Nucleic Acid Synthesis
Sigma Aldrich Fine Chemicals Biosciences 3 2 CGAMP DISODIUM ADEN 05UMOL
NC3875528 3 2 CGAMP DISODIUM ADEN 05UMOL
Bioss KD-Validated CTP synthase 1 Ra
CTP Synthase 1 Primary Antibody Unconjugated Public Immunogen Range 250-300/591 Host Species Rabbit Target Species Human Mouse Rat Clonality Monoclonal Applications WB FCM IC Concentration Lot dependent Size 50 ul Storage Buffer Supplied in PBS (pH 7 4) containing 50% glycerol and 0 02% sodium azide
Cayman Chemical AdenosIn 5-dIphosphate 250mg
A central component of energy storage, metabolism, and signal transduction in vivo; a precursor for ATP and agonist of purinergic receptors
Medchemexpress LLC Thymidine 5'-monophosphate-13C10,15N2 dilithium | 2483830-49-3 | 99.9% | 345.99 | 13C10H13Li215N2O8P | 10 MG
Thymidine 5'-monophosphate-13C10,15N2 dilithium is an isotopically labeled nucleotide provided as a concentrated solution. It carries uniform 13C and 15N labeling on the thymidine moiety and is used as a reference standard and tracer for analytical and structural studies in biochemical research.
- Isotopically labeled with 13C10 and 15N2.
- Provided as dilithium salt solution, colorless to light yellow.
- High purity: 99.9% suitable for analytical applications.
- Molecular weight 345.99 and CAS 2483830-49-3 for unambiguous identification.
- Packaged as a concentrated solution for convenient experimental use.
eMolecules Broadpharm / 2-Deoxycytidine-5-monophosphate disodium salt / 1g / 761707650 / BP-58813 / / 13085-50-2 / MFCD00672270 / 351.162 / C9H12N3Na2O7P
Broadpharm / 2-Deoxycytidine-5-monophosphate disodium salt / 1g / 761707650 / BP-58813 / / 13085-50-2 / MFCD00672270 / 351.162 / C9H12N3Na2O7P
Sigma Aldrich Fine Chemicals Biosciences Thymidine 5'-triphosphate sodium salt >=96% | 18423-43-3 | MFCD00080338 | 10MG
Thymidine 5'-triphosphate sodium salt >=96% | Purity: >=96% | Mol Wt: 504.15 | 18423-43-3 | MFCD00080338 | 10MG
Medchemexpress LLC 7-TFA-ap-7-Deaza-dG | 666847-77-4 | 98.0% | 415.32 g/mol | C16H16F3N5O5 | 5 MG
7-TFA-ap-7-Deaza-dG is a modified nucleoside (7-trifluoroacetyl 7-deaza-2'-deoxyguanosine) designed as a clickable building block for DNA and RNA synthesis and modification. It is provided in solid and solution formats and is accompanied by analytical documents (data sheet, COA, H NMR, RP-HPLC, MS, and SDS) to support research use.
- Contains an alkyne group enabling copper-catalyzed azide-alkyne cycloaddition (CuAAC).
- High reported purity for reproducible experimental results.
- Available in multiple formats, including small-scale solid and ready-to-use solutions.
- Comes with analytical documentation to verify identity and quality.
- Suitable as a building block or analogue in nucleic acid chemistry and click chemistry workflows.
Medchemexpress LLC Ninerafaxstat (trihydrochloride) | 2311824-72-1 | 99.7% | 524.9 g/mol | C22H32Cl3N3O5 | 5 MG
Ninerafaxstat trihydrochloride is a research small-molecule salt investigated as a cardiac mitochondrial agent. It is provided for laboratory and preclinical studies and is supplied in solid and solution formats with accompanying analytical documentation.
- Trihydrochloride salt form for improved stability and solubility.
- Molecular weight 524.9 g/mol; CAS 2311824-72-1.
- High purity (99.7%).
- Available as solid vials (e.g., 5 mg) and solution (10 mM in DMSO).
- Supplied with datasheet, COA, and SDS for traceability.
- Intended for research use only; not for human therapeutic use.
eMolecules Ambeed / 25-Dioxopyrrolidin-1-yl hept-6-ynoate / 250mg / 642079699 / A1161129 / / 917222-23-2 / MFCD29041721 / 223.228 / C11H13NO4
Ambeed / 25-Dioxopyrrolidin-1-yl hept-6-ynoate / 250mg / 642079699 / A1161129 / / 917222-23-2 / MFCD29041721 / 223.228 / C11H13NO4
![Medchemexpress LLC 4-chloro-3-[[(3-nitrophenyl)amino]sulfonyl]-benzoic acid | 412940-35-3 | MFCD01122300 | 98.0% | 356.74 g·mol⁻¹ | C13H9ClN2O6S | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000248615.png-250.jpg)
Medchemexpress LLC 4-chloro-3-[[(3-nitrophenyl)amino]sulfonyl]-benzoic acid | 412940-35-3 | MFCD01122300 | 98.0% | 356.74 g·mol⁻¹ | C13H9ClN2O6S | 10 MG
CTP inhibitor (Compound 792949) is a potent, selective inhibitor of citrate transport proteins (CTP/PMCT) used in biochemical research to investigate citrate transport and related metabolic pathways. The compound is supplied at high purity as a solid and is also available as a DMSO solution for in vitro experiments. For research use only.
- Potent, selective inhibition of citrate transport proteins.
- High purity appropriate for biochemical assays.
- Available in multiple milligram quantities and as a DMSO solution.
- Useful for studies of citrate transport and metabolic pathways.
- Provided for research use only; not for human consumption.
![Biolegend APC/Fire™ 750 anti-GATA3 [W19195B]; Isotype: Rat IgG2a, κ; Reactivity: Human, Mouse; Apps: ICFC; Size: 100 tests](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502567149.png-250.jpg)
Biolegend APC/Fire™ 750 anti-GATA3 [W19195B]; Isotype: Rat IgG2a, κ; Reactivity: Human, Mouse; Apps: ICFC; Size: 100 tests
APC/Fire™ 750 anti-GATA3 [W19195B]; Isotype: Rat IgG2a, κ; Reactivity: Human, Mouse; Apps: ICFC; Size: 100 tests
Cayman Chemical N6 N6-DImethyladenosIn 1g
A modified nucleoside; has been found in tRNA isolated from M. bovis; dimethylation of adjacent adenosine nucleosides is found in E. coli 16S rRNA and is important for the initiation of protein synthesis; inhibits the proliferation of L1210 leukemia cells in vitro (IC50 = 0.5 UG/ml) but does not have antitumor activity in vivo; a component of puromycin
Cayman Chemical NIcotInamIde 25mg
An amide form of niacin; precursor in the synthesis of the metabolic cofactor NAD+; an inhibitor of SIRT1 (IC50 = <50 µM); increases SPT activity and the biosynthesis of ceramide glucosylceramide, sphingomyelin, free fatty acids, and cholesterol in primary human keratinocytes at 10 µM; induces apoptosis in SNU-398, SNU-739, and HepG2 cells at 40 µM; prevents the formation of neoplastic lesions in a diethylnitrosamine-induced mouse model of HCC
Medchemexpress LLC Ctp inhibitor (compound 792949) | 412940-35-3 | MFCD00682824 | 98.0% | 356.74 g/mol | C13H9ClN2O6S | 50 MG
CTP inhibitor (Compound 792949) is a potent and selective inhibitor of the mitochondrial citrate transport protein (CTP). It reduces CTP activity while showing minimal inhibition of the plasma membrane citrate transporter (PMCT), and is supplied as an off-white to light yellow solid for research applications.
- Potent and selective inhibition of mitochondrial citrate transport protein (CTP).
- Minimal activity against plasma membrane citrate transporter (PMCT) at tested concentrations.
- High purity (98.0%).
- Molecular weight 356.74 g/mol.
- Available in multiple sizes, including 50 MG and DMSO solution formats.
- Off-white to light yellow solid appearance.
- Storage recommendations: 4°C protected from light; in solvent -80°C (6 months), -20°C (1 month).
- Intended for in vitro research use.