ST034307
ST034307 Basic information
- Product Name:
- ST034307
- Synonyms:
-
- ST034307
- 6-chloro-2-(trichloromethyl)-4H-chromen-4-one
- ST034307;ST-034307;ST 034307
- 6-Chloro-2-(trichloromethyl)-4H-1-benzopyran-4-one
- 4H-1-Benzopyran-4-one, 6-chloro-2-(trichloromethyl)-
- ST034307 >=98% (HPLC)
- Adenylate Cyclase,Inhibitor,ST 034307,inhibit,ST034307,ST-034307,Adenylyl cyclase
- ST034307, 10 mM in DMSO
- CAS:
- 133406-29-8
- MF:
- C10H4Cl4O2
- MW:
- 297.95
- Mol File:
- 133406-29-8.mol
ST034307 Chemical Properties
- Boiling point:
- 329.1±42.0 °C(Predicted)
- Density
- 1.674±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- solubility
- Soluble in DMSO (up to 30 mg/ml) or in Ethanol (up to 6 mg/ml)
- form
- solid
- color
- Yellow
- Stability:
- Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
ST034307 Usage And Synthesis
Description
ST-034307 (133406-29-8) is a?novel selective adenylyl cyclase 1 (AC1) inhibitor, IC50=2.3 μM . Inhibits calcium2+-stimulated cAMP accumulation in HEK cells stably transfected with AC11. It was also shown to inhibit AC1 stimulated by forskolin- and Gαs-coupled receptors in HEK-AC1 cells. ?It enhanced μ-opioid receptor-mediated inhibition of AC1 but it blocked heterologous sensitization of AC1 caused by chronic μ-opioid receptor activation.1,3?Displays analgesic properties in a mouse model of inflammatory pain.1?A useful tool for exploring the involvement of AC1 in cellular signalling.2
Uses
ST 034307 is a useful intermediate.
in vivo
ST034307 (0.25 μg) causes a significant relief of CFA-induced inflammatory pain in mice. ST034307 exhibits an estimated median effective dose (E50) value for analgesia of 0.28 μg in the mouse pain model[1].
storage
Store at -20°C
References
[1] TARSIS F. BRUST. Identification of a selective small-molecule inhibitor of type 1 adenylyl cyclase activity with analgesic properties[J]. Science Signaling, 2017, 10 467. DOI:10.1126/scisignal.aah5381
[2] ZHENG JIANG. Cyclic-Nucleotide- and HCN-Channel-Mediated Phototransduction in Intrinsically Photosensitive Retinal Ganglion Cells.[J]. Journal of Chemical Theory and Computation, 2018: 652-664.e12. DOI:10.1016/j.cell.2018.08.055
[3] WATTS V J. Selective Adenylyl Cyclase Type 1 Inhibitors as Potential Opioid Alternatives For Chronic Pain[J]. Neuropsychopharmacology, 2017, 43 1: 215-216. DOI:10.1038/npp.2017.190
ST034307Supplier
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