| 1. | Deprotonation of thiazole moiety in thiamine pyrophosphate results in ambivalent chemical reactivity
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| 2. | Farnesyl and geranyl pyrophosphate also serve as precursors for prenylated proteins.
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| 3. | Its mechanism of action involves inhibition of farnesyl pyrophosphate synthase activity.
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| 4. | Enzymatically, taxadiene is produced from geranylgeranyl pyrophosphate by taxadiene synthase.
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| 5. | However, the chemical is not phytotoxic, unlike tetraethyl pyrophosphate.
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| 6. | Mvp2 was shown to translocate 1 H + per pyrophosphate hydrolyzed.
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| 7. | Chemical structure for thiamine pyrophosphate and protein structure of transketolase.
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| 8. | Additional oxidation and cyclization clerodane pyrophosphate concludes the biosynthesis of salvinorin A.
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| 9. | Thiamine pyrophosphate ( TPP ) serves a functionally identical role.
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| 10. | A classic example is the cyclization of geranyl pyrophosphate to form limonene.
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