Phenols
![Alkali Scientific Riboflavin [Vitamin B2], 1 Kilogram](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000659679.jpg-250.jpg)
Alkali Scientific Riboflavin [Vitamin B2], 1 Kilogram
Riboflavin (Vitamin B2) is an essential water-soluble vitamin involved in cellular energy production, enzyme function, and the metabolism of fats, drugs, and steroids. This 1kg reagent is widely used in biochemical research to study metabolic processes, particularly those involving mitochondrial energy production and redox reactions. Riboflavin is also crucial for the synthesis of flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD), both of which are coenzymes in various enzymatic reactions. In laboratory applications, Riboflavin is used in assays involving redox chemistry, UV light studies, and research on vitamin deficiencies, cellular respiration, and energy metabolism.
Medchemexpress LLC Akt1 protein, human (active, Sf9, GST) | 100UG
Recombinant human AKT1 protein (active) expressed in Sf9 insect cells with an N-terminal GST tag. Supplied as a 0.22 μm filtered solution formulated in 50 mM HEPES (pH 7.5), 200 mM NaCl, 20% glycerol, 5 mM DTT, and trehalose; intended for research applications requiring active AKT1 kinase.
- Active kinase suitable for activity assays and signaling studies.
- Full-length sequence (M1-A480), approximately 82.2 kDa.
- N-terminal GST tag facilitates purification and detection.
- Expressed in Sf9 insect cells to support eukaryotic modifications.
- Supplied as a filtered solution in stabilizing buffer for handling and storage.
- Recommend aliquoting and avoiding repeated freeze-thaw cycles to preserve activity.
![Alkali Scientific Luria Agar [Miller's LB] 1 Gram Buffered Capsules, 500 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000661695.jpg-250.jpg)
Alkali Scientific Luria Agar [Miller's LB] 1 Gram Buffered Capsules, 500 G
Luria Agar [Miller's LB] 1 Gram Buffered Capsules, 500G is a microbial culture media used in a variety of laboratory applications, including bacterial cultivation and microbial research. The formulation contains a balanced nutrient mix that supports the growth of a wide range of microorganisms. These capsules are designed to be buffered, ensuring a stable pH environment that is crucial for consistent and reliable results. The 500g bottle provides a convenient volume for laboratories requiring moderate amounts of prepared media. The media is commonly used in microbiology labs for culturing bacteria, yeast, and fungi. It is available as a buffered capsule that can be easily dissolved in water.
Cambridge Isotope Laboratories 4 4-DDE (ring-13C12 99%) 100 ug/mL in nonane 1 2 mL
4 4-DDE (ring-13C12 99%) 100 ug/mL in nonane 1 2 mL
Medchemexpress LLC 2-Hydrazinobenzothiazole | 615-21-4 | 99.95% | C7H7N3S | 100 G
This compound, 2-Hydrazinobenzothiazole, is a potent IDO1 inhibitor with an IC50 of 8 μM. It interacts with the IDO1 haem through hydrazine and has potential for immune system related diseases research. It is supplied with a purity of 99.95%.
- Potent IDO1 inhibitor (IC50 of 8 μM)
- Interacts with IDO1 haem via hydrazine
- Suitable for immune system related diseases research
- Purity of 99.95%
- Solid appearance
- Molecular weight: 165.22
- Chemical formula: C7H7N3S
- CAS number: 615-21-4
Medchemexpress LLC Tropolone | 533-75-5 | MFCD00004158 | 100 G
Tropolone is a seven-membered non-benzenoid aromatic compound and a precursor of many Azulene derivatives. It is a potent mushroom tyrosinase inhibitor with an IC50 value of 0.4 μM. Tropolone exhibits broad anti-viral and anti-fungal activity and shows synergistic effects when co-treated with nucleos(t)ide analog drugs. It is also a promising candidate for research in osteosarcoma.
- Potent mushroom tyrosinase inhibitor with an IC50 of 0.4 μM
- Exhibits broad anti-viral and anti-fungal activity
- Precursor to Azulene derivatives
- Promising candidate for osteosarcoma research
- Solid appearance, off-white to light brown color
- Purity of 99.77%
Medchemexpress LLC Undecane | 1120-21-4 | 25 G
Undecane is a potent cAMP agonist with anti-allergic and anti-inflammatory activities. It inhibits degranulation and the secretion of histamine and TNF-α. It reverses increased levels of p38 phosphorylation, NF-κB transcriptional activity, and target cytokine/chemokine genes. Undecane can be used for the study of skin inflammatory disorders, such as atopic dermatitis.
- Potent cAMP agonist
- Exhibits anti-allergic and anti-inflammatory activities
- Inhibits degranulation and secretion of histamine and TNF-α
- Reverses p38 phosphorylation and NF-κB transcriptional activity
- Reduces mRNA expression of inflammatory cytokines
- Suitable for studying skin inflammatory disorders
Medchemexpress LLC TA-02 | 1784751-19-4 | 99.9% | 333.33 g/mol | C20H13F2N3 | 1 ML
TA-02 is a small-molecule inhibitor of p38 MAPK and an analog of SB 203580, reported to show potent biochemical activity (IC50 ≈ 20 nM). The compound is supplied with high purity and is offered in ready-to-use solution formats as well as solid quantities for research use in biochemical and cell-based assays.
- Potent p38 MAPK inhibition (IC50 ≈ 20 nM).
- High purity, suitable for research applications.
- Available as a 10 mM solution in DMSO for immediate use.
- Solid form available for custom dilution and formulation.
- Stable under recommended storage conditions for reliable results.
Medchemexpress LLC Kras G12d Inhibitor 14 | 2765254-39-3 | 98.88% | C20H19F3N4OS | 1 ML
KRAS G12D inhibitor 14 is a potent KRAS G12D inhibitor with a KD of 33 nM for binding to KRAS G12D protein. It decreases the active form of KRAS G12D (KRAS G12D-GTP) but not KRAS G13D. For research use only, not for sale to patients.
- Binds to KRAS G12D protein with a KD of 33 nM.
- Decreases the active form of KRAS G12D (KRAS G12D-GTP) but does not affect KRAS G13D.
- Shows antiproliferative activity with an IC50 of 2.1 μM against KRAS G12D-mutated cells.
- Causes efficient apoptosis in SW1990 and CT26 cancer cells.
- Down-regulates phosphorylated Raf and Erk in CT26 and SW1990 cancer cell lines.
- Exhibits significant antitumor efficacy in a CT26 tumor model with a tumor growth inhibition (TGI) of 42% or 53% at doses of 40 mg/kg or 60 mg/kg (i.p.), without apparent toxicity.
eMolecules 165534-43-0 | DEPBT | AstaTech | MFCD01236967 | 299.223 | C11H14N3O5P | 97.000 | CCOP(=O)(OCC)On1nnc2ccccc2c1=O | 100g | 384832716
DEPBT | AstaTech | 165534-43-0 | MFCD01236967 | 299.223 | C11H14N3O5P | 97.000 | CCOP(=O)(OCC)On1nnc2ccccc2c1=O | 100g | 384832716
Medchemexpress LLC 17-Phenyl trinor PGF 25mg | 130209-76-6 | 430.58 g/mol | C26H38O5 | 25 MG
17-Phenyl trinor PGF2α isopropyl ester (CAS 130209-76-6) is a prostaglandin analogue and FP receptor agonist supplied for laboratory research. It is the isopropyl ester derivative of 17-phenyl trinor PGF2α, provided as a white to off-white solid with high reported purity for use in receptor pharmacology, biochemical assays, and method development.
- High purity (~99.8%) suitable for research applications.
- White to off-white solid for straightforward handling and storage.
- Available in 25 mg packs for small-scale experiments.
- Functions as an FP receptor agonist for pharmacological studies.
- Molecular weight 430.58 g/mol; formula C26H38O5 for reference.
Apexbio Technology LLC Fenspiride HCl 5053-08-7 10mM (in 1mL DMSO)
Fenspiride hydrochloride (CAS 5053-08-7) is a small molecule antagonist of -adrenergic and histamine H1 receptors By inhibiting these signaling pathways Fenspiride HCl modulates bronchial smooth muscle tone and reduces inflammatory processes mediated by histamine and adrenergic activity This compound is utilized in biomedical research to investigate mechanisms of airway hyperreactivity neurogenic inflammation and the pharmacological modulation of respiratory tract disorders related to histaminergic and adrenergic signaling
Medchemexpress LLC Bis-Tos-PEG6 | 42749-27-9 | C26H38O11S2 | 500 MG
Bis-Tos-PEG6 is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs (Proteolysis Targeting Chimeras) consist of two different ligands connected by a linker: one ligand for an E3 ubiquitin ligase and another for the target protein. They utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Used in the synthesis of PROTACs.
- PEG-based PROTAC linker.
- Utilizes the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
Medchemexpress LLC Cathepsin C/DPPI protein, mouse (inactive, His-Myc) | >95.0% | 500UG
Recombinant mouse Cathepsin C/DPPI protein (inactive, His-Myc) provided lyophilized for research applications. The preparation is expressed in E. coli, formulated in 10 mM Tris-HCl, 1 mM EDTA, 6% trehalose (pH 8.0), and exhibits >95.0% purity by reducing SDS-PAGE. Supplied in multiple pack sizes and intended for storage frozen to preserve integrity.
- Inactive protein suitable for detection and structural studies.
- N-terminal 10xHis and C-terminal Myc tags for purification and detection.
- High purity (>95.0%) confirmed by reducing SDS-PAGE.
- Lyophilized formulation with trehalose for enhanced stability.
- Expressed in E. coli for cost-effective production.
- Stable when stored at -20°C; aliquot and freeze at -20°C or -80°C for extended storage.
eMolecules 59-67-6 | Niacin | Ambeed123.111 | C6H5NO2 | 98.000 | OC(=O)c1cccnc1 | 100g | 552650204
Niacin | Ambeed | 59-67-6123.111 | C6H5NO2 | 98.000 | OC(=O)c1cccnc1 | 100g | 552650204