Personal information

Other IDs

Scopus Author ID: 7004644249

Keywords

chemistry, medicinal chemistry, heterocyclic chemistry, history of chemistry, organic chemistry

Biography

Assoc. Prof. STANISLAV RADL, PhD
A versatile chemist with research, teaching, writing, and editing skills combined with industrial applied research experience
CAREER HISTORY
2013-to date Scientific Development Expert, Zentiva – A Sanofi company
2010 Assoc. Prof. of Organic Chemistry, Prague Institute of Chemical Technology
2006-to date Visiting lecturer (Medicinal Chemistry) at the Prague Institute of Chemical Technology
2005-2013 Head of the API Synthesis Development I Department, Zentiva, Prague
1995- 2005: Head of the Department of Organic Synthesis I of the Reseach Institute of Pharmacy and Biochemistry, Prague
1993-1994: Senior Research Scientist, Research Institute of Pharmacy and Biochemistry, Prague
1992-1993: Visiting Scientist, Hoffmann-La Roche, Nutley, U.S.A.
1990-1991: Senior Research Scientist, Research Institute of Pharmacy and Biochemistry, Prague
1987-1990: Head, Organic Synthesis-I department, Research Institute of Pharmacy and Biochemistry, Prague
1983-1986: Research Scientist, Research Institute of Pharmacy and Biochemistry, Prague
1978-1982: Postgraduate student, Research Institute of Pharmacy and Biochemistry (PhD Dissertation: Synthesis of new antiviral agents)
1970-1976: Student, Prague Institute of Chemical Technology, Faculty of Chemical Technology, Department of Organic Chemistry

PERSONAL DETAILS
Address: Zentiva, U kabelovny 130, 102 37, Prague 10. Czech Republic
Tel : 0420 2 67243741 Fax: 0420 2 67243741 Email: stanislav.radl@zentiva.cz
Date of Birth: 21 July 1951
RESEARCH PUBLICATIONS AND EDITING ACTIVITIES
Publications:
70 Original articles (Collect. Czech. Chem. Commun., Heterocycles, J. Heterocycl. Chem., Arch. Pharm.-Pharm. Med. Chem., Bioorg.Med. Chem. Lett., Gen. Physiol. Biophys., Cesk. Farm., Electronic Conference on Heterocyclic Chemistry '98, Org. Proc. Res. Dev., Synthesis, Tetrahedron Lett.)
38 Review articles (Advances in Heterocyclic Chemistry, Heterocycles, Current Medicinal Chemistry, Cesk. Farm., Drugs of the Future, Pharmacology and Therapeutics, Arch. Pharm.-Pharm. Med. Chem., Chem. Listy, Aldrichimica Acta, Janssen Chimica Acta, Vesmir)
1 Section in Comprehensive Heterocyclic Chemistry II (A. R. Katritzky, C. W. Rees, Eds)
1 Section in Comprehensive Heterocyclic Chemistry III (A. R. Katritzky, C. W. Rees, Eds)
1 Section in Comprehensive Functional Groups Transformations II (A. R. Katritzky, C. W. Rees, Eds)
1 Chapter in Science of Synthesis (Thieme)
1 Chapter in Selected Methods for Synthesis and Modification of Heterocycles (Kartsev V.G., Ed.).
5 Short monographs (Drugs of the Future)
4 Meeting Reports (Drugs of the Future, Drug News & Perspectives)
Textbook „Chemie léčiv“ (Cz), i.e. Medicinal Chemistry
Book „Farmakochemie“ (Cz), i.e. Pharmacochemistry,
2nd edition 2005 (cca 450 pages),
3rd edition is scheduled for Jan 2015 (cca 650 pages).
Section of Pharmacochemistry (480 entries) in „Encykopedický farmaceutický slovník“ (Cz), i.e. Encyclopedia of Pharmacy (cca 800 pages).
Co-author of more than 100 Czech Patent Applications, most of them also as WO, EP and/or US patents.
Editorial Boards:
Contributing Editor of Drugs of the Future (published by Prous Science Publishers, Barcelona, Spain, currently by Thompson Reuters)
Reviewer of ARKAT (an electronic publication published by Arkivoc)
1995-2012 Scientific editor of the Collection of Czechoslovak Chemical Communications (published by Czech Academy of Sciences, in 2012 transformed into ChemPlusChem)
Professional memberships:
Czech Chemical Society
International Society of Heterocyclic Chemistry
Fields of special interest:
Medicinal chemistry (especially antibacterial chemotherapy)
Heterocyclic chemistry (especially nitrogen-containing heterocycles)
Denitrocyclization reactions
Awards:
The Karel Preiss Annual Award of the Czech Chemical Society for 2004
Personality of Zentiva 2007
Gold Badge of the International Scientific Partnership Foundation, 2010

Activities

Collapse all

Employment (8)

Zentiva ks: Praha, CZ

2018-01-01 to present | Consultant (Development)
Employment
Source: Self-asserted source
Stanislav Radl

Zentiva - A Sanofi Company: Prague, CZ

2013 to 2017-12-31 | Scientific Development Expert (Chemistry Office)
Employment
Source: Self-asserted source
Stanislav Radl

Zentiva - A Sanofi Company: Prague, CZ

2005 to 2012 | Head (API DEvelopment I)
Employment
Source: Self-asserted source
Stanislav Radl

Research Institute of Pharmacy and Biochemistry: Prague, CZ

1995 to 2005 | Department Head (Organic Synthesis I)
Employment
Source: Self-asserted source
Stanislav Radl

Research Institute of Pharmacy and Biochemistry: Prague, CZ

1993-10-01 to 1994-12-31 | Senior Research Scientist (Organic Synthesis)
Employment
Source: Self-asserted source
Stanislav Radl

Hoffmann-La Roche Inc: Nutley, NJ, US

1992-01-01 to 1993-09-31 | Visiting Scientist (Medicinal Chemistry)
Employment
Source: Self-asserted source
Stanislav Radl

Research Institute of Pharmacy and Biochemistry: Prague, CZ

1987 to 1990 | Department Head (Organic Synthesis)
Employment
Source: Self-asserted source
Stanislav Radl

Research Institute of Pharmacy and Biochemistry: Prague, CZ

1983 to 1986 | Research Scientist (Organic Sznthesis)
Employment
Source: Self-asserted source
Stanislav Radl

Education and qualifications (2)

Research Institute of Pharmacy and Biochemistry: Prague, CZ

1978-09-01 to 1982-12-31 | CSc./PhD (Organic Synthesis)
Education
Source: Self-asserted source
Stanislav Radl

Prague Institute of Chemical Technology, Faculty of Chemical Technology[: Prague, CZ

1970-09-30 to 1976-06-31 | Ing/Mgr (Organic Chemistry)
Education
Source: Self-asserted source
Stanislav Radl

Works (50 of 73)

Items per page:
Page 1 of 2

Will the Drugs of the Future Be Small Molecules or Biological Drugs?

Chemické listy
2022-08-15 | Journal article
DOI: 10.54779/chl20220471
Contributors: Stanislav Rádl; Ondřej Dammer; Luděk Ridvan
Source: check_circle
Crossref

Drug-like Inhibitors of DC-SIGN Based on a Quinolone Scaffold

ACS Medicinal Chemistry Letters
2022-06-09 | Journal article
DOI: 10.1021/acsmedchemlett.2c00067
Part of ISSN: 1948-5875
Part of ISSN: 1948-5875
Source: Self-asserted source
Stanislav Radl

A Scalable Synthesis of Roxadustat (FG-4592)

Organic Process Research & Development
2022-03-18 | Journal article
DOI: 10.1021/acs.oprd.1c00281
Part of ISSN: 1083-6160
Part of ISSN: 1520-586X
Source: Self-asserted source
Stanislav Radl

Synthesis of Fingolimod Employing Regioselective Aziridine Ring-Opening Reaction as a Key Step

Organic Process Research & Development
2022-03-18 | Journal article
DOI: 10.1021/acs.oprd.1c00248
Part of ISSN: 1083-6160
Part of ISSN: 1520-586X
Source: Self-asserted source
Stanislav Radl

An Improved Synthesis of Elvitegravir

Journal of Heterocyclic Chemistry
2015 | Journal article
DOI: 10.1002/jhet.2477
EID:

2-s2.0-84940951180
Contributors: Rádl, S.; Stach, J.; Píša, O.; Cinibulk, J.; Havlíček, J.; Zajícová, M.; Pekárek, T.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Deuterated compounds as potential drugs | Deuterované sloučeniny jako potenciální léčiva

Chemicke Listy
2015 | Journal article
EID:

2-s2.0-84946089850
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

To err is human | Mýliti se je lidské

Chemicke Listy
2015 | Journal article
EID:

2-s2.0-84923036668
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Identification, characterization, synthesis and HPLC quantification of new process-related impurities and degradation products in retigabine

Journal of Pharmaceutical and Biomedical Analysis
2014 | Journal article
DOI: 10.1016/j.jpba.2014.01.042
EID:

2-s2.0-84894119470
Contributors: Douša, M.; Srbek, J.; Rádl, S.; Černý, J.; Klecán, O.; Havlíček, J.; Tkadlecová, M.; Pekárek, T.; Gibala, P.; Nováková, L.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis of 2-(4-isopropylthiazol-2-yl)-7-methoxy-8-methylquinolin-4-ol; A quinoline building block for simeprevir synthesis

Synthesis (Germany)
2014 | Journal article
DOI: 10.1055/s-0033-1340679
EID:

2-s2.0-84897051897
Contributors: Rádl, S.; Rezková, H.; Obadalová, I.; Srbek, J.; Břicháč, J.; Pekárek, T.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

The Bosutinib Case - Trust but Check Out | Případ bosutinib aneb důvěřuj, ale prověřuj

Chemicke Listy
2014 | Journal article
EID:

2-s2.0-84892972285
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Improved process for azilsartan medoxomil: A new angiotensin receptor blocker

Organic Process Research and Development
2013 | Journal article
DOI: 10.1021/op3002867
EID:

2-s2.0-84872703178
Contributors: Rádl, S.; Černý, J.; Stach, J.; Gablíková, Z.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Suvorexant: Dual orexin OX<inf>1</inf>/OX<inf>2</inf> receptor antagonist treatment of sleep disorders

Drugs of the Future
2013 | Journal article
DOI: 10.1358/dof.2013.038.01.1906425
EID:

2-s2.0-84930539587
Contributors: Radl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis of azilsartan and its selected potential impurities

Journal of Heterocyclic Chemistry
2013 | Journal article
DOI: 10.1002/jhet.1783
EID:

2-s2.0-84880959455
Contributors: Rádl, S.; Černý, J.; Stach, J.; Holec, J.; Píša, O.; Gablíková, Z.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Utilization of studies of drug side effects in development of modern drugs | Využití výsledků studií vedlejších účinků léčiv při vývoji moderních léčiv

Chemicke Listy
2013 | Journal article
EID:

2-s2.0-84883219766
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Identification, preparation and UHPLC determination of process-related impurity in zolmitriptan

Journal of Pharmaceutical and Biomedical Analysis
2012 | Journal article
DOI: 10.1016/j.jpba.2011.08.043
EID:

2-s2.0-80255133187
Contributors: Douša, M.; Gibala, P.; Rádl, S.; Klecán, O.; Mandelová, Z.; Břicháč, J.; Pekárek, T.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis of some impurities and/or degradation products of zaleplon

Journal of Heterocyclic Chemistry
2010 | Journal article
DOI: 10.1002/jhet.335
EID:

2-s2.0-77950336038
Contributors: Rádl, S.; Blahovcová, M.; Plaček, L.; Pekárek, T.; Havlíček, J.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthetic studies connected with the preparation of N-[3-(3- cyanopyrazolo[1,5-a]pyrimidin-5-yl)phenyl]-N-ethylacetamide, a zaleplon regioisomer

Heterocycles
2010 | Journal article
DOI: 10.3987/COM-09-S(S)129
EID:

2-s2.0-77955675196
Contributors: Rádl, S.; Blahovcová, M.; Tkadlecová, M.; Havlíček, J.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

An efficient synthesis of 6-(4-chlorophenyl)-2,2-dimethyl-7-phenyl-2,3- dihydro-lh-pyrrolizine, a key intermediate in the licofelone synthesis

Collection of Czechoslovak Chemical Communications
2009 | Journal article
DOI: 10.1135/cccc2009026
EID:

2-s2.0-69549135348
Contributors: Rádl, S.; Stach, J.; Černy, J.; Klecán, O.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Bicyclic Systems with Two Ring Junction Nitrogen Atoms

Comprehensive Heterocyclic Chemistry II: A Review of the Literature 1982-1995
2009 | Book
DOI: 10.1016/B978-008096518-5.00198-2
EID:

2-s2.0-84944076141
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Identification, synthesis and structural determination of some impurities of candesartan cilexetil

Collection of Czechoslovak Chemical Communications
2009 | Journal article
DOI: 10.1135/cccc2008072
EID:

2-s2.0-63849261479
Contributors: Havlĺček, J.; Mandelová, Z.; Weisemann, R.; Střelec, I.; Plaček, L.; Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and identification of some impurities of irbesartan

Acta Chimica Slovenica
2009 | Journal article
EID:

2-s2.0-70349427214
Contributors: Rádl, S.; Stach, J.; Havlíček, J.; Tkadlecová, M.; Plaček, L.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

A new synthesis of rizatriptan based on radical cyclization

Collection of Czechoslovak Chemical Communications
2008 | Journal article
DOI: 10.1135/cccc20080116
EID:

2-s2.0-41949115584
Contributors: Rádl, S.; Klecán, O.; Klvaňa, R.; Havlíček, J.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

A synthesis of licofelone using Fenton's reagent

Tetrahedron Letters
2008 | Journal article
DOI: 10.1016/j.tetlet.2008.06.078
EID:

2-s2.0-47549094297
Contributors: Rádl, S.; Černý, J.; Klecán, O.; Stach, J.; Plaček, L.; Mandelová, Z.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Bicyclic systems with two bridgehead (ring junction) nitrogen atoms

Comprehensive Heterocyclic Chemistry III
2008 | Book
EID:

2-s2.0-84906420362
Contributors: Radl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis of some impurities and/or degradation products of atorvastatin

Collection of Czechoslovak Chemical Communications
2008 | Journal article
DOI: 10.1135/cccc20080229
EID:

2-s2.0-43049146571
Contributors: Stach, J.; Havlíček, J.; Plaček, L.; Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthetic studies connected with the preparation of H+/K +-ATPase inhibitors rabeprazole and lansoprazole

Journal of Heterocyclic Chemistry
2006 | Journal article
DOI: 10.1002/jhet.5570430606
EID:

2-s2.0-33845457970
Contributors: Rádl, S.; Klecán, O.; Havlíček, J.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Modification of the Gewald methodology for the synthesis of 3-amino-2-(1H-1,2,3-benzotriazol-1-yl) substituted benzofurans, benzothiophenes and 1H-indoles

Arkivoc
2005 | Journal article
EID:

2-s2.0-23744510681
Contributors: Rádl, S.; Obadalová, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

The origin of a drug - Selected aspects of the research and development of synthetic drugs | Jak se rodí lék, aneb vybrané aspekty výzkumu a vývoje chemických léčiv

Chemicke Listy
2004 | Journal article
EID:

2-s2.0-11444250502
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Utilization of aromatic denitrocyclization reaction for the synthesis of 3-unsubstituted 1,4-dihydroquinolin-4-one derivatives

Collection of Czechoslovak Chemical Communications
2004 | Journal article
DOI: 10.1135/cccc20040822
EID:

2-s2.0-2442583473
Contributors: Rádl, S.; Obadalová, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

A new way to tert-Butyl [(4R,6R)-6-aminoethyl-2,2-dimethyl-1,3-dioxan-4-yl]acetate, a key intermediate of atorvastatin synthesis

Synthetic Communications
2003 | Journal article
DOI: 10.1081/SCC-120021507
EID:

2-s2.0-17944402728
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

An improved synthesis of 1,1-dimethylethyl 6-cyanomethyl-2,2-dimethyl-1,3-dioxane-4-acetate, a key intermediate for atorvastatin synthesis

Tetrahedron Letters
2002 | Journal article
DOI: 10.1016/S0040-4039(02)00175-2
EID:

2-s2.0-0037060950
Contributors: Rádl, S.; Stach, J.; Hajicek, J.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Aromatic nucleophilic denitrocyclization reactions

Advances in Heterocyclic Chemistry
2002 | Book
DOI: 10.1016/S0065-2725(02)83006-9
EID:

2-s2.0-0036440946
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Aromatic nucleophilic denitrocyclization reactions

Chemicke Listy
2001 | Journal article
EID:

2-s2.0-0041410296
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

A new approach to the synthesis of benzofuro[3,2-b]quinolines, benzothieno[3,2-b]quinolines and indolo[3,2-b]quinolines

Journal of Heterocyclic Chemistry
2000 | Journal article
EID:

2-s2.0-0033786416
Contributors: Radl, S.; Konvicka, P.; Vachal, P.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and analgesic activity of some 1-benzofurans, 1-benzothiophenes and indoles

Collection of Czechoslovak Chemical Communications
2000 | Journal article
EID:

2-s2.0-0034344030
Contributors: Rádl, S.; Hezký, P.; Urbánková, J.; Váchal, P.; Krejčí, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and analgesic activity of some quinazoline analogs of anpirtoline

Archiv der Pharmazie
2000 | Journal article
DOI: 10.1002/1521-4184(200011)333:11<381::AID-ARDP381>3.0.CO;2-A
EID:

2-s2.0-0033651738
Contributors: Rádl, S.; Hezky, P.; Proka, J.; Krejc, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and analgesic activity of some side-chain modified anpirtoline derivatives

Archiv der Pharmazie
2000 | Journal article
DOI: 10.1002/(SICI)1521-4184(20005)333:5<107::AID-ARDP107>3.0.CO;2-Y
EID:

2-s2.0-0343729420
Contributors: Rádl, S.; Hezky, P.; Proška, J.; Hejnová, L.; Krejcí, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and analgesic activity of some substituted 1-benzofurans and 1-benzothiophenes

Collection of Czechoslovak Chemical Communications
2000 | Journal article
EID:

2-s2.0-0034340219
Contributors: Rádl, S.; Hezký, P.; Konvička, P.; Krejčí, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and binding studies of some epibatidine analogues

Bioorganic and Medicinal Chemistry Letters
2000 | Journal article
DOI: 10.1016/S0960-894X(99)00575-2
EID:

2-s2.0-0342948833
Contributors: Rádl, S.; Hezký, P.; Hafner, W.; Buděšínský, M.; Hejnová, L.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis, analgesic activity, and binding properties of some epibatidine analogs with a tropine skeleton

Archiv der Pharmazie
2000 | Journal article
DOI: 10.1002/1521-4184(20006)333:6<167::AID-ARDP167>3.0.CO;2-8
EID:

2-s2.0-0343457949
Contributors: Rádl, S.; Hafner, W.; Budešínsky, M.; Hejnová, L.; Krejcí, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Molecular modification of anpirtoline, a non-opioid centrally acting analgesic

Collection of Czechoslovak Chemical Communications
1999 | Journal article
EID:

2-s2.0-0033241277
Contributors: Rádl, S.; Hafner, W.; Hezký, P.; Krejčí, I.; Proška, J.; Taimr, J.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and analgesic activity of some condensed analogs of anpirtoline

Archiv der Pharmazie
1999 | Journal article
DOI: 10.1002/(SICI)1521-4184(19996)332:6<208::AID-ARDP208>3.0.CO;2-0
EID:

2-s2.0-0342956832
Contributors: Rádl, S.; Kovárová, L.; Hezky, P.; Vosátka, V.; Königová, O.; Proǎka, J.; Krejcí, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and analgesic activity of some deaza derivatives of anpirtoline

Archiv der Pharmazie
1999 | Journal article
DOI: 10.1002/(SICI)1521-4184(19991)332:1<13::AID-ARDP13>3.0.CO;2-L
EID:

2-s2.0-0343413562
Contributors: Rádl, S.; Hezky, P.; Proška, J.; Krejcí, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis and antinociceptive activity of some 3-chlorophenyl-and 6-chloropyridin-2-yl derivatives

Collection of Czechoslovak Chemical Communications
1999 | Journal article
EID:

2-s2.0-0033241280
Contributors: Rádl, S.; Hafner, W.; Hezký, P.; Krejčí, I.; Proška, J.; Hájíček, J.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthesis of piperidine analogs of 1-(3- chlorophenyl)piperazine, a well known serotonin ligand

Journal of Heterocyclic Chemistry
1999 | Journal article
EID:

2-s2.0-0032853485
Contributors: Rádl, S.; Hezký, P.; Taimr, J.; Proška, J.; Krejčí, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Analgetically active substances derived from structures of anpirtoline and epibatidine

General Physiology and Biophysics
1998 | Journal article
EID:

2-s2.0-0031814202
Contributors: Rádl, S.; Hezký, P.; Proška, J.; Krejčí, I.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

1,2,4-triazoIine-3,5-diones

Advances in Heterocyclic Chemistry
1997 | Book
EID:

2-s2.0-0343537654
Contributors: Radl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Crisscross cycloaddition reactions

Aldrichimica Acta
1997 | Journal article
EID:

2-s2.0-0040651627
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

Synthetic studies connected with the preparation of 4-cyclopropyl-7-fluoro-6-(4-methylpiperazin-1-yl)-1,2,4,9-tetrahydrothiazolo[5, 4-b]quinoline-2,9-dione

Collection of Czechoslovak Chemical Communications
1997 | Journal article
EID:

2-s2.0-0040689312
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier

From chloroquine to antineoplastic drugs? The story of antibacterial quinolones

Archiv der Pharmazie
1996 | Journal article
EID:

2-s2.0-5844386254
Contributors: Rádl, S.
Source: Self-asserted source
Stanislav Radl via Scopus - Elsevier
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