Oxazinanes
Medchemexpress LLC 6,7-Dihydro-4-benzo[b]thiophenone | 13414-95-4 | 99.5% | C8H8OS | 1 ML
6,7-Dihydro-4-benzo[b]thiophenone is a biochemical reagent designed for various life science-related research applications. It serves as a versatile biological material or an organic compound for laboratory use.
- Suitable as a biological material or organic compound
- Intended for research use only
- Soluble in DMSO at 100 mg/mL
- Pure form stable at -20°C for 3 years or 4°C for 2 years
- In solvent, store at -80°C for 6 months or -20°C for 1 month
Accela Chembio Inc 2-morpholinobenzaldehyde | 5g | 58028-76-5 | MFCD00662562 | 97+% | Shelf Life: 1080 Days | Light Sensitive
2-morpholinobenzaldehyde | 5g | 58028-76-5 | MFCD00662562 | 97+% | Shelf Life: 1080 Days | Light Sensitive
Cayman Chemical GW 3965 hydrochloride
An orally-active agonist of LXRα and LXRβ, activating the human isoforms with EC50 values of 190 and 30 nM, respectively; alters LXR-regulated gene expression in mice and rats, affecting pathways related to glucose and lipid metabolism
TARGETMOL CHEMICALS INC Tiaspirone hydrochloride 1MG
Also available in 1 mL, 5 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Tiaspirone hydrochloride (BMY-13859 hydrochloride) exhibits antipsychotic activity. Tiaspirone hydrochloride influences the electrophysiological activity of dopaminergic neurons in the substantia nigra zona compacta (A9 DA cells) and ventral tegmental area (A10 DA cells) in the brain of the rat. Purity 99.98%
Medchemexpress LLC Decloxizine dihydrochloride | 13073-96-6 | 99.69% | C21H30Cl2N2O2 | 100 MG
Decloxizine dihydrochloride is a histamine 1 receptor antagonist.
- H1 receptor antagonist.
Medchemexpress LLC Amtb hydrochloride | 926023-82-7 | >98.0% | 430.99 | C23H27ClN2O2S | 1 ML
AMTB hydrochloride is a small-molecule TRPM8 channel blocker used in laboratory pharmacology and ion channel research. It has been applied in studies of overactive bladder and painful bladder syndrome and is reported to affect voltage-gated sodium channels in some assays.
- Selective TRPM8 channel blocker for ion channel studies.
- Reported activity in research on overactive bladder and painful bladder syndrome.
- Also inhibits voltage-gated sodium channels in some assays.
- Soluble in DMSO; manufacturer provides stock solution preparation for concentrations such as 10 mM.
- High purity available (≥98% by HPLC) and characterized by molecular weight 430.99.
Medchemexpress LLC Vacquinol-1 dihydrochloride (NSC13316 dihydrochloride) | 2309312-85-2 | 99.7% | 425.78 | 25 MG
Vacquinol-1 dihydrochloride (NSC13316) is a MKK4-specific activator that activates MAPK pathways. It specifically induces human glioblastoma cell (GC) death, attenuates tumor progression, and prolongs survival in a glioblastoma multiforme (GBM) mouse model. This compound also induces apoptosis in hepatocellular carcinoma (HCC) cells.
- MKK4-specific activator
- Activates MAPK pathways
- Induces glioblastoma cell death
- Attenuates tumor progression in glioblastoma multiforme mouse models
- Prolongs survival in glioblastoma multiforme mouse models
- Induces apoptosis in hepatocellular carcinoma cells
- Purity of 99.7%
- Appearance: white to off-white solid
Selleck Chemical LLC Sarpogrelate hydrochloride S3706-10mg
Sarpogrelate (MCI-9042) is a selective 5-HT2A antagonist with pKi values of 8 52 7 43 and 6 57 for 5-HT2A 5-HT2C and 5-HT2B receptors respectively
Selleck Chemical LLC MPTP hydrochloride S4732-200mg
MPTP hydrochloride is a dopaminergic neurotoxin and cause selective destruction of dopaminergic neurons in animal models of parkinsonism MPTP hydrochloride induces apoptosis MPTP hydrochloride can be used to induce animal models of Parkinson s disease
Medchemexpress LLC 3-Amino-2-oxazolidinone | 80-65-9 | MFCD00020871 | 98.0% | 102.09 | 1 ML
3-Amino-2-oxazolidinone (AOZ) is a metabolite of Furazolidone. It is consistently detected as an indicator of furazolidone residues in vivo. This compound is orally active.
- It is a metabolite of furazolidone.
- It is an indicator of furazolidone residues in vivo.
- The compound is orally active.
- It inhibits monoamine oxidase (MAO) via its metabolite in rats' brain and liver.
- It increases levels of monoamine neurotransmitters like norepinephrine and dopamine in the brain.
- It lowers blood pressure in renal hypertensive rats.