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Retro-indolicidin

Catalog No.: A48843
Bioactive Peptide
Retro-indolicidin is a bioactive peptide that functions as an antimicrobial agent. This synthetic reverse peptide, derived from indolicidin, consists of 13 amino acid residues and retains significant antimicrobial and protease inhibitory activities in vitro. Retro-indolicidin is applicable in research focused on antimicrobial properties, host defense mechanisms, and potential therapeutic strategies against microbial infections.
Retro-indolicidin 267890-59-5 Bioactive Peptide
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Research use only. We do not sell to patients.
Data Sheet SDS Compound Handling Instructions

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionRetro-indolicidin is a bioactive peptide that functions as an antimicrobial agent. This synthetic reverse peptide, derived from indolicidin, consists of 13 amino acid residues and retains significant antimicrobial and protease inhibitory activities in vitro. Retro-indolicidin is applicable in research focused on antimicrobial properties, host defense mechanisms, and potential therapeutic strategies against microbial infections.
Product Information
Catalog NumA48843
FormulaC100H132N26O13
Molecular Weight1906.28
CAS Number267890-59-5
SequenceArg-Arg-Trp-Pro-Trp-Trp-Pro-Trp-Lys-Trp-Pro-Leu-Ile-NH2
Sequence shorteningRRWPWWPWKWPLI-NH2
SMILESC([C@@H](C(=O)N1[C@H](C(N[C@@H](CC=2C=3C(NC2)=CC=CC3)C(N[C@H](C(N[C@@H](CC=4C=5C(NC4)=CC=CC5)C(=O)N6[C@H](C(N[C@H](C(N[C@@H]([C@H](CC)C)C(N)=O)=O)CC(C)C)=O)CCC6)=O)CCCCN)=O)=O)CCC1)NC([C@H](CC=7C=8C(NC7)=CC=CC8)NC(=O)[C@H]9N(C([C@H](CC=%10C=%11C(NC%10)=CC=CC%11)NC([C@@H](NC([C@H](CCCNC(=N)N)N)=O)CCCNC(=N)N)=O)=O)CCC9)=O)C=%12C=%13C(NC%12)=CC=CC%13
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