SCH-202676 structure
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Common Name | SCH-202676 | ||
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CAS Number | 70375-43-8 | Molecular Weight | 348.26100 | |
Density | N/A | Boiling Point | 392ºC at 760 mmHg | |
Molecular Formula | C15H14BrN3S | Melting Point | 240.0-240.8ºC(lit.) | |
MSDS | N/A | Flash Point | 190.9ºC |
Use of SCH-202676SCH-202676 is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). SCH-202676 has antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 µM[1][2][3][4]. |
Name | (Z)-N-(2,3-diphenyl-1,2,4-thiadiazol-5(2H)-ylidene)methanamine |
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Synonym | More Synonyms |
Description | SCH-202676 is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). SCH-202676 has antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 µM[1][2][3][4]. |
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Related Catalog | |
Target |
Adenosine A3 receptor |
In Vitro | SCH-202676 (compound 6a) 具有抗病毒活性并以时间依赖的方式抑制 3CLpro,在 0、5、10 和 20 分钟的 IC50 值分别为 0.409、0.302、0.206 和 0.191 µM[1]。 SCH-202676 (10 μM;90 min) 加强了大鼠前脑膜中 [35S]GTPγS 的标记[2]。 SCH-202676 抑制激动剂 [3H]UK-14,304 (HY-B0659) 和拮抗剂 [3H] 育亨宾 (Yohimbine,HY-12715) 与 α2a 肾上腺素能受体的结合[3]。 SCH-202676 (10 μM) 选择性地加速了激动剂在腺苷 A3 受体上的解离,减慢了拮抗剂在腺苷 Ai 受体上的解离,或加速了拮抗剂在腺苷 AzA 受体上的解离[4]。 |
References |
Boiling Point | 392ºC at 760 mmHg |
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Melting Point | 240.0-240.8ºC(lit.) |
Molecular Formula | C15H14BrN3S |
Molecular Weight | 348.26100 |
Flash Point | 190.9ºC |
Exact Mass | 347.00900 |
PSA | 58.42000 |
LogP | 4.08940 |
~% SCH-202676 CAS#:70375-43-8 |
Literature: Goerdeler,J. et al. Chemische Berichte, 1979 , vol. 112, p. 1288 - 1296 |
~% SCH-202676 CAS#:70375-43-8 |
Literature: Goerdeler,J. et al. Chemische Berichte, 1979 , vol. 112, p. 1288 - 1296 |
Precursor 2 | |
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DownStream 0 |
aurora ka-7903 |