Phenylhydrazines
Chem-Impex International, Inc. 1,5-Diphenylcarbazone compound with 1,5-Diphenylcarbazide | MFCD00013218 | 5G
1,5-Diphenylcarbazone compound with 1,5-Diphenylcarbazide, MFCD00013218, 5G
Medchemexpress LLC Valacyclovir hydrochloride | 124832-27-5 | 99.9% | 360.80 | 1 G
Valacyclovir hydrochloride (Valaciclovir hydrochloride) is an orally active antiviral agent effective against herpes simplex, herpes zoster, and herpes B. It inhibits HSV-1 W with a concentration of 50=2.9 μg/ml. Valacyclovir hydrochloride acts as a proagent of Aciclovir.
- Orally active antiviral agent
- Effective against herpes simplex, herpes zoster, and herpes B
- Inhibits HSV-1 W
- Proagent of Aciclovir
Medchemexpress LLC Medetomidine (hydrochloride) | 86347-15-1 | 99.8% | 236.74 | 1 ML
Medetomidine hydrochloride is an orally active α2-adrenoceptor agonist with sedative and analgesic effects. It can cause peripheral vasoconstriction through the activation of α2 adrenoceptors on blood vessels. It is for research use only.
- Orally active α2-adrenoceptor agonist (Ki: 1.08 nM)
- Sedative and analgesic effects
- Causes peripheral vasoconstriction through activation of α2 adrenoceptors
- Inhibits aldosterone release from adrenocortical cell suspension in vitro
- Activates a kicking response in Cyprids in vitro
- Increases cellular cAMP production by activating β-like receptors in CHO cells in vitro
- Induces sedation in cats in vivo
- Shows sedative and analgesic effects in dogs in vivo
- Protects against Diazinon-induced toxicosis in mice in vivo
Medchemexpress LLC 1-(3-fluorophenyl)-2-((2-((2,3,4-trifluorophenyl)methoxy)phenyl)methyl)pyrrolidine hydrochloride | 1227056-87-2 | 99.5% | 357.80 g/mol | C18H19ClF3NO | 5 MG
Ampreloxetine hydrochloride is an orally active, CNS-penetrant inhibitor of the norepinephrine transporter (NET) and the serotonin uptake transporter (SERT) supplied for research use. It is used in vitro and in vivo to investigate monoamine transporter pharmacology and CNS transporter-related mechanisms.
- Orally active inhibitor of norepinephrine and serotonin transporters.
- CNS-penetrant, suitable for in vivo and in vitro studies.
- Hydrochloride salt form for improved handling and solubility.
- High reported purity (99.5%).
- Supplied in milligram quantities for research applications.
- Useful for pharmacology, transporter mechanism, and CNS studies.
Medchemexpress LLC (S)-Remoxipride hydrochloride | 73220-03-8 | MFCD01743944 | >98.0% | 407.7 g/mol | C16H23BrN2O3.HCl | 25 MG
(S)-Remoxipride hydrochloride is the S-enantiomer salt of remoxipride, a selective dopamine D2 receptor antagonist used as a research reagent in receptor pharmacology and biochemical studies. The hydrochloride salt improves aqueous solubility and the material is typically provided in small, high-purity milligram quantities.
- Selective dopamine D2 receptor antagonist for receptor pharmacology studies.
- Enantiomerically defined S-form for stereoselective research.
- High purity suitable for biochemical and cellular assays.
- Hydrochloride salt form enhances solubility in aqueous media.
- Available in small milligram pack sizes for laboratory workflows.
Medchemexpress LLC 5-(dimethylamino)naphthalene-1-sulfonohydrazide | 33008-06-9 | 100.0% | 265.33 | 1 G
Dansyl hydrazine, also known as 5-(Dimethylamino)naphthalene-1-sulfonohydrazide, is a versatile biochemical reagent. It is commonly employed as a biological material or organic compound in various life science research applications, particularly where its properties can aid in detection and analysis.
- High purity (99.98%) for reliable experimental results.
- Clearly defined molecular weight (265.33) for accurate calculations.
- Identified by a unique CAS number (33008-06-9) for traceability.
- Presented as a solid for ease of handling.
- Specific storage recommendations to maintain product integrity.
- Useful in various life science research applications.
Medchemexpress LLC Ligustrazine hydrochloride | 76494-51-4 | 25 MG
Ligustrazine hydrochloride is a natural product primarily utilized for research. It has shown a protective effect on injured ECV304 cells, significantly increasing NOS and NO formation. This compound is intended for research use only, not for patient or medical applications.
- Protective effect on injured ECV304 cells
- Significantly increases NOS and NO formation
- Suitable for research applications
- Solid storage at 4°C, sealed and away from moisture
- In-solvent storage at -80°C for 6 months or -20°C for 1 month
Medchemexpress LLC Diclofensine hydrochloride | 34041-84-4 | 99.8% | 358.69 | 5 MG
Diclofensine (hydrochloride), also known as Ro 8-4650 hydrochloride, is an orally active neuronal monoamine uptake inhibitor. It effectively blocks the reuptake of dopamine, noradrenaline, and serotonin in rat brain synaptosomes, with IC50 values of 0.74, 2.3, and 3.7 nM, respectively. This compound has been shown to potentiate norepinephrine-induced hypertension while attenuating Tyramine-induced hypertension. It is recognized for producing psychostimulant and mood-elevating effects without the common issues of sudden disappearance or withdrawal reactions, making it a valuable tool in the research of moderate to severe depression.
- Blocks the uptake of dopamine, noradrenaline, and serotonin
- Potentiates norepinephrine-induced hypertension
- Attenuates Tyramine-induced hypertension
- Produces psychostimulant and mood-elevating effects
- Used in the research of moderate to severe depression
![Medchemexpress LLC 4-[2-[(2,4,6-trifluorophenoxy)methyl]phenyl]piperidine hydrochloride | 1227056-87-2 | 99.5% | 357.80 | C18H19ClF3NO | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000240014.png-250.jpg)
Medchemexpress LLC 4-[2-[(2,4,6-trifluorophenoxy)methyl]phenyl]piperidine hydrochloride | 1227056-87-2 | 99.5% | 357.80 | C18H19ClF3NO | 50 MG
Ampreloxetine hydrochloride is the hydrochloride salt of a small-molecule norepinephrine and serotonin reuptake inhibitor used for research into NET/SERT pharmacology and central nervous system activity. Supplied as a dry powder for laboratory use, it is intended for in vitro and preclinical studies.
- Hydrochloride salt form for improved stability.
- Potent norepinephrine and serotonin reuptake inhibition.
- Suitable for in vitro and preclinical research.
- Dry powder form for accurate dosing and formulation.
- High reported purity.
- Characterized by CAS 1227056-87-2 and molecular weight 357.80.
eMolecules 371-14-2 | Ambeed | (4-Fluorophenyl)hydrazine | 5g | 572929202 | A203677 | MFCD00041262 | 126.134 | C6H7FN2
Ambeed | N-(3-(4455-Tetramethyl-132-dioxaborolan-2-yl)phenyl)acrylamide | 250mg | 525048180 | A139594 | 874363-18-5 | MFCD22493996 | 273.140 | C15H20BNO3
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Medchemexpress LLC Ruboxistaurin hydrochloride | 169939-93-9 | 99.9% | 505.01 g/mol | C28H29ClN4O3 | 50 MG
Ruboxistaurin hydrochloride is the hydrochloride salt of ruboxistaurin, an orally active, selective protein kinase C beta (PKCβ) inhibitor supplied as a solid research reagent for biochemical and cell-based studies. It is intended for research use only and is not for human or clinical applications.
- Selective PKCβ inhibitor with low nanomolar potency (Ki ≈ 2 nM).
- High reported purity (≈99.9%).
- Orange to red solid appearance.
- Molecular weight 505.01 g/mol.
- Stable when stored sealed at 4°C; in solvent -80°C for up to 6 months.
- Suitable for biochemical and cell-based assays probing PKCβ signaling.
![Medchemexpress LLC Piperidine, 4-[2-[(2,4,6-trifluorophenoxy)methyl]phenyl]-, hydrochloride | 1227056-87-2 | 99.5% | 357.80 g·mol⁻¹ | C18H19ClF3NO | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000240486.png-250.jpg)
Medchemexpress LLC Piperidine, 4-[2-[(2,4,6-trifluorophenoxy)methyl]phenyl]-, hydrochloride | 1227056-87-2 | 99.5% | 357.80 g·mol⁻¹ | C18H19ClF3NO | 1 ML
Ampreloxetine hydrochloride (TD-9855) is a research-grade small molecule inhibitor of the norepinephrine transporter (NET) and serotonin transporter (SERT). It is CNS-penetrant and supplied for in-vitro research in solid form and as a ready-to-use 10 mM solution in DMSO; intended for research use only.
- Inhibits NET and SERT for neurotransmitter uptake studies.
- Supplied as a 10 mM solution in DMSO for immediate use.
- Also available as solid quantities for formulation or storage.
- High reported purity (99.5%).
- Molecular weight 357.80 g·mol⁻¹ for dose calculations.
- Intended for research use only.