Phenylhydrazines
Medchemexpress LLC Pipendoxifene hydrochloride | 245124-69-0 | 99.8% | C29H33ClN2O3 | 10MG
Pipendoxifene hydrochloride is a selective estrogen receptor modulator (SERM) used in preclinical research, including studies of breast cancer. Supplied as the hydrochloride salt, it is a white to yellow solid with high measured purity and recommended sealed storage to maintain stability. The compound is intended for research use and is provided with supporting safety documentation.
- Selective estrogen receptor modulator for ER-targeted studies.
- High purity suitable for research applications.
- White to yellow solid form for convenient handling.
- Multiple small-scale pack sizes available for screening.
- Stable when stored sealed at recommended temperatures.
- Provided with safety data sheet and technical information.
Medchemexpress LLC Almonertinib hydrochloride | 2134096-03-8 | 98.9% | 562.11 | 100 MG
Almonertinib hydrochloride is an orally available, irreversible, third-generation EGFR tyrosine kinase inhibitor with high selectivity for EGFR-sensitizing and T790M resistance mutations. It shows significant inhibitory activity against T790M, T790M/L858R, and T790M/Del19 (IC50: 0.37, 0.29, and 0.21 nM, respectively) and is less effective against wild type (3.39 nM). It is used for the research of non-small cell lung cancer.
- Orally available
- Irreversible
- Third-generation EGFR tyrosine kinase inhibitor
- High selectivity for EGFR-sensitizing and T790M resistance mutations
- Significant inhibitory activity against T790M, T790M/L858R, and T790M/Del19
- Effective against other EGFR sensitive mutations including G719X, del19, L858R, and L861Q
Medchemexpress LLC Trimethoprim (hydrochloride) | 60834-30-2 | 99.2% | 25 MG
Trimethoprim hydrochloride is a bacteriostatic antibiotic and an orally active dihydrofolate reductase inhibitor. It is effective against a broad spectrum of Gram-positive and Gram-negative aerobic bacteria, with potential for research into urinary tract infections, Shigellosis, and Pneumocystis pneumonia.
- Bacteriostatic antibiotic
- Orally active dihydrofolate reductase inhibitor
- Effective against Gram-positive and Gram-negative aerobic bacteria
- Inhibits dihydrofolate reductase (DHFR) activity
- Can inhibit influenza A virus infection when combined with zinc
Chemscene ChemScene | (4-Fluorophenyl)hydrazine | 10G | CS-0183141 | 0.96 | 371-14-2| MFCD00041262 | 126.13
ChemScene | (4-Fluorophenyl)hydrazine | 10G | CS-0183141 | 0.96 | 371-14-2| MFCD00041262 | 126.13
eMolecules Ambeed / o-Tolylhydrazine hydrochloride / 1g / 570567247 / A111609 / / 635-26-7 / MFCD00012925 / 158.630 / C7H11ClN2
Ambeed / o-Tolylhydrazine hydrochloride / 1g / 570567247 / A111609 / / 635-26-7 / MFCD00012925 / 158.630 / C7H11ClN2
Accela Chembio Inc 3-fluorophenylhydrazine Hydrochloride | 25g | 2924-16-5 | MFCD00012934 | 97+% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive/+4
3-fluorophenylhydrazine Hydrochloride | 25g | 2924-16-5 | MFCD00012934 | 97+% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive/+4
Medchemexpress LLC Medetomidine (hydrochloride) | 86347-15-1 | 99.9% | 236.74 | 50 MG
Medetomidine hydrochloride is an orally active α2-adrenoceptor agonist with a Ki of 1.08 nM. It exhibits sedative and analgesic effects and can induce peripheral vasoconstriction by activating α2 adrenoceptors on blood vessels.
- Orally active α2-adrenoceptor agonist (Ki: 1.08 nM).
- Possesses sedative and analgesic effects.
- Causes peripheral vasoconstriction through α2 adrenoceptor activation.
- Inhibits aldosterone release from adrenocortical cell suspension in vitro.
- Activates a kicking response in Cyprids in vitro.
- Increases cellular cAMP production by activating β-like receptors in CHO cells in vitro.
- Induces sedation in cats in vivo.
- Shows sedative and analgesic effects in dogs in vivo.
- Protects against Diazinon-induced toxicosis in mice in vivo.
Medchemexpress LLC Eflornithine (hydrochloride hydrate) | 96020-91-6 | 5 G
Eflornithine hydrochloride hydrate (DFMO hydrochloride hydrate) is a specific, irreversible inhibitor of the enzyme ornithine decarboxylase. It is used in the treatment of African trypanosomiasis and excessive facial hair growth in women. This product is intended for research and analytical applications.
- For research and analytical applications
- Specific, irreversible inhibitor of ornithine decarboxylase
- Recommended storage for powder: 4°C, sealed, away from moisture
- Recommended storage for in solvent: -80°C for 6 months; -20°C for 1 month, sealed, away from moisture
- Shipping at room temperature if less than 2 weeks
Medchemexpress LLC Omadacycline (hydrochloride) | 1196800-39-1 | 99.5% | 593.11 | 1 G
Omadacycline hydrochloride (PTK 0796) is a first-in-class orally active aminomethylcycline antibacterial, belonging to the tetracycline class of antibiotics. It inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit. This compound exhibits broad-spectrum antibacterial activity against aerobic and anaerobic Gram-positive and Gram-negative bacteria, as well as atypical bacteria. It is used in the research of acute bacterial skin and skin-structure infections, community-acquired pneumonia, and urinary tract infections.
- Exhibits broad-spectrum antibacterial activity.
- Effective against aerobic and anaerobic gram-positive and gram-negative bacteria.
- Shows activity against atypical bacteria.
- Inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit.
- Active against resistant strains including MRSA, VRE, beta-hemolytic streptococci, PRSP, and H. influenzae.
Medchemexpress LLC Tetracycline hydrochloride | 64-75-5 | 98.7% | 100 MG
Tetracycline hydrochloride | 64-75-5 | 98.7% | 100 MG
Medchemexpress LLC Pexidartinib hydrochloride | 2040295-03-0 | 99.8% | 454.28 | 500 MG
Pexidartinib hydrochloride (PLX-3397 hydrochloride) is a potent, orally active, selective, and ATP-competitive colony stimulating factor 1 receptor (CSF1R or M-CSFR) and c-Kit inhibitor. It induces cell apoptosis and exhibits anti-cancer activity, making it a valuable tool for cancer research.
- Potent, orally active, selective, and ATP-competitive inhibitor
- Targets CSF1R (M-CSFR) with an IC50 of 20 nM and c-Kit with an IC50 of 10 nM
- Exhibits 10- to 100-fold selectivity for these targets over other related kinases
- Induces cell apoptosis and shows anti-cancer activity
- Can deplete microglia cells in mice and reduces tissue macrophage levels
- For research use only
eMolecules 97108-50-4 | 2,5-Difluorophenylhydrazine | MFCD00013384 | 5g
Combi-Blocks | 2,5-Difluorophenylhydrazine | 5g | 482935591 | OR-2224 | 95.000 | 97108-50-4 | MFCD00013384 | 144.125 | C6H6F2N2
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Medchemexpress LLC Cardiogenol C hydrochloride | 1049741-55-0 | 99.8% | 296.75 g/mol | C13H17ClN4O2 | 10MG
Cardiogenol C hydrochloride is a cardiomyogenic small-molecule research compound used to induce differentiation of pluripotent stem cells into cardiomyocytes and to study cardiac development and repair. Supplied as the hydrochloride salt with high reported purity, it is provided in small laboratory pack sizes for research applications.
- Induces cardiomyogenic differentiation in embryonic and pluripotent stem cells.
- High reported purity (99.8%).
- Molecular formula C13H17ClN4O2; molecular weight 296.75 g/mol.
- Soluble in DMSO (≥59 mg/mL) and moderately soluble in water (≈2 mg/mL).
- Provided as a solid hydrochloride salt in small pack sizes suitable for laboratory use.
- Store solids at 4°C; solutions stable at -80°C for up to 6 months and -20°C for 1 month.
Medchemexpress LLC 3-nitrophenylhydrazine-13C6 hydrochloride | 1977535-33-3 | 98.3% | 195.56 | 13C6H8ClN3O2 | 5 MG
3-Nitrophenylhydrazine-13C6 hydrochloride is the 13C-labeled isotopologue of 3-nitrophenylhydrazine supplied as the hydrochloride salt. It serves as a tracer and internal standard for quantitative analytical workflows, and is commonly used after derivatization to enhance detection by NMR, GC-MS, and LC-MS.