Basic information Safety Supplier Related

ST034307

Basic information Safety Supplier Related

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
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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.
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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

MedChemexpress LLC
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021-58955995
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sales@medchemexpress.cn
Nanjing Dulai Biotechnology Co., Ltd.
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025-846993838003-8003 18013301590
Email
njduly@126.com
Shanghai SunSyn Pharmaceutical Co., Ltd.
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18621020637 18621020637;
Email
sales@sunsynpharma.com
Shanghai EFE Biological Technology Co., Ltd.
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021-65675885 18964387627
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info@efebio.com
Shanghai YuanYe Biotechnology Co., Ltd.
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021-61312847; 18021002903
Email
3008007409@qq.com
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ST034307(133406-29-8)Related Product Information