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| ATC_suffix = AB04 | | ATC_suffix = AB04 | ||
| PubChem = 16132438 | | PubChem = 16132438 | ||
| DrugBank = |
| DrugBank = DB00046 | ||
| UNII_Ref = {{fdacite|correct|FDA}} | | UNII_Ref = {{fdacite|correct|FDA}} | ||
| UNII = GFX7QIS1II | | UNII = <!-- blanked - oldvalue: GFX7QIS1II --> | ||
| KEGG = D04477 | | KEGG = D04477 | ||
| ChemSpiderID = NA | | ChemSpiderID = NA |
Revision as of 10:00, 31 October 2011
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Clinical data | |
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AHFS/Drugs.com | Monograph |
MedlinePlus | a697021 |
Routes of administration | Subcutaneous |
ATC code | |
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Chemical and physical data | |
Formula | C257H389N65O77S6 |
Molar mass | 5813.63 g/mol g·mol |
Insulin lispro (marketed by Eli Lilly and Company as "Humalog") is a fast acting insulin analogue; it was the first insulin analogue, and is similar to insulin aspart.
Engineered through recombinant DNA technology, the penultimate lysine and proline residues on the C-terminal end of the B-chain are reversed. This modification does not alter receptor binding, but blocks the formation of insulin dimers and hexamers. This allowed larger amounts of active monomeric insulin to be immediately available for postprandial injections.
Insulin lispro has one primary advantage over regular insulin for postprandial glucose control. It has a shortened delay of onset, allowing slightly more flexibility than regular insulin, which requires a longer waiting period before starting a meal after injection. Both preparations should be coupled with a longer acting insulin for good glycemic control.
References
- "Insulin Lispro: A Fast-Acting Insulin Analog". Retrieved 2007-06-08.
External links
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