ST 034307

Pricing Availability   Qty
说明: Adenylyl cyclase 1 (AC1) inhibitor; analgesic and active in vivo
化学名: 6-Chloro-2-(trichloromethyl)-4H-1-benzopyran-4-one
纯度: ≥98% (HPLC)
说明书
引用文献 (4)
评论

生物活性 for ST 034307

ST 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.

技术数据 for ST 034307

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.

溶解性数据 for ST 034307

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 29.8 100
ethanol 5.96 20

制备储备液 for ST 034307

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.

选择批次从而根据批次分子量重新计算:
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

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参考文献 for ST 034307

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


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关键词: ST 034307, ST 034307 supplier, ST034307, adenylyl, cyclase, inhibitors, inhibits, AC1, active, in, vivo, analgesic, cAMP, Adenylyl, Cyclase, 6271, Tocris Bioscience

4 篇 ST 034307 的引用文献

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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