Weight | 308.378 g/mol |
---|---|
Formula | C16H24N2O4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 4 |
Aromatic Rings | 1 |
Rotatable Bonds | 8 |
Bestatin (65391-42-6, 58970-76-6)
bestatin, (D-Leu)-(R-(R*,R*))-isomer · bestatin, (L-Leu)-(S-(R*,S*))-isomer, hydrochloride · bestatin, (L-Leu)-(R-(R*,R*))-isomer
Score:
#1213 in Biochemistry
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#3042 in Biology
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#3805 in Chemistry
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- BESTATIN, AN INHIBITOR OF AMINOPEPTIDASE B, PRODUCED BY ACTINOMYCETES (The Journal of Antibiotics, 1976)
- Inhibition of aminopeptidases by amastatin and bestatin derivatives. Effect of inhibitor structure on slow-binding processes. (Journal of Medicinal Chemistry, 1984)
- Inhibition of aminopeptidase B and leucine aminopeptidase by bestatin and its stereoisomer. (Archives of Biochemistry and Biophysics, 1976)
- Structure determination and refinement of bovine lens leucine aminopeptidase and its complex with bestatin (Journal of Molecular Biology, 1992)
- Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B. (Journal of Medicinal Chemistry, 1977)
- Enhancement of delayed-type hypersensitivity by bestatin, an inhibitor of aminopeptidase B and leucine aminopeptidase. (The Journal of Antibiotics, 1976)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - bestatin, (D-Leu)-(R-(R*,R*))-isomer
- bestatin, (L-Leu)-(S-(R*,S*))-isomer, hydrochloride
- bestatin, (L-Leu)-(R-(R*,R*))-isomer
- bestatin, (L-Leu)-(R-(R*,S*))-isomer
- bestatin, (D-Leu)-(R-(R*,S*))-isomer
- bestatin, (D-Leu)-(S-(R*,S*))-isomer
- 3-amino-2-hydroxy-4-phenylbutyryl-L-leucine
- bestatin, (L-Leu)-(S-(R*,R*))-isomer
- ubenimex
-
SMILESCC(C)CC(C(=O)O)NC(=O)C(C(CC1=CC=CC=C1)N)O
-
InChIKeyVGGGPCQERPFHOB-UHFFFAOYSA-N
- Pubchem - Bestatin
- Wikipedia - bestatin
Ubenimex (INN), also known more commonly as bestatin, is a competitive, reversible protease inhibitor. It is an inhibitor of arginyl aminopeptidase (aminopeptidase B), leukotriene A4 hydrolase (a zinc metalloprotease that displays both epoxide hydrolase and aminopeptidase activities), alanyl aminopeptidase (aminopeptidase M/N), leucyl/cystinyl aminopeptidase (oxytocinase/vasopressinase), and membrane dipeptidase (leukotriene D4 hydrolase). It is being studied for use in the treatment of acute myelocytic leukemia and lymphedema.
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