Oxazinanes
TARGETMOL CHEMICALS INC SC144 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. SC144 is an orally active small-molecule gp130 inhibitor. purity: 98%
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 CNDAC hydrochloride | 134665-72-8 | 98.0% | 288.69 | 1 ML
This compound is a metabolite and a nucleoside analog that has been shown to induce DNA damage and programmed cell death. It exhibits its effects by causing single-strand breaks in DNA which convert to double-strand breaks during cell replication. The compound has demonstrated inhibitory activity against various human cancer cell lines, as well as murine leukemia cells. In animal models, it has shown antitumor activity, increasing survival time and rate.
- Metabolite of an orally active agent.
- Nucleoside analog.
- Induces DNA damage.
- Induces apoptosis.
- Available as both solid and pre-made solution.
- High purity of over 98%.
Apexbio Technology LLC Flavoxate hydrochloride 3717-88-2 1g
Flavoxate hydrochloride (CAS 3717-88-2) is a synthetic small molecule that functions as an antagonist of muscarinic acetylcholine receptors (AChRs) By inhibiting muscarinic receptor-mediated signaling it disrupts smooth muscle contractions within the urinary tract Flavoxate hydrochloride is widely utilized in biomedical research to investigate mechanisms underlying bladder overactivity urinary tract disorders and cholinergic signaling pathways Its antispasmodic properties support studies focused on smooth muscle pharmacology and the modulation of acetylcholine-mediated responses