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Filtered Search Results
eMolecules 1010684-05-5 | 2-Cyclohexylethylzinc bromide, 0.50 M in THF | Synthonix256.490 | C8H15BrZn | 0.000 | [Br-].[Zn+]CCC1CCCCC1 | 50ml | 703157762
2-Cyclohexylethylzinc bromide, 0.50 M in THF | Synthonix | 1010684-05-5256.490 | C8H15BrZn | 0.000 | [Br-].[Zn+]CCC1CCCCC1 | 50ml | 703157762
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Medchemexpress LLC Varenicline hydrochloride | 230615-23-3 | 99.9% | 247.72 g/mol | C13H14ClN3 | 100 MG
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Varenicline hydrochloride is the hydrochloride salt of varenicline, an orally active partial agonist of α4β2 nicotinic acetylcholine receptors used in neuroscience and pharmacology research. It is provided for research and analytical applications in solid form and as prepared solutions for in vitro studies and assay development.
- Partial agonist at α4β2 nicotinic acetylcholine receptors, useful for receptor pharmacology studies.
- Supplied as a powder and in solution formats for flexible assay preparation.
- High purity suitable for analytical and biological assays.
- Characterized with confirmed CAS number and molecular weight for chemical identification.
- Suitable for use in studies of nicotine dependence and neuromodulation pathways.
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AdipoGen Violuric acid monohydrate
Chemical. CAS 26351-19-9. Formula C4H3N3O4 . H2O. Molecular Weight 175.1. Violuric acid has been used as an analytical reagent for spectrophotometric detection of cations, chromatographic separation and for cation oxidation .e.g Co2, Cu2, Fe2, etc. Violuric acid forms solid complexes chelates with many different cations and has attracted attention because simple salts of the violurate anion are deeply colored. The colours depend on the hydrate and the ratio of acid to cation, pH, temperature. Violuric acid is a redox mediator, and is used as reporter assay for assessing redox potentials during protein engineering. Violuric acid is effectively oxidized only by high-redox potential laccases HRPLs due to its high-redox potential. New colorimetric screening assays for the directed evolution of fungal laccases to improve the conversion of plant biomass have been described.
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eMolecules 1211592-70-9 | tert-Butyl 2-cyanomorpholine-4-carboxylate | Combi-Blocks, Inc. | MFCD18250325 | 212.249 | C10H16N2O3 | 98.000 | CC(C)(C)OC(=O)N1CCOC(C1)C#N | 5g | 569290839
tert-Butyl 2-cyanomorpholine-4-carboxylate | Combi-Blocks, Inc. | 1211592-70-9 | MFCD18250325 | 212.249 | C10H16N2O3 | 98.000 | CC(C)(C)OC(=O)N1CCOC(C1)C#N | 5g | 569290839
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eMolecules Synthonix (2-Naphthylmethyl)zinc bromide 0.50 M in THF 25ml 627353712 N73099 152329-44-7 [null] 286.480 C11H9BrZn
Synthonix (2-Naphthylmethyl)zinc bromide 0.50 M in THF 25ml 627353712 N73099 152329-44-7 [null] 286.480 C11H9BrZn
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eMolecules 1012041-98-3 | (Tetrahydropyran-4-ylmethyl)zinc bromide, 0.50 M in THF | Synthonix244.440 | C6H11BrOZn | 95.000 | [Br-].[Zn+]CC1CCOCC1 | 100ml | 798925414
(Tetrahydropyran-4-ylmethyl)zinc bromide, 0.50 M in THF | Synthonix | 1012041-98-3244.440 | C6H11BrOZn | 95.000 | [Br-].[Zn+]CC1CCOCC1 | 100ml | 798925414
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eMolecules 99027-88-0 | Benzyl 2-oxa-3-azabicyclo[2.2.1]hept-5-ene-3-carboxylate | Combi-Blocks, Inc. | MFCD22683220 | 231.251 | C13H13NO3 | 95.000 | O=C(OCc1ccccc1)N1OC2CC1C=C2 | 5g | 794200123
Benzyl 2-oxa-3-azabicyclo[2.2.1]hept-5-ene-3-carboxylate | Combi-Blocks, Inc. | 99027-88-0 | MFCD22683220 | 231.251 | C13H13NO3 | 95.000 | O=C(OCc1ccccc1)N1OC2CC1C=C2 | 5g | 794200123
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eMolecules 1207518-63-5 | methyl 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate | Advanced ChemBlocks | MFCD17016053 | 211.610 | C8H6ClN3O2 | 97.000 | COC(=O)c1c[nH]c2ncnc(Cl)c12 | 1g | 507809053
methyl 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate | Advanced ChemBlocks | 1207518-63-5 | MFCD17016053 | 211.610 | C8H6ClN3O2 | 97.000 | COC(=O)c1c[nH]c2ncnc(Cl)c12 | 1g | 507809053
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Medchemexpress LLC Scavenger receptor class B type I (SR-BI/SCARB1), human, HEK293-expressed, C-terminal His-tag | >95.0% | 5 UG
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Recombinant human scavenger receptor class B type I (SR-BI/SCARB1) expressed in HEK293 cells and supplied with a C-terminal His tag for research use in studies of lipid binding and HDL receptor function.
- HEK293-expressed recombinant human SR-BI covering P33-Y443.
- C-terminal His tag for affinity purification and detection.
- Purity greater than 95% as determined by reducing SDS-PAGE.
- Not recommended to reconstitute below 100 μg/mL in ddH2O.
- Store at -20°C; freeze aliquots at -20°C or -80°C for extended storage.
- Suitable for studies of HDL binding and receptor function.
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Medchemexpress LLC Alprenolol (hydrochloride) | 13707-88-5 | 99.8% | 100 MG
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Alprenolol ((RS)-Alprenolol; dl-Alprenolol) hydrochloride is an orally active non-selective β-adrenoceptor antagonist and an antagonist of 5-HT1A and 5-HT1B receptors. It is utilized as an anti-hypertensive, anti-anginal, and anti-arrhythmic agent.
- Orally active non-selective β-adrenoceptor antagonist.
- Antagonist of 5-HT1A and 5-HT1B receptors.
- Used as an anti-hypertensive agent.
- Used as an anti-anginal agent.
- Used as an anti-arrhythmic agent.
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eMolecules 301652-23-3 | 4-Methyl-2-(tributylstannyl)pyridine | Synthonix - Stock | MFCD07787403 | 382.179 | C18H33NSn | 96.000 | CCCC[Sn](CCCC)(CCCC)c1cc(C)ccn1 | 1g | 525920416
4-Methyl-2-(tributylstannyl)pyridine | Synthonix - Stock | 301652-23-3 | MFCD07787403 | 382.179 | C18H33NSn | 96.000 | CCCC[Sn](CCCC)(CCCC)c1cc(C)ccn1 | 1g | 525920416
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eMolecules 259807-88-0 | 3-Fluoro-4-(tributylstannyl)-pyridine | Synthonix - Stock | MFCD11044865 | 386.142 | C17H30FNSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1ccncc1F | 1g | 525917760
3-Fluoro-4-(tributylstannyl)-pyridine | Synthonix - Stock | 259807-88-0 | MFCD11044865 | 386.142 | C17H30FNSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1ccncc1F | 1g | 525917760
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TARGETMOL CHEMICALS INC ALPHA-NAPHTHOFLAVONE 50MG
Also available in 5 mg 10 mg 25 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. alpha-Naphthoflavone (78-benzoflavone) a synthetic flavonoid is a potent inhibitor of aromatase with an I50 value of 0.5 uM. purity: 99%
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Medchemexpress LLC (±)-BI-D | 1416258-16-6 | 98.1% | 10 MG
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(±)-BI-D is an allosteric HIV integrase inhibitor used in research to study integrase function and antiviral activity. It binds the LEDGF/p75 binding site on integrase and has demonstrated inhibition of HIV-Luc infection in cellular assays.
- Potent ALLINI mechanism of action.
- Binds LEDGF/p75 integrase site to disrupt viral integration.
- Demonstrated cellular activity (reported IC50s: 0.16 μM and 2.9 μM).
- Available as solid and as a 10 mM solution in DMSO for assay setup flexibility.
- High purity and defined molecular weight and formula for reproducible studies.
- Intended for biochemical and cellular research use only; not for human use.
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Medchemexpress LLC Celgosivir (hydrochloride) | 141117-12-6 | 98.0% | 295.76 | 10 MM * 1 ML
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Celgosivir hydrochloride is an α-glucosidase I inhibitor that inhibits bovine viral diarrhoea virus (BVDV) with an IC50 of 1.27 μM in an in vitro assay.
- Acts as an α-glucosidase I inhibitor.
- Exhibits antiviral activity.
- Potent against HIV-1.
- Active against BVDV.
- Active against DENV2.
- Active against DENV1, 3, and 4.
- Offers in vivo protection.
- Provides dose and schedule-dependent protection.
- Undergoes rapid metabolism.
- Appears as a solid, white to gray color.
- Ships at room temperature in continental US (may vary elsewhere). Store at 4°C, sealed, away from moisture. In solvent, store at -80°C for 6 months or -20°C for 1 month (sealed, away from moisture).
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