UDP-glucuronic acid
SMILES | O[C@@H]1[C@@H](COP(=O)(OP(=O)(O[C@H]2O[C@H](C(=O)O)[C@H]([C@@H]([C@H]2O)O)O)O)O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O |
InChIKey | HDYANYHVCAPMJV-LXQIFKJMSA-N |
Chemical properties
Hydrogen bond acceptors | 16 |
Hydrogen bond donors | 9 |
Rotatable bonds | 9 |
Molecular weight (Da) | 580.0 |
Drug properties
Molecular type | Small molecule |
Endogenous/Surrogate | Endogenous |
Approved drug | Yes |
Database connections
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
GLP-1 | GLP1R | Human | Glucagon | B1 | pKi | 6.9 | 6.95 | 7.0 | Guide to Pharmacology |
GLP-1 | GLP1R | Human | Glucagon | B1 | pKi | 8.15 | 8.15 | 8.15 | Drug Central |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
glucagon | GLR | Human | Glucagon | B1 | pEC50 | 9.0 | 9.0 | 9.0 | Guide to Pharmacology |
GLP-1 | GLP1R | Mouse | Glucagon | B1 | pEC50 | 8.59 | 9.47 | 10.36 | ChEMBL |
glucagon | GLR | Mouse | Glucagon | B1 | pEC50 | 10.7 | 10.7 | 10.7 | ChEMBL |
glucagon | GLR | Rat | Glucagon | B1 | pIC50 | 8.82 | 8.82 | 8.82 | ChEMBL |
glucagon | GLR | Rat | Glucagon | B1 | pEC50 | 8.1 | 8.2 | 8.3 | ChEMBL |
glucagon | GLR | Human | Glucagon | B1 | pEC50 | 9.01 | 10.03 | 10.67 | ChEMBL |
GLP-1 | GLP1R | Human | Glucagon | B1 | pEC50 | 7.39 | 8.97 | 10.36 | ChEMBL |
glucagon | GLR | Human | Glucagon | B1 | pEC50 | 8.05 | 8.05 | 8.05 | Drug Central |
glucagon | GLR | Rat | Glucagon | B1 | pIC50 | 8.05 | 8.05 | 8.05 | Drug Central |
GLP-1 | GLP1R | Mouse | Glucagon | B1 | pEC50 | 7.98 | 7.98 | 7.98 | Drug Central |
GLP-1 | F8V479 | Crab-eating macaque | Glucagon | B1 | pEC50 | 7.98 | 7.98 | 7.98 | Drug Central |
GLP-1 | F8V479 | Crab-eating macaque | Glucagon | B1 | pEC50 | 10.51 | 10.51 | 10.51 | ChEMBL |