Benzenoids
Medchemexpress LLC 4-Butoxyphenol | 122-94-1 | 166.22 | 250 G
4-Butoxyphenol is a biochemical reagent used as a biological material or organic compound for life science related research. It is intended for research use only and not for patient application.
- Molecular weight: 166.22
- Formula: C10H14O2
- Appearance: Solid
- Color: Light brown to brown
Medchemexpress LLC Disodium 5'-inosinate (IMP disodium salt) | 4691-65-0 | 99.74% | 100 G
Disodium 5'-inosinate (IMP disodium salt) is a nucleotide-based umami agent. Disodium 5'-inosinate can bind to umami receptors and stimulate taste nerves, allowing the brain to perceive umami. In addition, Disodium 5'-inosinate produces a transient behavioral excitement in mice.
- Responds to oral stimulation in rat solitary-tract nucleus neurons and is involved in encoding umami taste.
- Produced a behavioral excitement in mice showing an increased movement, jumping and squeaking in response to tactile stimuli and enhanced preening and increased reflex response.
Medchemexpress LLC Cyanosafracin B | 96996-50-8 | 96.01% | 549.62 | 50 MG
Cyanosafracin B is a starting material for the synthesis of Ecteinascidin ET-743 and Phthalascidin Pt-650.
- It is a solid.
- It appears light yellow to yellow in color.
- It is sourced from microorganisms.
- It is a marine natural product.
Medchemexpress LLC Etidocaine hydrochloride | 36637-19-1 | 99.9% | 100 MG
Etidocaine hydrochloride is a long-acting aminoamide local anesthetic agent used in research to suppress or relieve pain. It is intended for research use only and not for human or animal therapeutic use.
- Long-acting aminoamide local anesthetic agent
- Induces a significant increase in human fibroblasts survival in IGL-EDC formulations
- Did not show postinjection neurologic deficit when administered as a spinal injection at 0.0075% in adult Swiss Webster male mice
- Purity of 99.9%
- Molecular weight of 312.88
- Chemical formula C17H29ClN2O
- Appears as a solid
- White to off-white color
- Soluble in DMSO at 62.5 mg/mL
Medchemexpress LLC Imipramine hydrochloride | 113-52-0 | MFCD00012669 | 99.85% | 1 ML
Imipramine hydrochloride is an orally active tertiary amine tricyclic antidepressant. It acts as a Fascin1 inhibitor with antitumor activities and also inhibits the serotonin transporter with an IC50 value of 32 nM. This compound stimulates autophagy in U-87MG glioma cells and induces apoptosis in HL-60 cells. Additionally, it exhibits neuroprotective and immunomodulatory effects.
- Orally active tertiary amine tricyclic antidepressant.
- Fascin1 inhibitor with antitumor activities.
- Inhibits serotonin transporter (IC50 value of 32 nM).
- Stimulates U-87MG glioma cells autophagy.
- Induces HL-60 cell apoptosis.
- Shows neuroprotective effects.
- Exhibits immunomodulatory effects.
Medchemexpress LLC Antazoline hydrochloride | 2508-72-7 | 99.6% | 1 G
Antazoline hydrochloride is a histamine H1 receptor antagonist known for its anticholinergic and antiviral properties. It works by reversibly competing for histamine receptor sites, thereby blocking and inhibiting the H1 receptor to produce an antiallergic effect. This compound can effectively reduce HBV DNA in the extracellular supernatant in a dose-dependent manner and has also demonstrated an anti-arrhythmic effect in acute myocardial infarctions, making it suitable for research in cardiovascular diseases and HBV.
- Acts as a histamine H1 receptor antagonist
- Exhibits anticholinergic and antiviral properties
- Effectively reduces HBV DNA in HepAD38 and Huh7 cells
- Demonstrates anti-arrhythmic effects
- Suitable for research in cardiovascular diseases and HBV
Medchemexpress LLC Higenamine hydrochloride | 11041-94-4 | 307.77 | 500 MG
Higenamine hydrochloride is a selective inhibitor of LSD1 with an IC50 of 1.47 μM, naturally sourced from aconite. It exhibits anti-inflammatory and antibacterial properties and can mitigate IL-1β-induced apoptosis via the ROS-mediated PI3K/Akt signaling pathway. Additionally, it offers protective effects for brain cells against oxygen deprivation and stimulates bone formation in osteoporosis through the SMAD2/3 pathway. It is utilized in research for various conditions, including cancer, inflammation, and cardiorenal syndrome.
- Selective LSD1 inhibitor (IC50=1.47 μM)
- Derived from aconite
- Possesses anti-inflammatory activity
- Exhibits antibacterial activity
- Attenuates IL-1β-induced apoptosis
- Protects brain cells from oxygen deprivation
- Promotes bone formation in osteoporosis
- Relevant for studying cancer, inflammation, and cardiorenal syndrome