Compound Detail
CHEMBL88963
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O=S(=O)(c1ccccc1)C1CCN(Nc2nc(Cl)nc3c2ncn3[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)CC1
Basic Information
| ChEMBL ID | CHEMBL88963 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | YFHYXENKDUPFSL-WVSUBDOOSA-N |
3
Targets
4
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
525.0
MW (Da)
0.36
ALogP
12
HBA
4
HBD
162.9
PSA (Ų)
0.33
QED
2
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 9.15
Ki 2 meas. best 7.77
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Cavia porcellus CHEMBL369 | IC50 | 9.15 | 7.825 | 0.7 | 2 |
| Adenosine receptor A1 CHEMBL318 | Ki | 7.77 | 7.77 | 17.0 | 1 |
| Adenosine A2 receptor CHEMBL2094117 | Ki | 6.66 | 6.66 | 220.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Cavia porcellus | IC50 | = | 0.7 | nM | 9.15 | Tested for agonistic potency to inhibit stimulated cAMP accumulation in isolated... | - |
| Adenosine receptor A1 | Ki | = | 17.0 | nM | 7.77 | Tested for inhibition of adenosine A1 receptor binding to rat brain | - |
| Adenosine A2 receptor | Ki | = | 220.0 | nM | 6.66 | Tested for inhibition of adenosine A2 receptor binding to rat brain | - |
| Cavia porcellus | IC50 | = | 320.0 | nM | 6.5 | Tested for agonistic potency to inhibit contractile force in isolated guinea pig... | - |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| - | 10.1016/S0960-894X(01)80737-X | Cavia porcellus | 2 |
| - | 10.1016/S0960-894X(01)80737-X | Adenosine receptor A1 | 1 |
| - | 10.1016/S0960-894X(01)80737-X | Adenosine A2 receptor | 1 |
| - | 10.1016/S0960-894X(01)80737-X | No relevant target | 1 |
Data from ChEMBL 36 via Core Engine