Plipastatin A1

Catalog No.: A77158
Phospholipase A2 Iinhibitor
Plipastatin A1 is a lipopeptide that serves as an inhibitor of phospholipase A2. It demonstrates significant inhibitory effects on the conidial germination of Botrytis cinerea, leading to a reduction in the occurrence of gray mold on tomato leaves. This compound is valuable for research focused on agricultural pathogens and plant protection strategies against gray mold disease.
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Size Price Stock Qty
1mg
$935.00
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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
DescriptionPlipastatin A1 is a lipopeptide that serves as an inhibitor of phospholipase A2. It demonstrates significant inhibitory effects on the conidial germination of Botrytis cinerea, leading to a reduction in the occurrence of gray mold on tomato leaves. This compound is valuable for research focused on agricultural pathogens and plant protection strategies against gray mold disease.
Product Information
Catalog NumA77158
FormulaC72H110N12O20
Molecular Weight1463.71
CAS Number103651-09-8
Sequence{(3R)-3-hydroxy-1-oxohexadecyl}-Glu-{d-Orn}-Tyr-{d-Thr}-Glu-{d-Ala}-Pro-Gln-{d-Tyr}-Ile (Lactam bridge: Tyr3-Ile10)
Sequence shortening{(3R)-3-hydroxy-1-oxohexadecyl}-E-{d-Orn}-Y{d-Thr}-E-{d-Ala}-PQ{d-Tyr}-I (Lactam bridge: Tyr3-Ile10)
SMILESO=C([C@H](NC([C@@H](NC(C[C@@H](CCCCCCCCCCCCC)O)=O)CCC(O)=O)=O)CCCN)N[C@@H](CC1=CC=C(OC([C@@]([C@@H](C)CC)([H])NC([C@@H](CC2=CC=C(O)C=C2)NC3=O)=O)=O)C=C1)C(N[C@@]([C@H](O)C)([H])C(N[C@@H](CCC(O)=O)C(N[C@H](C)C(N4[C@@](C(N[C@H]3CCC(N)=O)=O)([H])CCC4)=O)=O)=O)=O
SynonymsFengycin IX; SNA-60-367-3
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