Purine nucleotides
Medchemexpress LLC Adenosine dialdehyde | 34240-05-6 | MFCD00056960 | 99.0% | 265.23 g/mol | C10H11N5O4 | 10MM 1ML
Adenosine dialdehyde is a purine nucleoside analogue that potently inhibits S-adenosylhomocysteine hydrolase (SAHH). It is used in biochemical assays and cancer research to study methylation-dependent pathways and can be supplied as a 10 mM solution in DMSO or as solid analytical standards.
![Medchemexpress LLC 2-amino-9-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one | 26578-09-6 | MFCD00064103 | 98.0% | 283.24 | C10H13N5O5 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000221802.png-250.jpg)
Medchemexpress LLC 2-amino-9-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one | 26578-09-6 | MFCD00064103 | 98.0% | 283.24 | C10H13N5O5 | 5 MG
L-Guanosine is the L-enantiomer of the purine nucleoside guanosine, provided as a research-grade small molecule for biochemical and antiviral studies and for preparing supramolecular hydrogels. The material is characterized with defined physicochemical properties and recommended storage and handling conditions.
- High purity: 98.0%.
- Molecular formula: C10H13N5O5; molecular weight: 283.24.
- Soluble in DMSO: approximately 100 mg/mL; ultrasonic assistance may be required.
- Storage recommendations: store at 4°C; in solution store at -80°C for long-term or -20°C short-term.
- Common applications: antiviral research, nucleoside chemistry, and hydrogel formation studies.
Research Products International Corp Adenosine 1.5 KG
Substance Name: 9-β-D-Ribofuranosyladenine
CAS Number: 58-61-7
Molecular Formula: C10H13N5O4
Molecular Weight: 267.2
Apexbio Technology LLC 7-Deaza-ATP(Synonyms: 7-Deazaadenosine triphosphate, 7-Deaza-ATP, 7-Deazaadenosine-5'-triphosphate), 100ul (100 mM).
7-Deaza-ATP is a chemically modified ATP analog wherein the nitrogen atom at position 7 of the adenine ring is replaced by a carbon atom This structural alteration modulates its interactions with enzymes and nucleic acid-binding proteins As a nucleotide analog 7-Deaza-ATP can be incorporated into DNA and RNA strands thereby influencing polymerase enzyme activity and subsequently affecting nucleotide synthesis replication and repair processes Due to these properties this molecule is applied in investigating nucleotide-protein binding specificity and the catalytic mechanisms of enzymes facilitating research towards nucleotide-targeted therapeutic strategies
Apexbio Technology LLC GTP-Binding Protein Fragment, G alpha 10mg
GTP-Binding Protein Fragment G alpha is a peptide fragment derived from the amino-terminal region of the alpha subunit of GTP-binding proteins It is designed to aid in elucidating the mechanisms of membrane association and -subunit interactions in cell signaling pathways GTP-Binding Protein Fragment G alpha exerts its biological activity by retaining membrane-binding properties independent of the nucleotide-binding state anchoring the protein to the cytoplasmic membrane surface This peptide fragment serves as an experimental tool to study membrane-association mechanisms and signal transduction pathways in biochemical and biomedical research Based on these properties GTP-Binding Protein Fragment G alpha holds research potential in investigating the molecular basis of G protein-mediated signal transduction and protein-membrane interactions
Medchemexpress LLC Guanosine-15N5 | 99.6% | 288.21 | 1 MG
Guanosine-15N5 is an isotopically labeled form of Guanosine, where 15N (nitrogen-15) replaces the natural nitrogen atoms in the molecule. Guanosine is a purine nucleoside, formed by the attachment of guanine to a ribose sugar via a β-N9-glycosidic bond. This compound is primarily intended for research purposes.
- 15N labeled compound
- Purine nucleoside
- Formed from guanine and ribose
- Possesses anti-HSV activity
- Suitable for research applications
Medchemexpress LLC 6-O-Methyl Guanosine | 7803-88-5 | 99.7% | 297.27 | 10 MG
6-O-Methyl Guanosine is a modified nucleoside that inhibits colony-forming ability in a malignant xeroderma pigmentosum cell line.
- Functions as a modified nucleoside
- Exhibits inhibition of colony-forming ability
- Relevant for nucleoside antimetabolite/analog research
Medchemexpress LLC Adenosine-13C10,15N5 | 202406-75-5 | MFCD28458760 | >98% | 25 MG
Adenosine-13C10,15N5 is a labeled adenosine, an endogenous purine nucleoside that acts as an important homeostatic regulator of physiological function and an anti-arrhythmic agent.
- Labeled adenosine
- Endogenous purine nucleoside
- Acts as an important homeostatic regulator of physiological function
- Functions as an anti-arrhythmic agent
- Modulates various physiological processes
- Activates G protein-coupled receptors (GPCRs), including adenosine receptors (ARs)
- Involved in energy metabolism
- Used in research for various diseases
Medchemexpress LLC Adenosine 2',3'-cyclic phosphate sodium | 37063-35-7 | 99.1% | 351.19 | 5 MG
Adenosine 2',3'-cyclic phosphate sodium is a 2',3'-cyclic purine nucleotide. It is deaminated by adenosine deaminase and can be degraded to 2'-AMP and 3'-AMP.
- Efficiently hydrolyzed by the monocations of alkylenediamines at pH 9.0, 50°C.
- Deaminated by adenosine deaminase from Drosophila larvae.
Medchemexpress LLC Adenosine amine congener (ADAC) | 96760-69-9 | 99.23% | 25 MG
Adenosine amine congener (ADAC) is a selective A1 adenosine receptor agonist. It can ameliorate noise- and cisplatin-induced cochlear injury and demonstrates neuroprotective effects.
- Selective A1 adenosine receptor agonist
- Ameliorates noise- and cisplatin-induced cochlear injury
- Has neuroprotective effects
- Reduces oxidative stress in noise-exposed cochlea
- Protects sensory hair cells
- Reduces cisplatin-induced apoptosis in cochlear tissues
- Inhibits glutamate release via presynaptic A1 receptors
- Inhibits voltage-gated Ca2+ channels
- Mitigates noise-induced hearing loss in a dose- and time-dependent manner
Medchemexpress LLC Guanosine 5'-triphosphate trisodium salt hydrate | 207300-85-4 | 95.0% | 200 MG
Guanosine 5'-triphosphate trisodium salt hydrate is an activator of the signal transducing G proteins. It also serves as an energy-rich precursor of mononucleotide units in the enzymatic biosynthesis of DNA and RNA. The chemical formula is C10H13N5Na3O14P3·xH2O and it appears as a white to off-white solid.
- Activator of signal transducing G proteins
- Energy-rich precursor of mononucleotide units
- Involved in enzymatic biosynthesis of DNA and RNA
- Appears as a white to off-white solid
Medchemexpress LLC GTP-14564 | 34823-86-4 | 99.9% | 234.25 | 100 MG
GTP-14564 is a tyrosine kinase inhibitor that targets internal tandem duplication (ITD) and FLT3. It inhibits FLT3 ligand-dependent growth in Ba/F3 leukemia cells.
- Tyrosine kinase inhibitor
- Targets internal tandem duplication (ITD) and FLT3
- Inhibits FLT3 ligand-dependent growth in Ba/F3 leukemia cells
- For research use only
Medchemexpress LLC TNP-ATP triethylammonium | 61368-63-6 | 98.7% | 1123.03 | 50 MG
TNP-ATP triethylammonium is a selective P2X receptor antagonist. It shows antinociceptive effects in rats. For research use only. We do not sell to patients.
- Selective P2X receptor antagonist.
- Exhibits antinociceptive effects in rats.
- High purity for reliable research.
- Suitable for in vitro and in vivo studies.
- Available in a convenient 1 MG quantity.
Medchemexpress LLC GTP-14564 | 34823-86-4 | 99.9% | 234.25 | 50 MG
GTP-14564 is a tyrosine kinase inhibitor that targets internal tandem duplication (ITD) and FLT3. It inhibits FLT3 ligand-dependent growth in Ba/F3 leukemia cells. It is a potential research tool for studying FLT3-related leukemia.
- Tyrosine kinase inhibitor
- Targets internal tandem duplication (ITD)
- Targets FLT3
- Inhibits FLT3 ligand-dependent growth in Ba/F3 leukemia cells
- Appearance: solid
- Color: off-white to yellow