6-phenyl-4-sulfanylidene-1H-1,3,5-triazin-2-one
Modify Date: 2025-09-17 17:59:30
6-phenyl-4-sulfanylidene-1H-1,3,5-triazin-2-one structure
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Common Name | 6-phenyl-4-sulfanylidene-1H-1,3,5-triazin-2-one | ||
|---|---|---|---|---|
| CAS Number | 32622-40-5 | Molecular Weight | 205.23600 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C9H7N3OS | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | 6-phenyl-4-sulfanylidene-1H-1,3,5-triazin-2-one |
|---|---|
| Synonym | More Synonyms |
| Molecular Formula | C9H7N3OS |
|---|---|
| Molecular Weight | 205.23600 |
| Exact Mass | 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... CAS#:32622-40-5 |
| Literature: 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... CAS#:32622-40-5 |
| Literature: Wang, Qingmin; Liu, Gang; Shao, Ruilian; Huang, Runqiu Heteroatom Chemistry, 2003 , vol. 14, # 6 p. 542 - 545 |
CAS#:7459-63-4|
Name: Inhibition of human liver cathepsin H expressed in Escherichia coli assessed as forma...
Source: ChEMBL
Target: Pro-cathepsin H
External Id: CHEMBL1837248
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Name: Inhibition of human recombinant cathepsin B assessed as formation of fluorescent degr...
Source: ChEMBL
Target: Cathepsin B
External Id: CHEMBL1837247
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Name: Inhibition of human recombinant cathepsin L expressed in Escherichia coli assessed as...
Source: ChEMBL
Target: Procathepsin L
External Id: CHEMBL1837249
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Name: Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: HCMV UL50
External Id: HMS1262
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Name: Dicer-mediated maturation of pre-microRNA
Source: Center for Chemical Genomics, University of Michigan
Target: N/A
External Id: TargetID_659_CEMA
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Name: Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: ORF 73 [Human herpesvirus 8 type M]
External Id: HMS791
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Name: Inhibition of human DNA topoisomerase IIalpha using plasmid pNO1 as a substrate after...
Source: ChEMBL
Target: DNA topoisomerase 2-alpha
External Id: CHEMBL3595291
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Name: High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS1303
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Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
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Name: A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: 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 |