| Weight | 1349.506 g/mol |
|---|---|
| Formula | C71H84N10O17 |
| Hydrogen Acceptors | 19 |
| Hydrogen Donors | 6 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 7 |
Pristinamycin (11006-76-1)
Score:
#213 in Microbiology
,
#2083 in Biology
,
#2556 in Chemistry
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- In vitro development of resistance to telithromycin (HMR 3647), four macrolides, clindamycin, and pristinamycin in Streptococcus pneumoniae. (Antimicrobial Agents and Chemotherapy, 2000)
- High prevalence of colonization with vancomycin- and pristinamycin-resistant enterococci in healthy humans and pigs in The Netherlands: is the addition of antibiotics to animal feeds to blame? (Journal of Antimicrobial Chemotherapy, 1997)
- Purification of the two-enzyme system catalyzing the oxidation of the D-proline residue of pristinamycin IIB during the last step of pristinamycin IIA biosynthesis. (Journal of Bacteriology, 1995)
- Pristinamycin I biosynthesis in Streptomyces pristinaespiralis: molecular characterization of the first two structural peptide synthetase genes. (Journal of Bacteriology, 1997)
- Identification and analysis of genes from Streptomyces pristinaespiralis encoding enzymes involved in the biosynthesis of the 4dimethylaminolphenylalanine precursor of pristinamycin I (Molecular Microbiology, 1997)
- Cloning and analysis of structural genes from Streptomyces pristinaespiralis encoding enzymes involved in the conversion of pristinamycin IIB to pristinamycin IIA (PIIA): PIIA synthase and NADH:riboflavin 5'-phosphate oxidoreductase. (Journal of Bacteriology, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC1C(=O)N2CCCC2C(=O)N(C(C(=O)N3CCC(=O)CC3C(=O)NC(C(=O)OC(C(C(=O)N1)NC(=O)C4=C(C=CC=N4)O)C)C5=CC=CC=C5)CC6=CC=CC=C6)C.CC1C=CC(=O)NCC=CC(=CC(CC(=O)CC2=NC(=CO2)C(=O)N3CCC=C3C(=O)OC1C(C)C)O)C
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InChIKeyMVTQIFVKRXBCHS-UHFFFAOYSA-N
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