Helvecardin B

Catalog No.: A47499
Antibiotic
Helvecardin B is a glycopeptide antibiotic that exerts its effects by disrupting bacterial cell wall synthesis. It demonstrates potent activity against both aerobic and anaerobic Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). Helvecardin B is useful in microbiological studies and antibiotic resistance research, contributing to the understanding of mechanisms underlying bacterial infections and treatment strategies.
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5mg
10mg
50mg
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Free Delivery on orders over $500
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
DescriptionHelvecardin B is a glycopeptide antibiotic that exerts its effects by disrupting bacterial cell wall synthesis. It demonstrates potent activity against both aerobic and anaerobic Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). Helvecardin B is useful in microbiological studies and antibiotic resistance research, contributing to the understanding of mechanisms underlying bacterial infections and treatment strategies.
Product Information
Catalog NumA47499
FormulaC84H93Cl2N9O31
Molecular Weight1795.58
CAS Number119979-34-9
SMILES[H][C@]1(NC([C@@H]([C@@H](C2=CC=C(OC3=CC4=CC(OC5=CC=C([C@H]([C@@]6(NC([C@](NC([C@@]4(NC1=O)[H])=O)(C7=CC=C(C(C8=C([C@H](NC6=O)C(O)=O)C=C(C=C8O)O)=C7)O)[H])=O)[H])O[C@H]9C[C@H]([C@H]([C@@H](O9)C)O)N)C=C5Cl)=C3O[C@@H]%10O[C@@H](C([C@@H]([C@H]%10O[C@H]%11C[C@H]([C@H]([C@@H](O%11)C)O)N)O)O)CO)C=C2)O)NC([C@@H](C%12=CC=C(C=C%12)O[C@@H]%13O[C@H]([C@@H]([C@H]([C@H]%13O)OC)O)C)NC)=O)=O)C%14=CC(Cl)=C(C=C%14)O
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