Organonitrogen Compounds
Bioworld Choline Chloride, 100 g
Choline Chloride An acyl group acceptor Technical Information:Also known as (2-Hydroxyethyl) trimethylammonium chlorideSensitivity: HygroscopicSubstance is listed in Toxic Substance Control Act (TSCA) inventoryAppearance: White crystalline powderDensity : 1.1 g/cm3 at 20 °C (lit.)IUPAC_Name: 2-hydroxy-N,N,N-trimethylethanaminium chloride OR (2-hydroxyethyl)trimethylammonium chlorideMelting Point: 302-305 °C (lit.)(dec.)RTECS Number: KH2975000
Chem-Impex International, Inc. Histamine dihydrochloride salt | 56-92-8 | MFCD00012703 | 100G
Histamine dihydrochloride salt, 56-92-8, MFCD00012703, 100G
eMolecules 1-(4-PYRIDYL)-1-BUTYLAMINE | 1179877-52-1 | MFCD12153946 | 1g
AstaTech | 1-(4-PYRIDYL)-1-BUTYLAMINE | 1g | 248479180 | 31766 | 95.000 | 1179877-52-1 | MFCD12153946 | 150.225 | C9H14N2
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eMolecules 2377151-10-3 | Medchem Express | ZL0580 | 5mg | 527574223 | HY-126428 | 532.54 | C25H23F3N4O4S
Medchem Express | Cefuroxime (sodium) | 500mg | 491484622 | HY-B1256 | 56238-63-2 | MFCD09878727 | 446.370 | C16H15N4NaO8S
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Medchemexpress LLC CAY 10465 | 688348-33-6 | 98.3% | 317.13 | 1 ML
CAY 10465 is a selective and high-affinity AhR agonist with a Ki of 0.2 nM. It demonstrates no effect on the estrogen receptor (Ki >100000 nM). This compound reduces apolipoprotein A-I (apo A-I) levels in HepG2 cells and inhibits the synthesis of the protein.
- Selective and high-affinity AhR agonist
- No effect on estrogen receptor
- Reduces apolipoprotein A-I levels in HepG2 cells
- Inhibits protein synthesis
Selleck Chemical LLC 1-Methylpyrrolidine
1-Methylpyrrolidine is extensively used in the synthesis of pyrrolidine based ionic liquids
TARGETMOL CHEMICALS INC Cisatracurium besylate 50MG
Also available in 1 mL, 10 mg, 25 mg, 100 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Cisatracurium besylate (51W89) is a nondepolarizing skeletal muscle relaxant intended for intravenous administration. Purity 98%
eMolecules 3040-34-4 | Ambeed | 3-Hydroxy-3-methylindolin-2-one | 250mg | 794180291 | A845860 | MFCD10699556 | 163.176 | C9H9NO2
Ambeed | 2-Hydroxy-2-methyl-1-phenylpropan-1-one | 10g | 523728631 | A201838 | 7473-98-5 | MFCD00040710 | 164.204 | C10H12O2
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Medchemexpress LLC Phenylbiguanide | 55-57-2 | MFCD00035040 | 100.0% | 213.67 g/mol | C8H12ClN5 | 100 G
Phenylbiguanide hydrochloride is a research-grade small molecule used as a selective agonist of the 5-HT3 receptor in pharmacology and neuronal signaling studies. It exhibits an EC50 of approximately 3.0 μM and has documented solubility and stability data suitable for laboratory use.
- Selective 5-HT3 receptor agonist (EC50 ≈ 3.0 μM).
- Chemical identity: CAS 55-57-2; formula C8H12ClN5; molecular weight 213.67 g/mol.
- High purity for research applications (COA reports 99.96%).
- Soluble in DMSO (≈40 mg/mL); formulations reported for in vivo dosing.
- Stable as solid at room temperature; defined solvent storage conditions available.
- Suitable for GPCR and neuronal signaling assays and related pharmacology studies.
![Medchemexpress LLC N,N-dimethyl-1-[4-(4-methylpyrazol-1-yl)-3-pyridinyl]piperidine-4-carboxamide | 1613480-70-8 | 99.6% | 313.40 g/mol | C17H23N5O | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000221563.png-250.jpg)
Medchemexpress LLC N,N-dimethyl-1-[4-(4-methylpyrazol-1-yl)-3-pyridinyl]piperidine-4-carboxamide | 1613480-70-8 | 99.6% | 313.40 g/mol | C17H23N5O | 5 MG
Cholesterol 24-hydroxylase-IN-1 is a potent, selective small-molecule inhibitor of cholesterol 24-hydroxylase (CYP46A1) used in biochemical and pharmacological research. The compound is analytically characterized with a defined molecular formula and high purity, enabling use in enzyme inhibition studies and mechanistic investigations.
- Potent, selective inhibitor of cholesterol 24-hydroxylase.
- Suitable for biochemical and pharmacological research applications.
- High purity (>99.5% by LCMS) supporting analytical use.
- Molecular weight 313.40 g/mol; formula C17H23N5O.
- Supplied as a 5 mg research pack.
Apexbio Technology LLC KW 2449 1000669-72-6 10mg
KW 2449 (CAS 1000669-72-6) is a multi-targeted kinase inhibitor with potent activity against FLT3 (IC50 6 6 nM) ABL (14 nM) Aurora kinases (4 nM) and FGFR (48 nM) It inhibits both wild-type and T315I-mutated ABL tyrosine kinase In vitro KW 2449 disrupts proliferation through modulation of distinct signaling pathways it downregulates FLT3/STAT5 phosphorylation and induces G1-phase arrest and apoptosis in FLT3-mutated leukemia cells while promoting G2/M arrest via reduced histone H3 phosphorylation in FLT3 wild-type cells KW 2449 is applied in research investigating kinase-driven leukemias and resistance mechanisms to targeted therapies
Matrix Scientific 3-HYDROXYPIPERIDINE-5G
3-Hydroxypiperidine, 98%; 5g,C5H11NO, MFCD00014591, mw 101.15, [6859-99-0]