Phenylhydrazines
Medchemexpress LLC Ethopropazine hydrochloride | 1094-08-2 | MFCD00012653 | 99.3% | 348.93 g/mol | C19H25ClN2S | 50 MG
Ethopropazine hydrochloride is the hydrochloride salt of a phenothiazine-class compound used in research as a butyrylcholinesterase (BChE) inhibitor and a non-selective muscarinic and NMDA antagonist. It is applied in neuroscience studies, including Parkinson's disease and analgesia models, for its anticholinergic and neuropharmacological effects.
- High purity: 99.3%.
- Molecular weight: 348.93 g/mol.
- Chemical formula: C19H25ClN2S.
- CAS number: 1094-08-2.
- Available as a 50 mg research pack.
- Useful as a BChE inhibitor in neuropharmacology studies.
Medchemexpress LLC Valacyclovir hydrochloride | 124832-27-5 | 98.7% | 360.80 | 1 ML
Valacyclovir hydrochloride is an orally active antiviral agent effective against herpes simplex, herpes zoster, and herpes B. It inhibits HSV-1 with an IC50 of 2.9 μg/mL and is a proagent of Aciclovir.
- Orally active antiviral agent
- Effective against herpes simplex, herpes zoster, and herpes B
- Inhibits HSV-1 with an IC50 of 2.9 μg/mL
- Proagent of Aciclovir
- Soluble in water and DMSO
- Appearance is a white to off-white solid
Medchemexpress LLC Valacyclovir hydrochloride | 124832-27-5 | 99.9% | 360.80 | 100 MG
Valacyclovir hydrochloride is an orally active antiviral agent for herpes simplex, herpes zoster, and herpes B. It inhibits HSV-1 W (50=2.9 μg/ml) and is a proagent of Aciclovir.
- IC50 and target: HSV-1, 2.9 μg/mL (IC50).
- In vitro: Uptake is concentration dependent and saturable, with hPEPT1 dominating intestinal transport.
- In vivo: Effective for treating genital herpes (1 g twice daily) and recurrences. A 1 g daily dose is as effective as 2 g daily and can be administered once a day. Studies in immunosuppressed mice showed reduced erythema, eliminated ear paralysis, ear lesions, and death.
Medchemexpress LLC Pexidartinib (hydrochloride) | 2040295-03-0 | 99.8% | 454.28 | 20 G
Pexidartinib hydrochloride is a potent, orally active, selective, and ATP-competitive colony stimulating factor 1 receptor (CSF1R or M-CSFR) and c-Kit inhibitor. It exhibits 10- to 100-fold selectivity for CSF1R and c-Kit over other related kinases and induces cell apoptosis with anti-cancer activity.
- Potent, orally active, selective, and ATP-competitive CSF1R and c-Kit inhibitor.
- Exhibits 10- to 100-fold selectivity for CSF1R and c-Kit over other related kinases.
- Induces cell apoptosis and has anti-cancer activity.
- Can be used to deplete microglia cells in mice.
- Reduces tissue macrophage levels without affecting glucose homeostasis in mice.
Chem-Impex International, Inc. 1,5-Diphenylcarbazone compound with 1,5-Diphenylcarbazide | MFCD00013218 | 5G
1,5-Diphenylcarbazone compound with 1,5-Diphenylcarbazide, MFCD00013218, 5G