Aminophenols
![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 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 2mg | 564356412](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000128908.jpg-250.jpg)
eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 2mg | 564356412
Medetomidine Hydrochloride | Key Organics/BIONET | 86347-15-1236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 2mg | 564356412
Medchemexpress LLC MK-3207 hydrochloride | 957116-20-0 | MFCD16038934 | 98.1% | 594.05 g/mol | C31H30ClF2N5O3 | 5 MG
MK-3207 hydrochloride is a potent, orally bioavailable antagonist of the calcitonin gene-related peptide (CGRP) receptor used in preclinical research to investigate CGRP-mediated signaling, migraine models, and receptor pharmacology.
- High affinity CGRP receptor antagonist (IC50 0.12 nM; Ki 0.024 nM).
- Purity 98.1%.
- Molecular formula C31H30ClF2N5O3; molecular weight 594.05 g/mol.
- Registered CAS number 957116-20-0.
- Suitable for in vitro and in vivo preclinical studies.
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.
Medchemexpress LLC R 59-022 hydrochlori 10mg | 93076-98-3 | 10MG
R 59-022 (DKGI-I) hydrochloride is a DGK inhibitor (IC50 2 8 M) R 59-022 hydrochloride inhibits the phosphorylation of OAG to OAPA R 59-022 hydrochloride is a 5-HT Receptor antagonist and activates protein kinase C (PKC) R 59-022 hydrochloride potentiates thrombin-induced diacylglycerol production in platelets and inhibits phosphatidic acid production in neutrophils[1 [2 [3 [4
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 CGP71683 hydrochloride | 192322-50-2 | MFCD07783999 | 99.4% | 512.07 g/mol | C26H30ClN5O2S | 50 MG
CGP71683 hydrochloride is a selective, non-peptide neuropeptide Y (NPY) Y5 receptor antagonist used for in vitro pharmacology and receptor signaling studies. The compound is supplied as a white solid and as a 10 mM solution in DMSO and is reported with high purity for research applications.
- Selective NPY Y5 receptor antagonist with low nanomolar affinity.
- Reported high purity suitable for research use.
- Available as a solid and as a 10 mM solution in DMSO for assay convenience.
- Molecular weight 512.07 g/mol aiding stoichiometric calculations.
- CAS registry number 192322-50-2 for unambiguous identification.
- Intended for biochemical and pharmacological studies in vitro.
Medchemexpress LLC RS100329 hydrochloride | 1215654-26-4 | MFCD00953081 | 99.6% | 462.89 g·mol⁻1 | C20H26ClF3N4O3 | 50 MG
RS100329 hydrochloride is the hydrochloride salt of RS100329, a potent and selective α1A-adrenoceptor antagonist used in pharmacological research. It is supplied as a white to off-white solid with high reported purity, and is suitable for in vitro and in vivo studies of α1A-adrenoceptor signaling and pharmacology.
- High purity (99.57%), white to off-white solid.
- Selective α1A-adrenoceptor antagonist for receptor pharmacology studies.
- Suitable for in vitro and in vivo research applications.
- Molecular weight 462.89 g·mol⁻1; formula C20H26ClF3N4O3.
- Store at 4°C and protect from light; solutions: -80°C (6 months) or -20°C (1 month).
- Supplied in 50 mg quantities.
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 RS100329 hydrochloride (2,4(1H,3H)-pyrimidinedione derivative) | 1215654-26-4 | 99.6% | 462.89 | C20H26ClF3N4O3 | 1 ML
RS100329 hydrochloride is a potent, selective α1A-adrenoceptor antagonist provided for in vitro receptor pharmacology and biochemical assays. It is available as a pre-made 10 mM solution in DMSO (1 mL) and in multiple solid sizes, with accompanying analytical documentation for research use.
- Potent, selective α1A-adrenoceptor antagonist suitable for in vitro studies.
- Available as 10 mM DMSO solution (1 mL) and as solid in multiple mg sizes.
- High purity (99.57%) appropriate for biochemical assays.
- Molecular weight 462.89 and formula C20H26ClF3N4O3.
- Supplied with data sheet, certificate of analysis, and safety data sheet.
- Intended for research use; follow laboratory safety and SDS guidance.
Medchemexpress LLC Ly266097 hydrochloride | 172895-39-5 | MFCD00949080 | 99.6% | 407.33 | C21H24Cl2N2O2 | 10 MG
LY266097 hydrochloride is a selective 5-HT2B receptor antagonist supplied as the hydrochloride salt for laboratory research. It is used to study serotonin 5-HT2 receptor pharmacology and is provided at high purity for in vitro and preclinical applications.
- Selective 5-HT2B receptor antagonist.
- Reported pKi values: 5-HT2A 7.7; 5-HT2B 9.8; 5-HT2C 7.6.
- High purity (99.6%) suitable for research use.
- Supplied as a hydrochloride salt in small milligram quantities for laboratory studies.
- Molecular formula C21H24Cl2N2O2; molecular weight 407.33.
Medchemexpress LLC Fasudil hydrochloride | 105628-07-7 | MFCD00943198 | 100.0% | 327.83 g/mol | C14H18ClN3O2S | 1 G
Fasudil hydrochloride is the hydrochloride salt of fasudil, a small-molecule Rho kinase (ROCK) inhibitor used in biochemical and cellular research to probe cytoskeletal dynamics, vascular tone, and related signaling pathways. It is provided as a high-purity solid suitable for laboratory research.
- RhoA/ROCK inhibitor for biochemical and cellular studies.
- CAS number 105628-07-7 and molecular weight 327.83 g/mol.
- Molecular formula C14H18ClN3O2S.
- High purity (~99.97%) suitable for research use.
- Solid, white to off-white appearance; soluble in DMSO and water.
- Recommended storage: 4°C sealed; in solvent: -80°C (1 year) or -20°C (6 months).
- Offered in laboratory pack sizes including 1 g.
Medchemexpress LLC 4-[(S)-amino(carboxy)methyl]-3-methylbenzoic acid hydrochloride | 2829282-00-8 | MFCD02262124 | 99.4% | 245.66 g/mol | C10H12ClNO4 | 1 ML
LY367385 hydrochloride is a selective mGluR1a antagonist supplied as a hydrochloride salt for research use. It is available as a solid and as a ready-to-use 10 mM solution in DMSO (1 mL vial), suitable for in vitro pharmacology and biochemical assays.
- High purity (99.4%) for reproducible assay results.
- Available as 10 mM solution in DMSO for convenient dosing.
- Also supplied as solid for custom formulation and storage.
- Molecular weight 245.66 g/mol and formula C10H12ClNO4.
- CAS number 2829282-00-8 for unambiguous substance identification.