Hydrochlorides
Medchemexpress LLC 1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol hydrochloride | 62717-42-4 | MFCD00069248 | 99.5% | 291.77 g/mol | C16H18ClNO2 | 500MG
SKF 38393 hydrochloride is a selective agonist of the dopamine D1 receptor used as a research reagent to study D1-mediated signaling. It is supplied as a solid (also available as a 10 mM solution in DMSO) with analytical-grade purity and intended for research use only.
- CAS number 62717-42-4.
- Chemical formula C16H18ClNO2.
- Molecular weight 291.77 g/mol.
- D1 receptor IC50 ~110 nM.
- Purity approximately 99.5%.
- Available as solid quantities including 500 mg and larger sizes.
- Provided for research use only; not for human or clinical use.
Medchemexpress LLC Zt 52656a hydrochloride | 115730-24-0 | 99.98% | 390.87 | C19H26ClF3N2O | 10 MG
ZT 52656A hydrochloride is the hydrochloride salt of a selective kappa-opioid receptor agonist used in research on kappa opioid receptor pharmacology. It is reported for prevention or alleviation of ocular pain and is supplied for in vitro and in vivo experimental use.
- Selective kappa-opioid receptor agonist, useful for KOR pharmacology studies.
- High reported purity of 99.98% for consistent experimental results.
- Chemical formula C19H26ClF3N2O and molecular weight 390.87 aid in dosing and calculations.
- Available in multiple pack sizes and as a DMSO solution for flexible experimental use.
- Provided as the hydrochloride salt to improve solubility in aqueous media.
![Medchemexpress LLC 5-isoxazoleacetic acid, a-amino-3-chloro-4,5-dihydro-, monohydrochloride, [S-(R*,R*)]- | 161922-40-3 | MFCD32874156 | 99.1% | 215.03 g·mol⁻¹ | C5H8Cl2N2O3 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000303494.png-250.jpg)
Medchemexpress LLC 5-isoxazoleacetic acid, a-amino-3-chloro-4,5-dihydro-, monohydrochloride, [S-(R*,R*)]- | 161922-40-3 | MFCD32874156 | 99.1% | 215.03 g·mol⁻¹ | C5H8Cl2N2O3 | 25 MG
Acivicin hydrochloride is the hydrochloride salt of acivicin, a natural product γ-glutamyl transpeptidase (GGT) inhibitor used as a biochemical research reagent. It is supplied as a solid and in solution formats for laboratory use, with defined storage conditions to preserve stability and activity.
- High confirmed purity (HPLC): 99.1%.
- Molecular weight 215.03 g·mol⁻¹ and formula C5H8Cl2N2O3.
- Available in mg-scale packs and solution aliquots for assay flexibility.
- Suitable for biochemical studies targeting GGT and related pathways.
- Storage recommendations: 4°C under nitrogen; in solvent -80°C (6 months) or -20°C (1 month).
eMolecules 1092304-80-7 | 8-(TRIFLUOROMETHYL)QUINOLIN-2-AMINE | MFCD11108677 | 1g
Pharmablock | (1S4S)-2-benzyl-25-diazabicyclo[2.2.1]heptanedihydrobromide | 250mg | 761745250 | PBTEN13579-1 | 116258-17-4 | 350.098 | C12H18Br2N2
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eMolecules 1390654-84-8 | 2-(BROMOMETHYL)-1-METHYLPIPERIDINE HBR | AstaTech | MFCD00179635 | 273.012 | C7H15Br2N | 95.000 | Br.CN1CCCCC1CBr | 1g | 449792075
2-(BROMOMETHYL)-1-METHYLPIPERIDINE HBR | AstaTech | 1390654-84-8 | MFCD00179635 | 273.012 | C7H15Br2N | 95.000 | Br.CN1CCCCC1CBr | 1g | 449792075
eMolecules 21987-29-1 | 4,4-Difluoropiperidine | ChemScene | MFCD03094281 | 121.131 | C5H9F2N | 97.000 | FC1(F)CCNCC1 | 1g | 569143771
4,4-Difluoropiperidine | ChemScene | 21987-29-1 | MFCD03094281 | 121.131 | C5H9F2N | 97.000 | FC1(F)CCNCC1 | 1g | 569143771
Medchemexpress LLC Benzamil hydrochloride | 161804-20-2 | 99.7% | 50 MG
Benzamil hydrochloride is an Amiloride analogue that acts as a Na+/Ca2+ exchanger (NCX) inhibitor (IC50~100 nM). It also functions as a non-selective Deg/epithelial sodium channels (ENaC) blocker and can enhance myogenic vasoconstriction. This product inhibits TRPP3-mediated Ca2+-activated currents with an IC50 of 1.1 μM.
- Inhibits neuronal and heterologously expressed small conductance Ca2+-activated K+ channels.
- Shown to improve survival in stroke-prone spontaneously hypertensive rats (SHRSP) when treated at 0.7 mg/kg/day (s.c.).
Medchemexpress LLC Roxindole hydrochloride | 108050-82-4 | MFCD09265259 | 99.0% | 382.93 g/mol | C23H27ClN2O | 10 MG
Roxindole hydrochloride is the hydrochloride salt of roxindole, a dopaminergic and serotonergic research compound used in receptor pharmacology and neuropharmacology studies. It functions primarily as a dopamine autoreceptor agonist with activity at multiple dopamine receptor subtypes and serotonergic sites, and is provided as solid material or as a DMSO solution for laboratory use.
- Dopamine autoreceptor agonist with activity at D2-like receptors.
- Shows affinity for 5-HT1A serotonergic sites.
- Supplied as solid and solution pack sizes for experimental flexibility.
- Molecular weight 382.93 g/mol; formula C23H27ClN2O.
- Storage recommended at -20°C; protect from light and store under inert gas.
Medchemexpress LLC 5,7-dimethoxy-3-(4-pyridinyl)quinoline dihydrochloride | 1123491-15-5 | MFCD02262123 | 99.1% | 339.22 g/mol | C16H16Cl2N2O2 | 5 MG
DMPQ dihydrochloride is the dihydrochloride salt of 5,7-dimethoxy-3-(4-pyridinyl)quinoline. It is a small-molecule inhibitor that selectively targets human platelet-derived growth factor receptor β (PDGFRβ) with reported biochemical potency, and is supplied as a light yellow to yellow solid for research use in biochemical and cell-based assays.
- Potent PDGFRβ inhibition with reported IC50 of 80 nM.
- High reported purity suitable for biochemical assays.
- Solid form, convenient for weighing and formulation.
- Available in multiple small pack sizes for research applications.
Medchemexpress LLC Benzenepropanamine, γ-(2-methoxyphenoxy)-N-methyl- | 53179-07-0 | 98.56% | 50 MG
Nisoxetine is a potent and selective inhibitor of noradrenaline transporter (NET), with a Kd of 0.76 nM. It is an antidepressant and local anesthetic, capable of blocking voltage-gated sodium channels. It is suitable for laboratory research and experimentation in various biological activities.
- Potent and selective inhibitor of noradrenaline transporter (NET)
- Kd of 0.76 nM (NET)
- Antidepressant properties
- Local anesthetic properties
- Blocks voltage-gated sodium channels
Medchemexpress LLC Verubulin hydrochloride | 917369-31-4 | 98.7% | 100 MG
Verubulin hydrochloride is the hydrochloride salt of verubulin (MPC-6827), a blood-brain barrier permeable microtubule-disrupting agent with demonstrated in vitro and in vivo anticancer activity. It is supplied for research use in solid and solution formats.
- Blood-brain barrier permeable microtubule disruptor.
- Demonstrated cytotoxic activity in MX-1 breast and other xenograft models.
- Available as solid and as solution in DMSO; pack sizes typically range from 5 mg to 500 mg.
- High purity (approx. 98.7%).
- Molecular formula C17H18ClN3O; molecular weight 315.8 g/mol.
- For research use only; not for human or veterinary use.
Medchemexpress LLC Dapoxetine hydrochloride | 129938-20-1 | 100.0% | 1 ML
Dapoxetine (LY-210448) hydrochloride is an orally active and selective serotonin reuptake inhibitor (SSRI) that can be utilized for research related to premature ejaculation (PE).
- Orally active and selective serotonin reuptake inhibitor (SSRI).
- Applicable for research of premature ejaculation (PE).
- Binds to 5-HT, norepinephrine, and dopamine reuptake transporters.
- Inhibits 5-HT, norepinephrine, and dopamine uptake with an order of potency: 5-HT > norepinephrine ≈ dopamine.
- Demonstrates an IC50 of 1.12 nM for inhibiting the uptake of [3H]5-HT by the 5-HT reuptake transporter.
- Shows IC50 values of 202 nM and 1720 nM for inhibiting the uptake of [3H]norepinephrine and [3H]dopamine, respectively.
- Significantly inhibits testosterone-mediated increase in prostate weight and attenuates testosterone-induced prostatic hyperplasia in rats.
Medchemexpress LLC Harmalol hydrochloride | 6028-07-5 | 1 ML
Harmalol hydrochloride is a beta carboline alkaloid found in medicinal plants like *Peganum harmala*. It is a main metabolite of Harmaline and significantly inhibits the dioxin-mediated induction of CYP1A1 at both transcriptional and posttranslational levels. This compound also exhibits antioxidant and hydroxyl radical-scavenging properties.
- Purity: 99.91%
- Inhibits dioxin-mediated induction of CYP1A1
- Possesses antioxidant and hydroxyl radical-scavenging properties
- For research use only
Medchemexpress LLC EG01377 dihydrochloride | 2749438-61-5 | 99.0% | 659.60 | 1 MG
EG01377 dihydrochloride | 2749438-61-5 | 99.0% | 659.60 | 1 MG
Apexbio Technology LLC Tirofiban 144494-65-5 5mg
Tirofiban is a selective non-peptide antagonist targeting platelet glycoprotein (GP) IIb/IIIa receptors a heterodimeric complex abundantly expressed on platelet surfaces responsible for mediating fibrinogen binding and platelet aggregation It acts through competitive inhibition of fibrinogen binding at GP IIb/IIIa sites thereby suppressing platelet cross-linking and aggregation induced by agonists like ADP In vitro studies demonstrate that Tirofiban inhibits ADP-induced platelet aggregation with an IC50 value of approximately 9 nM showing significantly lower affinity for integrin v 3 (vitronectin receptor) Tirofiban is frequently applied in biomedical research investigating platelet aggregation mechanisms and thrombotic events