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2-pyrrolino-DOX
Known as:
2-pyrrolinodoxorubicin
, 3'-deamino-3'-(2''-pyrroline-1''-yl)doxorubicin trifluoroacetate
National Institutes of Health
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2008
2008
Therapy of experimental hepatic cancers with cytotoxic peptide analogs targeted to receptors for luteinizing hormone-releasing hormone, somatostatin or bombesin
K. Szepesházi
,
A. Schally
,
A. Treszl
,
S. Seitz
,
G. Halmos
Anti-Cancer Drugs
2008
Corpus ID: 205527312
As there is no effective systemic therapy for advanced hepatocellular carcinoma (HCC), we investigated the presence of receptors…
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2005
2005
Effective Inhibition of Experimental Human Ovarian Cancers with a Targeted Cytotoxic Bombesin Analogue AN-215
J. Engel
,
Gunhild Keller
,
A. Schally
,
G. Halmos
,
Brian D Hammann
,
A. Nagy
Clinical Cancer Research
2005
Corpus ID: 9508822
Purpose: To determine whether the cytotoxic analogue of bombesin/gastrin-releasing peptide (GRP) AN-215 can inhibit the in vivo…
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2004
2004
Effective treatment of experimental androgen sensitive and androgen independent intraosseous prostate cancer with targeted cytotoxic somatostatin analogue AN-238.
Markus Letsch
,
A. Schally
,
K. Szepesházi
,
G. Halmos
,
A. Nagy
Journal of Urology
2004
Corpus ID: 25152830
PURPOSE The targeted cytotoxic somatostatin analogue AN-238, consisting of 2-pyrrolinodoxorubicin (AN-201) linked to carrier…
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Highly Cited
2002
Highly Cited
2002
Targeted cytotoxic somatostatin analogue AN-238 inhibits somatostatin receptor-positive experimental colon cancers independently of their p53 status.
K. Szepesházi
,
A. Schally
,
+6 authors
A. Nagy
Cancer Research
2002
Corpus ID: 40346255
The resistance of advanced colorectal cancers to therapy is often related to mutations in the p53 tumor suppressor gene. Because…
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2002
2002
Independently of Their p 53 Status Somatostatin Receptor-positive Experimental Colon Cancers Targeted Cytotoxic Somatostatin Analogue AN-238 Inhibits Updated
K. Szepesházi
,
A. Schally
,
+6 authors
A. Nagy
2002
Corpus ID: 13554808
The resistance of advanced colorectal cancers to therapy is often related to mutations in the p53 tumor suppressor gene. Because…
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Review
2001
Review
2001
Targeted cytotoxic analogs of luteinizing hormone-releasing hormone: a reply.
A. Schally
,
A. Nagy
European Journal of Endocrinology
2001
Corpus ID: 9990670
We read with great interest the Highlight Review by Dr CG rundker entitled 'Cytotoxic luteinizing hormone- releasing hormone…
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Highly Cited
2000
Highly Cited
2000
Inhibition of metastatic renal cell carcinomas expressing somatostatin receptors by a targeted cytotoxic analogue of somatostatin AN-238.
A. Płonowski
,
A. V. Schally
,
A. Nagy
,
H. Kiaris
,
F. Hebert
,
G. Halmos
Cancer Research
2000
Corpus ID: 18920511
The effectiveness of chemotherapy targeted to somatostatin (SST) receptors based on cytotoxic SST analogue AN-238, consisting of…
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1999
1999
Selective induction of apoptosis by the cytotoxic analog AN-207 in cells expressing recombinant receptor for luteinizing hormone-releasing hormone.
D. Danila
,
A. Schally
,
A. Nagy
,
J. Alexander
Proceedings of the National Academy of Sciences…
1999
Corpus ID: 19918752
The selectivity of ligands specific for certain cells can be used to preferentially target chemotherapeutic compounds to…
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Review
1999
Review
1999
Analogue AN-238 Cancer and Its Metastases by Cytotoxic Somatostatin Inhibition of PC-3 Human Androgen-independent Prostate
A. Płonowski
,
A. Schally
,
A. Nagy
,
Baodong Sun
,
K. Szepesházi
1999
Corpus ID: 16848685
We evaluated whether AN-238, the cytotoxic analogue of somatostatin (SST) consisting of the radical 2-pyrrolinodoxorubicin (AN…
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1998
1998
Synthesis and biological evaluation of cytotoxic analogs of somatostatin containing doxorubicin or its intensely potent derivative, 2-pyrrolinodoxorubicin (targeted chemotherapeutic agentsyhybrid…
A. Nagy
,
V. Schally
,
G. Halmos
,
P. Armatis
,
R. Cai
1998
Corpus ID: 87721972
To create cytotoxic hybrid analogs of soma- tostatin (SST), octapeptides RC-160 (D-Phe-Cys-Tyr-D-Trp- Lys-Val-Cys-Trp-NH2) and RC…
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