Hydrochlorides
![Medchemexpress LLC Ethanone, 1-[2-(1-pyrrolidinylmethyl)-1-piperidinyl]-2-[4-(trifluoromethyl)phenyl] hydrochloride | 115730-24-0 | 100.0% | 390.87 | C19H26ClF3N2O | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000248299.png-250.jpg)
Medchemexpress LLC Ethanone, 1-[2-(1-pyrrolidinylmethyl)-1-piperidinyl]-2-[4-(trifluoromethyl)phenyl] hydrochloride | 115730-24-0 | 100.0% | 390.87 | C19H26ClF3N2O | 50 MG
ZT 52656A hydrochloride is the hydrochloride salt of a selective kappa opioid receptor agonist described for ocular analgesia. It is supplied as a solid research reagent for laboratory and preclinical studies and is not for human or clinical use.
- Selective kappa opioid receptor agonist suitable for ocular pain studies.
- High reported purity (99.98%) for consistent experimental results.
- Solid, white to off-white form for easy handling and weighing.
- Molecular weight 390.87 and formula C19H26ClF3N2O for reference.
- Recommended storage: 4°C sealed; in solvent: -80°C (up to 6 months) or -20°C (up to 1 month).
- Packaged quantities suitable for small-scale laboratory experiments.
Medchemexpress LLC preQ1 dihydrochlorid 10mg | 86694-45-3 | 252.10 | C7H11Cl2N5O | 10 MG
preQ1 dihydrochloride is a guanine-derived nucleobase used as a precursor in the biosynthesis of queuine and as a ligand for PreQ1 riboswitch studies. Supplied as the dihydrochloride salt for research use, the compound has defined solubility and storage recommendations.
- Precursor in queuine biosynthesis and useful for tRNA modification studies.
- Binds the PreQ1 riboswitch aptamer with high affinity.
- Solubility: DMSO 125 mg/mL; water 15 mg/mL (may require ultrasonic agitation).
- Solid storage recommended at 4°C in a sealed container, protected from moisture and light.
- In-solution stability: store at -80°C for up to 6 months or -20°C for up to 1 month when sealed.
Medchemexpress LLC T-3775440 hydrochloride | 1422535-52-1 | 99.1% | 346.85 g·mol⁻¹ | C18H23ClN4O | 25 MG
T-3775440 hydrochloride is a potent, irreversible inhibitor of lysine-specific histone demethylase 1 (LSD1) with an IC50 of 2.1 nM. It shows selective inhibition of LSD1 versus MAO enzymes, reduces proliferation in multiple cell lines, and has demonstrated antitumor effects in xenograft models. Supplied as a high-purity research chemical for preclinical biochemical and cellular studies.
- Potent LSD1 inhibition (IC50 2.1 nM).
- Irreversible mechanism of action.
- High purity (~99.1%).
- Suitable for biochemical assays and cell-based studies.
- Available as solid and solution formats for flexible use.
- Stable when stored under recommended conditions.
Medchemexpress LLC SB-399885 hydrochloride | 402713-81-9 | 98.3% | 482.81 g/mol | C18H22Cl3N3O4S | 10 MG
SB-399885 hydrochloride is a research-grade small molecule hydrochloride salt that acts as a selective 5-HT6 (serotonin) receptor antagonist. It is supplied as a solid for laboratory research, suitable for in vitro and in vivo pharmacology and behavioral studies. CAS 402713-81-9; molecular weight 482.81 g/mol.
- High purity suitable for research use.
- Hydrochloride salt form for improved solubility.
- Applicable to in vitro receptor pharmacology and in vivo behavioral assays.
- Supplied with a supplier datasheet for handling and storage information.
- Available in small bench-scale pack sizes for preclinical studies.
Medchemexpress LLC Bestatin hydrochloride (Ubenimex hydrochloride) | 65391-42-6 | MFCD00058004 | 99.9% | 100 MG
Bestatin hydrochloride is an inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase, used for cancer research. Bestatin hydrochloride is also known to have several biological activities, including:
- Inhibitor of CD13 (aminopeptidase N)/APN and leukotriene A4 hydrolase
- Enhances ATRA-induced differentiation in ATRA-sensitive APL NB4 cells
- Inhibits ATRA-driven phosphorylation of p38 MAPK
- Slows cell cycle progression in D. discoideum
- Inhibits mitosis and inherent multinuclearity in D. discoideum
- Reduces CD13 expression in diabetic mice
- Inhibits MMP-9 specific gelationolytic band densities in diabetic mice
- Inhibits VEGF and heparanase expression in diabetic mice
- Increases splenocytes producing hemolytic anti-SRBC antibodies (at 0.1 mg/kg)
![Medchemexpress LLC N-[[1-(dimethylamino)cyclopentyl]methyl]-3,5-dimethoxy-4-(phenylmethoxy)benzamide hydrochloride | 495076-64-7 | 99.9% | 448.98 g/mol | C24H33ClN2O4 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000240661.png-250.jpg)
Medchemexpress LLC N-[[1-(dimethylamino)cyclopentyl]methyl]-3,5-dimethoxy-4-(phenylmethoxy)benzamide hydrochloride | 495076-64-7 | 99.9% | 448.98 g/mol | C24H33ClN2O4 | 5 MG
Org 25543 hydrochloride is the hydrochloride salt of a selective and irreversible glycine transporter 2 (GlyT2) inhibitor (IC50 16 nM) used as a research reagent to study glycine transport and analgesic mechanisms in preclinical models. It is supplied as a solid, high-purity material and should be stored sealed at -20°C to preserve stability.
- Selective GlyT2 inhibition (IC50 16 nM).
- Demonstrated analgesic activity in rodent neuropathic pain models.
- High purity (>99.9%).
- Solid form suitable for formulation and dosing in preclinical work.
- Recommended storage at -20°C, sealed and protected from moisture.
- Available in small research quantities for screening and pharmacology studies.
Medchemexpress LLC SB-258585 hydrochloride | 1216468-02-8 | 99.7% | 523.82 g/mol | C18H23ClIN3O3S | 10 MG
SB-258585 hydrochloride is a research compound used as a high-affinity ligand and antagonist for the serotonin 5-HT6 receptor (CAS 1216468-02-8). Supplied as the hydrochloride salt, it has molecular formula C18H23ClIN3O3S, molecular weight 523.82 g/mol, and is provided for in vitro and ex vivo pharmacological and receptor-binding studies.
- High-affinity antagonist of the serotonin 5-HT6 receptor.
- High reported purity, suitable for analytical and biological assays.
- Appropriate for radioligand binding and receptor labeling studies.
- Supplied in small-mass research quantities for laboratory use.
- Molecular weight 523.82 g/mol and defined molecular formula.
Chem-Impex International, Inc. O-Ethylhydroxylamine hydrochloride | MFCD00012956 | 25G
O-Ethylhydroxylamine hydrochloride, MFCD00012956, 25G
Chem-Impex International, Inc. O-Ethylhydroxylamine hydrochloride | MFCD00012956 | 1G
O-Ethylhydroxylamine hydrochloride, MFCD00012956, 1G
Medchemexpress LLC Bepridil hydrochloride hydrate | 74764-40-2 | 99.9% | 421.02 | 1 ML
Bepridil hydrochloride hydrate is a non-selective, long-acting Ca+ channel antagonist and Na+, K+ channel inhibitor. It possesses antianginal and type I antiarrhythmic effects and functions as a cardiac Na+/Ca2+ exchange (NCX1) inhibitor. It can be used for the research of cardiovascular disorders.
- Blocks Ca2+-dependent action potentials in vascular smooth muscle.
- Inhibits Ca currents and Na currents in cultured ventricular cells.
- Decreases IKs under blockade of IKr.
- Suitable for research into cardiovascular disorders.
Medchemexpress LLC Acivicin hydrochloride | 161922-40-3 | MFCD32874156 | 99.1% | 215.03 | C5H8Cl2N2O3 | 1 ML
Acivicin hydrochloride is a Streptomyces-derived natural product that inhibits γ-glutamyl transpeptidase (GGT). It has reported anti-cancer and anti-parasitic activities and is supplied in solid forms or as a ready-to-use 10 mM solution in DMSO for research applications.
- Acts as a γ-glutamyl transpeptidase (GGT) inhibitor.
- Derived from Streptomyces sviceus.
- Reported to cross the blood-brain barrier.
- Available as solid (mg scale) and 10 mM solution in DMSO.
- CAS number 161922-40-3.
- Chemical formula C5H8Cl2N2O3; molecular weight 215.03.
- Reported purity 99.12%.
- Solubility: DMSO 100 mg/mL; in vivo formulations and ≥2.5 mg/mL indicated.
- Storage guidance: 4°C for solids; in solvent -80°C (6 months) or -20°C (1 month) under nitrogen.
Medchemexpress LLC Epertinib hydrochloride | 2071195-74-7 | >98.0% | 596.48 g/mol | C30H28Cl2FN5O3 | 1 ML
Epertinib hydrochloride is the hydrochloride salt of epertinib, a reversible and selective tyrosine kinase inhibitor of EGFR, HER2, and HER4 used in oncology research. The product is supplied as a 10 mM solution in DMSO (1 mL) and as solid powders; consult the datasheet and safety information for handling and purity details.
- Potent, reversible inhibitor of EGFR, HER2, and HER4.
- Suitable for in vitro and in vivo oncology research.
- Available as a 10 mM DMSO solution for ready-to-use assays.
- Also available as solid for formulation or long-term storage.
- Molecular weight 596.48 g/mol and CAS number 2071195-74-7.
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.
Medchemexpress LLC YM-298198 hydrochloride | 1216398-09-2 | MFCD08703122 | ≥99.0% | 378.92 | C18H23ClN4OS | 10 MG
YM-298198 hydrochloride is the hydrochloride salt of a selective, high-affinity, non-competitive antagonist of metabotropic glutamate receptor 1 (mGluR1) supplied for research use in small quantities.
- Selective mGluR1 antagonist with Ki = 19 nM and IC50 = 16 nM in functional assays.
- High reported purity (≥99.0% for latest batches).
- Molecular formula C18H23ClN4OS and molecular weight 378.92.
- CAS number 1216398-09-2 for substance identification.
- Available in small pack sizes such as 10 mg for research applications.
- Recommended storage: -20°C sealed; in solvent: -80°C up to 6 months or -20°C up to 1 month, protected from moisture.