MRS1220
SMILES | O=C(Nc1nc2ccc(cc2c2n1nc(n2)c1ccco1)Cl)Cc1ccccc1 |
InChIKey | TWWFAXQOKNBUCR-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 6 |
Hydrogen bond donors | 1 |
Rotatable bonds | 4 |
Molecular weight (Da) | 403.1 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Database connections
Ligand site mutations | A3 |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
A2B | AA2BR | Human | Adenosine | A | pKi | 6.5 | 6.5 | 6.5 | Guide to Pharmacology |
A2A | AA2AR | Rat | Adenosine | A | pKi | 7.28 | 7.56 | 7.99 | ChEMBL |
A1 | AA1R | Rat | Adenosine | A | pKi | 6.52 | 6.9 | 7.28 | ChEMBL |
A3 | AA3R | Human | Adenosine | A | pKi | 5.77 | 8.64 | 9.94 | ChEMBL |
A3 | AA3R | Human | Adenosine | A | pKd | 10.01 | 10.06 | 10.11 | ChEMBL |
A2A | AA2AR | Human | Adenosine | A | pKi | 7.6 | 7.6 | 7.6 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pKi | 6.64 | 7.07 | 7.29 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pKd | 7.8 | 7.8 | 7.8 | ChEMBL |
A3 | AA3R | Human | Adenosine | A | pKi | 8.2 | 8.7 | 9.2 | Guide to Pharmacology |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
A3 | AA3R | Human | Adenosine | A | pEC50 | 7.44 | 7.44 | 7.44 | ChEMBL |
A3 | AA3R | Human | Adenosine | A | pIC50 | 8.14 | 9.07 | 10.01 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pEC50 | 7.32 | 7.32 | 7.32 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pIC50 | 7.32 | 7.32 | 7.32 | ChEMBL |
TSH | TSHR | Human | Glycoprotein hormone | A | Potency | 4.4 | 4.4 | 4.4 | ChEMBL |