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CP7-FP13-2

Catalog No.: A49862
Antibacterial Peptide
CP7-FP13-2 is an antibacterial peptide that targets virulence factors in bacteria. It effectively inhibits the formation of biofilms in Staphylococcus aureus, demonstrating potent antibacterial activity in in vivo mouse models. This compound is valuable for research applications focusing on microbial resistance and the development of alternative therapeutic strategies against bacterial infections.
CP7-FP13-2 3032621-32-9 Antibacterial 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
DescriptionCP7-FP13-2 is an antibacterial peptide that targets virulence factors in bacteria. It effectively inhibits the formation of biofilms in Staphylococcus aureus, demonstrating potent antibacterial activity in in vivo mouse models. This compound is valuable for research applications focusing on microbial resistance and the development of alternative therapeutic strategies against bacterial infections.
Product Information
Catalog NumA49862
FormulaC145H224N34O31S2
Molecular Weight3003.67
CAS Number3032621-32-9
SequenceCyclo(-Leu-Leu-Phe-Ala-(Dab))-Asn-Ile-Gly-Gly-Cys-(6-Maleimidocaproic acid)-Gly-Ile-Lys-Asn-Leu-Trp-Lys-Lys-Met-Ile-Lys-Leu-Trp-Tyr
Sequence shorteningCyclo(LLFA-(Dab))-NIGGC-(6-Maleimidocaproic acid)-GIKNLWKKMIKLWY
SMILESC([C@@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CC=1C=2C(NC1)=CC=CC2)C(N[C@@H](CC3=CC=C(O)C=C3)C(O)=O)=O)=O)CC(C)C)=O)CCCCN)=O)[C@H](CC)C)=O)CCSC)=O)CCCCN)=O)CCCCN)=O)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC(CNC(CCCCCN4C(=O)C(SC[C@@H](C(NCC(NCC(N[C@H](C(N[C@H](C(N[C@H]5CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC6=CC=CC=C6)NC(=O)[C@H](C)NC5=O)=O)CC(N)=O)=O)[C@H](CC)C)=O)=O)=O)N)CC4=O)=O)=O)[C@H](CC)C)=O)CCCCN)=O)CC(N)=O)=O)CC(C)C)=O)C=7C=8C(NC7)=CC=CC8
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Peptides
Microbiology > Antifection > Bacterial