Compound ID | 2097
Class: Pleuromutilin
Spectrum of activity: | Gram-positive |
Details of activity: | Binds to the peptidyl transferase component of the 50S subunit of ribosomes, thus inhibiting peptide bond formation. Active against Gram-positive bacteria. |
Description: | Semisynthetic pleuromutilin derivative. Used in veterinary medicine |
Year first mentioned: | 1997 |
Development status: | Approved for veterinary use off-patent |
Chemical structure(s): | |
Canonical SMILES: | C=C[C@]1(C)C[C@H]([C@]2(C)[C@H](C)CC[C@]3(CCC(=O)[C@@H]23)[C@@H](C)[C@@H]1O)OC(=O)CSC(C)(C)CNC(=O)[C@@H](C(C)C)N |
Isomeric SMILES: | C[C@@H]1CC[C@@]23CCC(=O)[C@H]2[C@@]1([C@@H](C[C@@]([C@H]([C@@H]3C)O)(C)C=C)OC(=O)CSC(C)(C)CNC(=O)[C@@H](C(C)C)N)C |
InChI: | InChI=1S/C31H52N2O5S/c1-10-29(8)15-22(38-23(35)16-39-28(6,7)17-33-27(37)24(32)18(2)3)30(9)19(4)11-13-31(20(5)26(29)36)14-12-21(34)25(30)31/h10,18-20,22,24-26,36H,1,11-17,32H2,2-9H3,(H,33,37)/t19-,20+,22-,24-,25+,26+,29-,30+,31+/m1/s1 |
InChI Key: | LLYYNOVSVPBRGV-MVNKZKPCSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/9850878 |
External links: | |
Main Source: | https://academic.oup.com/jac/article/69/8/2022/873861 |
Citation: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1426994/ |