Hydrochlorides
Medchemexpress LLC H-hyp-ome hydrochloride | 40216-83-9 | 98.0% | 181.62 g/mol | C6H12ClNO3 | 500 G
H-Hyp-OMe hydrochloride is the hydrochloride salt of the methyl ester of trans-4-hydroxy-L-proline, used as a non-cleavable ADC linker, a PROTAC linker building block, and a synthetic intermediate in medicinal chemistry.
- Hydrochloride salt form suitable for conjugation chemistry.
- Molecular weight 181.62 g/mol; formula C6H12ClNO3.
- Purity 98.0%.
- Available in bulk 500 g pack.
- SDS and COA PDFs available for handling and quality data.
Medchemexpress LLC YNT-185 dihydrochloride | 1804978-82-2 | 1804978-82-2 | 99.8% | 688.66 | 100 MG
YNT-185 dihydrochloride is a nonpeptide, selective orexin type-2 receptor (OX2R) agonist, with EC50 values of 0.028 μM for OX2R and 2.75 μM for OX1R. It ameliorates narcolepsy-cataplexy symptoms in mouse models and increases wakefulness in mice.
- Selective OX2R agonist
- Ameliorates narcolepsy-cataplexy symptoms
- Increases wakefulness
Medchemexpress LLC CP 93129 dihydrochloride | 879089-64-2 | 99.0% | 288.17 g·mol⁻1 | C12H15Cl2N3O | 1 MG
CP 93129 dihydrochloride is a selective 5-HT1B receptor agonist supplied for research use. It is used in pharmacology and neuroscience studies, including investigations related to Parkinson's disease, and is provided as a high-purity solid suitable for analytical, in vitro, and in vivo applications.
- Selective 5-HT1B receptor agonist suitable for receptor pharmacology studies.
- High purity (99.0%) for consistent experimental results.
- Molecular weight 288.17 g·mol⁻1 and formula C12H15Cl2N3O for precise calculations.
- Off-white to light yellow solid for convenient handling and storage.
- Recommended storage at 4°C, sealed and protected from moisture and light.
- Available in small, accurately weighed milligram quantities for dosing and assays.
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 Nifenalol hydrochloride | 5704-60-9 | 99.9% | 260.72 g/mol | C11H17ClN2O3 | 100 MG
Nifenalol hydrochloride is a research-grade β-adrenergic receptor antagonist (hydrochloride salt) used in pharmacology and cardiac electrophysiology studies. It is provided as a high-purity solid for biochemical and cellular assays, with recommended storage and solvent stability guidance supplied by the manufacturer.
- Chemical identity: CAS number 5704-60-9; formula C11H17ClN2O3; molecular weight 260.72 g/mol.
- Primary activity: β-adrenergic receptor antagonist demonstrating early afterdepolarization effects.
- High purity: 99.9% as listed by manufacturer.
- Available formats: solid and solution stocks, sold in multiple sizes including 100 MG.
- Storage recommendation: sealed, away from moisture and light; solids refrigerated at 4°C; in solvent store at -80°C (6 months) or -20°C (1 month).
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
Med Vet International Terbinafine Hcl (Lamisil) 250mg Tablet White Round 30 Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Terbinafine HCL (Lamisil) 250mg Tablet White Round 30 Tablets.
Medchemexpress LLC Ambroxol hydrochloride (Standard) | 23828-92-4 | 99.9% | 100 MG
Ambroxol hydrochloride (Standard) is an analytical standard and an active metabolite of Bromhexine with potent expectorant effects. It acts as a glucocerebrosidase (GCase) chaperone, increasing GCase activity and inducing lung autophagy. This product is intended for research and analytical applications, including studies related to Parkinson's disease and neuronopathic Gaucher disease.
- Analytical standard for research and analytical applications.
- Active metabolite with expectorant effects.
- Increases glucocerebrosidase activity.
- Induces lung autophagy.
- Potential for Parkinson disease research.
- Potential for neuronopathic Gaucher disease research.
- Used in qualitative research experiments.
- Used in quantitative research experiments.
- Used in methodological research experiments in HPLC, GC and MS.
Medchemexpress LLC 2-(4-(4-(Aminomethyl)-1-oxo-1,2-dihydrophthalazin-6-yl)-1-methyl-1H-pyrazol-5-yl)-3-fluoro-1-naphthonitrile hydrochloride | 99.88% | 460.89 | 25 MG
MRTX9768 hydrochloride is a potent, selective, orally active, first-in-class PRMT5-MTA complex inhibitor.
- Potent, selective, orally active, first-in-class PRMT5-MTA complex inhibitor.
- Inhibits SDMA and cell proliferation in HCT116 MTAP-del cells.
- Selectively targets MTAP/CDKN2A-deleted tumors, such as glioblastoma.
- Demonstrates dose-dependent inhibition of SDMA in MTAP-del tumors in xenograft studies.
- Exhibits a favorable ADME profile with good bioavailability in mice and dogs.
Medchemexpress LLC L-368,899 hydrochloride | 160312-62-9 | 99.97% | 591.23 | 100 MG
L-368,899 hydrochloride is a potent, selective, orally bioavailable, non-peptide oxytocin receptor antagonist. It has IC50s of 8.9 nM for rat uterus and 26 nM for human uterus oxytocin receptor. This compound is used as a tocolytic agent.
- Potent oxytocin receptor antagonist.
- Selective for oxytocin receptor.
- Orally bioavailable.
- Non-peptide structure.
- Used as a tocolytic agent.
- Less active on VP receptor in human liver and kidney, and rat liver and kidney.
- Exhibits similar pharmacokinetics in rats and dogs with a t1/2 of 2 hours after a single IV injection.
- Plasma clearance between 23 and 36 ml/min/kg in rats or dogs.
- Vdss values of 2.0 and 2.6 liters/kg for rats and 3.4 to 4.9 liters/kg for dogs.
- Oral bioavailabilities in rats: 14% (female) and 18% (male) at 5 mg/kg; 17% (female) and 41% (male) at 25 mg/kg.
Sigma Aldrich Fine Chemicals Biosciences 3-Pyridylacetic acid hydrochloride 98% | 6419-36-9 | MFCD00012819 | 1G
3-Pyridylacetic acid hydrochloride 98% | Purity: 98% | Mol Wt: 173.6 | 6419-36-9 | MFCD00012819 | 1G
Medchemexpress LLC Dasatinib hydrochloride | 854001-07-3 | 99.3% | 524.47 g/mol | C22H27Cl2N7O2S | 500 MG
Dasatinib hydrochloride is the hydrochloride salt of dasatinib, a potent ATP-competitive dual Src/Bcr-Abl kinase inhibitor used in cancer research and cell signaling studies. It is supplied as a high-purity research reagent intended for in vitro and in vivo kinase inhibition assays and related biochemical applications.
- Potent ATP-competitive inhibitor of Src and Bcr-Abl kinases.
- Suitable for in vitro and in vivo research applications.
- Hydrochloride salt for improved solubility and handling.
- High purity (99.31% by HPLC) for reliable experimental results.
- Molecular formula C22H27Cl2N7O2S; molecular weight 524.47 g/mol.
- Available in a 500 mg research package.
Medchemexpress LLC Dapoxetine hydrochloride | 129938-20-1 | 99.96% | 50 MG
Dapoxetine hydrochloride is an orally active and selective serotonin reuptake inhibitor (SSRI) used for premature ejaculation (PE) research. It binds to 5-HT, norepinephrine, and dopamine reuptake transporters.
- Inhibits 5-HT, norepinephrine, and dopamine uptake
- Can be used for premature ejaculation (PE) research
- Oral gavage significantly inhibits testosterone-mediated increase in prostate weight in rats
Medchemexpress LLC Zt 52656a hydrochloride | 115730-24-0 | MFCD00673899 | 100.0% | 390.87 g/mol | C19H26ClF3N2O | 1 ML
ZT 52656A hydrochloride is a selective kappa opioid receptor agonist used in research to prevent or alleviate ocular pain. The compound is provided as a solid or as a ready-to-use 10 mM solution in DMSO, with high reported purity and manufacturer guidance for storage to maintain stability.
- Selective kappa opioid receptor agonist suitable for ocular pain studies.
- Available as solid or pre-dissolved 10 mM solution in DMSO for convenience.
- High reported purity for consistent experimental results.
- Multiple pack sizes accommodate small- and large-scale experiments.
- Defined storage recommendations help preserve compound stability in solid and solution forms.
Medchemexpress LLC AQ-13 dihydrochloride | 169815-40-1 | MFCD01938526 | 98.1% | 364.74 g/mol | C16H24Cl3N3 | 10 MG
AQ-13 dihydrochloride is an aminoquinoline-class antimalarial research compound supplied as the dihydrochloride salt. It is used primarily in in vitro studies against drug-resistant Plasmodium falciparum and in investigations of aminoquinoline mechanism of action and resistance.