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Filtered Search Results
Medchemexpress LLC Benzocaine (hydrochloride) | 23239-88-5 | MFCD00012999 | 99.8% | 201.65 | C9H12ClNO2 | 1mL
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Benzocaine (hydrochloride) is an orally active local agent that can suppress or relieve pain that acts on voltage-gated Na channels at a common receptor with an IC50 value of 0 8 mM at 30 mV Additionally Benzocaine (hydrochloride) non-competitively inhibits Ca-ATPase binding with Ca2 with an IC50 of 47 1 mM Benzocaine (hydrochloride) can be used in research within the field of neuromuscular regulation[1][2][3]
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![eMolecules 1274868-09-5 | 3,5-Dichlorophenylzinc bromide, 0.50 M in THF | Synthonix291.270 | C6H3BrCl2Zn | 97.000 | [Br-].Clc1cc(Cl)cc([Zn+])c1 | 50ml | 703157777](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502694872.jpg-250.jpg)
eMolecules 1274868-09-5 | 3,5-Dichlorophenylzinc bromide, 0.50 M in THF | Synthonix291.270 | C6H3BrCl2Zn | 97.000 | [Br-].Clc1cc(Cl)cc([Zn+])c1 | 50ml | 703157777
3,5-Dichlorophenylzinc bromide, 0.50 M in THF | Synthonix | 1274868-09-5291.270 | C6H3BrCl2Zn | 97.000 | [Br-].Clc1cc(Cl)cc([Zn+])c1 | 50ml | 703157777
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Medchemexpress LLC BI-4020 | 2664214-60-0 | 98.82% | 50 MG
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BI-4020 is a fourth-generation, orally active, and non-covalent EGFR tyrosine kinase inhibitor. It exhibits high kinome selectivity and favorable DMPK properties. This compound is stable under recommended storage conditions.
- Inhibits the triple mutant EGFR del19 T790M C797S variant (IC50=0.2 nM in BaF3 cell lines).
- Inhibits the double mutant EGFR del19 T790M and primary mutant EGFR del19 (IC50=1 nM).
- Shows activity against EGFR wt (IC50=190 nM).
- For research use only by suitably qualified experienced scientists.
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Medchemexpress LLC L-Tyrosine, 3-hydroxy-, methyl ester, hydrochloride (1:1) | 1421-65-4 | 99.8% | 247.68 | 1 G
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Melevodopa hydrochloride is an effervescent Levodopa prodrug. Levodopa is an orally active metabolic precursor of neurotransmitters dopamine and has anti-allodynic effects and the potential for Parkinson's disease.
- Solid appearance
- White to off-white color
- Soluble in DMSO
- Store at 4°C under nitrogen
- Store in solvent at -80°C for 6 months, or -20°C for 1 month under nitrogen
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Medchemexpress LLC Octopamine hydrochloride | 770-05-8 | 99.9% | 1 ML
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Octopamine ((±)-p-Octopamine) hydrochloride, a biogenic monoamine structurally related to noradrenaline, acts as a neurohormone, a neuromodulator and a neurotransmitter in invertebrates. It can stimulate alpha2-adrenoceptors (ARs) in Chinese hamster ovary cells transfected with human alpha2-ARs. Research indicates Octopamine hydrochloride increases glycogenolysis, glycolysis, oxygen uptake, gluconeogenesis and the portal perfusion pressure.
- Acts as a neurohormone, neuromodulator, and neurotransmitter in invertebrates.
- Stimulates alpha2-adrenoceptors (ARs).
- Increases glycogenolysis and glycolysis.
- Enhances oxygen uptake.
- Boosts gluconeogenesis.
- Elevates portal perfusion pressure.
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Medchemexpress LLC Loperamide hydrochloride (Standard) | 34552-83-5 | 99.9% | 100 MG
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Loperamide hydrochloride (Standard) is the analytical standard of Loperamide (hydrochloride). It acts as an opioid receptor agonist and is recognized as a selective and competitive human intestinal carboxylesterases (hiCE) inhibitor, exhibiting an anti-diarrheal effect. This product is intended for research and analytical applications.
- Used as a reference standard for assay purposes.
- Commonly utilized in qualitative, quantitative, and methodological research experiments.
- Suitable for techniques such as HPLC, GC, and MS.
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Medchemexpress LLC Octopamine hydrochloride | 770-05-8 | MFCD00012881 | 99.90% | 5 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. This compound is known to affect various physiological processes, including metabolism and neuroregulation. It achieves its effects by binding to specific G protein-coupled receptors.
- Regulates sensory input desensitization, arousal, and complex behaviors like learning and memory.
- Modulates endocrine gland activity.
- Mobilizes lipids and carbohydrates as a neurohormone.
- Stimulates alpha2-adrenoceptors.
- Increases glycogenolysis, glycolysis, oxygen uptake, gluconeogenesis, and portal perfusion pressure.
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Medchemexpress LLC Loperamide hydrochloride | 34552-83-5 | 99.8% | 500 MG
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Loperamide hydrochloride is an opioid receptor agonist and a selective human intestinal carboxylesterases (hiCE) inhibitor, known for its anti-diarrheal effect. This compound has a molecular formula of C29H34Cl2N2O2 and a molecular weight of 513.50. It is intended for research use only and has not been fully validated for medical applications.
- Opioid receptor agonist
- Selective and competitive human intestinal carboxylesterases inhibitor
- Demonstrates anti-diarrheal properties
- Induces ER stress and autophagy in certain cell lines (in vitro)
- Decreases specific protein lipidation levels in ATF4 KO cells (in vitro)
- Suitable for laboratory research purposes
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Medchemexpress LLC BI 653048 | 1198784-72-3 | 99.8% | 25 MG
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BI 653048 is a chemical probe, a selective and orally active nonsteroidal glucocorticoid (GC) agonist with an IC50 value of 55 nM. It also acts as an HCV NS3 protease inhibitor.
- Inhibits CP1A2, CYP2D6, CYP2C9, CYP2C19, and CYP3A4 isoforms' activity.
- Reduces affinity for the hERG ion channel (IC50 > 30 μM).
- Can reduce viral loads infected with the hepatitis C virus.
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(CCCC)c1ccc(OCC)nc1 | 500mg | 525932231](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696423.jpg-250.jpg)
eMolecules 2265921-92-2 | 2-Ethoxy-5-(tributylstannyl)pyridine | Synthonix - Stock412.205 | C19H35NOSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1ccc(OCC)nc1 | 500mg | 525932231
2-Ethoxy-5-(tributylstannyl)pyridine | Synthonix - Stock | 2265921-92-2412.205 | C19H35NOSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1ccc(OCC)nc1 | 500mg | 525932231
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eMolecules Synthonix Propylzinc bromide 0.50 M in THF 100ml 627353818 P73474 156567-57-6 MFCD00671996 188.370 C3H7BrZn
Synthonix Propylzinc bromide 0.50 M in THF 100ml 627353818 P73474 156567-57-6 MFCD00671996 188.370 C3H7BrZn
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![eMolecules 521093-90-3 | 4-Cyano-3-fluorophenylzinc bromide, 0.50 M in THF | Synthonix | MFCD02260164 | 265.390 | C7H3BrFNZn | 0.000 | [Br-].Fc1cc([Zn+])ccc1C#N | 100ml | 532652709](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696276.jpg-250.jpg)
eMolecules 521093-90-3 | 4-Cyano-3-fluorophenylzinc bromide, 0.50 M in THF | Synthonix | MFCD02260164 | 265.390 | C7H3BrFNZn | 0.000 | [Br-].Fc1cc([Zn+])ccc1C#N | 100ml | 532652709
4-Cyano-3-fluorophenylzinc bromide, 0.50 M in THF | Synthonix | 521093-90-3 | MFCD02260164 | 265.390 | C7H3BrFNZn | 0.000 | [Br-].Fc1cc([Zn+])ccc1C#N | 100ml | 532652709
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Medchemexpress LLC Moxisylyte (hydrochloride) | 964-52-3 | 99.7% | 1 ML
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Moxisylyte (hydrochloride) is a selective α1A-adrenergic receptor antagonist that competitively antagonizes norepinephrine activation. It relaxes penile cavernous smooth muscle and aids erectile function, also improving dysuria and reducing residual urine volume in patients with multiple system atrophy. It is intended for research related to erectile dysfunction and multiple system atrophy.
- Acts as a competitive α-adrenergic receptor antagonist
- Exerts concentration-dependent relaxant effect on isolated human corpus cavernosum tissues
- Applicable to research related to erectile dysfunction
- Applicable to research related to multiple system atrophy
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Medchemexpress LLC Fenclonine hydrochloride | 23633-07-0 | 98.6% | 236.10 | C9H11Cl2NO2 | 1mL
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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 535961-78-5 | 2-Fluoro-6-methylbenzoyl chloride | Combi-Blocks | MFCD06660278 | 172.580 | C8H6ClFO | 98.000 | Cc1cccc(F)c1C(Cl)=O | 5g | 267180322
2-Fluoro-6-methylbenzoyl chloride | Combi-Blocks | 535961-78-5 | MFCD06660278 | 172.580 | C8H6ClFO | 98.000 | Cc1cccc(F)c1C(Cl)=O | 5g | 267180322
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