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Chromanol derivatives--a novel class of CETP inhibitors.
Bioorg Med Chem Lett. 2011 Jan 1;21(1):488-91. doi: 10.1016/j.bmcl.2010.10.110. Epub 2010 Oct 26.
Bioorg Med Chem Lett. 2011.
PMID: 21084191
Design and synthesis of potent and selective azaindole-based Rho kinase (ROCK) inhibitors.
Schirok H, Kast R, Figueroa-Pérez S, Bennabi S, Gnoth MJ, Feurer A, Heckroth H, Thutewohl M, Paulsen H, Knorr A, Hütter J, Lobell M, Münter K, Geiss V, Ehmke H, Lang D, Radtke M, Mittendorf J, Stasch JP.
Schirok H, et al. Among authors: thutewohl m.
ChemMedChem. 2008 Dec;3(12):1893-904. doi: 10.1002/cmdc.200800211.
ChemMedChem. 2008.
PMID: 18973168
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Identification of mono- and bisubstrate inhibitors of protein farnesyltransferase and inducers of apoptosis from a pepticinnamin E library.
Thutewohl M, Kissau L, Popkirova B, Karaguni IM, Nowak T, Bate M, Kuhlmann J, Müller O, Waldmann H.
Thutewohl M, et al.
Bioorg Med Chem. 2003 Jun 12;11(12):2617-26. doi: 10.1016/s0968-0896(03)00160-3.
Bioorg Med Chem. 2003.
PMID: 12757727
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Solid-phase synthesis of a pepticinnamin E library.
Thutewohl M, Waldmann H.
Thutewohl M, et al.
Bioorg Med Chem. 2003 Jun 12;11(12):2591-615. doi: 10.1016/s0968-0896(03)00159-7.
Bioorg Med Chem. 2003.
PMID: 12757726
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Solid-phase synthesis and biological evaluation of a pepticinnamin E library.
Thutewohl M, Kissau L, Popkirova B, Karaguni IM, Nowak T, Bate M, Kuhlmann J, Müller O, Waldmann H.
Thutewohl M, et al.
Angew Chem Int Ed Engl. 2002 Oct 4;41(19):3616-20; 3516. doi: 10.1002/1521-3773(20021004)41:19<3616::AID-ANIE3616>3.0.CO;2-F.
Angew Chem Int Ed Engl. 2002.
PMID: 12370908
No abstract available.
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Identification of hPin1 inhibitors that induce apoptosis in a mammalian Ras transformed cell line.
Bayer E, Thutewohl M, Christner C, Tradler T, Osterkamp F, Waldmann H, Bayer P.
Bayer E, et al. Among authors: thutewohl m.
Chem Commun (Camb). 2005 Jan 28;(4):516-8. doi: 10.1039/b414037k. Epub 2004 Dec 6.
Chem Commun (Camb). 2005.
PMID: 15654388
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Identification and specificity profiling of protein prenyltransferase inhibitors using new fluorescent phosphoisoprenoids.
Dursina B, Reents R, Delon C, Wu Y, Kulharia M, Thutewohl M, Veligodsky A, Kalinin A, Evstifeev V, Ciobanu D, Szedlacsek SE, Waldmann H, Goody RS, Alexandrov K.
Dursina B, et al. Among authors: thutewohl m.
J Am Chem Soc. 2006 Mar 8;128(9):2822-35. doi: 10.1021/ja052196e.
J Am Chem Soc. 2006.
PMID: 16506760
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Manumycin A and its analogues are irreversible inhibitors of neutral sphingomyelinase.
Arenz C, Thutewohl M, Block O, Waldmann H, Altenbach HJ, Giannis A.
Arenz C, et al. Among authors: thutewohl m.
Chembiochem. 2001 Feb 2;2(2):141-3. doi: 10.1002/1439-7633(20010202)2:2<141::AID-CBIC141>3.0.CO;2-P.
Chembiochem. 2001.
PMID: 11828438
No abstract available.
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