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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Ethyl trans-2-decenoate >=95%, stabilized, FG | 7367-88-6 | MFCD00015299 | 100G
Ethyl trans-2-decenoate >=95%, stabilized, FG | Purity: >=95% | Mol Wt: 198.3 | 7367-88-6 | MFCD00015299 | 100G
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eMolecules Ambeed / 2-Phenoxyethyl acrylate / 25g / 632809883 / A750164 / / 48145-04-6 / MFCD00053696 / 192.214 / C11H12O3
Ambeed / 2-Phenoxyethyl acrylate / 25g / 632809883 / A750164 / / 48145-04-6 / MFCD00053696 / 192.214 / C11H12O3
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![Biolegend Purified anti-Fumarase [9B1-4E1-8D5]; Isotype: Mouse IgG1, κ; Reactivity: Human; Apps: WB, IHC-P, ICC; Size: 25 ug](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502385169.PNG-250.jpg)
Biolegend Purified anti-Fumarase [9B1-4E1-8D5]; Isotype: Mouse IgG1, κ; Reactivity: Human; Apps: WB, IHC-P, ICC; Size: 25 ug
Purified anti-Fumarase [9B1-4E1-8D5]; Isotype: Mouse IgG1, κ; Reactivity: Human; Apps: WB, IHC-P, ICC; Size: 25 ug
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TARGETMOL CHEMICALS INC FLUPIRTINE MALEATE 200MG
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Also available in 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Flupirtine maleate (Katadolon maleate) a centrally acting non-opioid analgesia is the salt form of Flupirtine. It is an NMDA receptor antagonist and also a specific neuronal potassium channel opener. purity: 99%
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Medchemexpress LLC Indacaterol maleate | 753498-25-8 | MFCD20526769 | 99.8% | 508.56 g/mol | C28H32N2O7 | 5 MG
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Indacaterol maleate is the maleate salt of indacaterol, an ultra-long-acting β2-adrenergic receptor agonist. Supplied as an analytical standard, this solid reference material is intended for research use in assay development, method validation, and quality control testing.
- High purity (99.8%).
- Suitable for assay development and method validation.
- Confirmed identity by LC-MS consistent with structure.
- Stable solid form for accurate weighing and storage.
- Includes CAS 753498-25-8 and molecular weight 508.56 g/mol.
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Medchemexpress LLC Cinepazide Maleate | 26328-04-1 | 99.7% | C26H35N3O9 | 25 MG
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Cinepazide Maleate is a piperazine derivative that acts as a weak calcium channel blocker and a potent vasodilator. It is utilized in research for cerebrovascular diseases, including ischemic stroke and brain infarct.
- Acts as a weak calcium channel blocker
- Potent vasodilator
- Used for research on cerebrovascular diseases
- Suitable for ischemic stroke and brain infarct research
- For research use only
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Medchemexpress LLC Pirepemat fumarate | 2251806-70-7 | 98.3% | 329.30 | 50 MG
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Pirepemat fumarate is a cortical-preferring catecholamine- and cognition-promoting agent. It is utilized in the study of Parkinson's disease and is intended for research use only.
- Highest in vitro affinities for 5-HT and NA-related targets.
- Reverses deficits resulting from hypomonoaminergic function in vivo.
- Induces dose-dependent and regio-selective alterations in brain monoamine transmission indices and gene expression.
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eMolecules Ambeed / (Triisopropylsiloxy)methyl chloride / 100mg / 589771798 / A991979 / / 217300-17-9 / MFCD05865265 / 222.830 / C10H23ClOSi
Ambeed / (Triisopropylsiloxy)methyl chloride / 100mg / 589771798 / A991979 / / 217300-17-9 / MFCD05865265 / 222.830 / C10H23ClOSi
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Chem-Impex International, Inc. Dimethyl acetylenedicarboxylate | 762-42-5 | MFCD00008456 | 100G
Dimethyl acetylenedicarboxylate, 762-42-5, MFCD00008456, 100G
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Medchemexpress LLC Setiptiline maleate | 85650-57-3 | 99.9% | 377.43 | 50 MG
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Setiptiline maleate is a serotonin receptor antagonist and a tetracyclic antidepressant (TeCA) that acts as a noradrenergic and specific serotonergic antidepressant (NaSSA).
- Functions as a norepinephrine reuptake inhibitor.
- Acts as an α2-adrenergic receptor antagonist.
- Serves as a serotonin receptor antagonist, targeting 5-HT2A, 5-HT2C, and/or 5-HT3 subtypes.
- Acts as an H1 receptor inverse agonist/antihistamine.
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Ambeed 2-Chloroethyl methacrylate | 1888-94-4 | 148.59 g/mol | 10G
2-Chloroethyl methacrylate | 1888-94-4 | 148.59 g/mol | 10G
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Medchemexpress LLC BRL-44408 maleate | 681806-46-2 | 99.0% | 10 MG
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BRL-44408 maleate is a selective, blood-brain barrier-permeable α2A-adrenergic receptor antagonist with a Kᵢ value of 8.56 nM against human targets. It exhibits antidepressant and analgesic effects, and attenuates sepsis-induced acute lung injury by regulating neurotransmitter release or inhibiting signaling pathways. It can be used in studies related to acute respiratory distress syndrome, depression, and visceral pain.
- Selective α2A-adrenergic receptor antagonist
- Blood-brain barrier permeable
- Exhibits antidepressant and analgesic effects
- Attenuates sepsis-induced acute lung injury
- Regulates neurotransmitter release and inhibits signaling pathways
- Used in studies for acute respiratory distress syndrome, depression, and visceral pain
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Medchemexpress LLC IMMH-010 maleate | 2541982-47-0 | 99.8% | 756.04 | 1 MG
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IMMH-010 maleate is a prodrug that serves as a novel PD-L1 inhibitor, exhibiting potential antitumor activity for the treatment of neurological disorders and advanced malignant solid tumors. It is rapidly converted to its active form, YPD-29B, following oral administration. IMMH-010 maleate is poised for advancing research in the field of PD-L1 inhibitors and related therapeutic applications.
- Novel PD-L1 inhibitor
- Exhibits potential antitumor activity for neurological disorders and advanced malignant solid tumors
- Prodrug that rapidly converts to its active form, YPD-29B, following oral administration
- Poised for advancing research in the field of PD-L1 inhibitors and related therapeutic applications
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Medchemexpress LLC Zamifenacin fumarate | 127308-98-9 | 99.0% | 531.60 g/mol | C31H33NO7 | 25 MG
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Zamifenacin fumarate is the fumarate salt of zamifenacin, a gut-selective muscarinic M3 receptor antagonist used in research to study gastrointestinal motility. Supplied as a solid for laboratory research use only; not for human or clinical use.
- Potent gut-selective muscarinic M3 receptor antagonist.
- High purity: 99.0% (HPLC).
- White to off-white solid form for easy handling.
- Molecular weight 531.60 g/mol.
- Soluble in DMSO (100 mg/mL) and sparingly soluble in water with heating or ultrasonic treatment.
- Store sealed at 4°C; in solution store at -80°C (up to 6 months) or -20°C (1 month).
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Apexbio Technology LLC NB-598 Maleate 155294-62-5 50mg
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NB-598 Maleate is a small-molecule inhibitor targeting squalene epoxidase (SE) an essential enzyme in cholesterol biosynthesis It is designed to inhibit SE thereby disrupting the oxygenation of squalene and affecting downstream synthesis of cholesterol intermediates particularly within farnesol-dependent pathways leading to triglyceride biosynthesis NB-598 Maleate exerts its biological activity primarily through inhibition of squalene epoxidase In mouse pancreatic islet models NB-598 Maleate reduces insulin secretion under both basal and glucose-stimulated conditions Additionally this compound inhibits calcium voltage-dependent (CaV) ion channels in cellular assays Based on these pharmacological properties NB-598 Maleate holds research potential in studying cholesterol biosynthesis pathways lipid metabolism insulin regulation and the physiological role of CaV channels
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