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Page 1
Mannostatin A, a new glycoprotein-processing inhibitor.
Tropea JE, Kaushal GP, Pastuszak I, Mitchell M, Aoyagi T, Molyneux RJ, Elbein AD. Tropea JE, et al. Biochemistry. 1990 Oct 30;29(43):10062-9. doi: 10.1021/bi00495a008. Biochemistry. 1990. PMID: 2271638
However, it was virtually inactive toward mannosidase I. The N-acetylated derivative of mannostatin A had no inhibitory activity. In cell culture studies, mannostatin A also proved to be a potent inhibitor of glycoprotein processing. ...This observation is in keepin …
However, it was virtually inactive toward mannosidase I. The N-acetylated derivative of mannostatin A had no inhibitory activity. In …
Cyclopentanes from N-amino-glyconolactams. A synthesis of mannostatin A.
Hu G, Zimmermann M, Ramana CV, Vasella A. Hu G, et al. Chem Commun (Camb). 2003 Apr 21;(8):952-3. doi: 10.1039/b301213a. Chem Commun (Camb). 2003. PMID: 12744315
Oxidation of a N-amino-ribonolactam with lead tetraacetate yields two cyclopentanes; the major one was transformed into the alpha-mannosidase inhibitor mannostatin A....
Oxidation of a N-amino-ribonolactam with lead tetraacetate yields two cyclopentanes; the major one was transformed into the alpha-mannosidas …
Inhibition of Golgi mannosidase II with mannostatin A analogues: synthesis, biological evaluation, and structure-activity relationship studies.
Li B, Kawatkar SP, George S, Strachan H, Woods RJ, Siriwardena A, Moremen KW, Boons GJ. Li B, et al. Chembiochem. 2004 Sep 6;5(9):1220-7. doi: 10.1002/cbic.200300842. Chembiochem. 2004. PMID: 15368573
Mannostatin and aminocyclopentitetrol analogues with various substitutions at the amino function were synthesized. These compounds were tested as inhibitors of human Golgi and lysosomal alpha-mannosidases. Modification of the amine of mannostatin had only marginal e
Mannostatin and aminocyclopentitetrol analogues with various substitutions at the amino function were synthesized. These compounds we
The molecular basis of inhibition of Golgi alpha-mannosidase II by mannostatin A.
Kuntz DA, Zhong W, Guo J, Rose DR, Boons GJ. Kuntz DA, et al. Chembiochem. 2009 Jan 26;10(2):268-77. doi: 10.1002/cbic.200800538. Chembiochem. 2009. PMID: 19101978 Free PMC article.
Mannostatin A is a potent inhibitor of the mannose-trimming enzyme, Golgi alpha-mannosidase II (GMII), which acts late in the N-glycan processing pathway. ...Here, we report on the synthesis of new Mannostatin derivatives and analyze their binding in the active site
Mannostatin A is a potent inhibitor of the mannose-trimming enzyme, Golgi alpha-mannosidase II (GMII), which acts late in the N-glyca
Pd asymmetric allylic alkylation (AAA). A powerful synthetic tool.
Trost BM. Trost BM. Chem Pharm Bull (Tokyo). 2002 Jan;50(1):1-14. doi: 10.1248/cpb.50.1. Chem Pharm Bull (Tokyo). 2002. PMID: 11824567 Free article. Review.
These methods have already provided practical strategies towards numerous biological targets--some of which are adenosine and its enantiomer, aflatoxin B, aristeromycin, calanolide A and B, carbovir, cyclophellitol, ethambutol, galanthamine, mannostatin, neplanocin, phylla …
These methods have already provided practical strategies towards numerous biological targets--some of which are adenosine and its enantiomer …
Structural basis of the inhibition of Golgi alpha-mannosidase II by mannostatin A and the role of the thiomethyl moiety in ligand-protein interactions.
Kawatkar SP, Kuntz DA, Woods RJ, Rose DR, Boons GJ. Kawatkar SP, et al. J Am Chem Soc. 2006 Jun 28;128(25):8310-9. doi: 10.1021/ja061216p. J Am Chem Soc. 2006. PMID: 16787095 Free PMC article.
In the bound state, mannostatin A adopts a 2T1 twist envelope conformation, which is not significantly populated in solution. Possible conformations of the mannosyl oxacarbenium ion and an enzyme-linked intermediate have been compared to the conformation of mannostatin
In the bound state, mannostatin A adopts a 2T1 twist envelope conformation, which is not significantly populated in solution. Possibl …
Inhibition of experimental metastasis by enzyme inhibitors from microorganisms and plants.
Umezawa K. Umezawa K. Adv Enzyme Regul. 1996;36:267-81. doi: 10.1016/0065-2571(95)00014-3. Adv Enzyme Regul. 1996. PMID: 8869751 Review.
Alpha-glucosidase inhibitors such as epi-CPL and baicalein inhibited in vitro invasion and in vivo metastasis of mouse melanoma cells. A mannosidase inhibitor, mannostatin A, also inhibited in vitro invasion of mouse melanoma cells. Oncogene function inhibitors induce norm …
Alpha-glucosidase inhibitors such as epi-CPL and baicalein inhibited in vitro invasion and in vivo metastasis of mouse melanoma cells. A man …
Inhibition of tumor cell invasion in the Boyden chamber assay by a mannosidase inhibitor, mannostatin A.
Ochi Y, Atsumi S, Aoyagi T, Umezawa K. Ochi Y, et al. Anticancer Res. 1993 Sep-Oct;13(5A):1421-4. Anticancer Res. 1993. PMID: 8239514
Addition of mannostatin A to the cultured B16/F10 or K-ras-NIH3T3 cells inhibited cellular alpha-mannoside activity specifically. Mannostatin A-treated B16/F10 cells also showed decreased metastatic activity in vivo in C57Bl/6 mice....
Addition of mannostatin A to the cultured B16/F10 or K-ras-NIH3T3 cells inhibited cellular alpha-mannoside activity specifically. …
Synthesis and biological evaluation of alpha-mannosidase inhibitory activity of three deoxy derivatives of mannostatin A.
Ogawa S, Morikawa T. Ogawa S, et al. Bioorg Med Chem Lett. 1999 Jun 7;9(11):1499-504. doi: 10.1016/s0960-894x(99)00224-3. Bioorg Med Chem Lett. 1999. PMID: 10386924
Three deoxy derivatives of alpha-mannosidase inhibitor mannostatin A have been synthesized and their inhibitors activity for Jack beans alpha-mannosidase evaluated in order to elucidate roles of each hydroxyl groups of the inhibitor The 1- and 2-deoxy derivatives have pres …
Three deoxy derivatives of alpha-mannosidase inhibitor mannostatin A have been synthesized and their inhibitors activity for Jack bea …
22 results