BETAMETHASONE PHOSPHORIC ACID


SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)COP(=O)(O)O
InChIKey VQODGRNSFPNSQE-DVTGEIKXSA-N

Chemical properties

Hydrogen bond acceptors 6
Hydrogen bond donors 4
Rotatable bonds 4
Molecular weight (Da) 472.2

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug No

Database connections


Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M5 ACM5 Human Acetylcholine (muscarinic) A pKi 5.25 5.25 5.25 ChEMBL
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 5.78 5.78 5.78 ChEMBL
H1 HRH1 Human Histamine A pKi 5.93 5.93 5.93 ChEMBL
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 5.87 5.87 5.87 ChEMBL
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 5.78 5.78 5.78 ChEMBL
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 8.24 8.24 8.24 Drug Central
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 8.23 8.23 8.23 Drug Central
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 8.24 8.24 8.24 Drug Central
M5 ACM5 Human Acetylcholine (muscarinic) A pKi 8.28 8.28 8.28 Drug Central
H1 HRH1 Human Histamine A pKi 8.23 8.23 8.23 Drug Central
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M5 ACM5 Human Acetylcholine (muscarinic) A pIC50 5.11 5.11 5.11 ChEMBL
M4 ACM4 Human Acetylcholine (muscarinic) A pIC50 4.92 4.92 4.92 ChEMBL
H1 HRH1 Human Histamine A pIC50 5.0 5.0 5.0 ChEMBL
M3 ACM3 Human Acetylcholine (muscarinic) A pIC50 5.19 5.19 5.19 ChEMBL
M1 ACM1 Human Acetylcholine (muscarinic) A pIC50 5.16 5.16 5.16 ChEMBL