Aminophenols
Matrix Scientific 1-(4-HYDROXYPHENYL)PIPERAZI-10
1-(4-hydroxyphenyl)piperazine Mf C10h14n2o Mw 178.24 Cas 56621-48-8 Mdl MFCD00066156
![Medchemexpress LLC 7-[3-(4-(2,3-dimethylphenyl)piperazin-1-yl)propoxy]-1H-quinolin-2-one hydrochloride | 1329509-60-5 | 99.0% | 427.97 g·mol⁻¹ | C24H30ClN3O2 | 1 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000241642.png-250.jpg)
Medchemexpress LLC 7-[3-(4-(2,3-dimethylphenyl)piperazin-1-yl)propoxy]-1H-quinolin-2-one hydrochloride | 1329509-60-5 | 99.0% | 427.97 g·mol⁻¹ | C24H30ClN3O2 | 1 MG
OPC 4392 hydrochloride is a small-molecule dopamine receptor modulator used in preclinical pharmacology research. It functions as a presynaptic dopamine autoreceptor agonist and a postsynaptic D2 receptor antagonist, and has been applied in animal studies to reverse reserpine-induced dopamine depletion and reduce apomorphine-induced behaviors.
- Acts as presynaptic dopamine autoreceptor agonist and postsynaptic D2 antagonist.
- Demonstrated efficacy in reversing reserpine-induced dopamine depletion in animal studies.
- Inhibits apomorphine-induced stereotypic and climbing behaviors in rodent models.
- High purity (98.99%) suitable for research applications.
- White to off-white solid, convenient for handling and formulation.
- Recommended sealed storage away from moisture; in solvent store at -80°C for long-term preservation.
Medchemexpress LLC Fasudil hydrochloride | 105628-07-7 | MFCD00943198 | 100.0% | 327.83 g/mol | C14H18ClN3O2S | 100 MG
Fasudil hydrochloride is the hydrochloride salt of fasudil, a nonspecific RhoA/ROCK inhibitor used in research to investigate Rho-kinase-mediated signaling and kinase activity. It has CAS 105628-07-7, molecular formula C14H18ClN3O2S, and a molecular weight of 327.83 g/mol. The compound is supplied as a high-purity research reagent and is soluble in water and DMSO at the concentrations indicated on the product datasheet.
- Nonspecific RhoA/ROCK inhibitor for biochemical and cellular studies.
- Hydrochloride salt form for improved aqueous solubility.
- High purity (99.97%) suitable for research applications.
- Molecular weight 327.83 g/mol; formula C14H18ClN3O2S.
- Solubility: H2O 55 mg/mL (requires ultrasonic), DMSO ≥ 31 mg/mL.
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC Delapril hydrochloride | 83435-67-0 | MFCD00884619 | 98.0% | 489.00 | C26H33ClN2O5 | 50 MG
Delapril hydrochloride is the hydrochloride salt of delapril, a lipophilic angiotensin-converting enzyme (ACE) inhibitor commonly used in cardiovascular research. Supplied for research use only, the compound is characterized for identity and analytical purity to support experimental studies.
- Hydrochloride salt form for improved solubility and stability.
- High purity: 98.0% (NMR).
- Molecular formula C26H33ClN2O5; molecular weight 489.00.
- Available in solid quantities including 50 mg.
- Analytical documentation available: COA and SDS.
- Intended for in vitro and preclinical ACE inhibition studies.
Medchemexpress LLC AM-92016 hydrochloride | 133229-11-5 | 99.3% | 483.84 g/mol | C19H25Cl3N2O4S | 10 MG
AM-92016 hydrochloride is a research-grade small molecule that selectively blocks the rectifier potassium current (IK), delaying IK-mediated repolarization and restricting action potential duration. It is supplied as a high-purity solid intended for use in electrophysiology and ion-channel research.
- Specific blocker of rectifier potassium current (IK).
- Suitable for electrophysiology and ion-channel research.
- High purity (99.3%) for reliable experimental results.
- Solid, light yellow to yellow appearance.
- Storage: sealed at 4°C; in solvent -80°C (6 months) or -20°C (1 month).
- Pack size 10 mg for small-scale studies.
eMolecules Medchem Express / SKI-178 / 5mg / 599150633 / HY-12892 / / 1259484-97-3 / MFCD01913555 / 394.431 / C21H22N4O4
Medchem Express / SKI-178 / 5mg / 599150633 / HY-12892 / / 1259484-97-3 / MFCD01913555 / 394.431 / C21H22N4O4
Medchemexpress LLC UNC9994 hydrochloride | 2108826-33-9 | 99.5% | 457.84 | 10 MG
UNC9994 hydrochloride is a functionally selective, β-arrestin-biased dopamine D2 receptor (D2R) agonist. It selectively activates β-arrestin recruitment and signaling, demonstrating antipsychotic-like activity. It also acts as an antagonist of Gi-regulated cAMP production and a partial agonist for D2R/β-arrestin-2 interactions.
- Selectively activates β-arrestin recruitment and signaling.
- Antagonist of Gi-regulated cAMP production.
- Partial agonist for D2R/β-arrestin-2 interactions.
- Shows antipsychotic-like activity.
- Induces D2-mediated β-arrestin-2 translocation with EC50s of 6.1 nM and 448 nM.
- Acts as an antagonist at 5HT2A and 5HT2B receptors.
- Acts as an agonist at 5HT2C and 5HT1A receptors.
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 SKI-I | 5MG
SKI-I is a potent and selective inhibitor of human sphingosine kinase (SK) with an IC50 of 1 2 M for ST-hSK SKI-I also inhibits hERK2 (IC50 11 M) SKI-I induces apoptosis in tumor cell lines[1][2]
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 HY-112149 10mg Medchemexpress, ZL0420 CAS:2230496-80-5 Purity:>98%
Medchemexpress, HY-112149 10mg ZL0420 CAS:2230496-80-5 ZL0420 is a potent and selective bromodomain-containing protein 4 (BRD4) inhibitor with IC50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2. 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.
Medchemexpress LLC Ly-266,097 hydrochloride | 172895-39-5 | MFCD00949080 | ≥98.0% | 407.3 g/mol | C21H23ClN2O2 · HCl | 100 MG
LY266097 hydrochloride is the hydrochloride salt of LY266097, a selective antagonist of the serotonin 5-HT2B receptor used as a research tool in pharmacology and structural biology studies.
- Selective 5-HT2B receptor antagonist for receptor pharmacology studies.
- Supplied as the hydrochloride salt for improved solubility and handling.
- High purity suitable for in vitro and structural biology applications.
- Available in small research quantities for assay development and screening.
Medchemexpress LLC Rs 67333 hydrochloride | 168986-60-5 | 99.7% | 389.36 | C19H30Cl2N2O2 | 100 MG
RS 67333 hydrochloride is a research-grade 5-HT4 (serotonin 4) receptor partial agonist supplied as the hydrochloride salt for use in neuroscience and pharmacology studies. It is commonly used to probe 5-HT4 receptor function in vitro and in vivo, with reported neuroprotective and pro-cognitive activity.
- Partial agonist at 5-HT4 receptors, useful for receptor pharmacology studies.
- Hydrochloride salt form for improved solubility in aqueous media.
- High purity (99.68%) suitable for research applications.
- Characterized by CAS 168986-60-5 and defined molecular properties for formulation.
- Available in small research quantities (e.g., 100 MG) for in vitro and in vivo use.
- Relevant for studies of cognition, neuroprotection, and serotonergic signaling.
Medchemexpress LLC Nefopam (hydrochloride) | 23327-57-3 | 99.9% | 100 MG
Nefopam hydrochloride is a centrally-acting, non-opioid, and non-steroidal analgesic drug. It is derived from benzoxazocine and is used for the relief of moderate to severe pain. It targets β-catenin protein levels in mesenchymal cells both in-vitro and in-vivo, inhibiting β-catenin mediated signaling during skin wound repair.
- Centrally-acting analgesic
- Non-opioid and non-steroidal properties
- Aids in the relief of moderate to severe pain
- Inhibits β-catenin mediated signaling
- Derived from benzoxazocine
Medchemexpress LLC Cyclohexanecarboxylic acid, 1-phenyl-, 2-(4-morpholinyl)ethyl ester, hydrochloride (1:1) | 75136-54-8 | 99.8% | 353.88 | 1 ML
PRE-084 hydrochloride is a highly selective σ1 receptor (S1R) agonist, with an IC50 of 44 nM. It exhibits good neuroprotective effects, can improve motor function and motor neuron survival in mice, and can ameliorate myocardial ischemia-reperfusion injury in rats by activating the Akt-eNOS pathway.
- Highly selective σ1 receptor (S1R) agonist (IC50 of 44 nM).
- Exhibits neuroprotective effects.
- Improves motor function and motor neuron survival in mice.
- Ameliorates myocardial ischemia-reperfusion injury in rats by activating the Akt-eNOS pathway.