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IDR 1018 is an antibacterial peptide. It is active against P. aeruginosa and S. aureus (MICs = 19 and 5 µg/ml, respectively). IDR 1018 (20 µg/ml) decreases TNF-alpha secretion induced by LPS in isolated human peripheral blood mononuclear cells (PBMCs). It reduces biofilm formation by P. aeruginosa, A. baumannii, S. enterica, and methicillin-resistant S. aureus (MRSA) when used in combination with ceftazidime (Cay-14828). InChI: InChI=1S/C71H126N26O12.C2H4O2/c1-14-39(11)54(66(108)93-50(33-42-34-86-44-23-17-16-22-43(42)44)61(103)89-46(25-19-29-83-69(76)77)58(100)88-45(56(73)98)24-18-28-82-68(74)75)96-60(102)48(27-21-31-85-71(80)81)91-65(107)53(38(9)10)94-57(99)41(13)87-64(106)52(37(7)8)95-67(109)55(40(12)15-2)97-62(104)49(32-35(3)4)92-59(101)47(26-20-30-84-70(78)79)90-63(105)51(72)36(5)6,1-2(3)4/h16-17,22-23,34-41,45-55,86H,14-15,18-21,24-33,72H2,1-13H3,(H2,73,98)(H,87,106)(H,88,100)(H,89,103)(H,90,105)(H,91,107)(H,92,101)(H,93,108)(H,94,99)(H,95,109)(H,96,102)(H,97,104)(H4,74,75,82)(H4,76,77,83)(H4,78,79,84)(H4,80,81,85),1H3,(H,3,4)/t39-,40-,41-,45-,46-,47-,48-,49-,50-,51-,52-,53-,54-,55-,/m0./s1 InChIKey: LRGVZTXWLGHRPR-XIQVEKCESA-N SMILES: CC[C@@H]([C@@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N)=O)CCCNC(N)=N)=O)CCCNC(N)=N)=O)CC1=CNC2=C1C=CC=C2)=O)NC([C@@H](NC([C@H](C(C)C)NC([C@@H](NC([C@H](C(C)C)NC([C@H]([C@H](CC)C)NC([C@@H](NC([C@@H](NC([C@H](C(C)C)N)=O)CCCNC(N)=N)=O)CC(C)C)=O)=O)=O)C)=O)=O)CCCNC(N)=N)=O)C.CC(O)=O
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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