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Tunicamycin V

Cat. No. M38672
Tunicamycin V Structure
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Biological Activity

Tunicamycin V (Tunicamycin A) is a nucleoside natural product that inhibits bacterial phospho-N-acetylmuramyl-pentapeptide transferase (MraY) with an IC50 of 0.35 μM. Tunicamycin V has antibacterial activties.

Chemical Information
Molecular Weight 844.94
Formula C39H64N4O16
CAS Number 66054-36-2
Form Solid
Storage Powder -20°C
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Katsuhiko Mitachi et al. MethodsX. An improved total synthesis of tunicamycin V

[2] Katsuhiko Mitachi et al. Angew Chem Int Ed Engl. Concise Synthesis of Tunicamycin V and Discovery of a Cytostatic DPAGT1 Inhibitor

[3] Ning Zhang et al. FASEB J. N-glycosylation of CREBH improves lipid metabolism and attenuates lipotoxicity in NAFLD by modulating PPARα and SCD-1

[4] Kazuki Yamamoto et al. Bioorg Med Chem. Structural requirement of tunicamycin V for MraY inhibition

[5] Kazuki Yamamoto et al. Org Lett. Total Synthesis of Tunicamycin V

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