Phenylhydrazines
Medchemexpress LLC Raclopride-d5 hydrochloride | 1217623-85-2 | 99.8% | 352.27 | C15H16D5Cl3N2O3 | 1 MG
Raclopride-d5 hydrochloride is the deuterium-labeled (d5) isotopologue of raclopride supplied as the hydrochloride salt and intended for use as an analytical reference standard or stable-isotope internal standard for quantitative assays.
- Deuterated raclopride (d5) for use as an internal standard.
- Hydrochloride salt in solid form for stable handling.
- High purity (99.82%) suitable for analytical applications.
- Molecular weight 352.27 and formula C15H16D5Cl3N2O3.
- Available in small reference sizes (1 mg) for trace-level assays.
- Certificate of analysis and safety data sheet available for quality verification.
Medchemexpress LLC -PD 128907 hydroc 10mM | 300576-59-4 | 98.92% | 285.77 | 50 MG
(+)-PD 128907 hydrochloride is a selective dopamine D2/D3 receptor agonist. It demonstrates high selectivity for human and rat D3 receptors, with Ki values of 1.7 nM and 0.84 nM respectively, showing over 100-fold and 900-fold selectivity compared to human and rat D2 receptors. This compound is intended for research use only.
- Selective dopamine D2/D3 receptor agonist.
- Exhibits high affinity for D3 receptors in both human and rat models.
- Shows significant selectivity over D2 receptors.
- Decreases dialysate dopamine levels in wild-type mice, being more potent than in D3 knock-out mice.
Medchemexpress LLC Halofantrine hydrochloride | 36167-63-2 | 99.90% | C26H31Cl3F3NO | 1 ML
Halofantrine hydrochloride | 36167-63-2 | 99.90% | C26H31Cl3F3NO | 1 ML
Medchemexpress LLC Phentolamine hydrochloride | 73-05-2 | 99.9% | 100 MG
Phentolamine hydrochloride is an orally active, competitive α-adrenergic receptor-blocking agent. It functions as an antagonist with Ki values of 1.6 nM for α1-adrenergic receptors and 9 nM for α2-adrenergic receptors, making it suitable for research into vasodilation.
- Competitive α-adrenergic receptor antagonist
- Exhibits Ki of 1.6 nM for α1-adrenergic receptors
- Exhibits Ki of 9 nM for α2-adrenergic receptors
- Causes concentration-dependent relaxation (0.01-100 μM)
- Inhibits phenylephrine-induced contraction in vitro
- Inhibits epinephrine-induced hypertension and prolonged hypotension in cats
- Inhibits norepinephrine-induced blood pressure in cats
- For research use only
eMolecules 4751-99-9 | o-Tolylbiguanide hydrochloride | Oakwood Chemical | MFCD00050547 | 227.700 | C9H14ClN5 | 98.000 | Cl.Cc1ccccc1NC(=N)NC(N)=N | 1g | 537707739
o-Tolylbiguanide hydrochloride | Oakwood Chemical | 4751-99-9 | MFCD00050547 | 227.700 | C9H14ClN5 | 98.000 | Cl.Cc1ccccc1NC(=N)NC(N)=N | 1g | 537707739
Medchemexpress LLC Norfenefrine (hydrochloride) | 4779-94-6 | 98.9% | 250 MG
Norfenefrine hydrochloride is an orally active, endogenously found α-adrenergic agonist. It is suitable for research on female stress incontinence.
- Orally active
- Endogenously found α-adrenergic agonist
- Can be used for research of female stress incontinence
- Solid appearance
- White to off-white color
Medchemexpress LLC Thioridazine hydrochloride | 130-61-0 | 99.96% | 500 MG
Thioridazine hydrochloride is an orally active antagonist of dopamine receptor D2 family proteins, showing potent anti-psychotic and anti-anxiety activities. It is also a potent inhibitor of PI3K-Akt-mTOR signaling pathways with anti-angiogenic effects. Additionally, it demonstrates antiproliferative and apoptosis induction in various cancer cells, specifically targeting cancer stem cells (CSCs).
- Potent anti-psychotic and anti-anxiety activities
- Inhibitor of PI3K-Akt-mTOR signaling pathways
- Anti-angiogenic effects
- Antiproliferative and apoptosis induction in cancer cells
- Specifically targets cancer stem cells (CSCs)
Medchemexpress LLC Tetracycline hydrochloride | 64-75-5 | >99.2% | 50 MG
Tetracycline hydrochloride (Standard) is a broad-spectrum antibiotic with oral activity, primarily used as an analytical standard for research and analytical applications. It is effective against a wide range of bacteria, including gram-positive and gram-negative bacteria, chlamydiae, mycoplasmas, and rickettsiae, making it suitable for infection research.
- Broad-spectrum antibiotic
- Oral activity
- Effective against gram-positive and gram-negative bacteria, chlamydiae, mycoplasmas, and rickettsiae
- Suitable for infection research
- Intended for research and analytical applications
- Used in qualitative, quantitative, and methodological research experiments (HPLC, GC, MS)
Medchemexpress LLC Clomipramine hydrochloride (Chlorimipramine hydrochloride) | 17321-77-6 | 99.56% | 5 G
Clomipramine hydrochloride is a potent 5-HT reuptake blocker with an IC50 value of 1.5 nM. It is a tricyclic antidepressant primarily used for the research of depression and obsessive-compulsive disorder (OCD). It can inhibit the reuptake of both noradrenaline and 5-HT, with a stronger inhibition of 5-HT reuptake.
- Potent 5-HT reuptake blocker (IC50 = 1.5 nM)
- Tricyclic antidepressant
- Used for research of depression and obsessive compulsive disorder (OCD)
- Interferes with autophagic flux
- Reduces autophagy in neuronal primary cultures
- Elicits significant hyperglycemia in mice
- Reduces immobility in the forced swimming test in mice
- Inhibits marble burying behavior in mice
Medchemexpress LLC Clomipramine (hydrochloride) | 17321-77-6 | 99.6% | 1 ML
Clomipramine hydrochloride is a potent 5-HT reuptake blocker with an IC50 value of 1.5 nM. This tricyclic antidepressant is used in research for depression and obsessive compulsive disorder (OCD).
- Potent 5-HT reuptake blocker.
- Tricyclic antidepressant for depression and OCD research.
- Inhibits reuptake of both noradrenaline and 5-HT.
- Interferes with autophagic flux and compromises tumorigenic cell viability.
- Reduces autophagy in neuronal primary cultures.
- Elicits hyperglycemia in mice by blocking 5-HT2B and/or 5-HT2C receptors.
- Reduces immobility in the forced swimming test in mice.
- Inhibits marble burying behavior in mice.
Medchemexpress LLC Levofloxacin hydrochloride | 177325-13-2 | 99.0% | 1 G
Levofloxacin hydrochloride is an orally active antibiotic that inhibits DNA gyrase and topoisomerase IV activity, inducing apoptosis. It possesses broad-spectrum antibacterial activity and exhibits anticancer properties. It is widely used in research for infectious diseases and lung cancer.
- Inhibits DNA gyrase and topoisomerase IV activity
- Active against Gram-positive and Gram-negative bacteria
- Exhibits anticancer activity against lung cancer cells
- Provides anti-acnegenic, anxiogenic, and analgesic effects
- Shortens sleep duration in mice
- Used in research for tuberculosis, chronic periodontitis, bacterial infections, and BK viremia
eMolecules 1408076-34-5 | 4-methoxyazepane hydrochloride | MFCD21641983 | 1g
Ambeed | Methyl 2-(1H-indol-3-yl)-2-oxoacetate | 25g | 525137099 | A225489 | 18372-22-0 | MFCD00047173 | 203.197 | C11H9NO3
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