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Filtered Search Results
![eMolecules 352525-66-7 | 3-Chloro-4-methylphenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01311461 | 317.860 | C7H6ClIZn | 0.000 | [I-].Cc1ccc([Zn+])cc1Cl | 100ml | 532652687](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696296.jpg-250.jpg)
eMolecules 352525-66-7 | 3-Chloro-4-methylphenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01311461 | 317.860 | C7H6ClIZn | 0.000 | [I-].Cc1ccc([Zn+])cc1Cl | 100ml | 532652687
3-Chloro-4-methylphenylzinc iodide, 0.50 M in THF | Synthonix | 352525-66-7 | MFCD01311461 | 317.860 | C7H6ClIZn | 0.000 | [I-].Cc1ccc([Zn+])cc1Cl | 100ml | 532652687
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![eMolecules 738580-38-6 | 3,4-Dimethoxyphenylzinc iodide, 0.50 M in THF | Synthonix | MFCD07698716 | 329.440 | C8H9IO2Zn | 0.000 | [I-].COc1ccc([Zn+])cc1OC | 25ml | 627353611](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695355.jpg-250.jpg)
eMolecules 738580-38-6 | 3,4-Dimethoxyphenylzinc iodide, 0.50 M in THF | Synthonix | MFCD07698716 | 329.440 | C8H9IO2Zn | 0.000 | [I-].COc1ccc([Zn+])cc1OC | 25ml | 627353611
3,4-Dimethoxyphenylzinc iodide, 0.50 M in THF | Synthonix | 738580-38-6 | MFCD07698716 | 329.440 | C8H9IO2Zn | 0.000 | [I-].COc1ccc([Zn+])cc1OC | 25ml | 627353611
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Ambeed 1 6Dihydroxynaphthalene
1,6-Dihydroxynaphthalene, 575-44-0, 97%
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Medchemexpress LLC Adiphenine hydrochloride | 50-42-0 | 99.1% | 500 MG
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Adiphenine hydrochloride is a non-competitive inhibitor of the nicotinic acetylcholine receptor (nAChR). It exhibits anticonvulsant effects and has specific IC50 values for various nAChR subtypes including α1, α3β4, α4β2, and α4β4. In vivo, it prevents hindleg tonic-extensor components of maximal electroshock seizures (MES) in mice.
- Non-competitive inhibitor of nicotinic acetylcholine receptor (nAChR)
- Exhibits anticonvulsant effects
- Specific IC50 values for α1, α3β4, α4β2, and α4β4 nAChR subtypes
- Prevents hindleg tonic-extensor components of maximal electroshock seizures (MES) in mice
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Medchemexpress LLC Tizanidine (hydrochloride) | 64461-82-1 | 99.93 % | 1 ML
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Tizanidine hydrochloride is a skeletal muscle relaxant that acts as an orally effective central α2-adrenoceptor agonist. It primarily relaxes muscles by inhibiting the release of excitatory amino acids from spinal cord interneurons. Additionally, it exhibits anti-injury activity, can inhibit gastrointestinal (GI) transport, and has been shown to inhibit proliferation, migration, and invasion of lung cancer cells, inducing cell apoptosis. This compound is used to treat spasticity from conditions such as multiple sclerosis (MS), stroke, and spinal cord injury (SCI).
- Skeletal muscle relaxant
- Central α2-adrenoceptor agonist
- Inhibits excitatory amino acid release
- Exhibits anti-injury activity
- Inhibits gastrointestinal (GI) transport
- Inhibits lung cancer cell proliferation, migration, and invasion
- Induces cell apoptosis
- Treats spasticity from multiple sclerosis, stroke, and spinal cord injury
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Medchemexpress LLC Cephalexin hydrochloride | 59695-59-9 | 99.8% | 1 ML
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Cephalexin hydrochloride is a potent, orally active, new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. It demonstrates antibacterial activity against a wide variety of gram-positive and gram-negative bacteria by targeting penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. It is utilized in research for conditions such as pneumonia, strep throat, and bacterial endocarditis.
- Disrupts polymer peptidoglycan (PG) biogenesis
- Inhibits a broad spectrum of gram-positive and gram-negative organisms
- Has antibacterial activity in male Swiss-Webster mice with infected bacterial
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Medchemexpress LLC Buflomedil (hydrochloride) | 35543-24-9 | 99.8% | 500 MG
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Buflomedil hydrochloride is a vasodilator agent and an orally active α1A-adrenoceptor antagonist. It is characterized by its Ki values of 4.06 μM for α1A-AR and 6.84 μM for α1B-AR. This compound is primarily used for the study of peripheral circulatory disorders.
- Vasodilator agent
- Orally active α1A-adrenoceptor antagonist
- Useful for studying peripheral circulatory disorders
- High purity of 99.8%
- Appears as a white to off-white solid
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Medchemexpress LLC Octopamine hydrochloride | 770-05-8 | 99.9% | 1 G
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Octopamine hydrochloride is a biogenic monoamine structurally related to noradrenaline. It functions as a neurohormone, neuromodulator, and neurotransmitter in invertebrates, stimulating alpha2-adrenoceptors and increasing various metabolic processes. It mediates behaviors like learning and memory, regulates endocrine gland activity, and mobilizes lipids and carbohydrates through specific G protein-coupled receptors.
- Acts as a neurohormone, neuromodulator, and neurotransmitter
- Stimulates alpha2-adrenoceptors (ARs)
- Increases glycogenolysis, glycolysis, oxygen uptake, gluconeogenesis, and portal perfusion pressure
- Regulates sensory input desensitization, arousal, and rhythmic behaviors
- Involved in complex behaviors like learning and memory
- Regulates endocrine gland activity
- Induces lipid and carbohydrate mobilization
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Medchemexpress LLC Ivabradine hydrochloride | 148849-67-6 | 99.7% | 1 ML
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Ivabradine hydrochloride is a potent and orally active HCN (hyperpolarization-activated cyclic nucleotide-gated) channel blocker. It inhibits the cardiac pacemaker current (If), reducing heart rate dose-dependently without modifying blood pressure. This compound demonstrates anticonvulsant, anti-ischaemic, and anti-anginal activities.
- Potent and orally active HCN channel blocker
- Inhibits cardiac pacemaker current (If)
- Reduces heart rate dose-dependently
- Exhibits anticonvulsant activity
- Shows anti-ischaemic and anti-anginal effects
- Investigated in clinical trials for conditions such as heart failure and atrial fibrillation
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(CCCC)c1ccccn1 | 5g | 525923890](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696584.jpg-250.jpg)
eMolecules 17997-47-6 | 2-(Tributylstannyl)pyridine | Synthonix - Stock | MFCD00052052 | 368.152 | C17H31NSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1ccccn1 | 5g | 525923890
2-(Tributylstannyl)pyridine | Synthonix - Stock | 17997-47-6 | MFCD00052052 | 368.152 | C17H31NSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1ccccn1 | 5g | 525923890
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![eMolecules 13139-86-1 | 4-Methoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD00013515 | 211.341 | C7H7BrMgO | 0.000 | [Br-].COc1ccc([Mg+])cc1 | 100ml | 437237330](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502697559.jpg-250.jpg)
eMolecules 13139-86-1 | 4-Methoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD00013515 | 211.341 | C7H7BrMgO | 0.000 | [Br-].COc1ccc([Mg+])cc1 | 100ml | 437237330
4-Methoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 13139-86-1 | MFCD00013515 | 211.341 | C7H7BrMgO | 0.000 | [Br-].COc1ccc([Mg+])cc1 | 100ml | 437237330
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![eMolecules 312693-24-6 | 3-Methylphenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01311453 | 283.420 | C7H7IZn | 0.000 | [I-].Cc1cccc([Zn+])c1 | 50ml | 532652912](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696081.jpg-250.jpg)
eMolecules 312693-24-6 | 3-Methylphenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01311453 | 283.420 | C7H7IZn | 0.000 | [I-].Cc1cccc([Zn+])c1 | 50ml | 532652912
3-Methylphenylzinc iodide, 0.50 M in THF | Synthonix | 312693-24-6 | MFCD01311453 | 283.420 | C7H7IZn | 0.000 | [I-].Cc1cccc([Zn+])c1 | 50ml | 532652912
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eMolecules 75-62-7 | Bromotrichloromethane | Aladdin Scientific Corporation | MFCD00000783 | 198.270 | CBrCl3 | 97.000 | ClC(Cl)(Cl)Br | 25g | 845120327
Bromotrichloromethane | Aladdin Scientific Corporation | 75-62-7 | MFCD00000783 | 198.270 | CBrCl3 | 97.000 | ClC(Cl)(Cl)Br | 25g | 845120327
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Medchemexpress LLC Adiphenine hydrochloride | 50-42-0 | MFCD00008899 | 99.1% | 1 ML
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Adiphenine hydrochloride is a non-competitive inhibitor of nicotinic acetylcholine receptor (nAChR), exhibiting specific IC50s for various receptor subtypes. This compound has also demonstrated anticonvulsant effects in studies.
- Non-competitive inhibitor of nicotinic acetylcholine receptor (nAChR)
- Exhibits anticonvulsant effects
- Blocks function of α1*-nAChR, α3α4*-nAChR, α4β2- and α4β4-nAChR in various cell lines
- Decreases frequency of ACh-induced single-channel currents
- Prevents hindleg tonic-extensor component of maximal electroshock seizures in mice
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Medchemexpress LLC 1-naphthalenesulfonic acid, 3,4-dihydro-3,4-dioxo-, potassium salt | 5908-27-0 | MFCD00001699 | 99.8% | 276.31 | C10H5KO5S | 1g
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Potassium 1 2-naphthoquinone-4-sulphonate (Compound 16) is a 6-phosphogluconate dehydrogenase (6PGDH) inhibitor with an IC50 of 53 M Potassium 1 2-naphthoquinone-4-sulphonate can be used in the study of human African trypanosomiasis[1]
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