Monosaccharides
Medchemexpress LLC L-ribulose | 2042-27-5 | 99.9% | 1 MG
L-ribulose is an isomer of L-ribose provided as a 1 M aqueous solution for research use; it serves as a precursor for synthesis of rare sugars and L-nucleoside analogues.
- 1 M concentration in water.
- CAS number 2042-27-5.
- Purity 99.9% (as supplied).
- Molecular formula C5H10O5; molecular weight 150.13 g/mol.
- Supplied in micro-quantities suitable for synthesis and analytical work.
- Intended for research use only.
Bioworld 5-Fluorouridine, 100 mg
SpecificationsA proapoptotic and cytotoxic nucleoside analogSynonyms: 5-Fluorouracil 1β-D-ribofuranoside, FUrdShipped at ambient temperatureAppearance: SolidDensity : ~1.8 g/cm3 (Predicted)Melting Point: 182 °C
![eMolecules 1949-78-6 | L-Lyxose | Combi-Blocks | MFCD00064111 | 150.130 | C5H10O5 | 97.000 | O[C@H]1COC(O)[C@H](O)[C@@H]1O | 1g | 482932055](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502184379.JPG-250.jpg)
eMolecules 1949-78-6 | L-Lyxose | Combi-Blocks | MFCD00064111 | 150.130 | C5H10O5 | 97.000 | O[C@H]1COC(O)[C@H](O)[C@@H]1O | 1g | 482932055
L-Lyxose | Combi-Blocks | 1949-78-6 | MFCD00064111 | 150.130 | C5H10O5 | 97.000 | O[C@H]1COC(O)[C@H](O)[C@@H]1O | 1g | 482932055
Medchemexpress LLC D-ribose (mixture of isomers) | 50-69-1 | MFCD00135453 | 98.3% | 150.13 g·mol⁻¹ | C5H10O5 | 100 MG
D-ribose (mixture of isomers) is a solid reference standard intended for analytical and research use. It is an aldopentose sugar involved in ATP and nucleotide metabolism and is supplied with accompanying quality documentation for method development, validation, and quantitative analysis.
- High purity 98.29% for analytical use.
- Molecular formula C5H10O5 and molecular weight 150.13 g·mol⁻¹.
- Available in small package sizes suitable for standards and assays.
- Supplied with certificate of analysis and safety data sheet.
- Stored and shipped at room temperature unless otherwise specified.
Medchemexpress LLC Phosphocreatine disodium | 922-32-7 | 98.0% | 1 ML
Phosphocreatine is an organic compound found in vertebrate skeletal muscles. It enhances antioxidant activity, activates the TAK1 pathway to protect the heart, normalizes mitochondrial function, and reduces oxidative stress via the Akt-mediated Nrf2/HO-1 pathway. It also provides renal protection by suppressing Apoptosis and Reactive Oxygen Species (ROS) generation through the ERK-mediated Nrf-2/HO-1 pathway.
- Enhances antioxidant activity.
- Activates the TAK1 pathway to protect the heart.
- Normalizes mitochondrial function.
- Reduces oxidative stress via Akt mediated Nrf2/HO-1 pathway.
- Provides renal protection by suppressing Apoptosis and ROS generation through ERK mediated Nrf-2/HO-1 pathway.
- Human endogenous metabolite.
Medchemexpress LLC K-Ras ligand-linker conjugate 6 | 2378261-89-1 | C42H60N8O7 | 10MG
K-Ras ligand-Linker Conjugate 6 is a small-molecule ligand-linker designed as an intermediate for targeted protein degradation research. It links a K-Ras-binding ligand to a PROTAC linker to enable synthesis of K-Ras degraders for cellular degradation studies.
- High purity confirmed by HPLC (98.9%).
- Characterized by mass spectrometry consistent with structure.
- Molecular formula C42H60N8O7 and molecular weight 788.98 g/mol.
- Suitable for PROTAC synthesis and K-Ras degrader development.
- Available in multiple small-scale pack sizes (5 mg-100 mg) for research use.
AdipoGen BQC
Chemical. CAS 207124-63-8. Formula C20H10K2N2O4 . 3H2O. MW 474.55. 2,2´-Biquinoline-4,4´-dicarboxylic acid dipotassium salt BQC is a water soluble biquinoline-based ligand. The oxidation of alcohols to the corresponding aldehydes and ketones, which can be performed by a variety of methods, remains one of the most important reactions in organic synthesis. BOC is used in the aerobic oxidation of alcohols primary, secondary and benzylic in the presence of palladium catalysts. The catalytic system composed of CuCl2 and BQC was found to be highly efficient for the selective oxidation of secondary benzylic, allylic and propargylic alcohols to the corresponding ketones, with aqueous t-butyl hydroperoxide under phase-transfer catalysis conditions. The catalytic system is stable and can be recycled and reused several times without loss of activity.
Medchemexpress LLC Phosphoric acid, dipotassium salt, trihydrate | 16788-57-1 | MFCD00149926 | 99.2% | 228.22 g/mol | H7K2O7P | 500 G
Dipotassium hydrogen phosphate trihydrate is an inorganic salt commonly used as a buffering agent and source of potassium and phosphate in laboratory, pharmaceutical, and industrial applications. It is supplied as a white to off-white crystalline solid and is used in buffer preparation, cell culture media formulation, and analytical reagent systems.
- Used as a buffer and pH regulator in aqueous systems.
- Provides a source of phosphate and potassium ions.
- Suitable for buffer preparation and cell culture media formulation.
- Off-white crystalline solid with high purity.
- Available in laboratory pack sizes including 500 g.
Cambridge Isotope Laboratories D-Glucose-6-phosphate disodium salt hydrate (U-13C6 99%) 0 1 mg
D-Glucose-6-phosphate disodium salt hydrate (U-13C6 99%) 0 1 mg
Apexbio Technology LLC Methotrexate disodium 7413-34-5 500mg
Methotrexate disodium (CAS 7413-34-5) is a small-molecule inhibitor targeting dihydrofolate reductase (DHFR) It is designed to inhibit DHFR activity thereby disrupting the enzymatic reduction of dihydrofolate to tetrahydrofolate and impairing DNA and RNA biosynthesis Methotrexate disodium exerts its biological activity primarily through DHFR inhibition In in vitro studies methotrexate disodium demonstrates inhibitory activity with an IC50 value in the nanomolar range (approximately 5 to 50 nM depending on assay conditions and cell models) Based on these pharmacological properties methotrexate disodium holds research potential in autoimmune disorders such as rheumatoid arthritis and psoriasis as well as in antineoplastic studies involving acute lymphoblastic leukemia
Apexbio Technology LLC Carbenoxolone disodium 7421-40-1 50mg
Carbenoxolone disodium (CAS 7421-40-1) is a small-molecule inhibitor targeting 11 -hydroxysteroid dehydrogenase (11 -HSD) It is designed to modulate glucocorticoid metabolism by suppressing the interconversion of corticosteroid hormones thereby regulating glucocorticoid access to steroid receptors Carbenoxolone disodium exerts its biological activity through inhibition of 11 -HSD enzymatic function In vitro studies demonstrate inhibitory activity with reported IC50 values ranging from 10 30 M depending on experimental conditions and target tissue Based on these pharmacological properties Carbenoxolone disodium holds research potential in neuroendocrine and cardiovascular studies exploring glucocorticoid-mediated signaling pathways