DPCPX
SMILES | CCCn1c2nc([nH]c2c(=O)n(c1=O)CCC)C1CCCC1 |
InChIKey | FFBDFADSZUINTG-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 5 |
Hydrogen bond donors | 1 |
Rotatable bonds | 5 |
Molecular weight (Da) | 304.2 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | Yes |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
A1 | AA1R | Human | Adenosine | A | pKi | 7.4 | 8.3 | 9.2 | Guide to Pharmacology |
A2A | AA2AR | Human | Adenosine | A | pKi | 6.6 | 6.9 | 7.2 | Guide to Pharmacology |
A2B | AA2BR | Human | Adenosine | A | pKi | 6.9 | 7.1 | 7.3 | Guide to Pharmacology |
A3 | AA3R | Human | Adenosine | A | pKi | 5.4 | 6.01 | 6.61 | Guide to Pharmacology |
A2B | AA2BR | Mouse | Adenosine | A | pKi | 7.06 | 7.06 | 7.06 | Guide to Pharmacology |
A2B | AA2BR | Rat | Adenosine | A | pKi | 6.7 | 6.71 | 6.73 | Guide to Pharmacology |
A3 | AA3R | Rat | Adenosine | A | pKi | 4.37 | 5.98 | 7.6 | Guide to Pharmacology |
A2A | AA2AR | Rat | Adenosine | A | pKi | 6.3 | 6.55 | 6.8 | Guide to Pharmacology |
A2B | AA2BR | Rat | Adenosine | A | pKi | 6.73 | 6.73 | 6.73 | ChEMBL |
A1 | AA1R | Guinea pig | Adenosine | A | pKi | 8.19 | 8.23 | 8.53 | ChEMBL |
A3 | AA3R | Rat | Adenosine | A | pKi | 5.28 | 5.28 | 5.28 | ChEMBL |
A1 | AA1R | Bovine | Adenosine | A | pKi | 9.3 | 9.41 | 9.81 | ChEMBL |
A2A | AA2AR | Rat | Adenosine | A | pKi | 6.15 | 6.46 | 6.8 | ChEMBL |
A1 | AA1R | Rat | Adenosine | A | pKi | 8.42 | 9.24 | 9.68 | ChEMBL |
A1 | AA1R | Rat | Adenosine | A | pKd | 8.24 | 8.24 | 8.24 | ChEMBL |
A2B | AA2BR | Human | Adenosine | A | pKi | 5.13 | 6.93 | 7.29 | ChEMBL |
A3 | AA3R | Human | Adenosine | A | pKi | 5.4 | 5.88 | 6.7 | ChEMBL |
A2A | AA2AR | Human | Adenosine | A | pKi | 6.1 | 6.66 | 7.25 | ChEMBL |
A2A | AA2AR | Human | Adenosine | A | pKd | 6.97 | 7.04 | 7.12 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pKi | 7.02 | 8.56 | 9.33 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pKd | 8.43 | 8.5 | 8.57 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pKi | 7.89 | 8.86 | 9.85 | PDSP Ki database |
A3 | AA3R | Human | Adenosine | A | pKi | 5.4 | 6.02 | 6.61 | PDSP Ki database |
A2A | AA2AR | Human | Adenosine | A | pKi | 6.8 | 6.85 | 6.89 | PDSP Ki database |
A2B | AA2BR | Human | Adenosine | A | pKi | 7.14 | 7.28 | 7.4 | PDSP Ki database |
A1 | AA1R | Rat | Adenosine | A | pKi | 6.47 | 8.89 | 9.74 | PDSP Ki database |
A1 | AA1R | Bovine | Adenosine | A | pKi | 10.15 | 10.22 | 10.3 | PDSP Ki database |
A1 | W5NSY2 | Sheep | Adenosine | A | pKi | 10.0 | 10.0 | 10.0 | PDSP Ki database |
A1 | AA1R | Guinea pig | Adenosine | A | pKi | 8.97 | 8.97 | 8.97 | PDSP Ki database |
A1 | I3LEN5 | Pig | Adenosine | A | pKi | 9.64 | 9.64 | 9.64 | PDSP Ki database |
A2A | AA2AR | Rat | Adenosine | A | pKi | 6.33 | 6.33 | 6.33 | PDSP Ki database |
μ | OPRM | Human | Opioid | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
A1 | AA1R | Rat | Adenosine | A | pKi | 9.0 | 9.37 | 9.74 | Guide to Pharmacology |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
A1 | AA1R | Guinea pig | Adenosine | A | pIC50 | 8.88 | 8.88 | 8.88 | ChEMBL |
A2A | AA2AR | Rat | Adenosine | A | pIC50 | 5.96 | 5.96 | 5.96 | ChEMBL |
A1 | AA1R | Rat | Adenosine | A | pIC50 | 8.22 | 8.29 | 8.33 | ChEMBL |
A2B | AA2BR | Human | Adenosine | A | pIC50 | 7.37 | 7.89 | 8.42 | ChEMBL |
A2A | AA2AR | Human | Adenosine | A | pIC50 | 6.58 | 6.71 | 6.88 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pIC50 | 7.6 | 8.46 | 9.3 | ChEMBL |
A1 | AA1R | Human | Adenosine | A | pEC50 | 6.03 | 7.43 | 8.82 | ChEMBL |
TSH | TSHR | Human | Glycoprotein hormone | A | Potency | 5.2 | 5.2 | 5.2 | ChEMBL |
M1 | ACM1 | Rat | Acetylcholine (muscarinic) | A | Potency | 4.65 | 4.65 | 4.65 | ChEMBL |