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Submit ReviewABT 639 is a CaV3.2 channel blocker (IC50 = 2.3 μM). Also blocks low voltage-activated (CaV3.1) currents in native rat DRG neurons (IC50 = 7.6 μM). Exhibits little or no activity at other ion channels and receptors. Displays antinociceptive effects in a mechanical hyperalgesia model in vivo. Orally bioavailable.
ABT 639 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。
分子量 | 455.91 |
公式 | C20H20ClF2N3O3S |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 1235560-28-7 |
PubChem ID | 46851313 |
InChI Key | AGPIHNZOZNKRGT-CYBMUJFWSA-N |
Smiles | [H][C@]12CCCN1CCN(C(C3=CC(S(=O)(NC4=C(C=CC=C4)F)=O)=C(C=C3Cl)F)=O)C2 |
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 | 9.12 | 20 |
以下数据基于产品分子量 455.91。 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 |
---|---|---|---|
0.2 mM | 10.97 mL | 54.84 mL | 109.67 mL |
1 mM | 2.19 mL | 10.97 mL | 21.93 mL |
2 mM | 1.1 mL | 5.48 mL | 10.97 mL |
10 mM | 0.22 mL | 1.1 mL | 2.19 mL |
参考文献是支持产品生物活性的出版物。
Zhang et al (2015) Optimization of ADME properties for sulfonamides leading to the discovery of a T-type calcium channel blocker, ABT-639. ACS Med.Chem.Lett. 6 641 PMID: 26101566
If you know of a relevant reference for ABT 639, please let us know.
关键词: ABT 639, ABT 639 supplier, ABT639, T-type, calcium, channel, blockers, blocks, CaV3.2, CaV3.1, antinociceptive, orally, bioavailable, Cav3.x, Channels, 6770, Tocris Bioscience
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