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Filtered Search Results
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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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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eMolecules 1049744-31-1 | 4-(2-Aminoacetyl)-piperazine-1-carboxamide hydrochloride | Oakwood Chemical | MFCD06411635 | 222.670 | C7H15ClN4O2 | 98.000 | Cl.NCC(=O)N1CCN(CC1)C(N)=O | 1g | 537678525
4-(2-Aminoacetyl)-piperazine-1-carboxamide hydrochloride | Oakwood Chemical | 1049744-31-1 | MFCD06411635 | 222.670 | C7H15ClN4O2 | 98.000 | Cl.NCC(=O)N1CCN(CC1)C(N)=O | 1g | 537678525
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Medchemexpress LLC Piperazine erastin | 1538593-71-3 | 99.1% | 645.19 g·mol⁻¹ | C35H41ClN6O4 | 1 MG
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Piperazine erastin is a small-molecule analog of erastin that triggers an iron-dependent form of non-apoptotic cell death known as ferroptosis. It is provided as a research reagent for cellular and biochemical studies investigating ferroptosis mechanisms and cancer biology.
- Induces iron-dependent ferroptosis in cell-based assays
- Suitable for studies of ferroptosis pathways and cancer research
- High purity appropriate for in vitro experiments
- Offered in small solid and solution quantities for laboratory use
- Stable when stored according to recommended temperature conditions
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TARGETMOL CHEMICALS INC Alexidine dihydrochloride
Also available in 1 mL, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Alexidine dihydrochloride has antifungal and antibiofilm activity against a diverse range of fungal pathogens. Alexidine dihydrochloride is an anticancer agent that targets a mitochondrial tyrosine phosphatase, PTPMT1, in mammalian cells and causes mitochondrial apoptosis. Thus, Alexidine dihydrochloride has the potential to be developed as a pan-antifungal, antibiofilm drug. Purity 98.31%
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Apexbio Technology LLC ABT 702 dihydrochloride 1188890-28-9 10mg
ABT 702 dihydrochloride is a small-molecule inhibitor targeting adenosine kinase (AK) It is designed to inhibit AK the primary enzyme responsible for phosphorylation and metabolic inactivation of endogenous adenosine thereby elevating extracellular adenosine levels and modulating adenosine-mediated signaling ABT 702 dihydrochloride exerts its biological activity primarily through selective inhibition of AK In vitro studies indicate that ABT 702 potently inhibits AK activity and adenosine phosphorylation in intact cells Based on these pharmacological properties ABT 702 dihydrochloride holds research potential in inflammation and pain management particularly within experimental models of inflammatory and neuropathic pain
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Selleck Chemical LLC INCB059872 dihydrochloride
INCB059872 dihydrochloride is a potent selective and irreversible inhibitor of Lysine-Specific Demethylase 1(LSD1) It exhibits potential antineoplastic activity and can be used in acute myeloid leukemia (AML) research
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Aobchem 1-[2 4-Bis(1-methylethyl)phenyl]-2-methyl-1-propanone | 95% | CAS 140210-27-1 | C16H24O | 250mg
1-[2 4-Bis(1-methylethyl)phenyl]-2-methyl-1-propanone | 95% | CAS 140210-27-1 | C16H24O | 250mg
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Medchemexpress LLC N4-acetylsulfamethazine | 100-90-3 | >95.0% | 320.37 g/mol | C14H16N4O3S | 5 MG
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N4-Acetylsulfamethazine is the N4-acetylated metabolite of sulfamethazine supplied for research use as a reference standard and reagent for metabolic, residue, and analytical studies. The material is an off-white to light-yellow solid and should be stored at low temperatures to maintain stability.
- Serves as a metabolite reference for sulfamethazine in metabolic and residue studies.
- Suitable as an analytical standard for HPLC and mass spectrometry assays.
- Off-white to light-yellow solid for easy visual identification.
- Powder stable at -20°C for long-term storage.
- Available in small sample quantities for method development and validation.
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