Aminophenols
eMolecules Ambeed / N2N2-Dimethylpyrimidine-25-diamine / 250mg / 552737660 / A497416 / / 56621-99-9 / MFCD11656641 / 138.174 / C6H10N4
Ambeed / N2N2-Dimethylpyrimidine-25-diamine / 250mg / 552737660 / A497416 / / 56621-99-9 / MFCD11656641 / 138.174 / C6H10N4
eMolecules Ethyl (3-amino-4-hydroxyphenyl)acetate | 86818-19-1 | MFCD00230584 | 1g
Apollo Scientific | Ethyl (3-amino-4-hydroxyphenyl)acetate | 1g | 562430875 | OR110954 | | 86818-19-1 | MFCD00230584 | 195.218 | C10H13NO3
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eMolecules JANEX-1 | 202475-60-3 | MFCD01862614 | 1g
AstaTech | JANEX-1 | 1g | 290663216 | 44061 | 95.000 | 202475-60-3 | MFCD01862614 | 297.314 | C16H15N3O3
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Medchemexpress LLC Hypidone hydrochloride | 1339058-04-6 | 99.7% | 334.84 g/mol | C18H23ClN2O2 | 100 MG
Hypidone hydrochloride is the hydrochloride salt of a research compound with potent serotonergic activity. It functions as a selective serotonin (5-HT) uptake inhibitor and a 5-HT1A receptor agonist, and has demonstrated oral activity in animal models of depression. Supplied as a powder for laboratory research use only; not for human or clinical use.
- High purity suitable for research applications.
- Dual mechanism: serotonin uptake inhibition and 5-HT1A receptor agonism.
- Demonstrated oral activity in animal depression models.
- Available in multiple pack sizes including small research quantities.
- Recommended sealed storage away from moisture; in solvent store at -80°C for long term.
Apexbio Technology LLC OTS964 hydrochloride 1338545-07-5 2mg
OTS964 hydrochloride (CAS 1338545-07-5) is a selective inhibitor of T-lymphokine-activated killer cell-originated protein kinase (TOPK) demonstrating an IC50 of 28 nM against its target As a dimethylated derivative of OTS514 OTS964 displays high affinity and selectivity for TOPK a serine/threonine kinase implicated in various human malignancies In vitro OTS964 potently suppresses proliferation of multiple TOPK-positive cancer cell lines (IC50 values ranging from 7 6 to 73 nM) while showing markedly reduced activity in TOPK-negative models In in vivo studies OTS964 administered intravenously to mice bearing LU-99 xenografts resulted in significant tumor growth inhibition without notable toxicity Research applications include studying TOPK-related oncogenic pathways and hematopoietic cell differentiation
![Medchemexpress LLC N-(4-hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide | 901770-40-9 | MFCD29037927 | 99.5% | C16H21N3O3S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000261035.png-250.jpg)
Medchemexpress LLC N-(4-hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide | 901770-40-9 | MFCD29037927 | 99.5% | C16H21N3O3S | 10MG
Biotin-4-aminophenol is a biotin-phenol analog used to generate biotinylated protein radicals for selective labeling of tyrosine residues in proteins. Supplied as a solid or as pre-dissolved 10 mM solutions in DMSO, it is intended for biochemical labeling and proteomics workflows where site-selective modification of proteins is required.
- Selective tyrosine labeling via radical-mediated conjugation.
- Efficient generation of biotinylated protein radicals for detection and enrichment.
- Available as solid or 10 mM solution in DMSO for experimental convenience.
- High purity suitable for biochemical and proteomics applications.
- White to off-white solid with good solubility in DMSO.
eMolecules AOBChem USA / 3-Bromo-26-dichlorophenylboronic acid / 250mg / 525249607 / 20159 / / 1451392-94-1 / MFCD17011992 / 269.710 / C6H4BBrCl2O2
AOBChem USA / 3-Bromo-26-dichlorophenylboronic acid / 250mg / 525249607 / 20159 / / 1451392-94-1 / MFCD17011992 / 269.710 / C6H4BBrCl2O2
Cayman Chemical Acetaminophen Inhibitors
An analgesic and antipyretic compound; an inhibitor of COX-2 that is selective over COX-1 (IC50s = 113.7 and 25.8 µM, respectively, in human blood ex vivo); induces ferroptotic cell death in primary mouse hepatocytes; has a metabolite that depletes glutathione reserves in the liver
Cayman Chemical Acetaminophen Inhibitors
An analgesic and antipyretic compound; an inhibitor of COX-2 that is selective over COX-1 (IC50s = 113.7 and 25.8 µM, respectively, in human blood ex vivo); induces ferroptotic cell death in primary mouse hepatocytes; has a metabolite that depletes glutathione reserves in the liver
TARGETMOL CHEMICALS INC AMRI-59 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. AMRI-59 is a potent inhibitor of PrxI with anti-tumor activity. purity: 97%
Medchemexpress LLC Bepridil hydrochloride | 68099-86-5 | MFCD00065498 | 99.8% | 403.0 g/mol | C24H35ClN2O | 25 MG
Bepridil hydrochloride is a non-selective calcium channel blocker with antianginal activity, commonly used in cardiovascular and ion channel research to study calcium-mediated cardiac effects. The compound is provided as the hydrochloride salt (CAS 68099-86-5) with molecular formula C24H35ClN2O and molecular weight 403.0 g/mol.
- Non-selective calcium channel blocker used in cardiac and ion channel studies.
- Useful for investigating calcium-dependent electrophysiology and myocardial contractility.
- Hydrochloride salt form enhances solubility for assay preparation.
- Intended for in vitro and ex vivo research applications.
- Well-characterized chemical identifiers: CAS 68099-86-5; molecular formula C24H35ClN2O; molecular weight 403.0 g/mol.