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1. Imetelstat
1. Grn163l
2. F60ne4xb53
3. 5'-(o-(2-hydroxy-3-((1-oxohexadecyl)amino)propyl) Hydrogen Phosphorothioate)-d(3'-amino-3'-deoxy-p-thio)(t-a-g-g-g-t-t-a-g-a-c-a-a)
4. Grn163l Peptide
5. Imetelstat [inn]
6. Imetelstat [usan]
7. Imetelstat [who-dd]
8. Unii-f60ne4xb53
9. Grn 163l
10. Grn-163l
Molecular Weight | 4610 g/mol |
---|---|
Molecular Formula | C148H211N68O53P13S13 |
XLogP3 | -1.1 |
Hydrogen Bond Donor Count | 45 |
Hydrogen Bond Acceptor Count | 107 |
Rotatable Bond Count | 95 |
Exact Mass | 4607.8897749 g/mol |
Monoisotopic Mass | 4606.8864201 g/mol |
Topological Polar Surface Area | 2010 Ų |
Heavy Atom Count | 295 |
Formal Charge | 0 |
Complexity | 11900 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 39 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Investigated for use/treatment in leukemia (lymphoid) and solid tumors.
Enzyme Inhibitors
Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)
GRN163L has been characterized preclinically and shown to inhibit telomerase in human tumor cells of many cancer types. It targets the template region, or active site, of telomerase. GRN163L does not exhibit antisense activity (binding to messenger RNA), but rather directly bind to the RNA component of telomerase at the active site of the enzyme, thereby acting like a conventional pharmaceutical drug. Inhibiting telomerase activity should result in telomere shortening and therefore cause aging and death of cancer cells.
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