Phenols
Medchemexpress LLC Daurk-4 hydrochloride | 00-00-0 | 99.4% | C52H53Cl2FN8O12 | 10MG
dAURK-4 hydrochloride is a PROTAC derivative designed to selectively degrade Aurora A kinase (AURKA). It is supplied as a hydrochloride salt for research use in oncology and cell-cycle investigations, offering high purity and validated storage recommendations for small-scale laboratory studies.
- Potent and selective degrader of Aurora A kinase.
- High chemical purity suitable for research applications.
- Available as a hydrochloride salt for improved handling.
- Supplied in small quantities appropriate for in vitro studies.
- Detailed storage guidance provided to preserve stability.
Medchemexpress LLC Metixene hydrochloride hydrate | 7081-40-5 | 99.9% | 25 MG
Metixene hydrochloride hydrate is an anticholinergic, antiparkinsonian research standard used as a muscarinic acetylcholine receptor antagonist in pharmacology and neuroscience studies. It is supplied as the hydrochloride hydrate salt for improved stability and solubility and is typically provided in small quantities for laboratory research.
- Acts as a muscarinic acetylcholine receptor (mAChR) antagonist for receptor binding and functional assays.
- High purity suitable for analytical and biochemical applications (≈99.9%).
- Molecular weight 363.94 g/mol and formula C20H26ClNOS.
- Available in small package sizes such as 25 MG for laboratory use.
- Provided as a hydrochloride hydrate salt to aid solubility in common solvents.
Medchemexpress LLC (R)-2-hydroxy-3-(tetradecanoyl-d7-oxy)propyl (2-(trimethylammonio)ethyl) phosphate | 00-00-0 | 95.4% | 474.62 | C22H39D7NO7P | 5 MG
LysoPC(14:0/0:0)-d7 is a deuterium-labeled lysophosphatidylcholine used as an isotope-labeled endogenous metabolite standard for analytical and quantitative lipidomics studies. It is provided as a white to off-white solid and is intended for use as an internal standard in mass spectrometry workflows.
- Deuterium-labeled lyso-phosphatidylcholine for isotope-dilution assays.
- Molecular formula C22H39D7NO7P and molecular weight 474.62.
- Purity 95.4% by HPLC as reported on the certificate of analysis.
- Appearance white to off-white solid suitable for analytical use.
- Storage: powder -20°C up to 3 years, 4°C up to 2 years; in solvent -80°C up to 6 months.
- Intended for use as an endogenous metabolite/internal standard in lipidomics and quantitative assays.
![Medchemexpress LLC 2-pyridinemethanol, α-[3-[(2R,6S)-2,6-dimethyl-1-piperidinyl]propyl]-α-phenyl hydrochloride | 61477-94-9 | MFCD01691662 | 98.8% | 374.95 g/mol | C22H31ClN2O | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000213617.png-250.jpg)
Medchemexpress LLC 2-pyridinemethanol, α-[3-[(2R,6S)-2,6-dimethyl-1-piperidinyl]propyl]-α-phenyl hydrochloride | 61477-94-9 | MFCD01691662 | 98.8% | 374.95 g/mol | C22H31ClN2O | 50 MG
Pirmenol hydrochloride is the hydrochloride salt of pirmenol, an orally active antiarrhythmic compound used in cardiovascular research to study cardiac arrhythmias and ion channel modulation. It acts on muscarinic acetylcholine receptors to inhibit IK.ACh and is supplied as a solid for laboratory use.
- Orally active antiarrhythmic compound used in research.
- Inhibits IK.ACh by blocking muscarinic acetylcholine receptors (IC50 ~0.1 μM).
- Provided as a white to yellow solid suitable for biochemical assays.
- High reported purity (~98.8%) for analytical and pharmacology studies.
- Recommended storage: solid at 4°C under inert gas; solutions at -20°C to -80°C.
Medchemexpress LLC Pre-084 hydrochloride | 75136-54-8 | 99.92% | 353.88 | 50 MG
PRE-084 hydrochloride is a highly selective σ1 receptor (S1R) agonist with an IC50 of 44 nM. It demonstrates neuroprotective effects, improves motor function, and enhances motor neuron survival in mice. Additionally, it can mitigate myocardial ischemia-reperfusion injury in rats by activating the Akt-eNOS pathway.
- Highly selective σ1 receptor (S1R) agonist.
- Exhibits neuroprotective effects.
- Can improve motor function and motor neuron survival.
- Ameliorates myocardial ischemia-reperfusion injury by activating the Akt-eNOS pathway.
Medchemexpress LLC Mt-7716 hydrochloride | 1215859-93-0 | MFCD07778657 | 99.1% | 477.00 g·mol⁻¹ | C27H29ClN4O2 | 100 MG
MT-7716 hydrochloride is a selective non-peptide nociceptin receptor (NOP) agonist supplied as the hydrochloride salt for research use. It is investigated for reducing alcohol-seeking behavior and relapse, and is provided as a solid reagent for in vitro and in vivo pharmacology studies.
- Selective non-peptide nociceptin (NOP) receptor agonist.
- Investigated for reduction of alcohol seeking and relapse prevention.
- Provided as the hydrochloride salt in solid form for research applications.
- High purity (≈99.1%) suitable for analytical and pharmacology studies.
- Molecular formula C27H29ClN4O2, molecular weight 477.00 g·mol⁻¹.
- Storage: 4°C sealed, away from moisture; in solvent, -80°C (6 months) or -20°C (1 month).
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.
Medchemexpress LLC HLCL-61 hydrochloride | 1158279-20-9 | MFCD09446681 | 99.9% | 380.91 g/mol | C23H25ClN2O | 25 MG
HLCL-61 hydrochloride is a research-grade small-molecule inhibitor of protein arginine methyltransferase 5 (PRMT5), supplied as a hydrochloride salt for laboratory use only. It is intended for in vitro and preclinical research and is not for human or veterinary use.
- Inhibits PRMT5 activity in biochemical and cellular assays.
- High reported purity of 99.87%.
- Molecular weight is 380.91 g/mol.
- Identified by CAS number 1158279-20-9 for unambiguous chemical identification.
- Available in milligram quantities suitable for laboratory studies, including a 25 mg pack size.
Medchemexpress LLC Cgp55845 hydrochloride | 149184-22-5 | MFCD09266221 | 99.1% | 438.71 g/mol | C18H23Cl3NO3P | 5 MG
CGP55845 hydrochloride is the hydrochloride salt of CGP55845, a potent and selective GABAB receptor antagonist with low-nanomolar potency (IC50 ≈ 5-6 nM). It is supplied as a solid for research use in receptor pharmacology and neurological studies.
- Potent GABAB receptor antagonist with low-nanomolar activity.
- High purity (99.1%) suitable for research applications.
- Molecular weight 438.71 g/mol, well characterized.
- CAS number 149184-22-5 for unambiguous identification.
- Provided as the hydrochloride salt in a 5 mg pack for small-scale experiments.
Medchemexpress LLC HJC0416 hydrochloride | 2415263-08-8 | 98.7% | 429.32 g/mol | C18H18Cl2N2O4S | 25MG
HJC0416 hydrochloride is the hydrochloride salt of HJC0416, a potent, orally active small-molecule STAT3 inhibitor used in preclinical anticancer research. Supplied as a white to off-white solid with high chemical purity, it is intended for in vitro and in vivo studies assessing STAT3 pathway modulation.
- Potent STAT3 inhibition in preclinical models.
- Oral activity demonstrated in animal studies.
- High purity suitable for research applications.
- Available in small research pack sizes, including 25 mg.
- Store protected from light and under inert gas at recommended temperatures.
Medchemexpress LLC Bepridil hydrochloride | 68099-86-5 | MFCD00868313 | 99.8% | 403.0 g/mol | C24H35ClN2O | 50 MG
Bepridil hydrochloride is the mono-hydrochloride salt of bepridil, a non-selective calcium channel blocker with antianginal activity. This product is offered as an analytical standard for research and analytical applications.
- Calcium channel blocker, with antianginal activity.
- Intended for research and analytical use.
- High purity (reported ≈99.8%).
- Hydrochloride salt form for increased solubility in polar solvents.
- Chemical formula: C24H35ClN2O; molecular weight: 403.0 g/mol; CAS: 68099-86-5.
Medchemexpress LLC AM-92016 hydrochloride | 133229-11-5 | MFCD00673947 | 99.3% | 483.84 | C19H25Cl3N2O4S | 1 ML
AM-92016 hydrochloride is a small-molecule blocker of delayed rectifier potassium currents (IK), commonly used in electrophysiology and cardiovascular research to modulate action potential duration. It is supplied both as a solid and as a ready-to-use solution to support in vitro pharmacology and ion-channel assays.
- Blocks delayed rectifier potassium channels (IK) and shortens action potential duration.
- Supplied as a 10 mM solution in DMSO or as a dry solid for custom preparation.
- High purity suitable for research use (reported ~99.3%).
- Molecular weight 483.84 and CAS 133229-11-5 for clear identification.
- Available in small-quantity formats compatible with pharmacological assays.
Medchemexpress LLC UNC9994 hydrochloride | 2108826-33-9 | 99.5% | 457.84 | 50 MG
UNC9994 hydrochloride | 2108826-33-9 | 99.5% | 457.84 | 50 MG
Medchemexpress LLC HY-100689 5mg Medchemexpress, Propyl pyrazole triol CAS:263717-53-9 Purity:>98%
Medchemexpress, HY-100689 5mg Propyl pyrazole triol CAS:263717-53-9 Propyl pyrazole triol (PPT) is an estrogen receptor alpha (ERα) agonist. The relative binding affinity of Propyl pyrazole triol for ERα (ERα: 49%) around 410 times higher compared with estrogen receptor beta (ERβ: 0.12%) [1] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Cayman Chemical Acetaminophen, Purity: ≥98%, CAS: 103-90-2, 250 g
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