Hydrochlorides
Selleck Chemical LLC Duloxetine S5071-25mg
Duloxetine (LY-248686) is a potent inhibitor of serotonin (5-hydroxytryptamine 5-HT) and noradrenaline (NE) uptake in vitro and in vivo and is 3- to 5-times more effective at inhibiting 5-HT uptake
Sigma Aldrich Fine Chemicals Biosciences o-Phenylenediamine dihydrochloride peroxidase substrate | 615-28-1 | MFCD00012966 | 25G
o-Phenylenediamine dihydrochloride peroxidase substrate | Mol Wt: 181.06 | 615-28-1 | MFCD00012966 | 25G
Medchemexpress LLC Lycorine Hydrochloride Monohydrate | 6150-58-9 | 99.2% | 341.79 | 100 MG
Lycorine Hydrochloride Monohydrate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
- Biochemical reagent.
- Can be used as a biological material.
- Can be used as an organic compound for life science related research.
Medchemexpress LLC GSK-LSD1 dihydrochloride | 2102933-95-7 | 99.5% | 289.24 g/mol | C14H22Cl2N2 | 1 ML
GSK-LSD1 dihydrochloride is a potent, selective, and irreversible inhibitor of lysine-specific demethylase 1 (LSD1) with an IC50 of 16 nM. It is intended for research use to probe LSD1 function, study gene expression changes, and evaluate effects on cancer cell proliferation. Supplied as a high-purity solid or as a solution in DMSO.
Medchemexpress LLC Etazolate hydrochloride | 35838-58-5 | MFCD00209848 | 98.0% | 325.79 | C14H20ClN5O2 | 5 MG
Etazolate hydrochloride is a pyrazolopyridine research compound that functions as a selective phosphodiesterase-4 (PDE4) inhibitor, a GABAA receptor regulator, and an α-secretase activator. It is used in neuropharmacology and inflammation studies to probe cAMP signaling, amyloid precursor protein processing, and behavioral pharmacology.
Chem-Impex International, Inc. 3-Butyn-1-amine hydrochloride | 88211-50-1 | MFCD06658391 | 1G
3-Butyn-1-amine hydrochloride, 88211-50-1, MFCD06658391, 1G
Medchemexpress LLC N-(1,3-diphenylpyrazol-5-yl)-4-nitrobenzamide | 890764-36-0 | MFCD12546140 | 99.6% | 384.39 g/mol | C22H16N4O3 | 10 MG
VU-29 is a research-stage positive allosteric modulator of the metabotropic glutamate receptor 5 (mGlu5), used in preclinical pharmacology to selectively potentiate mGlu5 signaling. It is supplied as a powder with high chemical purity and is intended for in vitro and in vivo formulation following recommended solvent systems and storage conditions.
- Positive allosteric modulator of mGlu5 receptor, suitable for receptor pharmacology studies.
- High purity (99.6%) for reliable experimental results.
- Powder form for flexible dosing and formulation.
- Soluble in DMSO at 50 mg/mL; recommended vehicle progression for in vivo administration.
- Stable under recommended storage conditions for extended shelf life in powder form.
Medchemexpress LLC Ly-272015 hydrochloride | 172895-15-7 | 99.5% | 372.89 | C21H25ClN2O2 | 25 MG
LY-272015 hydrochloride is the hydrochloride salt of LY-272015, an orally active and selective 5-HT2B receptor antagonist supplied as a high-purity solid for laboratory research. It is used to probe serotonergic signaling and downstream ERK2 phosphorylation in preclinical studies.
- Orally active, selective 5-HT2B receptor antagonist.
- Useful for research into serotonergic signaling and ERK2 phosphorylation.
- High purity (about 99.5%) for reliable experimental results.
- Off-white to light yellow solid, suitable for analytical handling.
- Stable when stored sealed at 4°C; in solvent: -80°C for 6 months, -20°C for 1 month.
- Available in small research quantities, including 25 MG.
Sigma Aldrich Fine Chemicals Biosciences o-Phenylenediamine dihydrochloride | 615-28-1 | MFCD00012966 | 50 tablets
o-Phenylenediamine dihydrochloride | Mol Wt: 181.06 | 615-28-1 | MFCD00012966 | 50 tablets
Chem-Impex International, Inc. N-Z-1,5-pentanediamine hydrochloride | 18807-74-4 | MFCD00270152 | 1G
N-Z-1,5-pentanediamine hydrochloride, 18807-74-4, MFCD00270152, 1G
eMolecules 8-(TRIFLUOROMETHYL)QUINOLIN-6-AMINE | 1080640-91-0 | MFCD11052592 | 1g
AstaTech | 8-(TRIFLUOROMETHYL)QUINOLIN-6-AMINE | 1g | 410713139 | 95707 | 95.000 | 1080640-91-0 | MFCD11052592 | 212.175 | C10H7F3N2
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Apexbio Technology LLC RS 127445 HCl 199864-87-4 10mg
RS 127445 HCl (CAS 199864-87-4) is a small-molecule antagonist targeting the serotonin 5-HT2B receptor a member of the G-protein coupled receptor family It is designed to selectively block 5-HT2B receptor activity thereby modulating intracellular signaling pathways such as calcium elevation and inositol phosphate production RS 127445 HCl exerts its biological activity primarily through selective antagonism of the 5-HT2B receptor In isolated tissue preparations such as rat stomach fundus and jugular vein RS 127445 HCl inhibits serotonin-induced contraction Based on these pharmacological properties RS 127445 HCl holds research potential in studies of 5-HT2B receptor function and related physiological processes
eMolecules Medchem Express (US) Y-27632 (dihydrochloride) (Standard) 100mg 874279628 HY-10583R 129830-38-2 MFCD03490488 320 260 C14H23Cl2N3O
Medchem Express (US) Y-27632 (dihydrochloride) (Standard) 100mg 874279628 HY-10583R 129830-38-2 MFCD03490488 320 260 C14H23Cl2N3O
Medchemexpress LLC 1,3-propanediol, 2-amino-2-(1-nonyl-1H-1,2,3-triazol-4-yl) hydrochloride | 2376132-24-8 | 99.9% | 320.86 | C14H29ClN4O2 | 10 MG
KARI 201 hydrochloride is a dual-action small-molecule research compound that functions as a selective, brain-penetrant acid sphingomyelinase (ASM) inhibitor and a ghrelin receptor (GHSR) agonist. It is intended for preclinical in vitro and in vivo studies and is supplied as a solid for laboratory research use only.
- Selective acid sphingomyelinase inhibitor.
- Ghrelin receptor agonist with brain penetration.
- High purity, 99.9% (HPLC).
- Molecular weight 320.86 g·mol-1.
- Supplied as a 10 mg solid; store sealed at -20°C.
- For research use only; not for human or diagnostic use.
Medchemexpress LLC Prodipine hydrochloride | 31314-39-3 | 99.8% | 315.9 g/mol | C20H26ClN | 10 MG
Prodipine hydrochloride is a diphenyl-phosphonate derivative used as a research DPP-IV inhibitor. It has been characterized in vitro and in vivo for inhibition of dipeptidyl peptidase IV and is supplied for laboratory research use.
- Inhibits dipeptidyl peptidase IV (DPP-IV) in vitro and in vivo.
- Reported IC50 values: purified rabbit DPP-IV 4.5 μM; rabbit plasma DPP-IV 30 μM.
- High reported purity (99.8%).
- Molecular formula C20H26ClN; molecular weight 315.9 g/mol.
- Intended for biochemical and pharmacological research use only.
- Available in small research pack sizes suitable for assay work.