eledoisin
SMILES | None |
InChIKey | AYLPVIWBPZMVSH-FCKMLYJASA-N |
Sequence | XPSKDAFIGLM |
Chemical properties
Hydrogen bond acceptors | None |
Hydrogen bond donors | None |
Rotatable bonds | None |
Molecular weight (Da) |
Drug properties
Molecular type | Peptide |
Physiological/Surrogate | Surrogate |
Approved drug | Yes |
Database connections
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
NK3 | NK3R | Human | Tachykinin | A | pIC50 | 6.2 | 6.4 | 6.6 | Guide to Pharmacology |
NK1 | NK1R | Human | Tachykinin | A | pIC50 | 8.07 | 8.07 | 8.07 | Drug Central |
NK1 | NK1R | Human | Tachykinin | A | pIC50 | 8.6 | 8.6 | 8.6 | Guide to Pharmacology |
NK3 | NK3R | Human | Tachykinin | A | pEC50 | 8.02 | 8.02 | 8.02 | Drug Central |
NK3 | NK3R | Human | Tachykinin | A | pIC50 | 7.02 | 7.02 | 7.02 | ChEMBL |
NK3 | NK3R | Human | Tachykinin | A | pEC50 | 8.18 | 8.69 | 9.66 | ChEMBL |