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Pyrrhocoricin

Catalog No.: A49392
Bioactive Peptide
Pyrrhocoricin is a bioactive peptide with antimicrobial activity primarily against Gram-negative bacteria. This compound exhibits potential as an antibiotic agent, making it valuable for research in infectious diseases and antibiotic development. Its unique mechanism of action and specificity offer insights into peptide-based therapeutics and bacterial resistance studies.
Pyrrhocoricin 224569-84-0 Bioactive Peptide
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Research use only. We do not sell to patients.
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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
DescriptionPyrrhocoricin is a bioactive peptide with antimicrobial activity primarily against Gram-negative bacteria. This compound exhibits potential as an antibiotic agent, making it valuable for research in infectious diseases and antibiotic development. Its unique mechanism of action and specificity offer insights into peptide-based therapeutics and bacterial resistance studies.
Product Information
Catalog NumA49392
FormulaC119H190N34O38
Molecular Weight2704.99
CAS Number224569-84-0
SequenceVal-Asp-Lys-Gly-Ser-Tyr-Leu-Pro-Arg-Pro-{O-[2-(acetylamino)-2-deoxy-3-O-β-D-galactopyranosyl-α-D-galactopyranosyl]-Thr}-Pro-Pro-Arg-Pro-Ile-Tyr-Asn-Arg-Asn-NH2
Sequence shorteningVDKGSYLPRPXPPRPIYNRN-NH2 (X=O-[2-(acetylamino)-2-deoxy-3-O-β-D-galactopyranosyl-α-D-galactopyranosyl]-Thr)
SMILESN(C(C)=O)[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]([C@@H](C(=O)N3[C@H](C(=O)N4[C@H](C(N[C@H](C(=O)N5[C@H](C(N[C@H](C(N[C@@H](CC6=CC=C(O)C=C6)C(N[C@H](C(N[C@H](C(N[C@@H](CC(N)=O)C(N)=O)=O)CCCNC(=N)N)=O)CC(N)=O)=O)=O)[C@H](CC)C)=O)CCC5)CCCNC(=N)N)=O)CCC4)CCC3)NC(=O)[C@H]7N(C([C@@H](NC(=O)[C@H]8N(C([C@@H](NC([C@H](CC9=CC=C(O)C=C9)NC([C@@H](NC(CNC([C@@H](NC([C@@H](NC([C@H](C(C)C)N)=O)CC(O)=O)=O)CCCCN)=O)=O)CO)=O)=O)CC(C)C)=O)CCC8)CCCNC(=N)N)=O)CCC7)C
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