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Filtered Search Results
Medchemexpress LLC Cipralisant maleate | 223420-20-0 | 99.8% | 332.4 g/mol | C18H24N2O4 | 5 MG
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Cipralisant maleate is the maleate salt of cipralisant, a potent and selective histamine H3 receptor ligand that functions as a full antagonist in vivo and an agonist in vitro. Supplied for research use in neuroscience and pharmacology, the compound offers high purity, good DMSO solubility, and defined storage conditions for stability.
- Potent, selective histamine H3 receptor antagonist in vivo.
- Agonist activity observed in vitro.
- High reported purity (99.84%).
- Soluble in DMSO at ≥ 100 mg/mL.
- Molecular weight 332.4 g/mol.
- Recommended storage: powder -20°C for long term, 4°C for short term.
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TARGETMOL CHEMICALS INC Thioperamide maleate 10MG
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Also available in 1 mL, 1 mg, 5 mg, 25 mg and bulk. Please contact Fisher for quotes. Thioperamide maleate (MR-12842 maleate) is an effective and selective H3 receptor antagonist (Ki = 4.3 nM) that inhibits [3H]histamine synthesis (Ki = 31 nM). Purity 99.88%
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Chem-Impex International, Inc. Dimethyl acetylenedicarboxylate | 762-42-5 | MFCD00008456 | 5G
Dimethyl acetylenedicarboxylate, 762-42-5, MFCD00008456, 5G
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Selleck Chemical LLC Perhexiline maleate
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Perhexiline maleate is a potent inhibitor of carnitine palmitoyltransferase 1 (CPT1) with IC50s of 77 M and 148 M for rat heart CPT1 and liver CPT1 respectively and also inhibits carnitine palmitoyltransferase 2 (CPT2)
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Selleck Chemical LLC Trimebutine maleate
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Trimebutine maleate is the maleate salt form of trimebutine which is a spasmolytic agent that regulates intestinal and colonic motility and relieves abdominal pain with antimuscarinic and weak mu opioid agonist effects
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(C)C(C)(C)C)NC(=O)OC(C)(C)C | 500mg | 794076077](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502477968.JPG-250.jpg)
eMolecules 112418-19-6 | Methyl N-(tert-butoxycarbonyl)-O-(tert-butyldimethylsilyl)-D-serinate | Synthonix | MFCD28403203 | 333.500 | C15H31NO5Si | 98.000 | COC(=O)[C@@H](CO[Si](C)(C)C(C)(C)C)NC(=O)OC(C)(C)C | 500mg | 794076077
Methyl N-(tert-butoxycarbonyl)-O-(tert-butyldimethylsilyl)-D-serinate | Synthonix | 112418-19-6 | MFCD28403203 | 333.500 | C15H31NO5Si | 98.000 | COC(=O)[C@@H](CO[Si](C)(C)C(C)(C)C)NC(=O)OC(C)(C)C | 500mg | 794076077
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eMolecules 922-67-8 | Methyl propiolate | Oakwood Chemicals | MFCD00008572 | 84.074 | C4H4O2 | 97.000 | COC(=O)C#C | 5g | 480136915
Methyl propiolate | Oakwood Chemicals | 922-67-8 | MFCD00008572 | 84.074 | C4H4O2 | 97.000 | COC(=O)C#C | 5g | 480136915
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eMolecules 922-67-8 | Methyl propiolate | AA Blocks LLC | MFCD00008572 | 84.074 | C4H4O2 | 0.000 | COC(=O)C#C | 10g | 448665143
Methyl propiolate | AA Blocks LLC | 922-67-8 | MFCD00008572 | 84.074 | C4H4O2 | 0.000 | COC(=O)C#C | 10g | 448665143
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eMolecules 922-67-8 | Methyl propiolate | Combi-Blocks | MFCD00008572 | 84.074 | C4H4O2 | 97.000 | COC(=O)C#C | 25g | 117536327
Methyl propiolate | Combi-Blocks | 922-67-8 | MFCD00008572 | 84.074 | C4H4O2 | 97.000 | COC(=O)C#C | 25g | 117536327
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Medchemexpress LLC ER-27319 (maleate) | 1204480-26-1 | 99.4% | 396.44 | 50 MG
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ER-27319 (maleate), an acridone derivative, is a potent and selective SYK inhibitor. It inhibits the tyrosine phosphorylation of SYK and its activity, and can be used for study in allergic diseases. It also inhibits the release of antigen-induced allergic mediators from human and rat mast cells with an IC50 of 10 μM.
- Potent and selective SYK inhibitor
- Inhibits tyrosine phosphorylation of SYK
- Inhibits release of antigen-induced allergic mediators
- Suitable for study in allergic diseases
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Medchemexpress LLC Zamifenacin fumarate | 127308-98-9 | 99.0% | 531.60 g/mol | C31H33NO7 | 5 MG
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Zamifenacin fumarate is the fumarate salt of zamifenacin (UK-76654), a gut-selective muscarinic M3 receptor antagonist used in research to study gastrointestinal motility. It is provided as a high-purity solid for use in in vitro and in vivo pharmacology studies targeting colonic motility.
- Potent gut-selective muscarinic M3 receptor antagonist that reduces colonic motility.
- High purity suitable for research applications (99.0%).
- Solid, white to off-white form for convenient handling and dosing.
- Molecular weight 531.60 g/mol, molecular formula C31H33NO7.
- Recommended storage at 4°C; in solution, -80°C for long-term stability.
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Apexbio Technology LLC Rosiglitazone maleate(Synonyms: Avandia, BRL 49653, BRL49653C, Rosiglitazone maleate salt, BRL49653, RGZ, Rosiglizole maleate), 25mg, CAS: 155141-29-0.
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Rosiglitazone maleate (CAS 155141-29-0) is the maleate salt formulation of rosiglitazone a thiazolidinedione compound targeting the nuclear receptor peroxisome proliferator-activated receptor gamma (PPAR ) By selective activation of PPAR rosiglitazone increases insulin sensitivity of peripheral tissues facilitating glucose uptake and reduction of blood glucose levels Due to its insulin-sensitizing activity rosiglitazone maleate serves as an important research tool in diabetes and metabolic syndrome investigations However recent clinical studies also report associations with adverse cardiovascular events fluid retention and anemia underscoring considerations for risk-benefit evaluation in ongoing research
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Cayman Chemical FluoresceIn dIacetate 25g
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A cell-permeable fluorogenic cell viability probe; cleaved by intracellular esterases to produce fluorescein which displays excitation/emission maxima of 490/520 nm, respectively
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Apexbio Technology LLC Ethynodiol diacetate 297-76-7 10mM (in 1mL DMSO)
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Ethynodiol diacetate (297-76-7) is a small-molecule agonist targeting progesterone receptors It is designed to selectively bind and activate these receptors thereby modulating gene transcription pathways and influencing reproductive tissue responses Ethynodiol diacetate exerts its biological activity primarily through selective activation of progesterone receptors Based on these pharmacological properties Ethynodiol diacetate holds research potential in studies investigating hormonal regulation contraceptive mechanisms and modulation of the reproductive system
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Cayman Chemical FluoresceIn dIacetate 10g
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A cell-permeable fluorogenic cell viability probe; cleaved by intracellular esterases to produce fluorescein which displays excitation/emission maxima of 490/520 nm, respectively
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