Nucleosides and Analogues
Medchemexpress LLC Uridine 3',5'-diphosphate | 2922-95-4 | 99.7% | 404.16 g/mol | C9H14N2O12P2 | 10 MG
Uridine 3',5'-diphosphate is a nucleotide derivative used as a competitive RNase inhibitor in biochemical research. It is supplied as a powdered reagent for laboratory use and is intended for research purposes only. Key chemical identifiers include CAS 2922-95-4, molecular formula C9H14N2O12P2, and molecular weight 404.16 g/mol.
- High purity (99.65%).
- Powder form suitable for long-term storage.
- Stable at -20°C for extended storage; in solvent stability guidelines available.
- Functionally used as a competitive RNase inhibitor in biochemical assays.
- Well-characterized molecular identity for reproducible research results.
- Intended for research use only; not for clinical or human use.
Apexbio Technology LLC Lamivudine 134678-17-4 50mg
Lamivudine is a nucleoside analog that acts primarily as a reverse transcriptase inhibitor disrupting viral replication by interfering with RNA-dependent DNA polymerase activity It inhibits human immunodeficiency virus type 1 (HIV-1) reverse transcriptase with an IC50 value of approximately 0 316 M Lamivudine also suppresses replication of simian retrovirus (SRV-1 and SRV-2) while exhibiting negligible activity on foamy viruses and amphotropic murine leukemia virus (MLV-A) Due to its antiviral mechanism and dual inhibitory effect against both HIV-1 and hepatitis B virus (HBV) lamivudine is frequently utilized in research involving retroviral infection models particularly HIV-1 and HBV coinfection studies to evaluate viral dynamics antiviral efficacy and biochemical responses
Medchemexpress LLC BRM/BRG1 ATP Inhibitor-2 | 2368900-77-8 | 99.7% | C₂₀H₂₀N₄O₂S₂ | 25 MG
BRM/BRG1 ATP Inhibitor-2 is a BRG1/BRM ATPase inhibitor for the research of BAF-related disorders. This product is intended for research use only and not for sale to patients.
- BRG1/BRM ATPase inhibitor
- Used for research of BAF-related disorders
- Targets epigenetic reader domain
- Involved in epigenetics pathway
Apexbio Technology LLC 7-Deaza-ATP(Synonyms: 7-Deazaadenosine triphosphate, 7-Deaza-ATP, 7-Deazaadenosine-5'-triphosphate), 50ul (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
Medchemexpress LLC Nicotinamide riboside-d4 (triflate) | 98.0% | 408.34 | C12H11D4F3N2O8S | 1mg
Nicotinamide riboside-d4 (triflate) (Nicotinamide riboside-d4 triflate (d3-major)a/b mixture) is deuterium labeled Nicotinamide riboside (triflate)[1]
Medchemexpress LLC D-glucosamine 6-phosphate sodium | 70442-23-8 | MFCD00069826 | 99.9% | 281.13 | C6H13NNaO8P | 10mg
D-Glucosamine 6-phosphate (sodium) (GlcN6P-Na) is a class of biochemical reagents used in glycobiology research Glycobiology studies the structure synthesis biology and evolution of sugars It involves carbohydrate chemistry enzymology of glycan formation and degradation protein-glycan recognition and the role of glycans in biological systems This field is closely related to basic research biomedicine and biotechnology[1]
TARGETMOL CHEMICALS INC ADENOSINE AMINE CONGENER 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Adenosine amine congener (ADAC) (ADAC) is an agonist of selective A1 adenosine receptor. purity: 98%
Medchemexpress LLC D-Glucosamine 6-phosphate | 3616-42-0 | 259.15 | 100 MG
D-Glucosamine 6-phosphate is an endogenous metabolite that can be synthesized by glutamine fructose-6-phosphate amidotransferase (GFAT). It can be used for the research of diabetes mellitus and is for research use only.
- Endogenous metabolite
- Synthesized by glutamine fructose-6-phosphate amidotransferase (GFAT)
- Used for the research of diabetes mellitus
- Purity: 99.97%
- Appearance: solid
- Color: white to off-white
- Structure classification: saccharides, monosaccharides
- Initial source: endogenous metabolite, human gut microbiota metabolites
- Solubility in vitro: H2O : 125 mg/mL (482.35 mM; need ultrasonic)
Medchemexpress LLC D-Glucosamine 6-phosphate | 3616-42-0 | 259.15 | 50 MG
D-Glucosamine 6-phosphate is an endogenous metabolite that can be synthesized by glutamine fructose-6-phosphate amidotransferase (GFAT). It is utilized for research into diabetes mellitus.
- Endogenous metabolite
- Synthesized by glutamine fructose-6-phosphate amidotransferase (GFAT)
- Applicable for research of diabetes mellitus
- Molecular weight of 259.15
- Chemical formula is C6H14NO8P
- CAS number is 3616-42-0
- Appears as a white to off-white solid
- High purity of 99.97%
- Soluble in H2O at 125 mg/mL
- Store at -20°C, sealed, away from moisture and light
Biotium Primary Antibody CA15 3 CD227 EMA MUC1 VU-4H5 CF740 1/EA
MAb VU-4H5 reacts with MUC1 a large transmembrane glycoprotein expressed on the ductal surface of normal glandular epithelia The dominant epitope of MAb VU4H5 is APDTR as established with epitope fingerprinting VU-4H5 preferentially binds to under-glycosylated tumor MUC1 The extracellular domain of MUC1 largely consists of a highly conserved O-glycosylated 20 amino acids tandem repeat which can occur 30-100 times per molecule depending on the length of the allele involved In the vast majority of human carcinomas this protein is upregulated and poorly glycosylated and appears on the cell surface in a non-polarized fashion Antibody to EMA is useful as a pan-epithelial marker for detecting early metastatic loci of carcinoma in bone marrow or liver
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
TARGETMOL CHEMICALS INC ADENOSINE DIALDEHYDE ADO 50MG
Also available in 5 mg 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Adenosine Dialdehyde (Periodate-oxidized adenosine) is a purine nucleoside analogue. Adenosine Dialdehyde is a potent inhibitor of S-Adenosylhomocysteine hydrolase (SAHH) (Ki=3.3 nM). Adenosine Dialdehyde exhibits potent anti-tumor activity in vivo. purity: 95%
eMolecules Combi-Blocks Nicotinamide 1kg 457916668 NA-0257 98 000 98-92-0 MFCD00006395 122 127 C6H6N2O
Combi-Blocks Nicotinamide 1kg 457916668 NA-0257 98 000 98-92-0 MFCD00006395 122 127 C6H6N2O