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Filtered Search Results
eMolecules 15022-18-1 | WuXi ChemSupply | 1-thiophen-2-ylpropan-2-one | 5g | 599164764 | LN00166067 | MFCD00125263 | 140.200 | C7H8OS
WuXi ChemSupply 1-thiophen-2-ylpropan-2-one 5g 599164764 LN00166067 15022-18-1 MFCD00125263 140.200 C7H8OS
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eMolecules 21900-37-8 | 2,6-Dimethylbenzoyl chloride | Oakwood Chemical | MFCD00052854 | 168.620 | C9H9ClO | 98.000 | Cc1cccc(C)c1C(Cl)=O | 5g | 537676214
2,6-Dimethylbenzoyl chloride | Oakwood Chemical | 21900-37-8 | MFCD00052854 | 168.620 | C9H9ClO | 98.000 | Cc1cccc(C)c1C(Cl)=O | 5g | 537676214
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Medchemexpress LLC Sodium naphthalen-1-yl phosphate hydrate | 207569-06-0 | MFCD00150614 | >95.0% | 286.13 g/mol | C10H9O4P·xH2O·2Na | 1 G
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Sodium naphthalen-1-yl phosphate hydrate is a biochemical reagent used in life-science research. It is supplied as a solid, white to off-white powder and is intended for research use only.
- Solid, white to off-white powder.
- Used as a biochemical reagent for life-science research.
- Available in 100 mg to 1 g pack sizes.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- CAS number: 207569-06-0; molecular weight approximately 286.13 g/mol.
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eMolecules 127349-68-2 | 4-tert-Butylbenzylmagnesium bromide, 0.25 M in 2-MeTHF | Synthonix - Stock251.450 | C11H15BrMg | 0.000 | [Br-].CC(C)(C)c1ccc(C[Mg+])cc1 | 50ml | 507876232
4-tert-Butylbenzylmagnesium bromide, 0.25 M in 2-MeTHF | Synthonix - Stock | 127349-68-2251.450 | C11H15BrMg | 0.000 | [Br-].CC(C)(C)c1ccc(C[Mg+])cc1 | 50ml | 507876232
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eMolecules 112780-67-3 | 3-Fluoro-4-methoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock229.331 | C7H6BrFMgO | 0.000 | [Br-].COc1ccc([Mg+])cc1F | 100ml | 437237248
3-Fluoro-4-methoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 112780-67-3229.331 | C7H6BrFMgO | 0.000 | [Br-].COc1ccc([Mg+])cc1F | 100ml | 437237248
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eMolecules 518990-00-6 | 3-Cyano-4-fluorophenylzinc bromide, 0.50 M in THF | Synthonix | MFCD02260165 | 265.390 | C7H3BrFNZn | 0.000 | [Br-].Fc1ccc([Zn+])cc1C#N | 25ml | 627353558
3-Cyano-4-fluorophenylzinc bromide, 0.50 M in THF | Synthonix | 518990-00-6 | MFCD02260165 | 265.390 | C7H3BrFNZn | 0.000 | [Br-].Fc1ccc([Zn+])cc1C#N | 25ml | 627353558
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Medchemexpress LLC Netarsudil hydrochloride | 1253952-02-1 | 99.9% | 100 MG
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Netarsudil hydrochloride is a competitive inhibitor of Rho-associated protein kinases (ROCK I and ROCK II) and a reversible inhibitor of the norepinephrine transporter (NET). It is primarily used in the study of ocular hypertension and primary open-angle glaucoma, reducing intraocular pressure by inhibiting ROCK and reducing aqueous humor production by inhibiting NET.
- Inhibits ROCK I and ROCK II
- Reversible inhibitor of norepinephrine transporter (NET)
- Reduces intraocular pressure
- Increases aqueous humor outflow ease
- Reduces aqueous humor production
- Causes relaxation of trabecular meshwork cells
- Dilation of episcleral veins
- Metabolizes to active compound Netarsudil-M1
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eMolecules 259807-97-1 | 3-Methyl-2-(tributylstannyl)pyridine | Synthonix - Stock | MFCD07787404 | 382.179 | C18H33NSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1ncccc1C | 5g | 525920424
3-Methyl-2-(tributylstannyl)pyridine | Synthonix - Stock | 259807-97-1 | MFCD07787404 | 382.179 | C18H33NSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1ncccc1C | 5g | 525920424
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eMolecules 185416-17-5 | 4-Methoxy-3,5-dimethylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD01319917 | 239.395 | C9H11BrMgO | 97.000 | [Br-].COc1c(C)cc([Mg+])cc1C | 50ml | 437237346
4-Methoxy-3,5-dimethylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 185416-17-5 | MFCD01319917 | 239.395 | C9H11BrMgO | 97.000 | [Br-].COc1c(C)cc([Mg+])cc1C | 50ml | 437237346
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eMolecules 63488-08-4 | 2-iso-Propylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD06201611 | 223.396 | C9H11BrMg | 0.000 | [Br-].CC(C)c1ccccc1[Mg+] | 50ml | 437237405
2-iso-Propylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 63488-08-4 | MFCD06201611 | 223.396 | C9H11BrMg | 0.000 | [Br-].CC(C)c1ccccc1[Mg+] | 50ml | 437237405
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eMolecules 32721-06-5 | (6-Bromo-naphthalen-2-yl)-aceticacid | Ochem Incorporation | MFCD11110483 | 265.106 | C12H9BrO2 | 95.000 | OC(=O)Cc1ccc2cc(Br)ccc2c1 | 1g | 873779868
(6-Bromo-naphthalen-2-yl)-aceticacid | Ochem Incorporation | 32721-06-5 | MFCD11110483 | 265.106 | C12H9BrO2 | 95.000 | OC(=O)Cc1ccc2cc(Br)ccc2c1 | 1g | 873779868
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eMolecules 87942-08-3 | 4-Propylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock223.396 | C9H11BrMg | 0.000 | [Br-].CCCc1ccc([Mg+])cc1 | 50ml | 437237414
4-Propylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 87942-08-3223.396 | C9H11BrMg | 0.000 | [Br-].CCCc1ccc([Mg+])cc1 | 50ml | 437237414
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Medchemexpress LLC Crizotinib hydrochloride | 1415560-69-8 | 99.7% | C21H23Cl3FN5O | 100 MG
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Crizotinib hydrochloride is an orally bioavailable, selective, and ATP-competitive dual ALK and c-Met inhibitor. It also acts as a ROS proto-oncogene 1 (ROS1) inhibitor, demonstrating effective tumor growth inhibition. In cell-based assays, it inhibits tyrosine phosphorylation of NPM-ALK with an IC50 of 24 nM and tyrosine phosphorylation of c-Met with an IC50 of 11 nM.
- Inhibits ALK with an IC50 of 20 nM
- Inhibits c-Met with an IC50 of 8 nM
- Potently prevents cell proliferation, leading to G(1)-S-phase cell cycle arrest and apoptosis induction in ALK-positive ALCL cells
- Causes marked regression of large established tumors in GTL-16 model
- Significantly reduces CD31-positive endothelial cells in GTL-16 tumors
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eMolecules 62351-47-7 | 3,5-Difluorophenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD00672005 | 217.296 | C6H3BrF2Mg | 0.000 | [Br-].Fc1cc(F)cc([Mg+])c1 | 500ml | 437237116
3,5-Difluorophenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 62351-47-7 | MFCD00672005 | 217.296 | C6H3BrF2Mg | 0.000 | [Br-].Fc1cc(F)cc([Mg+])c1 | 500ml | 437237116
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Medchemexpress LLC Mebeverine hydrochloride | 2753-45-9 | 99.9% | C25H36ClNO5 | 25 MG
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Mebeverine hydrochloride is a β-phenylethylamine derivative and a musculotropic agent that potently blocks intestinal peristalsis. It directly blocks voltage-operated sodium channels and inhibits intracellular calcium accumulation.
- Potent blocker of intestinal peristalsis
- Directly blocks voltage-operated sodium channels
- Inhibits intracellular calcium accumulation
- Relevant for metabolic or endocrine disease research
- Targets sodium channels
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