Organic Acids
Chem-Impex International, Inc. D-(+)-Malic acid | 636-61-3 | MFCD00004245 | 25G
D-(+)-Malic acid, 636-61-3, MFCD00004245, 25G
Medchemexpress LLC Pam2CSK4 (TFA) | 99.5% | 1271.82 (free base) | 5 MG
Pam2CSK4 (TFA) is a lipopeptide that acts as a TLR6-independent TLR2 ligand and agonist. It promotes platelet aggregation and increases platelet adhesion to collagen-coated surfaces in a TLR2/NF-κB/BTK-dependent manner. Pam2CSK4 (TFA) also activates iNOS expression and NO production in mouse macrophages.
- Acts as a TLR6-independent TLR2 ligand and agonist.
- Promotes platelet aggregation.
- Increases platelet adhesion to collagen-coated surfaces.
- Activates iNOS expression and NO production in mouse macrophages.
Medchemexpress LLC Sar441255 TFA | 99.9% | 4866.56 (free base) | 1 MG
SAR441255 TFA is a potent unimolecular peptide GLP-1/GIP/GCG receptor triagonist. It demonstrates high potency with balanced activation of all three target receptors. This compound shows positive acute glucoregulatory effects in diabetic obese monkeys, indicating its potential for metabolic and endocrine disease research, particularly in areas like obesity and type 2 diabetes.
- Potent unimolecular peptide receptor triagonist.
- Displays high potency with balanced activation of three target receptors.
- Shows positive acute glucoregulatory effects in diabetic obese monkeys.
- Relevant for research in metabolic diseases, including obesity and type 2 diabetes.
Medchemexpress LLC Charybdotoxin TFA | 96.8% | 4295.89 (free acid) | 100 UG
Charybdotoxin TFA is a 37-amino acid peptide that functions as a potassium channel blocker. This compound is a valuable tool for research involving potassium channels.
- Acts as a potassium channel blocker
- 37-amino acid peptide
- Useful for studying potassium channels
- Storage conditions for powder: -80°C for 2 years, -20°C for 1 year
- Storage conditions for in solvent: -80°C for 6 months, -20°C for 1 month
- Sealed storage, away from moisture and light required for both forms
Medchemexpress LLC Pepinh-MYD TFA | 1421052-89-2 | 98.9% | 3388.03 | 5 MG
Pepinh-MYD TFA is a MyD88 inhibitor designed to interfere with MyD88-mediated TLR signaling pathways. It contains a domain sequence from MyD88 TIR and a protein transduction sequence, enabling cell membrane penetration and inhibition of related immune responses. This compound shows potential for studying the role of MyD88 in viral infections, including COVID-19.
- Acts as a MyD88 inhibitor
- Contains a domain sequence from MyD88 TIR
- Includes a protein transduction sequence for cell membrane penetration
- Interferes with MyD88-mediated TLR signaling pathways
- Inhibits immune responses
- Suitable for studying the role of MyD88 in viral infections
- Applicable in COVID-19 anti-virus research
Medchemexpress LLC ATX-II TFA | 99.7% | 4934.62 | 500 UG
ATX-II TFA is a selective sodium channel modulator toxin that enhances late sodium current, prevents full sodium channel inactivation, and generates persistent current fractions. It has a pro-arrhythmic effect, slowing intrinsic heart rate and prolonging QT interval. This compound is suitable for research on atrial fibrillation, long QT syndrome, and long QT3 syndrome.
![eMolecules 13200-83-4 | formyl-L-proline | Synthonix | MFCD00037321 | 143.142 | C6H9NO3 | 98.000 | OC(=O)[C@@H]1CCCN1C=O | 500mg | 794075379](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502442246.PNG-250.jpg)
eMolecules 13200-83-4 | formyl-L-proline | Synthonix | MFCD00037321 | 143.142 | C6H9NO3 | 98.000 | OC(=O)[C@@H]1CCCN1C=O | 500mg | 794075379
formyl-L-proline | Synthonix | 13200-83-4 | MFCD00037321 | 143.142 | C6H9NO3 | 98.000 | OC(=O)[C@@H]1CCCN1C=O | 500mg | 794075379
Medchemexpress LLC Malic enzyme inhibitor ME1 | 522649-59-8 | 99.7% | 351.40 | 1 MG
Malic enzyme inhibitor ME1 is a potent inhibitor of Malic enzyme (ME1) with an IC50 of 0.15 μM. It is intended for research use only and has been shown to significantly impact cell viability and proliferation in various cell lines.
- Potent inhibitor of Malic enzyme (ME1) with an IC50 of 0.15 μM
- Significantly reduces total cell numbers and cell viability/metabolic activity in MTS cells
- Dose-dependently reduces the number of colonies formed by HCT116 and HT29 cells
- Suitable for research applications
Crescent Chemical Co Inc CACODYLIC ACID-NA-SALT-3H2O
Cacodylic acid-Na-salt-3H2O research grade For buffers, especially for bactericidal buffers used in electron microscopy. Size - 500G Storage Conditions - +15 °C TO +30 °C Catalog Number - 15540.03 CAS 6131-99-3
Medchemexpress LLC Cef20 (Tfa) | 99.3% | 1057.19 | 25 MG
CEF20 TFA is an HLA-A*0201-restricted epitope from cytomegalovirus pp65 (495-503).
- High purity of 99.31%
- Molecular weight of 1057.19
- Solid appearance
- White to off-white color
- Sequence: Asn-Leu-Val-Pro-Met-Val-Ala-Thr-Val (NLVPMVATV)
- Soluble in DMSO
- Store in sealed container, away from moisture
- Powder storage: -80°C for 2 years, -20°C for 1 year
- Storage in solvent: -80°C for 6 months, -20°C for 1 month
Medchemexpress LLC Clovibactin TFA | 97.1% | 903.08 | 100 UG
Clovibactin TFA is the TFA salt form of Clovibactin. It is an antibiotic effective against drug-resistant bacterial pathogens without detectable resistance. Clovibactin TFA inhibits cell wall synthesis by targeting pyrophosphate of peptidoglycan precursors.
- Effective against drug-resistant bacterial pathogens
- Exhibits no detectable resistance
- Inhibits cell wall synthesis
- Targets pyrophosphate of peptidoglycan precursors
Medchemexpress LLC Lagipra peptide (TFA) | 98.2% | 5756.50 (free base) | 1 MG
LAGIPRA peptide TFA is a long-acting GIP1R agonist. It enhances insulin sensitivity by augmenting glucose disposal and reduces branched-chain amino acids (BCAAs) and ketoacids. This peptide has potential for the research of type 2 diabetes.
- Long-acting GIP1R agonist
- Enhances insulin sensitivity
- Reduces branched-chain amino acids (BCAAs)
- Reduces ketoacids
- Potential for type 2 diabetes research
Medchemexpress LLC Maleic hydrazide | 123-33-1 | 99.9% | C4H4N2O2 | 50 G
Maleic hydrazide is a systemic plant growth regulator and herbicide, known for inhibiting nucleic acid and protein synthesis. It exhibits low acute toxicity via oral, dermal, and inhalation routes, and has shown minimal cytotoxicity on Vero cells compared to Hep2 and HepG2 cells.
- Systemic plant growth regulator and herbicide
- Inhibits nucleic acid and protein synthesis
- Low acute toxicity
- Minimal cytotoxicity on Vero cells