CHEMBL5179081
SMILES | CCCC[C@@H]1NC(=O)[C@@H]2CSc3nnc(c4c3CCC3C(CC4)C3COC(=O)NCCOCCOCCNC(=O)c3ccc4c(c3)C(=O)OC43c4ccc(O)cc4Oc4cc(O)ccc43)SC[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](Cc3c[nH]c4ccccc34)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc3ccccc3)NC(=O)[C@H](Cc3cnc[nH]3)NC(=O)CNC1=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N2 |
InChIKey | QCXXYYAQEUNASC-MNUZRXMESA-N |
Chemical properties
Hydrogen bond acceptors | 36 |
Hydrogen bond donors | 36 |
Rotatable bonds | 45 |
Molecular weight (Da) | 2788.2 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Database connections
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
MC1 | MSHR | Human | Melanocortin | A | pKi | 8.55 | 8.55 | 8.55 | ChEMBL |
MC3 | MC3R | Human | Melanocortin | A | pKi | 7.51 | 7.51 | 7.51 | ChEMBL |
MC4 | MC4R | Human | Melanocortin | A | pKi | 6.58 | 6.58 | 6.58 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
MC1 | MSHR | Human | Melanocortin | A | pEC50 | 9.62 | 9.62 | 9.62 | ChEMBL |
MC5 | MC5R | Human | Melanocortin | A | pIC50 | 5.79 | 5.79 | 5.79 | ChEMBL |
MC3 | MC3R | Human | Melanocortin | A | pEC50 | 9.02 | 9.02 | 9.02 | ChEMBL |
MC4 | MC4R | Human | Melanocortin | A | pEC50 | 7.78 | 7.78 | 7.78 | ChEMBL |