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Filtered Search Results
eMolecules 1233318-32-5 | 5-Methyl-2-thienylzinc bromide, 0.50 M in THF | Synthonix | MFCD08064068 | 242.440 | C5H5BrSZn | 0.000 | [Br-].Cc1ccc([Zn+])s1 | 50ml | 532652928
5-Methyl-2-thienylzinc bromide, 0.50 M in THF | Synthonix | 1233318-32-5 | MFCD08064068 | 242.440 | C5H5BrSZn | 0.000 | [Br-].Cc1ccc([Zn+])s1 | 50ml | 532652928
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000586189 BI-9564 25MG
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Medchemexpress LLC Phenylalanine, 4-chloro-, hydrochloride | 23633-07-0 | 98.6% | 236.10 | C9H11Cl2NO2 | 1g
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Fenclonine hydrochloride is a selective and irreversible tryptophan hydroxylase inhibitor which is a rate-limiting enzyme in the biosynthesis of serotonin Fenclonine hydrochloride can be used in carcinoid syndrome research[1][2][3]
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eMolecules 756822-47-6 | 4-[Bis(trimethylsilyl)amino]phenylmagnesium bromide, 0.50 M in THF | Synthonix | MFCD18253642 | 340.694 | C12H22BrMgNSi2 | 0.000 | [Br-].C[Si](C)(C)N(c1ccc([Mg+])cc1)[Si](C)(C)C | 50ml | 721997561
4-[Bis(trimethylsilyl)amino]phenylmagnesium bromide, 0.50 M in THF | Synthonix | 756822-47-6 | MFCD18253642 | 340.694 | C12H22BrMgNSi2 | 0.000 | [Br-].C[Si](C)(C)N(c1ccc([Mg+])cc1)[Si](C)(C)C | 50ml | 721997561
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eMolecules 581-71-5 | 3-Hydroxynaphthalene-2-carbaldehyde | Combi-Blocks, Inc. | MFCD00079346 | 172.183 | C11H8O2 | 98.000 | Oc1cc2ccccc2cc1C=O | 5g | 603141634
3-Hydroxynaphthalene-2-carbaldehyde | Combi-Blocks, Inc. | 581-71-5 | MFCD00079346 | 172.183 | C11H8O2 | 98.000 | Oc1cc2ccccc2cc1C=O | 5g | 603141634
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eMolecules 1967019-73-3 | (Tetrahydropyran-4-ylmethyl)magnesium bromide, 0.50 M in THF | Synthonix203.362 | C6H11BrMgO | 0.000 | [Br-].[Mg+]CC1CCOCC1 | 25ml | 798925409
(Tetrahydropyran-4-ylmethyl)magnesium bromide, 0.50 M in THF | Synthonix | 1967019-73-3203.362 | C6H11BrMgO | 0.000 | [Br-].[Mg+]CC1CCOCC1 | 25ml | 798925409
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5000697200 GUANFACINE HYDROCHL 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000693154 ETHAVERINE HYDROCHL 10MM/1ML
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Medchemexpress LLC Dipivefrin hydrochloride | 64019-93-8 | MFCD00793796 | 98.4% | 1 ML
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Dipivefrin hydrochloride is an antiglaucoma proagent that is hydrolyzed to epinephrine, the active compound, by esterases in the cornea. This product is for research use only and not intended for patient use.
- Functions as an antiglaucoma proagent
- Hydrolyzed to active compound epinephrine by corneal esterases
- Intended for research use only
- Store solid at -20°C under nitrogen, away from moisture
- Store in solvent at -80°C for 6 months or -20°C for 1 month under nitrogen, away from moisture
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Apexbio Technology LLC BI-D1870 501437-28-1 10mM (in 1mL DMSO)
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BI-D1870 (CAS 501437-28-1) is a cell-permeable small molecule inhibitor that selectively targets the p90 ribosomal S6 kinase (RSK) family comprising RSK1 RSK2 RSK3 and RSK4 It functions as an ATP-competitive inhibitor exhibiting IC50 values of 31 nM 24 nM 18 nM and 15 nM against RSK1 RSK2 RSK3 and RSK4 respectively BI-D1870 demonstrates over 500-fold greater selectivity for RSK isoforms compared to other AGC kinases In cellular assays such as with Rat-2 cells it has been shown to induce phosphorylation of ERK1/ERK2 and subsequent CREB phosphorylation BI-D1870 is widely utilized for investigating RSK-mediated signal transduction and downstream cellular processes in biomedical research
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eMolecules 206446-38-0 | 1-t-Butoxycarbonylazetedin-3-ylzinc iodide, 0.50 M in THF | Synthonix - Stock348.490 | C8H14INO2Zn | 0.000 | [I-].CC(C)(C)OC(=O)N1CC([Zn+])C1 | 50ml | 347518886
1-t-Butoxycarbonylazetedin-3-ylzinc iodide, 0.50 M in THF | Synthonix - Stock | 206446-38-0348.490 | C8H14INO2Zn | 0.000 | [I-].CC(C)(C)OC(=O)N1CC([Zn+])C1 | 50ml | 347518886
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Apexbio Technology LLC MK-571 115104-28-4 10mg
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MK-571 (CAS 115104-28-4) also known as L-660711 is a selective antagonist of the leukotriene D4 (LTD4) receptor a G protein-coupled receptor activated by cysteinyl leukotrienes involved in inflammatory responses MK-571 demonstrates high affinity for the LTD4 receptor with reported Ki values of 0 22 nM in guinea pig lung and 2 1 nM in human lung membranes It effectively antagonizes LTD4- and LTE4-induced contractions in guinea pig and human airway tissues as indicated by pA2 values ranging from 8 5 to 10 5 In vivo MK-571 reduces airway hyperresponsiveness and leukocyte infiltration in animal models of pulmonary inflammation Additionally MK-571 acts as a specific inhibitor of multidrug resistance protein 1 (MRP1) supporting its use in studies of leukotriene signaling and drug transport mechanisms
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Medchemexpress LLC 4-[4-[(dimethylamino)methyl]-3,5-dimethoxyphenyl]-2-methyl-2,7-naphthyridin-1(2H)-one | 1883429-21-7 | ≥98.0% | 353.41 | C20H23N3O3 | 25 MG
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BI-7273 is a potent, cell-permeable small-molecule inhibitor of bromodomain-containing proteins BRD9 and BRD7, developed for research use in epigenetics and oncology. It demonstrates low-nanomolar biochemical potency and high binding affinity, and is suitable as a tool compound for biochemical, cellular, and in vivo studies.
- Potent biochemical activity (BRD9 IC50 ~19 nM; BRD7 IC50 ~117 nM).
- High binding affinity (BRD9 Kd ~0.75 nM; BRD7 Kd ~0.3 nM).
- Cell-permeable and active in cellular assays.
- Suitable for in vitro and in vivo experiments.
- Soluble in DMSO at 10 mg/mL; ultrasonic may be required.
- Stable as a powder when stored at -20°C; follow supplier storage recommendations.
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eMolecules 1416437-22-3 | 2-(Methylsulfonyl)-5-(tributylstannyl)thiazole | Synthonix - Stock | MFCD01319035 | 452.260 | C16H31NO2S2Sn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cnc(s1)S(C)(=O)=O | 5g | 525921487
2-(Methylsulfonyl)-5-(tributylstannyl)thiazole | Synthonix - Stock | 1416437-22-3 | MFCD01319035 | 452.260 | C16H31NO2S2Sn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cnc(s1)S(C)(=O)=O | 5g | 525921487
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000656209 DFHBI-BI 1MG
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