6-phenyl-4-sulfanylidene-1H-1,3,5-triazin-2-one结构式
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常用名 | 6-phenyl-4-sulfanylidene-1H-1,3,5-triazin-2-one | 英文名 | 6-phenyl-4-sulfanylidene-1H-1,3,5-triazin-2-one |
|---|---|---|---|---|
| CAS号 | 32622-40-5 | 分子量 | 205.23600 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C9H7N3OS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 6-phenyl-4-sulfanylidene-1H-1,3,5-triazin-2-one |
|---|---|
| 英文别名 | 更多 |
| 分子式 | C9H7N3OS |
|---|---|
| 分子量 | 205.23600 |
| 精确质量 | 205.03100 |
| PSA | 97.70000 |
| LogP | 1.53290 |
| InChIKey | SOOHREIWXFQLAH-UHFFFAOYSA-N |
| SMILES | O=c1[nH]c(-c2ccccc2)nc(=S)[nH]1 |
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~83%
6-phenyl-4-sulf... 32622-40-5 |
| 文献:Sosic, Izidor; Stefane, Bogdan; Kovac, Andreja; Turk, Samo; Blanot, Didier; Gobec, Stanislav Heterocycles, 2010 , vol. 81, # 1 p. 91 - 115 |
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~74%
6-phenyl-4-sulf... 32622-40-5 |
| 文献:Wang, Qingmin; Liu, Gang; Shao, Ruilian; Huang, Runqiu Heteroatom Chemistry, 2003 , vol. 14, # 6 p. 542 - 545 |
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实验名称:Inhibition of human liver cathepsin H expressed in Escherichia coli assessed as forma...
来源:ChEMBL
靶标:Pro-cathepsin H
External Id:CHEMBL1837248
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实验名称:Inhibition of human recombinant cathepsin B assessed as formation of fluorescent degr...
来源:ChEMBL
靶标:Cathepsin B
External Id:CHEMBL1837247
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实验名称:Inhibition of human recombinant cathepsin L expressed in Escherichia coli assessed as...
来源:ChEMBL
靶标:Procathepsin L
External Id:CHEMBL1837249
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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
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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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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
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实验名称:Inhibition of human DNA topoisomerase IIalpha using plasmid pNO1 as a substrate after...
来源:ChEMBL
靶标:DNA topoisomerase 2-alpha
External Id:CHEMBL3595291
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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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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
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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
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| HMS1665I07 |
| F2184-0190 |
| 6-phenyl-4-thioxo-1,3,5-triazine-2-one |