Ilomastat, also known as GM6001 and galardin, is a broad-spectrum matrix metalloproteinase inhibitor with potential anticancer activity. GM6001 is a member of the hydroxamic acid class of reversible metallopeptidase inhibitors. The anionic state of the hydroxamic acid group forms a bidentate complex with the active site zinc. Examples of enzymes that ilomastat inhibit include thermolysin, peptide deformylase, and anthrax lethal factor endopeptidase (LF) produced by the bacterium Bacillus anthracis.
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Name | Ilomastat |
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Iupac Chemical Name | (R)-N1-((S)-3-(1H-indol-3-yl)-1-(methylamino)-1-oxopropan-2-yl)-N4-hydroxy-2-isobutylsuccinamide |
Synonyms | GM6001 ; GM-6001 |
Molecular Formula | C20H28N4O4 |
Molecular Weight | 388.46072 |
Smile | N1C=C(C2=CC=CC=C12)C[C@@H](C(=O)NC)NC([C@@H](CC(=O)NO)CC(C)C)=O |
InChiKey | NITYDPDXAAFEIT-DYVFJYSZSA-N |
InChi | InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/m1/s1 |
CAS Number | 142880-36-2 |
Related CAS |
Packaging | Price | Availability | Purity | Shipping Time |
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Formulation | Solid powder |
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Purity | 98% by HPLC |
Storage | -20 ºC for 3 years |
Solubility | Soluble in DMSO |
Handling | |
Shipping Condition | Shipped under ambient temperature |
HS Code |
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Mechanism | |
Cell study | |
Animal study | |
Clinical study |