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Submit ReviewST 034307 is an adenylyl cyclase 1 (AC1) inhibitor (IC50 = 2.3 μM). Exhibits some selectivity for AC1 over other AC isoforms, with no significant activity against AC8. Inhibits Ca2+/calmodulin-stimulated cAMP accumulation in hippocampal homogenates. Enhances μ opioid receptor (MOR)-mediated inhibition of AC1 in cellular assays and inhibits development and maintenance of MOR-mediated sensitization of AC1. ST 034307 relieves pain without causing tolerance in mouse models of pain. Active in vivo. Analgesic.
分子量 | 297.95 |
公式 | C10H4Cl4O2 |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 133406-29-8 |
PubChem ID | 867466 |
InChI Key | NTDHYMSVCBGQJF-UHFFFAOYSA-N |
Smiles | ClC1=CC=C2OC(C(Cl)(Cl)Cl)=CC(C2=C1)=O |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 29.8 | 100 | |
ethanol | 5.96 | 20 |
以下数据基于产品分子量 297.95。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 3.36 mL | 16.78 mL | 33.56 mL |
5 mM | 0.67 mL | 3.36 mL | 6.71 mL |
10 mM | 0.34 mL | 1.68 mL | 3.36 mL |
50 mM | 0.07 mL | 0.34 mL | 0.67 mL |
参考文献是支持产品生物活性的出版物。
Brust et al (2017) Identification of a selective small-molecule inhibitor of type 1 adenylyl cyclase activity with analgesic properties. Sci.Signal. 10 eaah5381 PMID: 28223412
If you know of a relevant reference for ST 034307, please let us know.
关键词: ST 034307, ST 034307 supplier, ST034307, adenylyl, cyclase, inhibitors, inhibits, AC1, active, in, vivo, analgesic, cAMP, Adenylyl, Cyclase, 6271, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 ST 034307 的部分引用包括:
Cheng et al (2019) Antinociceptive effects of the adenylyl cyclase inhibitor ST034307 on tooth-movement-induced nociception in rats. Arch Oral Biol. 98 81 PMID: 30465937
Val J et al (2022) Reduced activity of adenylyl cyclase 1 attenuates morphine induced hyperalgesia and inflammatory pain in mice. Front Pharmacol 13 937741 PMID: 36120355
Giacoletti et al (2022) A selective adenylyl cyclase 1 inhibitor relieves pain without causing tolerance. Front.Pharmacol. 13 935588 PMID: 35899113
Bose et al (2021) Cross-talk between cAMP and Ca2+ signalling in cardiac pacemaker cells involves IP3-evoked Ca2+ release and stimulation of adenylyl cyclase 1. BioRXiv - not yet peer reviewed
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