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Filtered Search Results
eMolecules 2633-66-1 | 2,4,6-Trimethylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD00009663 | 223.396 | C9H11BrMg | 0.000 | [Br-].Cc1cc(C)c([Mg+])c(C)c1 | 100ml | 437237439
2,4,6-Trimethylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 2633-66-1 | MFCD00009663 | 223.396 | C9H11BrMg | 0.000 | [Br-].Cc1cc(C)c([Mg+])c(C)c1 | 100ml | 437237439
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eMolecules 1105511-65-6 | 2-Methoxy-3-(tributylstannyl)pyrazine | Synthonix - Stock | MFCD09025812 | 399.166 | C17H32N2OSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1nccnc1OC | 5g | 525920560
2-Methoxy-3-(tributylstannyl)pyrazine | Synthonix - Stock | 1105511-65-6 | MFCD09025812 | 399.166 | C17H32N2OSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1nccnc1OC | 5g | 525920560
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eMolecules 672325-70-1 | 3-Bromo-2-thienylzinc bromide, 0.50 M in THF | Synthonix | MFCD02260168 | 307.310 | C4H2Br2SZn | 0.000 | [Br-].[Zn+]c1sccc1Br | 50ml | 532652616
3-Bromo-2-thienylzinc bromide, 0.50 M in THF | Synthonix | 672325-70-1 | MFCD02260168 | 307.310 | C4H2Br2SZn | 0.000 | [Br-].[Zn+]c1sccc1Br | 50ml | 532652616
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Medchemexpress LLC PHA-767491 HYDROCHL 10MM 1ML
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PHA-767491 HYDROCHL 10MM 1ML
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Medchemexpress LLC LIXUMISTAT HYDROCHL 10MM 1ML
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LIXUMISTAT HYDROCHL 10MM 1ML
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Medchemexpress LLC A-1-2 FUCOSIDASE BI 1KU
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A-1-2 FUCOSIDASE BI 1KU
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eMolecules 160732-56-9 | 1-Azido-1,2-benziodoxol-3(1H)-one, 40% in diatomaceous earth | Synthonix - Stock | MFCD04038996 | 289.032 | C7H4IN3O2 | 95.000 | [N-]=[N+]=N[I]1OC(=O)c2ccccc12 | 5g | 525906036
1-Azido-1,2-benziodoxol-3(1H)-one, 40% in diatomaceous earth | Synthonix - Stock | 160732-56-9 | MFCD04038996 | 289.032 | C7H4IN3O2 | 95.000 | [N-]=[N+]=N[I]1OC(=O)c2ccccc12 | 5g | 525906036
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Medchemexpress LLC Fenspiride hydrochloride | 5053-08-7 | 99.1% | C15H21ClN2O2 | 1 ML
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Fenspiride hydrochloride is an orally active, non-steroidal anti-inflammatory agent that acts as an antagonist of the H1-histamine receptor. It inhibits phosphodiesterase 3 (PDE3), phosphodiesterase 4 (PDE4), and phosphodiesterase 5 (PDE5) activities. This compound can be used for research related to respiratory diseases.
- Antagonist of the H1-histamine receptor
- Inhibits phosphodiesterase 3, phosphodiesterase 4, and phosphodiesterase 5 activities
- Useful for research on respiratory diseases
- Inhibits histamine-induced contraction of isolated guinea pig trachea (in vitro)
- Reduces lipopolysaccharide-induced tumor necrosis factor concentrations (in vivo)
- Reduces primed stimulation of alveolar macrophages (in vivo)
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 308796-27-2 | 4-(Methylthio)phenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01863641 | 315.480 | C7H7ISZn | 95.000 | [I-].CSc1ccc([Zn+])cc1 | 100ml | 721997568
4-(Methylthio)phenylzinc iodide, 0.50 M in THF | Synthonix | 308796-27-2 | MFCD01863641 | 315.480 | C7H7ISZn | 95.000 | [I-].CSc1ccc([Zn+])cc1 | 100ml | 721997568
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eMolecules 1142215-67-5 | 4-Chlorophenethylzinc bromide, 0.50 M in THF | Synthonix284.890 | C8H8BrClZn | 0.000 | [Br-].Clc1ccc(CC[Zn+])cc1 | 25ml | 627353563
4-Chlorophenethylzinc bromide, 0.50 M in THF | Synthonix | 1142215-67-5284.890 | C8H8BrClZn | 0.000 | [Br-].Clc1ccc(CC[Zn+])cc1 | 25ml | 627353563
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Medchemexpress LLC Valnemulin hydrochloride | 133868-46-9 | 98.1% | C31H53ClN2O5S | 1 ML
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Valnemulin hydrochloride is an orally effective truncated pleurotin antibiotic. It inhibits bacterial protein synthesis by binding to peptidyl transferase in the 50s ribosome subunit. This antibiotic has shown efficacy in eliminating Mycobacterium bovis in experimental bovine models of Mycoplasma bovis infection and can reduce mortality in epidemic rabbit enteropathy.
- Inhibits bacterial protein synthesis
- Effectively eliminates Mycobacterium bovis in bovine models
- Reduces mortality in epidemic rabbit enteropathy
- Supports rapid diminution of clinical signs and restoration of appetite in calves
- No adverse effects on rabbit growth performance
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eMolecules 160732-56-9 | 1-Azido-1,2-benziodoxol-3(1H)-one, 40% in diatomaceous earth | Synthonix - Stock | MFCD04038996 | 289.032 | C7H4IN3O2 | 95.000 | [N-]=[N+]=N[I]1OC(=O)c2ccccc12 | 500mg | 525932163
1-Azido-1,2-benziodoxol-3(1H)-one, 40% in diatomaceous earth | Synthonix - Stock | 160732-56-9 | MFCD04038996 | 289.032 | C7H4IN3O2 | 95.000 | [N-]=[N+]=N[I]1OC(=O)c2ccccc12 | 500mg | 525932163
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Apexbio Technology LLC BI 6015 93987-29-2 10mg
BI 6015 is a small-molecule antagonist targeting hepatocyte nuclear factor 4 alpha (HNF4 ) a nuclear receptor implicated in transcriptional regulation within liver intestinal and pancreatic -cells It is designed to inhibit HNF4 -mediated transcriptional activation thereby modulating gene expression related to glucose and lipid metabolism BI 6015 exerts its biological activity primarily through direct antagonism of HNF4 leading to reduced transcriptional activation and lowering endogenous HNF4 protein levels In cell-based studies BI 6015 demonstrates inhibition of insulin promoter activity and suppression of endogenous insulin expression in T6PNE cells as well as decreased HNF4 protein in MIN6 and HepG2 cells Based on these pharmacological properties BI 6015 holds research potential in the study of diabetes and hepatic metabolic regulation
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eMolecules 455-13-0 | 4-Iodobenzotrifluoride | Accela ChemBio (ASD) | MFCD00039398 | 272.009 | C7H4F3I | 98.000 | FC(F)(F)c1ccc(I)cc1 | 100g | 444756518
4-Iodobenzotrifluoride | Accela ChemBio (ASD) | 455-13-0 | MFCD00039398 | 272.009 | C7H4F3I | 98.000 | FC(F)(F)c1ccc(I)cc1 | 100g | 444756518
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eMolecules 172035-86-8 | 3-Thienylmagnesium iodide, 0.5 M in THF | Synthonix - Stock | MFCD03427252 | 234.340 | C4H3IMgS | 97.000 | [I-].[Mg+]c1ccsc1 | 100ml | 507877786
3-Thienylmagnesium iodide, 0.5 M in THF | Synthonix - Stock | 172035-86-8 | MFCD03427252 | 234.340 | C4H3IMgS | 97.000 | [I-].[Mg+]c1ccsc1 | 100ml | 507877786
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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