CXCL12α
| SMILES | None |
| InChIKey | None |
| Sequence | KPVSLSYRCPCRFFESHVARANVKHLKILNTPNCALQIVARLKNNNRQVCIDPKLKWIQEYLEKALNK |
Chemical properties
| Hydrogen bond acceptors | None |
| Hydrogen bond donors | None |
| Rotatable bonds | None |
| Molecular weight (Da) |
Drug properties
| Molecular type | Peptide |
| Physiological/Surrogate | Endogenous |
| Approved drug | No |
Database connections
| Structure pdb | 7SK3 |
Bioactivities
| Receptor | Activity | Source | |||||||
|---|---|---|---|---|---|---|---|---|---|
| GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
| CXCR3 | CXCR3 | Human | Chemokine | A | pKi | 6.4 | 6.4 | 6.4 | Guide to Pharmacology |
| CXCR4 | CXCR4 | Human | Chemokine | A | pKd | 7.7 | 7.95 | 8.2 | Guide to Pharmacology |
| Receptor | Activity | Source | |||||||
|---|---|---|---|---|---|---|---|---|---|
| GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
| CXCR4 | CXCR4 | Human | Chemokine | A | pIC50 | 9.3 | 9.3 | 9.3 | Guide to Pharmacology |
| ACKR3 | ACKR3 | Human | Chemokine | A | pEC50 | 7.52 | 7.71 | 7.9 | Guide to Pharmacology |