Microsomal aminopeptidase
Microsomal aminopeptidase structure
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Common Name | Microsomal aminopeptidase | ||
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| CAS Number | 9054-63-1 | Molecular Weight | 200.31776 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C12H24O2 | Melting Point | N/A | |
| MSDS | USA | Flash Point | N/A | |
Use of Microsomal aminopeptidaseMicrosomal aminopeptidase (microsomal aminoptidase) was first reported from C. elegans. The Microsomal aminopeptidase is beneficial for the development of molecular vaccines against parasitic nematodes[1]. |
| Name | Aminopeptidase |
|---|---|
| Synonym | More Synonyms |
| Description | Microsomal aminopeptidase (microsomal aminoptidase) was first reported from C. elegans. The Microsomal aminopeptidase is beneficial for the development of molecular vaccines against parasitic nematodes[1]. |
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| Related Catalog | |
| References |
| Molecular Formula | C12H24O2 |
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| Molecular Weight | 200.31776 |
| Appearance of Characters | powder | white |
| Storage condition | 2-8°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Safety Phrases | 22-24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
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Sodium solute symporter and cadherin proteins act as Bacillus thuringiensis Cry3Ba toxin functional receptors in Tribolium castaneum.
J. Biol. Chem. 288(25) , 18013-21, (2013) Understanding how Bacillus thuringiensis (Bt) toxins interact with proteins in the midgut of susceptible coleopteran insects is crucial to fully explain the molecular bases of Bt specificity and insec... |
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Novel leucine ureido derivatives as inhibitors of aminopeptidase N (APN).
Bioorg. Med. Chem. 21(7) , 1621-7, (2013) Aminopeptidase N (APN/CD13) over expressed on tumor cells, plays a critical role in tumor invasion, metastasis, and tumor angiogenesis. Here we described the design, synthesis and preliminary activity... |
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Synthesis and structure-activity relationships of phosphonic arginine mimetics as inhibitors of the M1 and M17 aminopeptidases from Plasmodium falciparum.
J. Med. Chem. 56(12) , 5213-7, (2013) The malaria parasite Plasmodium falciparum employs two metallo-aminopeptidases, PfA-M1 and PfA-M17, which are essential for parasite survival. Compounds that inhibit the activity of either enzyme repr... |
| MFCD00131501 |