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Filtered Search Results
Medchemexpress LLC Histone H4 Human/Xe 500ug
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Histone H4 proteins are core components of nucleosomes which compact DNA into chromatin and regulate DNA accessibility during cellular processes Histones including H4 play critical roles in transcriptional regulation DNA repair replication and chromosome stability Histone H4 Protein Human/Xenopus laevis is the recombinant Xenopus laevis-derived Histone H4 protein expressed by E coli with tag free
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Apexbio Technology LLC Phytic acid 83-86-3 250mg
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Phytic acid (CAS 83-86-3) is a naturally occurring polyphosphorylated carbohydrate predominantly isolated from plant seeds It functions as a chelating agent binding mineral ions such as iron and calcium thereby modulating their bioavailability Through its antioxidant properties and regulation of cellular signaling pathways phytic acid is investigated for roles in cell proliferation apoptosis and metabolism Its utility extends to studies on mineral absorption cancer biology and oxidative stress The compound is soluble in water ethanol and acetone and it should be stored in a tightly sealed container under cool dry conditions to maintain stability
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eMolecules Ambeed / 1H-Benzo[d]imidazole-5-carboxylic acid / 1g / 525056506 / A145671 / / 15788-16-6 / MFCD00011555 / 162.148 / C8H6N2O2
Ambeed / 1H-Benzo[d]imidazole-5-carboxylic acid / 1g / 525056506 / A145671 / / 15788-16-6 / MFCD00011555 / 162.148 / C8H6N2O2
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Medchemexpress LLC HOOC-PEG-SH MW 2000 250mg
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HOOC-PEG-SH (MW 2000) (HOOC-PEG-Thiol (MW 2000)) is a reactive thiol PEG derivative with a terminal carboxyl group The carboxyl group can react with amine or hydroxyl groups to form a stable amide bond or an unstable ester bond The PEG linkage between the thiol and carboxyl groups has good water solubility flexible linker distance and higher stability[1]
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eMolecules Ambeed 2-Methoxyacetimidamide hydrochloride 250mg 521408831 A151005 0 000 1903-91-9 MFCD08752294 124 570 C3H9ClN2O
Ambeed 2-Methoxyacetimidamide hydrochloride 250mg 521408831 A151005 0 000 1903-91-9 MFCD08752294 124 570 C3H9ClN2O
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Medchemexpress LLC 4-dimethylaminopyridine N-oxide | 1005-31-8 | MFCD00143310 | 98.0% | 138.17 g/mol | C7H10N2O | 250 MG
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4-Dimethylaminopyridine N-oxide is an oxidizing reagent used in organic synthesis, particularly for the oxidation of alkyl halides. It is supplied as a solid, research-grade chemical (CAS 1005-31-8) with a molecular weight of 138.17 g/mol and is intended for laboratory research and method development.
- Efficient oxidant for alkyl halides
- Solid form suitable for bench-scale handling
- Available in small pack sizes for research use
- Commonly used in synthetic method development
- Provided for research use only
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eMolecules Ambeed 6-(Trifluoromethoxy)pyridin-3-amine 250mg 570568388 A195888 0 000 135900-33-3 MFCD07374879 178 114 C6H5F3N2O
Ambeed 6-(Trifluoromethoxy)pyridin-3-amine 250mg 570568388 A195888 0 000 135900-33-3 MFCD07374879 178 114 C6H5F3N2O
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Apexbio Technology LLC Pimozide 2062-78-4 250mg
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Pimozide (CAS 2062-78-4) is a small-molecule antagonist targeting dopamine receptors including D2 D3 and D4 subtypes It is designed to inhibit dopamine receptor signaling thereby modulating dopaminergic pathways Pimozide exerts its biological activity primarily through antagonistic binding to dopamine receptors It demonstrates inhibition with Ki values of approximately 2 4 nM (D2) 0 2 nM (D3) and 1 8 nM (D4) In animal studies administration of pimozide reduced dopamine-driven behaviors such as food-motivated activity and cocaine reinforcement Based on these pharmacological properties pimozide holds research potential in neurological and psychiatric disorders including schizophrenia Tourette s syndrome dopamine-related motor disorders and delusional psychosis
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Apexbio Technology LLC CJ-42794(Synonyms: CJ42794, CJ 42794, CJ-42794, EP4 antagonist CJ-42794, CAS 847728-01-2), 250mg, CAS: 847728-01-2.
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CJ-42794 (CAS 847728-01-2) is a potent and selective antagonist targeting prostaglandin E receptor subtype 4 (EP4) It exhibits high affinity for EP4 receptors (Ki 3 16 nM) with significantly lower potency at EP2 receptors (Ki 631 nM) and negligible affinity for EP1 or EP3 By blocking EP4-mediated signaling CJ-42794 prevents prostaglandin E2-induced intracellular cAMP elevation thereby reversing PGE2-dependent inhibition of inflammatory responses such as lipopolysaccharide-induced TNF- secretion In animal models administration of CJ-42794 delays gastric ulcer healing through suppression of VEGF expression and angiogenesis This compound serves as a valuable tool for investigating EP4-associated physiological and pathological processes
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eMolecules AA Blocks LLC 3-Oxotetrahydrofuran 250mg 642063177 AA002LGB 0 000 22929-52-8 MFCD07778393 86 090 C4H6O2
AA Blocks LLC 3-Oxotetrahydrofuran 250mg 642063177 AA002LGB 0 000 22929-52-8 MFCD07778393 86 090 C4H6O2
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Medchemexpress LLC Ethyl Tridecanoate 25g
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Ethyl Tridecanoate is an ester compound with a fruity odor commonly used as a flavoring agent in the food and beverage industry In addition it can be used as an intermediate in the synthesis of various organic compounds including fragrances pharmaceuticals and agrochemicals Its unique chemical properties make it an important ingredient in a variety of industrial processes notably in the production of cosmetics personal care products and cleaning agents
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Apexbio Technology LLC DOTMA 104872-42-6 250mg
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DOTMA (CAS 104872-42-6) is a tetramethylated DOTA analogue structurally classified as a cationic lipid It imparts a positive surface charge to liposomes thus enhancing electrostatic interactions with negatively charged cellular membranes This property facilitates cellular uptake enabling its use as a non-viral vector for nucleic acid delivery including siRNA microRNA and oligonucleotides DOTMA is widely utilized in both in vitro and in vivo gene transfection studies contributing to research in gene therapy and nucleic acid-based therapeutics
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Ambeed Meso5 10 15 20Tetraphenyl21H 2
Meso-5,10,15,20-Tetraphenyl-21H,23H-porphineironu-oxodimer, 12582-61-5, 97%
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Apexbio Technology LLC KN-92 hydrochloride 1431698-47-3 200mg
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KN-92 hydrochloride is an inactive structural analog of the Ca /calmodulin-dependent protein kinase II (CaMKII) inhibitor KN-93 serving primarily as a comparative control compound in biological research Unlike KN-93 KN-92 hydrochloride lacks meaningful inhibitory activity against CaMKII exhibiting a much higher Ki value ( 100 M) In experimental models it is utilized to distinguish CaMKII-dependent molecular and physiological responses particularly in studies of early afterdepolarizations (EADs) and cardiac repolarization events Based on these properties KN-92 hydrochloride is applied as a negative control in cardiac electrophysiological research
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Chemscene ChemScene | 2-Bromopyrimidine-5-carboxylic acid | 2.5G | CS-0101938 | 0.98 | 1224885-47-5| MFCD28670600 | 203
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ChemScene | 2-Bromopyrimidine-5-carboxylic acid | 2.5G | CS-0101938 | 0.98 | 1224885-47-5| MFCD28670600 | 203
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