carbacyclin


SMILES CCCCC[C@@H](/C=C/[C@H]1[C@H](O)C[C@H]2[C@@H]1C/C(=C\CCCC(=O)O)/C2)O
InChIKey XZFRIPGNUQRGPI-WLPVIMDJSA-N

Chemical properties

Hydrogen bond acceptors 3
Hydrogen bond donors 3
Rotatable bonds 10
Molecular weight (Da) 350.2

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
H3 HRH3 Human Histamine A pKi 8.8 9.25 9.7 Guide to Pharmacology
H4 HRH4 Human Histamine A pKi 7.6 7.8 8.0 Guide to Pharmacology
H3 HRH3 Rat Histamine A pKi 8.8 8.85 8.9 Guide to Pharmacology
H3 HRH3 Mouse Histamine A pKi 9.8 9.8 9.8 Guide to Pharmacology
H3 HRH3 Guinea pig Histamine A pKi 9.4 9.4 9.4 ChEMBL
H4 HRH4 Human Histamine A pKi 7.66 7.68 7.7 ChEMBL
H3 HRH3 Human Histamine A pKi 9.3 9.37 9.52 ChEMBL
H3 HRH3 Human Histamine A pKi 5.0 8.12 9.4 PDSP Ki database
H3 HRH3 Rat Histamine A pKi 8.85 9.07 9.3 PDSP Ki database
H4 HRH4 Human Histamine A pKi 7.7 7.81 8.05 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
H4 HRH4 Human Histamine A pEC50 7.25 7.53 7.8 ChEMBL
H3 HRH3 Human Histamine A pEC50 9.17 9.73 10.4 ChEMBL