mezlocillin


SMILES CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](NC(=O)N3CCN(C3=O)S(C)(=O)=O)C3=CC=CC=C3)C(=O)N2[C@H]1C(O)=O
InChIKey YPBATNHYBCGSSN-VWPFQQQWSA-N

Chemical properties

Hydrogen bond acceptors 8
Hydrogen bond donors 3
Rotatable bonds 6
Molecular weight (Da) 539.1

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
CB2 CNR2 Human Cannabinoid A pKi 8.38 8.38 8.38 Drug Central
DP1 PD2R Human Prostanoid A pKi 8.31 8.31 8.31 Drug Central
DP2 PD2R2 Human Prostanoid A pKi 8.2 8.2 8.2 Drug Central
EP1 PE2R1 Human Prostanoid A pKi 8.36 8.36 8.36 Drug Central
EP2 PE2R2 Human Prostanoid A pKi 8.18 8.18 8.18 Drug Central
EP3 PE2R3 Human Prostanoid A pKi 8.36 8.36 8.36 Drug Central
EP4 PE2R4 Human Prostanoid A pKi 8.36 8.36 8.36 Drug Central
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
CB1 CNR1 Human Cannabinoid A pIC50 8.4 8.4 8.4 Drug Central
A3 AA3R Human Adenosine A pIC50 8.31 8.31 8.31 Drug Central