Halomethanes
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Filtered Search Results
Medchemexpress LLC Omzotirome 10mg | 1092551-88-6 | 10MG
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Omzotirome (TRC150094) a functional analog of iodothyronines can be used for the research of hyperlipidaemia (WO2008149379)[1 [2
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Medchemexpress LLC RN-1665 | 1803003-65-7 | 99.9% | 513.54 | 25 MG
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RN-1665 is an orally active TRPV4 antagonist that exhibits excellent selectivity for related TRP receptors such as TRPV1, TRPV3, and TRPM8. It serves as a TRPV4 probe for focus screens, with IC50 values of 0.26 μM and 0.39 μM for human (hTRPV4) and rat (rTRPV4), respectively.
- Orally active TRPV4 antagonist.
- Shows excellent selectivity for related TRP receptors like TRPV1, TRPV3, and TRPM8.
- Serves as a TRPV4 probe for focus screens.
- IC50 of 0.26 μM for human TRPV4.
- IC50 of 0.39 μM for rat TRPV4.
- Soluble in DMSO (100 mg/mL).
- Powder stable for 3 years at -20°C and 2 years at 4°C.
- In solvent, stable for 6 months at -80°C and 1 month at -20°C.
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eMolecules ChemScene / Bicyclo[4.2.0]octa-135-triene-3-carbaldehyde / 250mg / 632277807 / CS-0044063 / 0.000 / 112892-88-3 / MFCD09842341 / 132.162 / C9H8O
ChemScene / Bicyclo[4.2.0]octa-135-triene-3-carbaldehyde / 250mg / 632277807 / CS-0044063 / 0.000 / 112892-88-3 / MFCD09842341 / 132.162 / C9H8O
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Medchemexpress LLC Pralidoxime (iodide) | 94-63-3 | 25 MG
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Pralidoxime iodide is a potent reactivator of acetylcholinesterase (AChE). It reactivates nerve agent-inhibited AChE via direct nucleophilic attack by the oxime moiety on the phosphorus center of the bound nerve agent. Pralidoxime iodide is an antidote for organophosphate poisoning.
- Potent reactivator of acetylcholinesterase (AChE).
- Reactivates nerve agent-inhibited AChE via direct nucleophilic attack by the oxime moiety on the phosphorus center of the bound nerve agent.
- Antidote for organophosphate poisoning.
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Medchemexpress LLC Thymol iodide | 552-22-7 | 1 G
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Thymol iodide is an iodine derivative of thymol, functioning as a mild preservative and fungicide. It serves as an iodine source for intensive rotifer culture, enabling rotifers to achieve and maintain high iodine content similar to copepods during storage. Research shows it does not enhance pleurodesis efficacy in rabbits after intrapleural injection.
- Iodine derivative of thymol.
- Acts as a mild preservative.
- Functions as a fungicide.
- Used as an iodine source in the intensive culture of rotifers.
- Enables rotifers to reach iodine levels similar to copepods.
- Maintains a high iodine content in rotifers during storage.
- Does not enhance pleurodesis efficacy in rabbits.
- Enriches rotifer iodine content to copepod levels with low dietary replacement (0.36-2.03%).
- Maintains stable iodine retention in rotifers for up to 18 hours.
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Medchemexpress LLC Acetylshengmanol Arabinoside | 402513-88-6 | 5 MG
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Acetylshengmanol Arabinoside is a high-purity chemical compound (99.89%) isolated from Cimicifugae rhizoma. This white to off-white solid has a molecular weight of 662.85 and a chemical formula of C₃₇H₅₈O₁₀. It is intended for research use in laboratories and for the manufacture of substances, and is not for sale to patients.
- Isolated from Cimicifugae rhizoma
- For research use only
- Purity of 99.89%
- Solid, white to off-white appearance
- Store at 4°C, protect from light
- Store in solvent at -80°C for 6 months or -20°C for 1 month, protect from light
- Shipped at room temperature if less than 2 weeks
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eMolecules Medchem Express / Thymopentin (acetate) / 5mg / 515744480 / HY-N7122A / / 89318-88-7 / MFCD00133107 / 739.828 / C32H53N9O11
Medchem Express / Thymopentin (acetate) / 5mg / 515744480 / HY-N7122A / / 89318-88-7 / MFCD00133107 / 739.828 / C32H53N9O11
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Medchemexpress LLC 1H,5H-Imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one, 2,3,10,10a-tetrahydro-1-[(3-methyl-4-isoxazolyl)carbonyl]-10a-(6-methyl-3-pyridinyl)-, (10aS)- | 1323077-88-8 | 99.7% | 377.40 | 1 MG
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Enzaplatovir (BTA-C585) is an orally bioavailable inhibitor for respiratory syncytial virus (RSV) infection and is described as a small-molecule RSV entry inhibitor. It is used for respiratory syncytial virus (RSV) infection and is relevant for RSV-associated lower respiratory tract infection (LRTI).
- Orally bioavailable
- Inhibitor for respiratory syncytial virus (RSV) infection
- Small-molecule RSV entry inhibitor
- Used for respiratory syncytial virus infection
- Relevant for RSV-associated lower respiratory tract infection (LRTI)
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Medchemexpress LLC Pralidoxime (iodide) | 94-63-3 | 98.0% | 250 MG
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Pralidoxime iodide is a potent reactivator of acetylcholinesterase (AChE). It reactivates nerve agent-inhibited AChE through direct nucleophilic attack by the oxime moiety on the phosphorus center of the bound nerve agent. It is also an antidote for organophosphate poisoning.
- Potent reactivator of acetylcholinesterase (AChE).
- Reactivates nerve agent-inhibited AChE.
- Antidote for organophosphate poisoning.
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Medchemexpress LLC 2-cyclohexen-1-one, 3-(15-hydroxypentadecyl)-2,4,4-trimethyl- | 220757-88-0 | 99.1% | 364.60 | C24H44O2 | 5 MG
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tCFA15 is a trimethyl cyclohexenonic long-chain fatty alcohol reported to promote neuronal differentiation and modulate Notch signaling. It is supplied as a pure-form research reagent with molecular formula C24H44O2 and molecular weight 364.60, and has documented analytical purity and storage stability.
- Promotes neuronal differentiation and modulates Notch signaling.
- High purity (99.12% by LCMS).
- Long-chain fatty alcohol structure with a 15-carbon side chain.
- Stable in pure form for extended storage at -20°C.
- Intended for research use in neuronal and stem cell pathway studies.
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eMolecules AstaTech / 2-PHENYLOXAZOLE / 0.25g / 233627069 / 36029 / 95.000 / 20662-88-8 / MFCD00461764 / 145.161 / C9H7NO
AstaTech / 2-PHENYLOXAZOLE / 0.25g / 233627069 / 36029 / 95.000 / 20662-88-8 / MFCD00461764 / 145.161 / C9H7NO
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eMolecules Ambeed / 34-difluorobenzoylchloride / 5g / 569096044 / A378696 / / 76903-88-3 / MFCD00009930 / 176.550 / C7H3ClF2O
Ambeed / 34-difluorobenzoylchloride / 5g / 569096044 / A378696 / / 76903-88-3 / MFCD00009930 / 176.550 / C7H3ClF2O
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eMolecules AstaTech / 2-IODOBENZENESULFONIC ACID MONOHYDRATE / 1g / 410713444 / CK2361 / 95.000 / 63059-25-6 / MFCD30534311 / 302.080 / C6H7IO4S
AstaTech / 2-IODOBENZENESULFONIC ACID MONOHYDRATE / 1g / 410713444 / CK2361 / 95.000 / 63059-25-6 / MFCD30534311 / 302.080 / C6H7IO4S
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Medchemexpress LLC Beperidium iodide | 86434-57-3 | 100.0% | 527.44 g·mol⁻¹ | C23H34IN3O3 | 10 MG
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Beperidium iodide is a research-grade muscarinic acetylcholine receptor antagonist reported with a pA2 of 7.93. Supplied as the iodide salt, it is intended for laboratory research use only and provides a defined, high-purity material for receptor pharmacology studies.
- High purity suitable for research applications (reported 99.97%).
- Identified by CAS 86434-57-3 for unambiguous chemical identification.
- Chemical formula C23H34IN3O3 and molecular weight 527.44 g·mol⁻¹.
- Available in small mass quantities for assay development and screening.
- Provided as the iodide salt optimized for receptor-binding studies.
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Medchemexpress LLC Methylene blue | 61-73-4 | MFCD00012111 | 95.0% | C16H18ClN3S | 100 MG
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Methylene blue is an inhibitor of guanylyl cyclase (sGC), monoamine oxidase A (MAO-A), and NO synthase (NOS). It acts as a vasopressor and is commonly used as a dye in various medical procedures. This REDOX cycling compound is capable of crossing the blood-brain barrier and is also a Tau aggregation inhibitor. It helps reduce cerebral edema, mitigate microglial activation, and decrease neuroinflammation.
- Inhibits guanylyl cyclase (sGC), monoamine oxidase A (MAO-A), and NO synthase (NOS)
- Acts as a vasopressor
- Commonly used as a dye in medical procedures
- Impacts prepulse inhibition through the nitric oxide synthase/guanylate cyclase signaling pathway
- Functions as a REDOX cycling compound
- Capable of crossing the blood-brain barrier
- Acts as a Tau aggregation inhibitor
- Helps reduce cerebral edema
- Mitigates microglial activation
- Decreases neuroinflammation
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