucial fungal mechanisms including cell wall synthesis, membrane assembly, mRNA synthesis, lipid metabolism, and pathogenesis, influencing gene splicing.
- Inhibits exocellular keratinase production
- Inhibits exocellular lipase production
- Disrupts fungal cell wall synthesis
- Disrupts fungal membrane assembly
- Disrupts fungal mRNA synthesis
- Influences gene splicing
Strem, An Ascensus Company CAS# 19766-89-3. 25g. Sodium 2-ethylhexanoate, min. 97%. MFCD00014007
CAS# 19766-89-3. 25g. Sodium 2-ethylhexanoate, min. 97%. MFCD00014007. Molecular Weight: 166.20. Molecular Formula: NaOOCCH(C2H5)C4H9. Color/form: white pwdr. Strem# 93-1163. http://www.strem.com/catalog/v/93-1163/
Sigma Aldrich Fine Chemicals Biosciences Lauric acid natural, >=98%, FCC, FG | 143-07-7 | MFCD00002736 | 5KG
Lauric acid natural, >=98%, FCC, FG | Purity: >=98% | Mol Wt: 200.32 | 143-07-7 | MFCD00002736 | 5KG
eMolecules 73141-46-5 | 3-Hydroxy Sebacic Acid | Toronto Research Chemicals | MFCD18642141 | 218.249 | C10H18O5 | 95.000 | OC(CCCCCCC(O)=O)CC(O)=O | 100mg | 601596987
3-Hydroxy Sebacic Acid | Toronto Research Chemicals | 73141-46-5 | MFCD18642141 | 218.249 | C10H18O5 | 95.000 | OC(CCCCCCC(O)=O)CC(O)=O | 100mg | 601596987
Sigma Aldrich Fine Chemicals Biosciences Heptanoic acid natural, FG | 111-14-8 | MFCD00004426 |
Heptanoic acid natural, FG | Mol Wt: 130.18 | 111-14-8 | MFCD00004426 |
Medchemexpress LLC 10-Undecenoic acid, 98% (stabilized with TBC) | 112-38-9 | 98% | 10 G
10-Undecenoic acid (Undecylenic acid) is an antifungal agent that also exhibits neuroprotective and anticancer effects. It can inhibit Aβ oligomerization, scavenge Reactive Oxygen Species (ROS), and inhibit μ-calpain activity. Additionally, it shows activity against *C. albicans* biofilm formation and MRSA infection.
- Inhibits Aβ oligomerization
- Scavenges reactive oxygen species (ROS)
- Inhibits μ-calpain activity
- Demonstrates neuroprotective effects
- Shows anticancer effects on various tumors
- Inhibits *C. albicans* biofilm formation
- Inhibits MRSA infection
- Inhibits quorum sensing signals of *Bacillus subtilis* and *Pseudomonas aeruginosa*
NC(=O)OCC1c2ccccc2-c2ccccc12 | 100g | 374520935](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000170534.jpg-250.jpg)
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 | 100g | 374520935
Fmoc-L-propargylglycine | Combi-Blocks | 198561-07-8 | MFCD01075095 | 335.359 | C20H17NO4 | 98.000 | OC(=O)[C@H](CC#C)NC(=O)OCC1c2ccccc2-c2ccccc12 | 100g | 374520935
Medchemexpress LLC L-Propargylglycine | 23235-01-0 | 113.11 | 1 G
L-Propargylglycine, also known as (S)-2-Aminopent-4-ynoic acid, is a synthetic amino acid. It is utilized in the creation of folate-conjugates and their associated metal-chelate complexes. This compound functions as a click chemistry reagent, containing an Alkyne group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with molecules possessing Azide groups.
- Synthetic amino acid
- Used in the synthesis of folate-conjugates and metal-chelate complexes
- Functions as a click chemistry reagent
- Contains an Alkyne group for copper-catalyzed azide-alkyne cycloaddition with Azide groups
- For research use only
C(O)=O | 1g | 205396668](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000161657.jpg-250.jpg)
eMolecules 23235-01-0 | L-Propargylglycine | Combi-Blocks | MFCD00077855 | 113.116 | C5H7NO2 | 98.000 | N[C@@H](CC#C)C(O)=O | 1g | 205396668
L-Propargylglycine | Combi-Blocks | 23235-01-0 | MFCD00077855 | 113.116 | C5H7NO2 | 98.000 | N[C@@H](CC#C)C(O)=O | 1g | 205396668
Medchemexpress LLC 4-pentenoic acid, 2-amino-, (2S)- | 16338-48-0 | ≥98.0% | 115.13 | 5 G
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
Selleck Chemical LLC Itaconic acid S3095-100mg
Itaconic acid a macrophage-specific (M -specific) metabolite mediates crosstalk between macrophage metabolism and peritoneal tumors Itaconic acid is also a precursor of polymers chemicals and fuels that can be synthesized by many fungi