Phenols
Cambridge Isotope Laboratories Bisphenol E (unlabeled) 100 ug/mL in acetonitrile 1 2 mL
Bisphenol E (unlabeled) 100 ug/mL in acetonitrile 1 2 mL
Medchemexpress LLC Cefotaxime sodium | 64485-93-4 | 99.1% | C16H16N5NaO7S2 | 1 ML
Cefotaxime sodium is a β-lactamase stable, third-generation cephalosporin antibiotic. It demonstrates broad-spectrum antibiotic activity against numerous Gram-positive and Gram-negative bacteria.
- Exhibits MIC of 0.0625 mg/L for V. vulnificus CMCP6
- More effective in clearing V. vulnificus in vivo when combined with ciprofloxacin
- Lowers viable bacterial counts in liver when combined with ciprofloxacin
![Medchemexpress LLC Bicyclo[3.1.1]heptane-2-ethanol, 6,6-dimethyl- | 4747-61-9 | 98.1% | 168.28 | 500 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000365812-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Bicyclo[3.1.1]heptane-2-ethanol, 6,6-dimethyl- | 4747-61-9 | 98.1% | 168.28 | 500 G
Hydronopol is a saturated alcohol terpene derivative. It exhibits central inhibitory, anticonvulsant, analgesic, anticholinergic, and antihypertensive activities, making it suitable for research in neurological and cardiovascular diseases.
- Saturated alcohol terpene derivative
- Exhibits central inhibitory, anticonvulsant, analgesic, anticholinergic, and antihypertensive activities
- Can be used for research in neurological and cardiovascular diseases
Medchemexpress LLC Taranabant (1R,2R)stereoisomer | 701977-08-4 | 98.2% | 515.95 g/mol | C27H25ClF3N3O2 | 1 ML
Taranabant (1R,2R) stereoisomer is the R-enantiomer of taranabant, a potent and selective cannabinoid 1 (CB1) receptor inverse agonist supplied for research use. It is provided at high purity and is available both as a 10 mM solution in DMSO and in multiple solid sizes for in vitro pharmacology and biochemical studies.
- High purity (98.15%).
- CAS number 701977-08-4.
- Molecular weight 515.95 g/mol.
- Available as 10 mM solution in DMSO and solids (2 mg-500 mg).
- Suitable for in vitro pharmacology and receptor binding studies.
Medchemexpress LLC Varenicline dihydrochloride | 866823-63-4 | 99.2% | 284.18 g/mol | C13H15Cl2N3 | 50 MG
Varenicline dihydrochloride is a small-molecule partial agonist of neuronal nicotinic acetylcholine receptors, used as a research reagent to study α4β2, α6β2, and α7 receptor pharmacology and mechanisms of nicotine dependence. The dihydrochloride salt improves aqueous solubility for in vitro assays and analytical workflows.
- Potent partial agonist of α4β2 nicotinic receptors.
- Also active at α6β2 and α7 receptor subtypes.
- Suitable for in vitro pharmacology and signaling studies.
- High reported purity appropriate for research use.
- Dihydrochloride salt enhances solubility in aqueous media.
Medchemexpress LLC CPA inhibitor | 223532-02-3 | 99.78% | C18H19NO4 | 1 ML
CPA inhibitor (Compound 5) is a potent carboxypeptidase A (CPA) inhibitor with a Ki of 0.32 μM. It is for research use only and not sold to patients.
- Potent carboxypeptidase A (CPA) inhibitor
- Ki of 0.32 μM
- For research use only
Medchemexpress LLC 2-Aminomethylpyrimidine (hydrochloride) | 372118-67-7 | 99.2% | C5H8ClN3 | 100 G
2-Aminomethylpyrimidine hydrochloride is a synthetic intermediate useful for pharmaceutical synthesis. This compound is intended for research use only and is not sold to patients. It appears as a solid with a color ranging from off-white to light yellow.
- Useful for pharmaceutical synthesis
- Intended for research use only
- Appears as a solid
- Color is off-white to light yellow
- Stable under recommended storage conditions
Chemscene ChemScene | 4-Amino-3,5-dimethylphenol | 25G | CS-W019281 | 0.98 | 3096-70-6| MFCD01741459 | 137.18
ChemScene | 4-Amino-3,5-dimethylphenol | 25G | CS-W019281 | 0.98 | 3096-70-6| MFCD01741459 | 137.18
eMolecules ChemScene / 2-Fluoro-4-iodophenol / 10g / 536847430 / CS-W005152 / 0.000 / 2713-28-2 / MFCD11109769 / 238.000 / C6H4FIO
ChemScene / 2-Fluoro-4-iodophenol / 10g / 536847430 / CS-W005152 / 0.000 / 2713-28-2 / MFCD11109769 / 238.000 / C6H4FIO
Medchemexpress LLC MTR-106 | 1639357-93-9 | 99.4% | 525.62 | 5 MG
MTR-106 is a potent and orally active G-quadruplex stabilizer and RNA polymerase I inhibitor. It induces apoptosis and inhibits cell growth, making it suitable for cancer research.
- Potent and orally active G-quadruplex stabilizer
- RNA polymerase I inhibitor
- Induces apoptosis and inhibits cell growth
- Has antitumor activity in both HR-deficient cells and PARPi-resistant cells
- Induces cell cycle arrest and DNA damage
- Suppresses tumor growth in BRCA-deficient and PARPi-resistant xenografts in nude mice