Monosaccharides
Selleck Chemical LLC b-D-Glucose pentaacetate
-D-Glucose pentaacetate is an enantiomer of D-glucose pentaacetate
[C@@H](O)[C@@H](O)[C@H](O)C=O | 5g | 705364792](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000158903.jpg-250.jpg)
eMolecules 2438-80-4 | L-(-)-Fucose | Accela ChemBio (ASD) | MFCD00135607 | 164.157 | C6H12O5 | 98.000 | C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C=O | 5g | 705364792
L-(-)-Fucose | Accela ChemBio (ASD) | 2438-80-4 | MFCD00135607 | 164.157 | C6H12O5 | 98.000 | C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C=O | 5g | 705364792
Apexbio Technology LLC Meglumine 6284-40-8 50g
Meglumine (6284-40-8) is an aminoglycoside derivative that exhibits anti-inflammatory and anti-tumor activity It is suggested to interfere with pro-inflammatory signaling pathways thereby modulating inflammatory responses Meglumine exerts its biological activity primarily through modulation of these pathways No specific cellular targets activity type key metrics or experimental models are reported Based on these pharmacological properties meglumine serves as a pharmaceutical excipient and is utilized in the synthesis of radiographic imaging agents (e g meglumine iohexol meglumine iopamidol) for diagnostic imaging and biomedical research
Medchemexpress LLC Mannose triflate | 92051-23-5 | 98.0% | 480.36 | 100 MG
Mannose triflate is a glucose analog that serves as a precursor for 18F-FDG synthesis, which is utilized in PET applications. It facilitates the binding to 18F through an SN2 nucleophilic substitution reaction and finds application as an imaging technique for the detection of cancer.
- Is a glucose analog
- Serves as a precursor for 18F-FDG synthesis for PET applications
- Binds to 18F via SN2 nucleophilic substitution reaction
- Can be used for an imaging technique in detection of cancer
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
Cayman Chemical NADHsodIum salt hydrate 500mg
The reduced form of nicotinamide adenine dinucleotide that can donate electrons as part of a reducing reaction
Medchemexpress LLC Fludarabine (phosphate) | 75607-67-9 | 99.8% | C10H13FN5O7P | 50 MG
Fludarabine phosphate is an analogue of adenosine and deoxyadenosine. It competes with dATP for incorporation into DNA and inhibits DNA synthesis. This compound significantly reduces cell viability in a dose-dependent manner.
- Competes with dATP for incorporation into DNA
- Inhibits DNA synthesis
- Significantly reduces cell viability in a dose-dependent manner
- Causes complete regression of D54 tumors in mice
- For research use only
Medchemexpress LLC Phosphocreatine disodium hydrate | 19333-65-4 | 99.57% | 100 MG
Phosphocreatine (disodium hydrate) is an organic compound naturally found in the skeletal muscles of vertebrates. It demonstrates several protective effects:
- Enhances antioxidant activity.
- Activates the TAK1 pathway to protect the heart.
- Normalizes mitochondrial function and reduces oxidative stress through the Akt-mediated Nrf2/HO-1 pathway.
- Provides renal protection by suppressing apoptosis and reactive oxygen species (ROS) generation via the ERK-mediated Nrf-2/HO-1 pathway.
Medchemexpress LLC Olsalazine Disodium | 6054-98-4 | 99.8% | 1 ML
Olsalazine Disodium is an orally active prodrug of 5-ASA. It can inhibit cell proliferation, induce apoptosis, reduce DAI and MPO activity, and inhibit inflammatory cytokine levels. This product is used in research for cancer, inflammation, and metabolic diseases, including colorectal cancer, inflammatory bowel disease (IBD), and hyperuricemia.
- Orally active prodrug of 5-ASA
- Inhibits cell proliferation
- Induces apoptosis
- Reduces DAI and MPO activity
- Inhibits inflammatory cytokine levels
- Used in research for cancer, inflammation, and metabolic diseases