Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C44H52N8O10 |
Molecular Weight | 852.9313 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[C@H]1NC(=O)[C@@H](NC(=O)C2=NC=CC=C2O)[C@@H](C)OC(=O)[C@@H](NC(=O)[C@@H]3CC(=O)CCN3C(=O)[C@H](CC4=CC=C(NC)C=C4)N(C)C(=O)[C@@H]5CCCN5C1=O)C6=CC=CC=C6
InChI
InChIKey=PCOXSOQWQVRJCH-RIECGXCRSA-N
InChI=1S/C44H52N8O10/c1-5-30-41(58)51-21-10-13-31(51)42(59)50(4)33(23-26-15-17-28(45-3)18-16-26)43(60)52-22-19-29(53)24-32(52)38(55)49-36(27-11-7-6-8-12-27)44(61)62-25(2)35(39(56)47-30)48-40(57)37-34(54)14-9-20-46-37/h6-9,11-12,14-18,20,25,30-33,35-36,45,54H,5,10,13,19,21-24H2,1-4H3,(H,47,56)(H,48,57)(H,49,55)/t25-,30-,31+,32+,33+,35+,36+/m1/s1
Efepristin (RPR 106972) is an oral streptogramin consisting of two synergistic components RPR 112808 (pristinamycin IB) and RPR 106950 (pristinamycin IIB). It demonstrated activity against Gram-positive microorganisms in vitro and in vivo, including those with multi-drug resistance. The streptogramins inhibit bacterial growth by disrupting the translation of mRNA into protein.
Originator
Approval Year
PubMed
Title | Date | PubMed |
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In vitro antimicrobial activity and MIC quality control guidelines of RPR 106972 (RPR 112808/RPR106950): a novel orally administered streptogramin combination. The Quality Control Study Group. | 1997 Jul |
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Comparative activity of quinupristin/dalfopristin and RPR 106972 and the effect of medium on in-vitro test results. | 1998 Dec |
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In vitro activity of RPR 106972 alone and in combination with vancomycin, ampicillin, and gentamicin against multidrug-resistant enterococci. | 1998 Oct |
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Novel streptogramin antibiotics. | 2001 Feb |
Patents
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69RU1K50ZP
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SUB06465MIG
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57206-54-9
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5748661
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m524
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C166920
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100000080534
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CHEMBL2105803
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7472
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ACTIVE MOIETY