Compound Detail
CHEMBL606446
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Basic Information
| ChEMBL ID | CHEMBL606446 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | UZFAWASFVMCUEA-RJNFYWFKSA-N |
3
Targets
5
Activities
2
Assay Types
1
PK Parameters
6
Publications
0
Known Names
Molecular Properties
321.4
MW (Da)
0.06
ALogP
9
HBA
3
HBD
119.3
PSA (Ų)
0.68
QED
0
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
EC50 4 meas. best 5.72
Ki 1 meas. best 4.8
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| E6SM CHEMBL614149 | EC50 | 5.72 | 5.72 | 1900.0 | 1 |
| Adenosylhomocysteinase CHEMBL2664 | Ki | 4.8 | 4.8 | 16000.0 | 1 |
| HEL CHEMBL613888 | EC50 | 4.06 | 4.06 | 87000.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| T1/2 | 0.1167 | hr | - |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| E6SM | EC50 | = | 1900.0 | nM | 5.72 | Effective concentration required to inhibit Vaccinia virus-induced cytopathicity... | 11495586 |
| Adenosylhomocysteinase | Ki | = | 16000.0 | nM | 4.8 | Inhibition of purified recombinant human placental S-adenosyl-homocysteine hydro... | 11495586 |
| HEL | EC50 | = | 87000.0 | nM | 4.06 | Effective concentration required to inhibit Tyrosine kinase deficient (TK-) Vari... | 11495586 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 11495586 | 10.1021/jm0108350 | Vero | 9 |
| 11495586 | 10.1021/jm0108350 | HEL | 7 |
| 11495586 | 10.1021/jm0108350 | E6SM | 6 |
| 11495586 | 10.1021/jm0108350 | Adenosylhomocysteinase | 4 |
| 11495586 | 10.1021/jm0108350 | HeLa | 4 |
| 11495586 | 10.1021/jm0108350 | Unchecked | 1 |
Data from ChEMBL 36 via Core Engine