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Filtered Search Results
Aobchem 4-Ethoxycarbonyl-2-methoxyphenylboronic acid | ≥97% | CAS 603122-86-7 | C10H13BO5 | 10g
4-Ethoxycarbonyl-2-methoxyphenylboronic acid | ≥97% | CAS 603122-86-7 | C10H13BO5 | 10g
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Aobchem 1-Methylethyl 2-cyano-3-(4-fluorophenyl)-2-propenoate | 95% | CAS 328262-43-7 | C13H12FNO2 | 5g
1-Methylethyl 2-cyano-3-(4-fluorophenyl)-2-propenoate | 95% | CAS 328262-43-7 | C13H12FNO2 | 5g
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Aobchem 1-Methylethyl 2-cyano-3-(4-fluorophenyl)-2-propenoate | 95% | CAS 328262-43-7 | C13H12FNO2 | 1g
1-Methylethyl 2-cyano-3-(4-fluorophenyl)-2-propenoate | 95% | CAS 328262-43-7 | C13H12FNO2 | 1g
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Aobchem 2-(1-Methylethyl)-1 1 -biphenyl | 95% | CAS 19486-60-3 | C15H16 | 500mg
2-(1-Methylethyl)-1 1 -biphenyl | 95% | CAS 19486-60-3 | C15H16 | 500mg
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Aobchem 3 4-Dichloro-N-(1-methylethyl)benzenesulfonamide | 95% | CAS 28298-41-1 | C9H11Cl2NO2S | 500mg
3 4-Dichloro-N-(1-methylethyl)benzenesulfonamide | 95% | CAS 28298-41-1 | C9H11Cl2NO2S | 500mg
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Apexbio Technology LLC nor-Binaltorphimine dihydrochloride 113158-34-2 50mg
nor-Binaltorphimine dihydrochloride (CAS 113158-34-2) is a highly selective antagonist of the -opioid receptor By inhibiting -opioid receptor-mediated signaling pathways this compound modulates processes such as nociceptive transmission and regulation of affective states Its selectivity enables precise investigation of -opioid receptor function in experimental models nor-Binaltorphimine dihydrochloride is widely utilized in pain research and neuroscience to elucidate the physiological and behavioral roles of -opioid receptor signaling
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Apexbio Technology LLC IT1t dihydrochloride 1092776-63-0 5mg
IT1t dihydrochloride (CAS 1092776-63-0) is a small-molecule antagonist targeting the chemokine receptor CXCR4 It is designed to inhibit CXCR4-mediated signaling by disrupting interactions with its natural ligand CXCL12 as well as the HIV envelope protein gp120 thereby interfering with cellular chemotaxis and viral entry mechanisms IT1t dihydrochloride exerts its biological activity primarily by antagonizing CXCR4 to inhibit receptor-mediated Ca2 mobilization and virus attachment In in vitro assays IT1t dihydrochloride demonstrates potent inhibition with IC50 values of approximately 8 nM in human CXCR4 receptor binding assays 1 1 nM in Ca2 mobilization assays and 7 nM in HIV attachment assays Based on these pharmacological properties IT1t dihydrochloride holds research potential in CXCR4-related signaling and HIV entry studies
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TARGETMOL CHEMICALS INC Fluphenazine dihydrochloride
Also available in 1 mL, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Fluphenazine dihydrochloride (Prolixin) is an inhibitor of phenothiazine-class D1DR and D2DR; In studies, Fluphenazine can be used to probe the effects and metabolic process of this commonly used dopamine antagonist. Purity 100%
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Selleck Chemical LLC Y-39983 Dihydrochloride
Y-39983 (Y-33075)Dihydrochloride is a selective rho-associated protein kinase(ROCK) inhibitor with an IC50 of 3 6 nM
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Selleck Chemical LLC Vanoxerine dihydrochloride
Vanoxerine (GBR-12909) is a potent and selective inhibitor of the presynaptic dopamine uptake complex
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Selleck Chemical LLC Trimetazidine dihydrochloride S4543-500mg
Trimetazidine dihydrochloride (Yoshimilon Kyurinett Vastarel F) is a kind of drug for treatment of chronic ischemic disorders It improves myocardial glucose utilization through inhibition of fatty acid metabolism known as fatty acid oxidation inhibitor
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Medchemexpress LLC Pyridinium, 3-carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)-, inner salt (triethylamine) | 321-02-8 | 99.9% | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Nicotinic acid mononucleotide (NAM) acts as a SARM1 inhibitor and an intermediate in NAD+ biosynthesis, with an IC50 value of 93.3 μM against SARM1. It is intended for research use only.
- Acts as an allosteric SARM1 inhibitor.
- Plays a role in the biosynthesis of NAD+.
- Exerts protective effects on axons and delays axonal degeneration.
- Increases NAD+ levels in the body.
- Boosts the activity of Sirt1.
- Improves myocardial capillary density and alleviates myocardial fibrosis.
- Reverses diabetic cardiomyopathy in diabetic mice by increasing myocardial NAD+ levels.
- Applicable for research related to cancer, multiple sclerosis, diabetic cardiomyopathy, neurodegenerative diseases, and Huntington's disease.
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Apexbio Technology LLC N4-Methyl-dCTP(Synonyms: N4-Methyl-2'-deoxycytidine-5'-triphosphate, N4-Me-dCTP, 4-Methyl-dCTP), 100ul (100 mM).
N4-Methyl-dCTP is a cytosine-derived modified deoxynucleoside triphosphate capable of being enzymatically incorporated into DNA strands thereby introducing cytosine methylation modifications at specific genomic sites DNA methylation at the N4 position of cytosine is observed naturally across both prokaryotic and eukaryotic organisms and influences processes such as epigenetic gene expression regulation DNA replication and DNA damage repair Researchers use N4-Methyl-dCTP to incorporate defined methylation modifications enabling investigation into methylation-specific DNA-binding protein interactions DNA methylation patterning analyses and functional studies of epigenetic modification pathways
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eMolecules 134526-69-5 | (R)-2-Formyl-piperidine-1-carboxylic acid tert-butyl ester | J & W PharmLab LLC | MFCD06738714 | 213.277 | C11H19NO3 | 96.000 | CC(C)(C)OC(=O)N1CCCC[C@@H]1C=O | 1g | 525311286
(R)-2-Formyl-piperidine-1-carboxylic acid tert-butyl ester | J & W PharmLab LLC | 134526-69-5 | MFCD06738714 | 213.277 | C11H19NO3 | 96.000 | CC(C)(C)OC(=O)N1CCCC[C@@H]1C=O | 1g | 525311286
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TARGETMOL CHEMICALS INC Dilazep dihydrochloride 25MG
Also available in 1 mL, 5 mg, 10 mg, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Dilazep dihydrochloride is an adenosine uptake inhibitor. Dilazep dihydrochloride also inhibits the ischemic damage, membrane transport of nucleosides and platelet aggregation. Dilazep dihydrochloride has cerebral and coronary vasodilating action through enhancement of effect of adenosine. Purity 99.72%
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