Aminophenols
Aobchem 4-Bromo-N-(2-hydroxy-1 1-dimethylethyl)benzenesulfonamide | 95% | CAS 502484-72-2 | C10H14BrNO3S | 1g
4-Bromo-N-(2-hydroxy-1 1-dimethylethyl)benzenesulfonamide | 95% | CAS 502484-72-2 | C10H14BrNO3S | 1g
Aobchem 4-Bromo-N-(2-hydroxy-1 1-dimethylethyl)benzenesulfonamide | 95% | CAS 502484-72-2 | C10H14BrNO3S | 250mg
4-Bromo-N-(2-hydroxy-1 1-dimethylethyl)benzenesulfonamide | 95% | CAS 502484-72-2 | C10H14BrNO3S | 250mg
Aobchem 3-Bromo-1 4-difluoro-2 5-dimethoxybenzene | 95% | C8H7BrF2O2 | 1g
3-Bromo-1 4-difluoro-2 5-dimethoxybenzene | 95% | C8H7BrF2O2 | 1g
Aobchem 1-Bromo-3 4-difluoro-2 5-dimethylbenzene | 95% | CAS 2969357-28-4 | C8H7BrF2 | 500mg
1-Bromo-3 4-difluoro-2 5-dimethylbenzene | 95% | CAS 2969357-28-4 | C8H7BrF2 | 500mg
Aobchem 1-Bromo-3 5-difluoro-2 4-dimethoxybenzene | 95% | CAS 2969447-54-7 | C8H7BrF2O2 | 250mg
1-Bromo-3 5-difluoro-2 4-dimethoxybenzene | 95% | CAS 2969447-54-7 | C8H7BrF2O2 | 250mg
Medchemexpress LLC L-NAME (hydrochloride) | 51298-62-5 | 99.9% | 269.69 | 25 G
L-NAME hydrochloride inhibits NOS with an IC50 of 70 μM. It is a precursor to the NOS inhibitor L-NOARG, which has an IC50 value of 1.4 μM. This product is intended for research use only and can be used to induce hypertension and preeclampsia models.
- Inhibits NOS with an IC50 of 70 μM.
- Functions as a precursor to the NOS inhibitor L-NOARG.
- Suitable for inducing hypertension models.
- Suitable for inducing preeclampsia models.
- Exhibits a purity of 99.89%.
Medchemexpress LLC RGX-104 hydrochloride | 610318-03-1 | 99.9% | 632.54 | 10 MG
RGX-104 hydrochloride is a small-molecule LXR agonist that modulates innate immunity through the transcriptional activation of the ApoE gene. It is intended for research use only.
- Modulates innate immunity via transcriptional activation of the ApoE gene.
- Potential anti-cancer activity through suppression of various cancer types, including lung cancer, melanoma, glioblastoma, ovarian, renal cell, triple-negative breast, and colon cancer.
- Induces tumor regression in some cases.
- Available in various quantities.
Medchemexpress LLC SKI-178 | 1259484-97-3 | 99.3% | 50 MG
SKI-178 is a potent inhibitor of both sphingosine kinase-1 (SphK1) and sphingosine kinase-2 (SphK2). It demonstrates cytotoxicity in various cancer cell lines, including agent-sensitive and multi-agent resistant types, with IC50 concentrations ranging from 0.1 to 1.8 μM. This compound has been shown to induce apoptosis in human acute myeloid leukemia cell lines in a CDK1-dependent manner and correlates with prolonged Bcl-2 phosphorylation. In in-vivo studies, SKI-178 inhibited leukemic progression in the MLL-AF9 mouse model, leading to a decrease in white blood cell counts.
- Potent SphK1 and SphK2 inhibitor
- Exhibits cytotoxicity in various cancer cell lines
- Induces apoptosis in human acute myeloid leukemia cells
- Correlates with prolonged Bcl-2 phosphorylation
- Inhibits leukemic progression in MLL-AF9 mouse model
Medchemexpress LLC RS100329 hydrochloride | 1215654-26-4 | 99.6% | 462.89 g/mol | C20H26ClF3N4O3 | 25 MG
RS100329 hydrochloride is the hydrochloride salt of RS100329, a potent and selective α1A-adrenoceptor antagonist used in pharmacological research, including studies of urethral reflex contractions and benign prostatic hyperplasia. It is supplied as a solid research chemical with high reported purity and defined storage recommendations.
- Potent, selective α1A-adrenoceptor antagonist (pKi 9.6 for α1A).
- High purity (≈99.6% by HPLC), suitable for biochemical assays.
- Well-characterized small molecule: molecular weight 462.89 g/mol, formula C20H26ClF3N4O3.
- Provided as a solid hydrochloride salt for accurate dosing in experiments.
- Recommended storage: 4°C protected from light; in solvent, -80°C (6 months) or -20°C (1 month).
eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 40mg | 564356423
Medetomidine Hydrochloride | Key Organics/BIONET | 86347-15-1236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 40mg | 564356423
Medchemexpress LLC Bi-9627 (hydrochloride) | 1422252-46-7 | 98.01% | 392.80 | 1 ML
BI-9627 hydrochloride is a potent inhibitor of sodium-hydrogen exchanger isoform 1 (NHE1), exhibiting high selectivity over NHE2 and no measurable activity against NHE3. This compound shows low agent-agent interaction potential, excellent pharmacokinetics, and potent activity in isolated heart models of ischemia-reperfusion injury. It is intended for research use only.
- Decreases autophagy in HTR-8/SVneo cells.
- Significantly reduces the pHi of human sperm and partially reverses the effect of DMA.
- Prolongs Ca2+ recovery time in KO hiPSC-CMs.
- Shows low DDI potential.
- Excellent pharmacokinetics in rat and dog.
- Potent activity in isolated heart models of ischemia-reperfusion injury.