| pubmed-article:19058272 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19058272 | lifeskim:mentions | umls-concept:C0003232 | lld:lifeskim |
| pubmed-article:19058272 | lifeskim:mentions | umls-concept:C0332437 | lld:lifeskim |
| pubmed-article:19058272 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:19058272 | lifeskim:mentions | umls-concept:C0349590 | lld:lifeskim |
| pubmed-article:19058272 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:19058272 | pubmed:dateCreated | 2009-1-5 | lld:pubmed |
| pubmed-article:19058272 | pubmed:abstractText | The conventional notion that peptides are poor candidates for orally available drugs because of protease-sensitive peptide bonds, intrinsic hydrophilicity, and ionic charges contrasts with the diversity of antibiotic natural products with peptide-based frameworks that are synthesized and utilized by Nature. Several of these antibiotics, including penicillin and vancomycin, are employed to treat bacterial infections in humans and have been best-selling therapeutics for decades. Others might provide new platforms for the design of novel therapeutics to combat emerging antibiotic-resistant bacterial pathogens. | lld:pubmed |
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