-
1
-
-
0024288739
-
Stereoselective synthesis of (1-alkoxyalkyl) alpha- and beta- d -glucopyranosiduronates (acetal-glucopyranosiduronates): A new approach to specific cytostatics for the treatment of cancer
-
L. F. Tietze was one of the first researchers to propose the use of glucuronide prodrugs for selective cancer chemotherapy: Tietze, L.; Seele, R.; Leiting, B.; Krach, T. Stereoselective synthesis of (1-alkoxyalkyl) alpha- and beta- d -glucopyranosiduronates (acetal-glucopyranosiduronates): a new approach to specific cytostatics for the treatment of cancer Carbohydr. Res. 1988, 180, 253-262
-
(1988)
Carbohydr. Res.
, vol.180
, pp. 253-262
-
-
Tietze, L.1
Seele, R.2
Leiting, B.3
Krach, T.4
-
2
-
-
0036015566
-
Beta-glucuronidase-mediated drug release
-
DOI 10.2174/1381612023394485
-
de Graaf, M.; Boven, E.; Scheeren, H. W.; Haisma, H. J.; Pinedo, H. M. Beta-glucuronidase-mediated drug release Curr. Pharm. Des. 2002, 8, 1391-1403 (Pubitemid 34591354)
-
(2002)
Current Pharmaceutical Design
, vol.8
, Issue.15
, pp. 1391-1403
-
-
De Graaf, M.1
Boven, E.2
Scheeren, H.W.3
Haisma, H.J.4
Pinedo, H.M.5
-
3
-
-
12244271023
-
Glucuronides in anti-cancer therapy
-
DOI 10.2174/1568011033353470
-
Chen, X.; Wu, B.; Wang, P. G. Glucuronides in anti-cancer therapy Curr. Med. Chem.: Anti-Cancer Agents 2003, 3, 139-150 (Pubitemid 36221734)
-
(2003)
Current Medicinal Chemistry - Anti-Cancer Agents
, vol.3
, Issue.2
, pp. 139-150
-
-
Chen, X.1
Wu, B.2
Wang, P.G.3
-
4
-
-
84855692081
-
A self-immolative dendritic glucuronide prodrug of doxorubicin
-
Grinda, M.; Clarhaut, J.; Renoux, B.; Tranoy-Opalinski, I.; Papot, S. A self-immolative dendritic glucuronide prodrug of doxorubicin MedChemComm 2012, 3, 68-70
-
(2012)
MedChemComm
, vol.3
, pp. 68-70
-
-
Grinda, M.1
Clarhaut, J.2
Renoux, B.3
Tranoy-Opalinski, I.4
Papot, S.5
-
5
-
-
79551469662
-
Synthesis and biological evaluation of prodrugs based on the natural antibiotic duocarmycin for use in ADEPT and PMT
-
Tietze, L. F.; Schmuck, K.; Schuster, H. J.; Müller, M.; Schuberth, I. Synthesis and biological evaluation of prodrugs based on the natural antibiotic duocarmycin for use in ADEPT and PMT Chem. - Eur. J. 2011, 17, 1922-1929
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 1922-1929
-
-
Tietze, L.F.1
Schmuck, K.2
Schuster, H.J.3
Müller, M.4
Schuberth, I.5
-
6
-
-
82955197381
-
A heterodimeric glucuronide prodrug for cancer tritherapy: The double role of the chemical amplifier
-
Grinda, M.; Clarhaut, J.; Tranoy-Opalinski, I.; Renoux, B.; Monvoisin, A.; Cronier, L.; Papot, S. A heterodimeric glucuronide prodrug for cancer tritherapy: the double role of the chemical amplifier ChemMedChem 2011, 6, 2137-2141
-
(2011)
ChemMedChem
, vol.6
, pp. 2137-2141
-
-
Grinda, M.1
Clarhaut, J.2
Tranoy-Opalinski, I.3
Renoux, B.4
Monvoisin, A.5
Cronier, L.6
Papot, S.7
-
7
-
-
84857511037
-
A new cyclopamine glucuronide prodrug with improved kinetics of drug release
-
Renoux, B.; Legigan, T.; Bensalma, S.; Chadéneau, C.; Muller, J.-M.; Papot, S. A new cyclopamine glucuronide prodrug with improved kinetics of drug release Org. Biomol. Chem. 2011, 9, 8459-8464
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 8459-8464
-
-
Renoux, B.1
Legigan, T.2
Bensalma, S.3
Chadéneau, C.4
Muller, J.-M.5
Papot, S.6
-
9
-
-
0001874589
-
-
Bosslet, K.; Czech, J.; Hoffmann, D. Tumor Target. 1995, 1, 45-50
-
(1995)
Tumor Target.
, vol.1
, pp. 45-50
-
-
Bosslet, K.1
Czech, J.2
Hoffmann, D.3
-
10
-
-
0031739137
-
The efficacy of the anthracycline prodrug daunorubicin-GA3 in human ovarian cancer xenografts
-
Houba, P. H. J.; Boven, E.; Erkelens, C. A. M.; Leenders, R. G. G.; Scheeren, J. W.; Pinedo, H. M.; Haisma, H. J. The efficacy of the anthracycline prodrug daunorubicin-GA3 in human ovarian cancer xenografts Br. J. Cancer 1998, 78, 1600-1606 (Pubitemid 28550045)
-
(1998)
British Journal of Cancer
, vol.78
, Issue.12
, pp. 1600-1606
-
-
Houba, P.H.J.1
Boven, E.2
Erkelens, C.A.M.3
Leenders, R.G.G.4
Scheeren, J.W.5
Pinedo, H.M.6
Haisma, H.J.7
-
11
-
-
0032521438
-
Elucidation of the mechanism enabling tumor selective prodrug monotherapy
-
Bosslet, K.; Straub, R.; Blumrich, M.; Czech, J.; Gerken, M.; Sperker, B.; Kroemer, H. K.; Gesson, J. P.; Koch, M.; Monneret, C. Elucidation of the mechanism enabling tumor selective prodrug monotherapy Cancer Res. 1998, 58, 1195-1201 (Pubitemid 28183208)
-
(1998)
Cancer Research
, vol.58
, Issue.6
, pp. 1195-1201
-
-
Bosslet, K.1
Straub, R.2
Blumrich, M.3
Czech, J.4
Gerken, M.5
Sperker, B.6
Kroemer, H.K.7
Gesson, J.-P.8
Koch, M.9
Monneret, C.10
-
12
-
-
0033868108
-
Comparison of three approaches to doxorubicin therapy: Free doxorubicin, liposomal doxorubicin, and β-glucuronidase-activated prodrug (HMR 1826)
-
Woessner, R.; An, Z.; Li, X.; Hoffman, R. M.; Dix, R.; Bitonti, A. Comparison of three approaches to doxorubicin therapy: free doxorubicin, liposomal doxorubicin, and β-glucuronidase-activated prodrug (HMR 1826) Anticancer Res. 2000, 20, 2289-2296 (Pubitemid 30614428)
-
(2000)
Anticancer Research
, vol.20
, Issue.4
, pp. 2289-2296
-
-
Woessner, R.1
An, Z.2
Li, X.3
Hoffman, R.M.4
Dix, R.5
Bitonti, A.6
-
13
-
-
0035106974
-
A novel doxorubicin-glucuronide prodrug DOX-GA3 for tumour-selective chemotherapy: Distribution and efficacy in experimental human ovarian cancer
-
DOI 10.1054/bjoc.2000.1640
-
Houba, P. H. J.; Boven, E.; Van Der Meulen-Muileman, I. H.; Leenders, R. G. G.; Scheeren, J. W.; Pinedo, H. M.; Haisma, H. J. A novel doxorubicin-glucuronide prodrug DOX-GA3 for tumour-selective chemotherapy: distribution and efficacy in experimental human ovarian cancer Br. J. Cancer 2001, 84, 550-557 (Pubitemid 32215885)
-
(2001)
British Journal of Cancer
, vol.84
, Issue.4
, pp. 550-557
-
-
Houba, P.H.J.1
Boven, E.2
Van Der Meulen-Muileman, I.H.3
Leenders, R.G.G.4
Scheeren, J.W.5
Pinedo, H.M.6
Haisma, H.J.7
-
14
-
-
68049083832
-
Antiangiogenesis targeting tumor microenvironment synergizes glucuronide prodrug antitumor activity
-
Juan, T. Y.; Roffler, S. R.; Hou, H. S.; Huang, S. M.; Chen, K. C.; Leu, Y. L.; Prijovich, Z. M.; Yu, C. P.; Wu, C. C.; Sun, G. H.; Cha, T. L. Antiangiogenesis targeting tumor microenvironment synergizes glucuronide prodrug antitumor activity Clin. Cancer Res. 2009, 15, 4600-4611
-
(2009)
Clin. Cancer Res.
, vol.15
, pp. 4600-4611
-
-
Juan, T.Y.1
Roffler, S.R.2
Hou, H.S.3
Huang, S.M.4
Chen, K.C.5
Leu, Y.L.6
Prijovich, Z.M.7
Yu, C.P.8
Wu, C.C.9
Sun, G.H.10
Cha, T.L.11
-
15
-
-
79953054576
-
The EPR effect: Unique features of tumor blood vessels for drug delivery, factors involved, and limitations and augmentation of the effect
-
Enhanced permeability and retention: Fang, J.; Nakamura, H.; Maeda, H. The EPR effect: unique features of tumor blood vessels for drug delivery, factors involved, and limitations and augmentation of the effect Adv. Drug Delivery Rev. 2011, 63, 136-151
-
(2011)
Adv. Drug Delivery Rev.
, vol.63
, pp. 136-151
-
-
Fang, J.1
Nakamura, H.2
Maeda, H.3
-
16
-
-
56949084877
-
Albumin as a drug carrier: Design of prodrugs, drug conjugates and nanoparticles
-
Review on albumin as a drug carrier: Kratz, F. Albumin as a drug carrier: design of prodrugs, drug conjugates and nanoparticles J. Controlled Release 2008, 132, 171-183
-
(2008)
J. Controlled Release
, vol.132
, pp. 171-183
-
-
Kratz, F.1
-
17
-
-
0037028050
-
Probing the cysteine-34 position of endogenous serum albumin with thiol-binding doxorubicin derivatives. Improved efficacy of an acid-sensitive doxorubicin derivative with specific albumin-binding properties compared to that of the parent compound
-
DOI 10.1021/jm020276c
-
Kratz, F.; Warnecke, A.; Scheuermann, K.; Stockmar, C.; Schwab, J.; Lazar, P.; Druckes, P.; Esser, N.; Drevs, J.; Rognan, D.; Bissantz, C.; Hinderling, C.; Folkers, G.; Fichtner, I.; Unger, C. Probing the cysteine-34 position of endogenous serum albumin with thiol-binding doxorubicin derivatives. Improved efficacy of an acid-sensitive doxorubicin derivative with specific albumin-binding properties compared to that of the parent compound J. Med. Chem. 2002, 45, 5523-5533 (Pubitemid 35424970)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.25
, pp. 5523-5533
-
-
Kratz, F.1
Warnecke, A.2
Scheuermann, K.3
Stockmar, C.4
Schwab, J.5
Lazar, P.6
Druckes, P.7
Esser, N.8
Drevs, J.9
Rognan, D.10
Bissantz, C.11
Hinderling, C.12
Folkers, G.13
Fichtner, I.14
Unger, C.15
-
18
-
-
9244222743
-
Synthesis and biological activity of water-soluble maleimide derivatives of the anticancer drug carboplatin designed as albumin-binding prodrugs
-
DOI 10.1021/bc049829j
-
Warnecke, A.; Fichtner, I.; Garmann, D.; Jaehde, U.; Kratz, F. Synthesis and biological activity of water-soluble maleimide derivatives of the anticancer drug carboplatin designed as albumin-binding prodrugs Bioconjugate Chem. 2004, 15, 1349-1359 (Pubitemid 39552025)
-
(2004)
Bioconjugate Chemistry
, vol.15
, Issue.6
, pp. 1349-1359
-
-
Warnecke, A.1
Fichtner, I.2
Garmann, D.3
Jaehde, U.4
Kratz, F.5
-
19
-
-
34347354414
-
Albumin-binding prodrugs of camptothecin and doxorubicin with an Ala-Leu-Ala-Leu-Linker that are cleaved by cathepsin B: Synthesis and antitumor efficacy
-
DOI 10.1021/bc0602735
-
Schmid, B.; Chung, D. E.; Warnecke, A.; Fichtner, I.; Kratz, F. Albumin-binding prodrugs of camptothecin and doxorubicin with an ala-leu-ala-leu-linker that are cleaved by cathepsin B: synthesis and antitumor efficacy Bioconjugate Chem. 2007, 18, 702-716 (Pubitemid 47010789)
-
(2007)
Bioconjugate Chemistry
, vol.18
, Issue.3
, pp. 702-716
-
-
Schmid, B.1
Chung, D.-E.2
Warnecke, A.3
Fichtner, I.4
Kratz, F.5
-
20
-
-
74149085146
-
INNO-206, the (6-maleimidocaproyl hydrazone derivative of doxorubicin), shows superior antitumor efficacy compared to doxorubicin in different tumor xenograft models and in an orthotopic pancreas carcinoma model
-
Graeser, R.; Esser, N.; Unger, H.; Fichtner, I.; Zhu, A.; Unger, C.; Kratz, F. INNO-206, the (6-maleimidocaproyl hydrazone derivative of doxorubicin), shows superior antitumor efficacy compared to doxorubicin in different tumor xenograft models and in an orthotopic pancreas carcinoma model Invest. New Drugs 2010, 28, 14-19
-
(2010)
Invest. New Drugs
, vol.28
, pp. 14-19
-
-
Graeser, R.1
Esser, N.2
Unger, H.3
Fichtner, I.4
Zhu, A.5
Unger, C.6
Kratz, F.7
-
21
-
-
77956154259
-
Optimization of an albumin-binding prodrug of doxorubicin that is cleaved by prostate-specific antigen
-
Elsadek, B.; Graeser, R.; Warnecke, A.; Unger, C.; Saleem, T.; El-Melegy, N.; Madkor, H.; Kratz, F. Optimization of an albumin-binding prodrug of doxorubicin that is cleaved by prostate-specific antigen ACS Med. Chem. Lett. 2010, 1, 234-238
-
(2010)
ACS Med. Chem. Lett.
, vol.1
, pp. 234-238
-
-
Elsadek, B.1
Graeser, R.2
Warnecke, A.3
Unger, C.4
Saleem, T.5
El-Melegy, N.6
Madkor, H.7
Kratz, F.8
-
22
-
-
78649634752
-
Development of a novel prodrug of paclitaxel that is cleaved by prostate-specific antigen: An in vitro and in vivo evaluation study
-
Elsadek, B.; Graeser, R.; Esser, N.; Schafer-Obodozie, C.; Abu Ajaj, K.; Unger, C.; Warnecke, A.; Saleem, T.; El-Melegy, N.; Madkor, H.; Kratz, F. Development of a novel prodrug of paclitaxel that is cleaved by prostate-specific antigen: an in vitro and in vivo evaluation study Eur. J. Cancer 2010, 46, 3434-3444
-
(2010)
Eur. J. Cancer
, vol.46
, pp. 3434-3444
-
-
Elsadek, B.1
Graeser, R.2
Esser, N.3
Schafer-Obodozie, C.4
Abu Ajaj, K.5
Unger, C.6
Warnecke, A.7
Saleem, T.8
El-Melegy, N.9
Madkor, H.10
Kratz, F.11
-
23
-
-
34548106304
-
Phase I and pharmacokinetic study of the (6-maleimidocaproyl)hydrazone derivative of doxorubicin
-
DOI 10.1158/1078-0432.CCR-06-2776
-
Unger, C.; Haring, B.; Medinger, M.; Drevs, J.; Steinbild, S.; Kratz, F.; Mross, K. Phase I and pharmacokinetic study of the (6-maleimidocaproyl) hydrazone derivative of doxorubicin Clin. Cancer Res. 2007, 13, 4858-4866 (Pubitemid 47294793)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.16
, pp. 4858-4866
-
-
Unger, C.1
Haring, B.2
Medinger, M.3
Drevs, J.4
Steinbild, S.5
Kratz, F.6
Mross, K.7
-
24
-
-
34249980937
-
DOXO-EMCH (INNO-206): The first albumin-binding prodrug of doxorubicin to enter clinical trials
-
DOI 10.1517/13543784.16.6.855
-
Kratz, F. DOXO-EMCH (INNO-206): the first albumin-binding prodrug of doxorubicin to enter clinical trials Expert Opin. Invest. Drugs 2007, 16, 855-866 (Pubitemid 46882358)
-
(2007)
Expert Opinion on Investigational Drugs
, vol.16
, Issue.6
, pp. 855-866
-
-
Kratz, F.1
-
25
-
-
0036080057
-
Design of selectively activated anticancer prodrugs: Elimination and cyclization strategies
-
DOI 10.2174/1568011023354173
-
Papot, S.; Tranoy, I.; Tillequin, F.; Florent, J. C.; Gesson, J. P. Design of selectively activated anticancer prodrugs: elimination and cyclization strategies Curr. Med. Chem.: Anti-Cancer Agents 2002, 2, 155-85 (Pubitemid 34649872)
-
(2002)
Current Medicinal Chemistry - Anti-Cancer Agents
, vol.2
, Issue.2
, pp. 155-185
-
-
Papot, S.1
Tranoy, I.2
Tillequin, F.3
Florent, J.-C.4
Gesson, J.-P.5
-
26
-
-
52749096860
-
Design of self-immolative linkers for tumour-activated prodrug therapy
-
Tranoy-Opalinski, I.; Fernandes, A.; Thomas, M.; Gesson, J. P.; Papot, S. Design of self-immolative linkers for tumour-activated prodrug therapy Anti-Cancer Agents Med. Chem. 2008, 8, 618-637
-
(2008)
Anti-Cancer Agents Med. Chem.
, vol.8
, pp. 618-637
-
-
Tranoy-Opalinski, I.1
Fernandes, A.2
Thomas, M.3
Gesson, J.P.4
Papot, S.5
-
27
-
-
33646924550
-
Development and properties of β-glucuronide linkers for monoclonal antibody-drug conjugates
-
DOI 10.1021/bc0600214
-
The first maleimide-containing glucuronide-linker was described in the following: Jeffrey, S. C.; Andreyka, J. B.; Bernhardt, S. X.; Kissler, K. M.; Kline, T.; Lenox, J. S.; Moser, R. F.; Nguyen, M. T.; Okeley, N. M.; Stone, I. J.; Zhang, X. Q.; Senter, P. D. Development and properties of beta-glucuronide linkers for monoclonal antibody-drug conjugates Bioconjugate Chem. 2006, 17, 831-840 (Pubitemid 43794395)
-
(2006)
Bioconjugate Chemistry
, vol.17
, Issue.3
, pp. 831-840
-
-
Jeffrey, S.C.1
Andreyka, J.B.2
Bernhardt, S.X.3
Kissler, K.M.4
Kline, T.5
Lenox, J.S.6
Moser, R.F.7
Nguyen, M.T.8
Okeley, N.M.9
Stone, I.J.10
Zhang, X.11
Senter, P.D.12
-
28
-
-
15144361344
-
Prodrugs of anthracyclines for use in antibody-directed enzyme prodrug therapy
-
DOI 10.1021/jm970589l
-
Florent, J. C.; Dong, X.; Gaudel, G.; Mitaku, S.; Monneret, C.; Gesson, J. P.; Jacquesy, J. C.; Mondon, M.; Renoux, B.; Andrianomenjanahary, S.; Michel, S.; Koch, M.; Tillequin, F.; Gerken, M.; Czech, J.; Straub, R.; Bosslet, K. Prodrugs of anthracyclines for use in antibody-directed enzyme prodrug therapy J. Med. Chem. 1998, 41, 3572-3581 (Pubitemid 28449340)
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, Issue.19
, pp. 3572-3581
-
-
Florent, J.-C.1
Dong, X.2
Gaudel, G.3
Mitaku, S.4
Monneret, C.5
Gesson, J.-P.6
Jacquesy, J.-C.7
Mondon, M.8
Renoux, B.9
Andrianomenjanahary, S.10
Michel, S.11
Koch, M.12
Tillequin, F.13
Gerken, M.14
Czech, J.15
Straub, R.16
Bosslet, K.17
-
29
-
-
0037099395
-
A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
-
DOI 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
-
Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective “ligation of azides and terminal alkynes Angew. Chem., Int. Ed. 2002, 41, 2596-2599 (Pubitemid 34803480)
-
(2002)
Angewandte Chemie - International Edition
, vol.41
, Issue.14
, pp. 2596-2599
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
30
-
-
0028348376
-
Tumor-selective prodrug activation by fusion protein-mediated catalysis
-
Elimination half-life of HMR 1826 is between 0.4 and 2.6 h: Bosslet, K.; Czech, J.; Hoffmann, D. Tumor-selective prodrug activation by fusion protein-mediated catalysis Cancer Res. 1994, 54, 2151-2159 (Pubitemid 24138689)
-
(1994)
Cancer Research
, vol.54
, Issue.8
, pp. 2151-2159
-
-
Bosslet, K.1
Czech, J.2
Hoffmann, D.3
|