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Filtered Search Results
Medchemexpress LLC Vicriviroc maleate | 599179-03-0 | MFCD09833218 | 99.9% | 649.70 | 1 ML
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Vicriviroc maleate is a potent, selective, and orally bioavailable CCR5 antagonist. It is CNS penetrated with a Ki of 2.5 nM. This compound effectively inhibits HIV-1 in PBMC cells across various strains.
- Potent and selective CCR5 antagonist
- Oral bioavailable and CNS penetrated
- Inhibits HIV-1 in PBMC cells
- Active against multiple HIV-1 strains
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Medchemexpress LLC 4-PPBP maleate | 201216-39-9 | 99.6% | 409.52 g/mol | C25H31NO4 | 50 MG
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4-PPBP maleate is a research-grade sigma-1 (σ1) receptor ligand and agonist used in neuroscience studies. It acts as a non-competitive, selective antagonist of NR1a/2B NMDA receptors and has been used in models of neuroprotection. The compound is supplied as a solid with high reported purity and defined storage recommendations for stability.
- Potent sigma-1 receptor ligand and agonist.
- Non-competitive, selective NR1a/2B NMDA receptor antagonist.
- Used in neuroprotection research models.
- High purity (99.6%).
- Supplied as a solid for convenient handling.
- Stable when stored sealed at 4°C; solvent storage conditions applicable.
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=O | 5g | 537664091](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502148529.JPG-250.jpg)
eMolecules 953-26-4 | Ethyl 4-nitrocinnamate | Oakwood Chemical | MFCD00007380 | 221.212 | C11H11NO4 | 98.000 | CCOC(=O)\C=C\c1ccc(cc1)[N+]([O-])=O | 5g | 537664091
Ethyl 4-nitrocinnamate | Oakwood Chemical | 953-26-4 | MFCD00007380 | 221.212 | C11H11NO4 | 98.000 | CCOC(=O)\C=C\c1ccc(cc1)[N+]([O-])=O | 5g | 537664091
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Medchemexpress LLC Lisuride maleate | 19875-60-6 | 99.97% | 454.52 | 50 MG
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Lisuride (maleate) is a potent dopamine agonist that is believed to act directly on dopaminergic receptors. It is an ergot derivative. This compound has been shown to alleviate premenstrual mastalgia without significant side effects. Lisuride (maleate) has been studied in vivo, demonstrating 3-4 times higher potency when administered intraperitoneally (i.p.) compared to orally (p.o.). It effectively antagonizes motor depression and hypothermia induced by reserpine. At dosages as low as 0.10 mg/kg i.p., it is comparable in effectiveness to apomorphine and D-amphetamine in causing significant hypothermia. The product is for research use only and not sold to patients.
- Potent dopamine agonist
- Ergot derivative
- Therapeutic potential for premenstrual mastalgia
- Suitable for research applications
- High purity
- Versatile formulations
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Medchemexpress LLC Sumanirole (maleate) | 179386-44-8 | 99.8% | 319.31 | C15H17N3O5 | 10 MG
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Sumanirole maleate is the maleate salt of sumanirole, a selective dopamine D2 receptor full agonist used in neuroscience and pharmacology research to investigate dopaminergic signaling and disease models. It is supplied as a white to off-white solid with high purity and specified molecular formula C15H17N3O5 (MW 319.31).
- Selective D2 receptor full agonist for receptor pharmacology studies.
- High purity suitable for analytical and biological assays.
- White to off-white solid appearance for easy visual inspection.
- Available in small research quantities appropriate for in vitro studies.
- Stable when stored sealed at 4°C; in solvent store at -80°C (6 months) or -20°C (1 month).
- CAS number 179386-44-8 for unambiguous chemical identification.
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TARGETMOL CHEMICALS INC Monatepil maleate 1MG
Also available in 5 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Monatepil maleate (AJ-2615 maleate) is an orally active Ca2+-channel and alpha1-adrenoceptor antagonist and non-competitive heparanoyl-coenzyme Acholesterol acyltransferase (ACAT) inhibitor with antihypertensive activity.Monatepil maleate is used in studies of hyperlipidemia and atherosclerosis. Monatepil maleate is used to study hyperlipidemia and atherosclerosis. Purity 96.28%
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Medchemexpress LLC PD-168077 maleate | 630117-19-0 | 99.6% | 450.49 | 100 MG
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PD-168077 maleate is a selective dopamine D4 receptor agonist with a Ki of 9 nM. It is for research use only. It shows high selectivity over other D2-like receptor family members and D1-like counterparts, as well as α1, α2, 5-HT1A, and 5-HT2A receptors. It evidences intrinsic activity at the D4 receptor and can induce locomotion in a dose-dependent manner. This product may be used in research related to neurological diseases, neurodegenerative diseases, depression, and Parkinson's disease.
- Selective dopamine D4 receptor agonist
- High selectivity over other receptor types
- Evidences intrinsic activity at the D4 receptor
- Induces locomotion in PD-168077-treated cells
- May be used in research for neurological diseases
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Medchemexpress LLC 4-PPBP maleate | 201216-39-9 | MFCD00209909 | 99.6% | 409.52 g·mol-1 | C25H31NO4 | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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4-PPBP maleate is a research-grade small-molecule sigma-1 receptor ligand and NMDA receptor modulator supplied as the maleate salt. It is intended for in vitro and preclinical studies and is not for human or clinical use. The compound is well characterized and provided with analytical purity suitable for laboratory research.
- Potent sigma-1 receptor ligand and agonist.
- Selective, non-competitive modulator of NR1a/2B NMDA receptors.
- Supplied as the maleate salt for stability and handling.
- High purity suitable for research applications (approximately 99.6%).
- Well-characterized molecular identity: C25H31NO4; MW 409.52 g·mol-1.
- Available in small laboratory pack sizes (25 mg).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Dizocilpine maleate | 77086-22-7 | C20H19NO4 | 100 MG
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Dizocilpine maleate is a potent, selective, and non-competitive NMDA receptor antagonist. It effectively blocks currents induced by N-Me-D-Asp and can be utilized in various research applications, including inducing schizophrenia models.
- Potent, selective, and non-competitive NMDA receptor antagonist
- Causes progressive, long-lasting blockade of current induced by N-Me-D-Asp
- Used to induce schizophrenia models
- Kd of 37.2 nM in rat brain membranes
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Apexbio Technology LLC Mepyramine maleate 59-33-6 10mM (in 1mL DMSO)
Mepyramine maleate (CAS 59-33-6) is a selective antagonist of the histamine H1 receptor exhibiting dissociation constants of 0 8 nM for H1 5200 nM for H2 and over 3000 nM for H3 receptors By blocking H1 receptor-mediated signaling it modulates pathways involved in allergic responses Mepyramine maleate is commonly utilized in experimental models of allergic diseases to investigate histamine-related mechanisms and to delineate the role of H1 receptor activity in immunological and inflammatory processes
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Pfaltz & Bauer DI(2-ETHYLHEXYL) FUMARAT 50G
Di(2-ethylhexyl) fumarate 50G CAS# 141-02-6
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Apexbio Technology LLC WAY-100635 maleate salt 1092679-51-0 100mg
WAY-100635 maleate salt (CAS 1092679-51-0) is a selective antagonist of the serotonin 5-HT1A receptor subtype It demonstrates high potency with a reported pIC50 value of 8 87 and displays over 100-fold selectivity relative to other serotonin receptor isoforms and common neurotransmitter receptor classes Due to its specific interaction with 5-HT1A receptors WAY-100635 maleate is frequently applied in neuroscience research to elucidate serotonin-mediated pathways and associated physiological or behavioral responses
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(C)OCCCCBr | 250mg | 527374902](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502430228.PNG-250.jpg)
eMolecules 89043-32-3 | 4-bromobutoxy-tert-butyl-dimethylsilane | Ambeed | MFCD20259686 | 267.282 | C10H23BrOSi | 97.000 | CC(C)(C)[Si](C)(C)OCCCCBr | 250mg | 527374902
4-bromobutoxy-tert-butyl-dimethylsilane | Ambeed | 89043-32-3 | MFCD20259686 | 267.282 | C10H23BrOSi | 97.000 | CC(C)(C)[Si](C)(C)OCCCCBr | 250mg | 527374902
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eMolecules 6525-45-7 | Ethyl 2-cyanobenzoate | Combi-Blocks | MFCD03423595 | 175.187 | C10H9NO2 | 96.000 | CCOC(=O)c1ccccc1C#N | 25g | 485192366
Ethyl 2-cyanobenzoate | Combi-Blocks | 6525-45-7 | MFCD03423595 | 175.187 | C10H9NO2 | 96.000 | CCOC(=O)c1ccccc1C#N | 25g | 485192366
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Medchemexpress LLC Fti-2153 | 344900-92-1 | MFCD32215316 | 99.8% | 466.60 | C25H30N4O3S | 50MG
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FTI-2153 is a potent, highly selective farnesyltransferase (FTase) inhibitor for research use. It inhibits FTase with an IC50 of 1.4 nM and is used to study protein prenylation and FTase-related cellular processes.
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