Nucleosides and Analogues
Sigma Aldrich Fine Chemicals Biosciences Adenosine 15N5 5 diphospha10MG
Adenosine 15N5 5 diphospha10MG
Medchemexpress LLC Adenosine antagonist-1 | 431040-19-6 | 99.8% | 359.41 g/mol | C18H13N7S | 50 MG
Adenosine antagonist-1 is a research-grade small molecule that acts as a selective adenosine A3 receptor (A3R) antagonist with reported anti-inflammatory activity. It is provided in solid and solution formats with analytical characterization suitable for in vitro pharmacology and receptor signaling studies.
- Adenosine A3 receptor (A3R) antagonist.
- Demonstrated anti-inflammatory activity.
- High purity suitable for research applications (99.79%).
- Molecular formula C18H13N7S and molecular weight 359.41 g/mol.
- Available as solid and DMSO solution formats for flexible dosing.
- Supplied for research use only; not for human use.
Medchemexpress LLC Adenosine 3',5'-diphosphate disodium | 75431-54-8 | 99.1% | 471.16 | 1 MG
Adenosine 3',5'-diphosphate disodium is an hydroxysteroid sulfotransferases inhibitor. It is for research use only and not sold to patients.
- Hydroxysteroid sulfotransferases inhibitor
- For research use only
- Not sold to patients
- Soluble in H2O at ≥ 25 mg/mL (53.06 mM)
- Store at -20°C, sealed, away from moisture
- In solvent, store at -80°C (6 months) or -20°C (1 month), sealed, away from moisture
Medchemexpress LLC Adenosine, 1-oxide | 146-92-9 | MFCD00037993 | 99.5% | 283.24 g/mol | C10H13N5O5 | 25 MG
Adenosine N1-oxide is a nucleoside derivative used in research as an orally active anti-inflammatory agent. It has been reported to promote osteogenic and adipocyte differentiation and is supplied as a purified research-grade solid with supporting documentation (COA, SDS).
- CAS 146-92-9
- Molecular formula C10H13N5O5
- Molecular weight 283.24 g/mol
- Purity 99.50%
- Available in small vial sizes for research use (e.g., 1-25 mg)
- Documentation: certificate of analysis and safety data sheet available
Medchemexpress LLC L-adenosine | 3080-29-3 | MFCD01075784 | 99.8% | 267.24 g/mol | C10H13N5O4 | 50 MG
L-adenosine is an enantiomeric analog of adenosine used as a research reagent and a weak adenosine deaminase (ADA) inhibitor (reported Ki = 385 μM). It is supplied as a high-purity solid for studies of adenosine uptake, accumulation, and ADA-related metabolism.
- High purity - 99.82% (reported).
- Suitable for adenosine uptake and accumulation studies.
- Weak ADA inhibitor (Ki ≈ 385 μM).
- Available as a 50 MG solid; additional pack sizes and DMSO solutions are offered.
- Molecular weight 267.24 g/mol; formula C10H13N5O4.
Apexbio Technology LLC Adenosine 5-triphosphate 34369-07-8 500mg
Adenosine 5-triphosphate (ATP CAS 34369-07-8) also known as ATP disodium salt hydrate is a nucleotide central to cellular energy transfer It functions as the primary intracellular energy carrier undergoing hydrolysis to release energy required for numerous biochemical processes including muscle contraction signal transduction and biosynthetic reactions ATP also serves as a substrate for kinases in phosphorylation events and plays a regulatory role in purinergic signaling pathways In biomedical research ATP is widely used to study cellular metabolism enzyme activities and receptor-mediated responses
Medchemexpress LLC Adenosine receptor inhibitor 2 | 2550401-76-6 | 99.1% | 406.28 | 1 MG
This compound is a potent adenosine receptor (AR) inhibitor, demonstrating dual affinity for A1 and A2A ARs. It exhibits higher affinity for the A1AR compared to the A2AAR.
- Potent AR inhibitor
- Dual affinity for A1 and A2A ARs
- Ki values: 52.2 nM for A1AR and 167 nM for A2AAR
- For research use only
Medchemexpress LLC Kinetin triphosphate tetrasodium | 00-00-0 | 99.9% | C15H16N5Na4O14P3 | 10MG
Kinetin triphosphate tetrasodium is an ATP analogue used in biochemical and kinase research, including investigations of mitochondrial quality control pathways. It is supplied as a tetrasodium salt in small milligram quantities and includes documentation for experimental use and handling.
- ATP analogue for kinase and enzymology assays.
- High purity (99.92%) suitable for sensitive biochemical studies.
- Soluble in water with recommended reconstitution guidance (100 mM preparations).
- Provided in small research quantities for experimental flexibility.
- Documentation includes datasheet, certificate of analysis, and safety data sheet.
Medchemexpress LLC Guanosine, 6-O-methyl- | 7803-88-5 | 99.7% | 297.27 | 25 MG
6-O-Methyl Guanosine is identified as a modified nucleoside. Research indicates its capacity to inhibit the colony-forming ability in a malignant xeroderma pigmentosum cell line, suggesting potential applications in cell biology studies related to cell proliferation and specific genetic disorders. This modified nucleoside provides a tool for investigating cellular mechanisms and could contribute to understanding pathways involved in malignancy.
- Modified nucleoside.
- Inhibits colony-forming ability in a malignant xeroderma pigmentosum cell line.
Medchemexpress LLC ATP-Red 1 | 1847485-97-5 | 561.48 | 25 MG
ATP-Red 1 is a multisite-binding switchable fluorescent probe that selectively and rapidly responds to intracellular concentrations of ATP in living cells.
- Multisite-binding switchable fluorescent probe
- Selectively and rapidly responds to intracellular concentrations of ATP in living cells
- Excitation/Emission wavelengths (Ex/Em) = 510/590 nm
Revvity Health Sciences Inc HTRF Human & Mouse Phospho-RSK1 (Thr359/Ser363) Detection Kit, 500 Assay Points
HTRF Human & Mouse Phospho-RSK1 (Thr359/Ser363) Detection Kit, 500 Assay Points
Medchemexpress LLC 7-Methyl-guanosine-5'-triphosphate sodium (m7GTP sodium) | 50 MG
7-Methyl-guanosine-5'-triphosphate (m7GTP) sodium is a guanosine 5'-phosphate.
- Potent cap-dependent translation inhibitor.
Medchemexpress LLC Guanosine 5'-diphosphate sodium | 43139-22-6 | 99.9% | 465.18 | 100 MG
Guanosine 5'-diphosphate (GDP) sodium, 96% (HPLC), is a nucleoside diphosphate that activates the adenosine 5'-triphosphate-sensitive K+ channel. It functions as an iron mobilizer by forming a complex with hepcidin, thereby inhibiting the hepcidin-ferroportin (FPN) interaction and modulating the IL-6/stat-3 pathway. This compound can ameliorate Turpentine-induced anemia of inflammation (AI) in mice when combined with FeSO4 and is suitable for AI research.
- Activates adenosine 5'-triphosphate-sensitive K+ channel.
- Functions as an iron mobilizer.
- Inhibits hepcidin-ferroportin interaction.
- Modulates the IL-6/stat-3 pathway.
- Ameliorates Turpentine-induced anemia of inflammation (AI) in mice when combined with FeSO4.
- Suitable for research applications.