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5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶

更新时间:2025-09-02 11:46:54

5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶结构式
5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶结构式
品牌特惠专场
常用名 5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶 英文名 5,7-dimethyl-2-(methylsulfanyl)-[1,2,4]triazolo[1,5-a]pyrimidine
CAS号 51646-19-6 分子量 194.25700
密度 N/A 沸点 N/A
分子式 C8H10N4S 熔点 N/A
MSDS N/A 闪点 N/A

 名称

中文名 5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶
英文名 5,7-dimethyl-2-methylsulfanyl-[1,2,4]triazolo[1,5-a]pyrimidine
英文别名 更多

 物理化学性质

分子式 C8H10N4S
分子量 194.25700
精确质量 194.06300
PSA 68.38000
LogP 1.46300
InChIKey BTLWCWRYAWSLNK-UHFFFAOYSA-N
SMILES CSc1nc2nc(C)cc(C)n2n1

 合成线路

~68%

5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶结构式

5,7-二甲基-2-(甲基硫烷...

51646-19-6

文献:STATegics, Inc.; PUNNONEN, Juha; SPENCER, Jeffrey R.; CHURCH, Timothy J.; TETTENBORN, Connie S.; LARIOSA-WILLINGHAM, Karen; LEONOUDAKIS, Dimitri; MILLER, James L. Patent: US2014/142122 A1, 2014 ; Location in patent: Paragraph 0570; 0571 ;

~77%

5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶结构式

5,7-二甲基-2-(甲基硫烷...

51646-19-6

文献:Novinson; Springer; O'Brien; Scholten; Miller; Robins Journal of Medicinal Chemistry, 1982 , vol. 25, # 4 p. 420 - 426

~%

5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶结构式

5,7-二甲基-2-(甲基硫烷...

51646-19-6

文献:Chen, Wen-Bin; Jin, Gui-Yu Heteroatom Chemistry, 2003 , vol. 14, # 7 p. 607 - 611

~%

5,7-二甲基-2-(甲基硫烷基)-[1,2,4]三唑并[1,5-a]嘧啶结构式

5,7-二甲基-2-(甲基硫烷...

51646-19-6

文献:Novinson; Springer; O'Brien; Scholten; Miller; Robins Journal of Medicinal Chemistry, 1982 , vol. 25, # 4 p. 420 - 426

 靶点实验

查看更多实验

实验名称:qHTS screening for TAG (triacylglycerol) accumulators in algae
来源:11812
靶标:N/A
External Id:FATTTLab-Algae-Lipid
实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
实验名称:Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:ORF 73 [Human herpesvirus 8 type M]
External Id:HMS791
实验名称:Inhibitory activity toward Phosphodiesterase isolated from rabbit lung
来源:ChEMBL
靶标:Phosphodiesterase; PDE3 & PDE4
External Id:CHEMBL761659
实验名称:Inhibitory activity toward phosphodiesterase isolated from rabbit kidney
来源:ChEMBL
靶标:Phosphodiesterase; PDE3 & PDE4
External Id:CHEMBL840878
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
实验名称:A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Chain A, Poliovirus Polymerase With Gtp
External Id:HMS750
实验名称:In vitro inhibition of Phosphodiesterase isolated from bovine heart.
来源:ChEMBL
靶标:Phosphodiesterase
External Id:CHEMBL763059
实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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 英文别名

HMS1584E07
5,7-dimethyl-2-(methylsulfanyl)[1,2,4]triazolo[1,5-a]pyrimidine
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