Aminophenols
![Medchemexpress LLC 4-Piperidinecarboxamide, N-hydroxy-1-(2-methoxyethyl)-4-[[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonyl]-, hydrochloride (1:1) | 226395-93-3 | 99.4% | 554.96 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Medchemexpress LLC 4-Piperidinecarboxamide, N-hydroxy-1-(2-methoxyethyl)-4-[[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonyl]-, hydrochloride (1:1) | 226395-93-3 | 99.4% | 554.96 | 10 MG
SD-2590 hydrochloride is a potent MMP inhibitor with IC50 values of <0.1, <0.1, 0.18, and 1.7 nM for MMP2, MMP13, MMP9, and MMP8, respectively. It inhibits dilation of the left ventricle in rats. This product is for research use only.
- Potent MMP inhibitor
- Inhibits dilation of the left ventricle in rats
- Solid appearance
- White to off-white color
- Ships at room temperature
- Store at -20°C, sealed, away from moisture
- Soluble in DMSO at 55.5 mg/mL
Medchemexpress LLC BN82002 hydrochloride | 1049740-43-3 | 99.4% | 395.88 | 50 MG
BN82002 hydrochloride is a potent, selective, and irreversible inhibitor of the CDC25 phosphatase family. It inhibits CDC25A, CDC25B2, CDC25B3, CDC25C, and 25C-cat with IC50 values of 2.4, 3.9, 6.3, 5.4, and 4.6 μM, respectively. The compound demonstrates approximately 20-fold greater selectivity over CD45 tyrosine phosphatase and inhibits cell proliferation in several human tumor cell lines in a concentration-dependent manner in the low micromolar range. Treatment with 50 μM BN82002 modestly affects cell cycle distribution, suggesting cell cycle arrest at various stages.
- Potent, selective, and irreversible inhibitor of CDC25 phosphatase family.
- Displays approximately 20-fold greater selectivity over CD45 tyrosine phosphatase.
- Inhibits cell proliferation in various human tumor cell lines.
- For research use only.
Medchemexpress LLC Scopine hydrochloride | 85700-55-6 | 99.7% | 5 MG
Scopine hydrochloride, also known by its synonym 6,7-Epoxytropine hydrochloride, is recognized as a metabolite of Scopolamine and functions as a brain-targeting compound. This compound has demonstrated the ability to significantly elevate the brain exposure of Chlorambucil and consequently amplify its anti-glioma activity. These properties make Scopine hydrochloride a candidate for targeted therapy research focused on brain gliomas.
- It is a metabolite of Scopolamine.
- It acts as a brain-targeting compound.
- It significantly increases the brain exposure of Chlorambucil.
- It enhances the anti-glioma activity of Chlorambucil.
- It is used in targeted therapy research for brain gliomas.
- CHLS (Scopine combined with Chlorambucil) exhibits significant anti-glioma activity in C6 cells.
- Its IC50 & target is the α adrenergic receptor.
eMolecules 103-90-2 | Acetaminophen (Standard) | Medchem Express (US) | MFCD00002328 | 151.165 | C8H9NO2 | 98.000 | CC(=O)Nc1ccc(O)cc1 | 100mg | 849677361
Acetaminophen (Standard) | Medchem Express (US) | 103-90-2 | MFCD00002328 | 151.165 | C8H9NO2 | 98.000 | CC(=O)Nc1ccc(O)cc1 | 100mg | 849677361
Medchemexpress LLC Lavendustin B | 125697-91-8 | 98.0% | 365.38 | 500 MG
Lavendustin B is an inhibitor of HIV-1 integrase interaction with LEDGF/p75 with an IC50 of 94.07 μM. It also acts as an ATP-competitive GLUT1 inhibitor with a Ki of 15 μM, and a weak inhibitor of tyrosine kinases.
- Purity: 98.02%
- Appearance: Solid
- Color: White to yellow
- In vitro solubility: 50 mg/mL (136.84 mM)
- Shipping: Room temperature (continental US)
- Powder storage: -20°C for 3 years, 4°C for 2 years
- In solvent storage: -80°C for 6 months, -20°C for 1 month
![eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 6mg | 564356415](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000127359.jpg-250.jpg)
eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 6mg | 564356415
Medetomidine Hydrochloride | Key Organics/BIONET | 86347-15-1236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 6mg | 564356415
Medchemexpress LLC His-Pro hydrochloride | 2415727-78-3 | 99.8% | 288.73 | 100 MG
His-Pro (Histidyl-proline) hydrochloride is a dipeptide consisting of histidyl and proline. It is for research use only and not sold to patients.
- Appearance: Solid
- Color: White to off-white
- Shipping: Room temperature in continental US
- Storage: Sealed storage, away from moisture and light. Powder: -80°C for 2 years, -20°C for 1 year. In solvent: -80°C for 6 months, -20°C for 1 month.
- Solubility (In Vitro): DMSO: 125 mg/mL (432.93 mM)
Medchemexpress LLC Ac-099 hydrochloride | 849335-07-5 | 99.9% | 301.10 g/mol | C9H9Cl2F3N4 | 10 MG
AC-099 hydrochloride is a research-grade small-molecule hydrochloride salt used in preclinical studies as a ligand for neuropeptide FF receptors. The compound is supplied as a solid and characterized by standard analytical data for laboratory use.
- Research use only; not for human or veterinary use.
- High reported purity, 99.9%.
- Chemical formula C9H9Cl2F3N4 and molecular weight 301.10 g/mol.
- Provided as a solid suitable for dissolution in common organic solvents.
- Common applications include receptor pharmacology and in vivo preclinical assays.
Medchemexpress LLC Guvacine hydrochloride | 6027-91-4 | 99.9% | 163.60 g·mol⁻¹ | C6H10ClNO2 | 100 MG
Guvacine hydrochloride is a research reagent used to inhibit GABA uptake in neuropharmacology and biochemical studies. It is supplied as a white to off-white solid and is available in both solid and small-solution formats for in vitro experiments.
- Functions as a GABA uptake inhibitor for neuropharmacology research.
- High purity (~99.9%) minimizes impurities in assays.
- Available as solids and as a DMSO solution for experimental flexibility.
- White to off-white solid suitable for analytical and in vitro use.
- Molecular weight 163.60 g·mol⁻¹ supports accurate stoichiometry calculations.
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 Imiloxan hydrochloride | 81167-22-8 | MFCD01074788 | >98.0% | 280.75 | C14H17ClN2O2 | 25 MG
Imiloxan hydrochloride is the hydrochloride salt of imiloxan, a potent and selective α2B-adrenoceptor antagonist used in pharmacology research. Supplied as a solid reagent, it is intended for distinguishing α2 receptor subtypes and for probing adrenergic signaling in both in vitro and in vivo studies.
- Potent, selective α2B-adrenoceptor antagonist for receptor pharmacology.
- Suitable for both in vitro and in vivo pharmacodynamic studies.
- High purity (≥98% HPLC) supporting reproducible results.
- Hydrochloride salt form improves aqueous solubility for dosing.
- Available in small research pack sizes appropriate for screening and dosing.
- Molecular formula C14H17ClN2O2; molecular weight 280.75 g/mol.
Medchemexpress LLC UNC9994 hydrochloride | 2108826-33-9 | 99.5% | 457.84 | 25 MG
UNC9994 hydrochloride is a functionally selective, β-arrestin-biased dopamine D2 receptor (D2R) agonist that selectively activates β-arrestin recruitment and signaling. It exhibits a binding affinity with a Ki of 79 nM for D2R. This compound also acts as an antagonist of Gi-regulated cAMP production and a partial agonist for D2R/β-arrestin-2 interactions. UNC9994 hydrochloride demonstrates antipsychotic-like activity. For research use only.
- Selectively activates β-arrestin recruitment and signaling
- Exhibits binding affinity with a Ki of 79 nM for D2R
- Acts as an antagonist of Gi-regulated cAMP production
- Functions as a partial agonist for D2R/β-arrestin-2 interactions
- Demonstrates antipsychotic-like activity
Medchemexpress LLC DiAzKs hydrochloride | 2421187-79-1 | 98.0% | 100 MG
DiAzKs hydrochloride, also known as H-L-Photo-lysine hydrochloride, is a diazirine-containing lysine amino acid and a photo-cross-linker. It can be site-selectively incorporated into proteins and is used to crosslink protein-protein interactions in vitro and in living cells. This compound acts as a UV light-activated photo-crosslinking probe.
- Site-selective incorporation into proteins.
- Used to crosslink protein-protein interactions in vitro and in living cells.
- Acts as a UV light-activated photo-crosslinking probe.
- Photo-lysine can capture and identify proteins that recognize lysine post-translational modifications (PTMs), including 'readers' and 'erasers' of histone modifications.
Medchemexpress LLC NPS-2143 hydrochloride | 324523-20-8 | MFCD16038896; MFCD04113010 | 100.0% | 445.38 g/mol | C24H26Cl2N2O2 | 50 MG
NPS-2143 hydrochloride is an orally active calcilytic small molecule that selectively antagonizes the calcium-sensing receptor (CaSR), inhibiting CaSR-mediated increases in intracellular Ca2+. It is supplied as a solid at high purity for use in biochemical and pharmacological research into CaSR signaling and related physiological pathways.
- Selective CaSR antagonist for CaSR signaling studies.
- Orally active calcilytic small molecule suitable for in vitro and in vivo research.
- High purity solid appropriate for research applications.
- Molecular weight 445.38 g/mol and chemical formula C24H26Cl2N2O2.
- Available in small research quantities, including 50 MG.
- Applicable to biochemical, cellular, and pharmacological assays.
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.