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Tunicamycin B

Catalog No.: A27679
Tunicamycin Derivative
Tunicamycin B is a derivative of Tunicamycin known for its antimicrobial properties. It demonstrates significant antibacterial activity against Bacillus thuringiensis strains BT01 and W102, with minimum inhibitory concentrations (MICs) of 0.125 and 0.063 μg/mL, respectively. Additionally, it exhibits antifungal activity against Candida albicans strains ATCC 96901 and CMCC (F) 98001, with MICs of 8.0 and 4.0 μg/mL, respectively. Tunicamycin B is suitable for research applications focused on antimicrobial mechanisms and efficacy.
Tunicamycin B 66081-36-5 Tunicamycin Derivative
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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
DescriptionTunicamycin B is a derivative of Tunicamycin known for its antimicrobial properties. It demonstrates significant antibacterial activity against Bacillus thuringiensis strains BT01 and W102, with minimum inhibitory concentrations (MICs) of 0.125 and 0.063 μg/mL, respectively. Additionally, it exhibits antifungal activity against Candida albicans strains ATCC 96901 and CMCC (F) 98001, with MICs of 8.0 and 4.0 μg/mL, respectively. Tunicamycin B is suitable for research applications focused on antimicrobial mechanisms and efficacy.
Product Information
Catalog NumA27679
FormulaC39H64N4O16
Molecular Weight844.94
CAS Number66081-36-5
SMILESO=C1C=CN([C@@H]2O[C@H]([C@H](O)C[C@H]3O[C@@H](O[C@@H]4[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@@H](CO)O4)[C@H](NC(/C=C/CCCCCCCCCCC(C)C)=O)[C@@H](O)[C@H]3O)[C@H](O)[C@@H]2O)C(N1)=O
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Microbiology > Antifection > Fungal