Hydrochlorides
eMolecules 3651-67-0 | N-Methylmorpholine hydrochloride | Combi-Blocks | MFCD00039042 | 137.610 | C5H12ClNO | 96.000 | Cl.CN1CCOCC1 | 1g | 303362220
N-Methylmorpholine hydrochloride | Combi-Blocks | 3651-67-0 | MFCD00039042 | 137.610 | C5H12ClNO | 96.000 | Cl.CN1CCOCC1 | 1g | 303362220
Medchemexpress LLC Naloxone (hydrochloride) | 357-08-4 | 100.0% | 363.84 | 500 MG
Naloxone hydrochloride is an antagonist of the Opioid receptor. It alleviates opioid-overdose-induced respiratory depression and may cause pulmonary edema and cardiac arrhythmias. It is for research use only and not sold to patients.
- Functions as an antagonist of the Opioid receptor.
- Helps to counteract respiratory depression caused by opioid overdose.
- Intended for research purposes.
Medchemexpress LLC Zm323881 hydrochloride | 193000-39-4 | C22H19ClFN3O2 | 25 MG
ZM323881 hydrochloride is a potent and selective VEGFR2 inhibitor with an IC50 of less than 2 nM. This anilinoquinazoline potently inhibits VEGFR2 (KDR) tyrosine kinase activity, showing excellent selectivity over other receptor tyrosine kinases. It inhibits VEGF-A-induced endothelial cell proliferation and VEGFR2 tyrosine phosphorylation.
- Potent and selective VEGFR2 inhibitor (IC50 < 2 nM)
- Inhibits VEGFR2 (KDR) tyrosine kinase activity
- Excellent selectivity over other receptor tyrosine kinases
- Inhibits VEGF-A-induced endothelial cell proliferation (IC50 = 8 nM)
- Inhibits VEGFR2 tyrosine phosphorylation
- Blocks activation of VEGFR-2, while sparing VEGFR-1, EGFR, PDGFR, and HGF receptor
- For research use only
eMolecules 1788058-41-2 | (R)-4-AMINOPYRROLIDIN-2-ONE HCL | MFCD20257112 | 1g
Medchem Express | Trametiglue | 5mg | 791206436 | HY-153181 | 2666940-97-0 | 666.470 | C25H24FIN6O5S
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool<|a>
Medchemexpress LLC Drp1i27 (dihydrochloride) | C20H28Cl2N6O | 25 MG
DRP1i27 dihydrochloride is a potent inhibitor of human Drp1 (dynamin-related protein 1). It binds to the GTPase site of Drp1 through hydrogen bonds to Gln34 and Asp218. This product targets Drp1-mediated mitochondrial fission in cell line models and offers protection against simulated ischemia-reperfusion injury.
- Potent inhibitor of human Drp1 (dynamin-related protein 1)
- Binds to the GTPase site of Drp1
- Targets Drp1-mediated mitochondrial fission in cell line models
- Protects against simulated ischemia-reperfusion injury
- Increases cellular networks of mitochondria in human and mouse fibroblasts in a Drp1-dependent manner
Medchemexpress LLC Bay-6672 hydrochloride | 2247520-31-4 | 98.0% | 581.33 | C26H28BrCl2N3O3 | 5 MG
BAY-6672 hydrochloride is a research-grade small molecule antagonist of the human Prostaglandin F (FP) receptor with a reported IC50 of 11 nM. Supplied as the hydrochloride salt and characterized at high purity, it is intended for in vitro pharmacology and biochemical studies and is available as a solid or as a 10 mM solution in DMSO. For research use only; not for human or clinical use.
- Potent FP receptor antagonist (IC50 = 11 nM).
- High purity suitable for pharmacological assays.
- Available as solid mg quantities and as a 10 mM DMSO solution.
- Characterized molecular weight and formula for identification.
- Intended for in vitro research use only.
Medchemexpress LLC CCT365623 hydrochloride | 2126136-98-7 | 98.1% | 443.99 | C18H18ClNO4S3 | 10MM 1ML
CCT365623 hydrochloride is an orally active lysyl oxidase (LOX) inhibitor supplied as a high-purity research reagent. It is available as solids and as a 10 mM solution in DMSO for use in biochemical and cellular assays, with molecular weight 443.99 g/mol and chemical formula C18H18ClNO4S3. Typical applications include LOX inhibition studies, signaling pathway research, and preclinical investigations.
- High purity, 98.1%.
- Available as 10 mM solution in DMSO (1 mL) and as solids (5-100 mg).
- Soluble in DMSO; ultrasonic agitation may improve dissolution.
- Molecular weight 443.99 g/mol.
- Suitable for biochemical and cellular LOX inhibition assays.
- Provided with certificate of analysis for batch verification.
- CAS number 2126136-98-7 for unambiguous identification.
Medchemexpress LLC TG 100572 hydrochloride | 867331-64-4 | 98.8% | 512.43 g/mol | C26H27Cl2N5O2 | 1 ML
TG 100572 Hydrochloride is the hydrochloride salt of a multi-targeted kinase inhibitor that blocks selected receptor tyrosine kinases and Src family kinases. It is provided for research use in biochemical and cell-based studies and is available as a ready-to-use solution or as a solid form.
- Multi-targeted kinase inhibitor active against receptor tyrosine kinases and Src family kinases.
- Supplied as a 10 mM solution in DMSO (1 mL) for immediate use.
- Also available as a solid with a pink to red appearance.
- High purity (~98.8%) suitable for research applications.
- Store sealed, away from moisture; in solvent store at -80°C for up to 6 months.
Medchemexpress LLC VU-1545 | 890764-63-3 | 99.0% | 402.38 | 50 MG
VU-1545 is a metabotropic glutamate receptor 5 positive allosteric modulator (mGluR5 PAM). It exhibits a Ki of 156 nM and an EC50 of 9.6 nM. This compound promotes AKT activation at concentrations of 0.1 and 1.0 μM and is intended for research use only.
- Functions as a metabotropic glutamate receptor 5 positive allosteric modulator (mGluR5 PAM).
- Demonstrates a Ki of 156 nM and an EC50 of 9.6 nM.
- Promotes AKT activation.
- Promotes Akt phosphorylation in neuronal cells.
- Solid appearance, light yellow to yellow color.
- 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.
Medchemexpress LLC Dopamine hydrochloride (standard) | 62-31-7 | 99.75% | 25 MG
Dopamine hydrochloride is an analytical standard intended for research and analytical applications. This catecholamine neurotransmitter is produced in the substantia nigra, ventral tegmental area, and hypothalamus of the brain. It plays important roles in the brain and body, acting through D2 dopamine receptors to induce endocytosis of VEGFR2, which is critical for promoting angiogenesis. The compound is used in qualitative, quantitative, and methodological research experiments.
- Analytical standard for research and analysis
- Catecholamine neurotransmitter
- Acts via D2 dopamine receptors
- Promotes angiogenesis
- Suitable for HPLC, GC, and MS experiments
- Molecular weight: 189.64
- Formula: C8H12ClNO2
- Appearance: Solid, white to off-white
- Classified as phenols and polyphenols
- Derived from microorganisms
- Endogenous metabolite
Medchemexpress LLC T-3775440 hydrochloride | 1422535-52-1 | 99.1% | 346.85 g/mol | C18H23ClN4O | 10 MG
T-3775440 hydrochloride is the hydrochloride salt of T-3775440, an irreversible lysine-specific demethylase 1 (LSD1) inhibitor used in biochemical and cellular research. It has a reported IC50 of 2.1 nM and is supplied as a solid salt for assay and mechanistic studies.
- Irreversible LSD1 inhibitor with reported IC50 = 2.1 nM.
- Hydrochloride salt form suitable for biochemical and cell-based assays.
- High purity suitable for research use (reported purity 99.13%).
- Molecular formula C18H23ClN4O; molecular weight 346.85 g/mol.
- Packaged in small research quantities for assay development and validation.
eMolecules 5407-57-8 | 1,2-ETHANEDIAMINE,N1-(7-CHLORO-4-QUINOLINYL) | AstaTech | MFCD02179802 | 221.690 | C11H12ClN3 | 95.000 | NCCNc1ccnc2cc(Cl)ccc12 | 1g | 282982525
1,2-ETHANEDIAMINE,N1-(7-CHLORO-4-QUINOLINYL) | AstaTech | 5407-57-8 | MFCD02179802 | 221.690 | C11H12ClN3 | 95.000 | NCCNc1ccnc2cc(Cl)ccc12 | 1g | 282982525
Medchemexpress LLC VU-1545 | 890764-63-3 | 99.0% | 402.38 | 100 MG
VU-1545 is a metabotropic glutamate receptor 5 positive allosteric modulator (mGluR5 PAM) with a Ki of 156 nM and an EC50 of 9.6 nM.
- Promotes AKT activation at concentrations of 0.1 and 1.0 μM.
- Neuroprotective in a mouse model of Huntington's disease.
- For research use only, not for sale to patients.
Medchemexpress LLC Co 101244 hydrochloride (PD 174494) | 193356-17-1 | 99.9% | 377.90 | C21H28ClNO3 | 50 MG
Co 101244 hydrochloride is the hydrochloride salt of a small-molecule NR2B-containing NMDA receptor antagonist supplied for research use. It is a light yellow to yellow solid with high purity and characterized molecular properties and storage/solubility data for in vitro and in vivo applications.
- Selective NR2B NMDA receptor antagonist useful for neuroscience research.
- High purity suitable for analytical and biological assays.
- Well-characterized solubility in DMSO for solution preparation.
- Stable when stored sealed at recommended temperatures.
- Available in multiple small-scale quantities for laboratory use.
Medchemexpress LLC Duloxetine metabolite Para-Naphthol Duloxetine | 949095-98-1 | 297.41 | 50 MG
Duloxetine metabolite Para-Naphthol Duloxetine is a metabolite of Duloxetine, a serotonin-norepinephrine reuptake inhibitor (SNRI). This product is intended for research use only and is not sold to patients.
- Metabolite of Duloxetine
- For research use only
- Molecular formula: C18H19NOS
- Appearance: Solid
- Color: White to off-white
- Store powder at -20°C for 3 years
- Store in solvent at -80°C for 6 months, or -20°C for 1 month