Interaction of Diphenyltin(IV) Dichloride with Some Selected Bioligands

The interaction of diphenyltin(IV) with selected bioligands having a variety of model functional groups were investigated using the potentiometric technique. The hydrolysis constants of diphenyltin(IV) cation and the step-wise formation constants of the complexes formed in solution were calculated u...

Full description

Saved in:
Bibliographic Details
Published inChemical & pharmaceutical bulletin Vol. 49; no. 3; pp. 253 - 257
Main Authors MOHAMED, Mahmoud Mohamed Ahmed, SHOUKRY, Mohamed Mohamed
Format Journal Article
LanguageEnglish
Published Tokyo The Pharmaceutical Society of Japan 01.03.2001
Maruzen
Japan Science and Technology Agency
Subjects
Algorithms
amino acid
Chemical Phenomena
Chemistry
Chemistry, Physical
dicarboxylic acid
diphenyltin(IV) dichloride
DNA constituent
Drug Carriers - chemistry
equilibrium study
Exact sciences and technology
Ge, sn, pb derivatives
Hydrogen-Ion Concentration
Indicators and Reagents
Ligands
Organic chemistry
Organometalloidal and organometallic compounds
Organotin Compounds - chemistry
peptide
Potentiometry
Preparations and properties
Equilibrium constant
Thiol
Organic ligand
Stability constant
Penicillamine
Sulfur containing aminoacid
α-Aminoacid
Tin IV Complexes
Medium effect
pH
Chloro complex
Aminothiol
Tin Organic compounds
Online AccessGet full text

Cover

Abstract The interaction of diphenyltin(IV) with selected bioligands having a variety of model functional groups were investigated using the potentiometric technique. The hydrolysis constants of diphenyltin(IV) cation and the step-wise formation constants of the complexes formed in solution were calculated using the non linear least-squares program MINIQUAD-75. The participation of different ligand functional groups in binding to organotin is discussed. The concentration distribution of the various complex species was evaluated as a function of pH.
AbstractList The interaction of diphenyltin(IV) with selected bioligands having a variety of model functional groups were investigated using the potentiometric technique. The hydrolysis constants of diphenyltin(IV) cation and the step-wise formation constants of the complexes formed in solution were calculated using the non linear least-squares program MINIQUAD-75. The participation of different ligand functional groups in binding to organotin is discussed. The concentration distribution of the various complex species was evaluated as a function of pH.
Author MOHAMED, Mahmoud Mohamed Ahmed
SHOUKRY, Mohamed Mohamed
Author_xml – sequence: 1
  fullname: MOHAMED, Mahmoud Mohamed Ahmed
  organization: Department of Chemistry, Faculty of Education, Assuit University
– sequence: 2
  fullname: SHOUKRY, Mohamed Mohamed
  organization: Department of Chemistry, Faculty of Science, Cairo University
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=933150$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/11253913$$D View this record in MEDLINE/PubMed
BookMark eNpd0NFqFDEUBuAgFbtdvfEBZECQWpg1mSSTyZW01daFghdVb0MmOdPNkk22SZbStzeyayveJITz8Z_wn6CjEAMg9JbgBenY8MlsxwWTi47TF2hGKBMt7zp6hGYYY9l2tKfH6CTnNcYdx4K-QseEVCwJnaHrZSiQtCkuhiZOzRe3XUF49MWF0-Wvj_VtVj4mZ6F5cGXV3MYNNLfgwRSwzYWL3t3pYPNr9HLSPsObwz1HP6--_rj81t58v15ent-0hklRWsENJmJgmk2cCNsPY0esJJMdBK4To8ceJCUDtz3VAyET4BFzqfmIhQU-0Tn6sM_dpni_g1zUxmUD3usAcZeV6KUgNbrC9__BddylUP-mCOsxZYTVDubobK9MijknmNQ2uY1Oj4pg9adcVctVTKpqK353iNyNG7DP9NDmPzt1NtpPSQfj8pOTlBKOq_q8V-tc9B08jXUqznj4u5Hujxr9PFnppCDQ31N9mAY
CODEN CPBTAL
CitedBy_id crossref_primary_10_1007_s10953_017_0654_3
crossref_primary_10_1515_REVIC_2005_25_1_79
crossref_primary_10_1021_je900975s
crossref_primary_10_1007_s10953_013_0104_9
crossref_primary_10_1080_00958972_2015_1007962
crossref_primary_10_1007_s10953_012_9854_z
crossref_primary_10_1080_00958970500270786
crossref_primary_10_1021_acs_est_0c02855
crossref_primary_10_1155_2013_106357
crossref_primary_10_1016_j_theochem_2010_06_016
crossref_primary_10_1007_s10953_016_0448_z
crossref_primary_10_1039_c2an35999e
crossref_primary_10_1080_10426500903120750
crossref_primary_10_1007_s11426_010_4034_8
crossref_primary_10_1080_00958972_2011_565755
Cites_doi 10.1139/v64-117
10.1002/aoc.590060103
10.1016/0162-0134(92)84053-P
10.1016/S0039-9140(96)02113-3
10.1021/ic00171a005
10.1016/S0022-0728(73)80379-1
10.1016/S0020-1693(97)06044-1
10.1007/978-3-642-74191-3_2
10.1080/00958979209409742
10.1016/S0020-1693(00)95610-X
10.1016/0039-9140(95)01708-9
10.1007/978-3-642-74191-3_5
ContentType Journal Article
Copyright 2001 The Pharmaceutical Society of Japan
2001 INIST-CNRS
Copyright Japan Science and Technology Agency 2001
Copyright_xml – notice: 2001 The Pharmaceutical Society of Japan
– notice: 2001 INIST-CNRS
– notice: Copyright Japan Science and Technology Agency 2001
DBID IQODW
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7TK
7TM
7U9
H94
7X8
DOI 10.1248/cpb.49.253
DatabaseName Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
Neurosciences Abstracts
Nucleic Acids Abstracts
Virology and AIDS Abstracts
AIDS and Cancer Research Abstracts
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
AIDS and Cancer Research Abstracts
Virology and AIDS Abstracts
Neurosciences Abstracts
Nucleic Acids Abstracts
MEDLINE - Academic
DatabaseTitleList MEDLINE

AIDS and Cancer Research Abstracts
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Pharmacy, Therapeutics, & Pharmacology
Chemistry
EISSN 1347-5223
EndPage 257
ExternalDocumentID 3133465431
10_1248_cpb_49_253
11253913
933150
article_cpb_49_3_49_3_253_article_char_en
Genre Journal Article
GroupedDBID ---
.55
.GJ
29B
2WC
3O-
53G
5GY
6J9
AABQG
AAUGY
ABTAH
ACGFO
ACIWK
ACPRK
ADBBV
AENEX
AFRAH
AI.
ALMA_UNASSIGNED_HOLDINGS
BAWUL
BKOMP
CS3
DIK
DU5
E3Z
EBS
EJD
F5P
GX1
HH5
JMI
JSF
JSH
KQ8
L7B
MOJWN
OK1
P2P
RJT
RZJ
TKC
TR2
VH1
X7J
X7M
XSB
ZE2
ZGI
ZY4
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7TK
7TM
7U9
H94
7X8
ID FETCH-LOGICAL-c497t-75c01784a4f517d68b21d91fd870c01cab6e93185d63a811fe0b059a5b07de5f3
ISSN 0009-2363
IngestDate Fri Aug 16 11:40:30 EDT 2024
Fri Sep 13 00:39:48 EDT 2024
Fri Aug 23 01:40:34 EDT 2024
Sat Sep 28 08:33:33 EDT 2024
Sun Oct 22 16:07:43 EDT 2023
Thu Aug 17 20:25:43 EDT 2023
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords Equilibrium constant
Thiol
Organic ligand
Stability constant
Penicillamine
Sulfur containing aminoacid
α-Aminoacid
Tin IV Complexes
Medium effect
pH
Chloro complex
Aminothiol
Tin Organic compounds
Language English
License CC BY 4.0
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c497t-75c01784a4f517d68b21d91fd870c01cab6e93185d63a811fe0b059a5b07de5f3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.jstage.jst.go.jp/article/cpb/49/3/49_3_253/_article/-char/en
PMID 11253913
PQID 1460341425
PQPubID 1996362
PageCount 5
ParticipantIDs proquest_miscellaneous_76971517
proquest_journals_1460341425
crossref_primary_10_1248_cpb_49_253
pubmed_primary_11253913
pascalfrancis_primary_933150
jstage_primary_article_cpb_49_3_49_3_253_article_char_en
PublicationCentury 2000
PublicationDate 2001-03-01
PublicationDateYYYYMMDD 2001-03-01
PublicationDate_xml – month: 03
  year: 2001
  text: 2001-03-01
  day: 01
PublicationDecade 2000
PublicationPlace Tokyo
PublicationPlace_xml – name: Tokyo
– name: Japan
PublicationTitle Chemical & pharmaceutical bulletin
PublicationTitleAlternate Chem. Pharm. Bull.
PublicationYear 2001
Publisher The Pharmaceutical Society of Japan
Maruzen
Japan Science and Technology Agency
Publisher_xml – name: The Pharmaceutical Society of Japan
– name: Maruzen
– name: Japan Science and Technology Agency
References 4) Tsangaris J.M., Williams D.R., App. Organometallic Chem., 6, 3 (1992).
3) Crowe A.J., “Tin Compounds and Their Potential as Pharmaceutical Agents,” Tin-Based Antitumour Drugs. NATO ASI Series, Vol. H37, Springer Verlag, Berlin, 1990, p. 69.
7) Shoukry M.M., Bull. Soc. Chem. Fr., 130, 177 (1993).
21) Natsume T., Aizawa S.I., Hatano K., Funahashi S., J. Chem. Soc., Dalton Trans., 1994, 2749.
2) Penninks A.H., Bol-Schoenmakers M., Seinen W. “Cellular Interaction of Organotin Compounds in Relation to Their Antitumour Activity,” ed. by Gielen M., Tin-Based Antitumour Drugs. NATO ASI Series, Vol. H37, Springer Verlag, Berlin, 1990, p. 169.
5) Shoukry M.M., J. Inorg. Biochem., 48, 271 (1992).
8) Shoukry M.M., Talanta, 43, 177 (1996).
18) Buzjs N., Gajda T., Nagy L., Kuzmann E., Vértes A., Burger K., Inorg. Chim. Acta, 274, 167 (1998).
22) Farooq O., Ahmed N., Malik A.V., J. Electroanal. Chem., 48, 475 (1973).
1) This paper is dedicated to Prof. Dr. M.H. Elnagdi on the occasion of his 60th birthday.
11) Al-Najjar A.A., Shehata M.R., Mohamed M.M.A., Shoukry M.M., Main Group Met. Chem., 22, 253 (1999).
6) Shoukry M.M., J. Coord. Chem., 25, 111 (1992).
9) Shoukry M.M., Mohamed M.M.A., Main Group Met. Chem., 20, 281 (1997).
17) Perrin D.D., “Stability Constants of Metal-Ion Complexes: Part B, Organic Ligands,” Pergamon Press, Oxford, 1979.
12) Bates R.G., “Determination of pH-Theory and Practice,” 2nd ed., Wiley, New York, 1975.
10) Shoukry M.M., Khairy E.M., Mohamed M.M.A., Talanta, 44, 1149 (1997).
20) Arena G., Purrello R., Rizzarelli E., Gianguzza A., Pellerito L., J. Chem. Soc., Dalton Trans., 1989, 773.
14) Motekaitis R.J., Martell A.E., Nelson D.A., Inorg. Chem., 23, 275 (1984).
15) Gans P., Sabatini A., Vacca A., Inorg. Chim. Acta, 18, 237 (1976).
23) Lim M.C., Inorg. Chem., 1981, 1377.
16) Pettit L., (University of Leeds), Personal Communication.
19) Tobias R.S., Yasuda M., Can. J. Chem., 42, 781 (1964).
13) Shoukry M.M., Hosny W.M., Khalil M.M., Transition Met. Chem., 20, 252 (1995).
12
Shoukry M.M. (7) 1993; 130
(6) 1992; 25
15
Tsangaris J.M., Williams D.R. (4) 1992; 6
16
Farooq O., Ahmed N., Malik A.V. (22) 1973; 48
17
18
(13) 1995; 20
Shoukry M.M., Mohamed M.M.A. (9) 1997; 20
Motekaitis R.J., Martell A.E., Nels (14) 1984; 23
Lim M.C. (23); 1981
1
2
3
5
Al-Najjar A.A., Shehata M.R., Moham (11) 1999; 22
8
Tobias R.S., Yasuda M. (19) 1964; 42
Natsume T., Aizawa S.I., Hatano K. (21); 1994
Arena G., Purrello R., Rizzarelli E (20); 1989
10
References_xml – ident: 17
– volume: 42
  start-page: 781
  issn: 0008-4042
  year: 1964
  ident: 19
  publication-title: Can. J. Chem.
  doi: 10.1139/v64-117
  contributor:
    fullname: Tobias R.S., Yasuda M.
– volume: 6
  start-page: 3
  year: 1992
  ident: 4
  publication-title: App. Organometallic Chem.
  doi: 10.1002/aoc.590060103
  contributor:
    fullname: Tsangaris J.M., Williams D.R.
– ident: 5
  doi: 10.1016/0162-0134(92)84053-P
– volume: 1989
  start-page: 773
  issn: 1472-7773
  ident: 20
  publication-title: J. Chem. Soc., Dalton Trans.
  contributor:
    fullname: Arena G., Purrello R., Rizzarelli E
– ident: 10
  doi: 10.1016/S0039-9140(96)02113-3
– volume: 23
  start-page: 275
  issn: 0020-1669
  issue: 3
  year: 1984
  ident: 14
  publication-title: Inorg. Chem.
  doi: 10.1021/ic00171a005
  contributor:
    fullname: Motekaitis R.J., Martell A.E., Nels
– ident: 1
– ident: 12
– volume: 48
  start-page: 475
  year: 1973
  ident: 22
  publication-title: J. Electroanal. Chem.
  doi: 10.1016/S0022-0728(73)80379-1
  contributor:
    fullname: Farooq O., Ahmed N., Malik A.V.
– volume: 22
  start-page: 253
  year: 1999
  ident: 11
  publication-title: Main Group Met. Chem.
  contributor:
    fullname: Al-Najjar A.A., Shehata M.R., Moham
– ident: 18
  doi: 10.1016/S0020-1693(97)06044-1
– volume: 20
  start-page: 281
  year: 1997
  ident: 9
  publication-title: Main Group Met. Chem.
  contributor:
    fullname: Shoukry M.M., Mohamed M.M.A.
– ident: 3
  doi: 10.1007/978-3-642-74191-3_2
– volume: 130
  start-page: 177
  year: 1993
  ident: 7
  publication-title: Bull. Soc. Chem. Fr.
  contributor:
    fullname: Shoukry M.M.
– ident: 16
– volume: 25
  start-page: 111
  issn: 0095-8972
  issue: 2
  year: 1992
  ident: 6
  publication-title: J. Coord. Chem.
  doi: 10.1080/00958979209409742
– volume: 1981
  start-page: 1377
  issn: 0020-1669
  ident: 23
  publication-title: Inorg. Chem.
  contributor:
    fullname: Lim M.C.
– ident: 15
  doi: 10.1016/S0020-1693(00)95610-X
– ident: 8
  doi: 10.1016/0039-9140(95)01708-9
– volume: 1994
  start-page: 2749
  issn: 1472-7773
  ident: 21
  publication-title: J. Chem. Soc., Dalton Trans.
  contributor:
    fullname: Natsume T., Aizawa S.I., Hatano K.
– ident: 2
  doi: 10.1007/978-3-642-74191-3_5
– volume: 20
  start-page: 252
  issn: 0340-4285
  issue: 3
  year: 1995
  ident: 13
  publication-title: Transition Met. Chem.
SSID ssj0025073
Score 1.7356641
Snippet The interaction of diphenyltin(IV) with selected bioligands having a variety of model functional groups were investigated using the potentiometric technique....
SourceID proquest
crossref
pubmed
pascalfrancis
jstage
SourceType Aggregation Database
Index Database
Publisher
StartPage 253
SubjectTerms Algorithms
amino acid
Chemical Phenomena
Chemistry
Chemistry, Physical
dicarboxylic acid
diphenyltin(IV) dichloride
DNA constituent
Drug Carriers - chemistry
equilibrium study
Exact sciences and technology
Ge, sn, pb derivatives
Hydrogen-Ion Concentration
Indicators and Reagents
Ligands
Organic chemistry
Organometalloidal and organometallic compounds
Organotin Compounds - chemistry
peptide
Potentiometry
Preparations and properties
Title Interaction of Diphenyltin(IV) Dichloride with Some Selected Bioligands
URI https://www.jstage.jst.go.jp/article/cpb/49/3/49_3_253/_article/-char/en
https://www.ncbi.nlm.nih.gov/pubmed/11253913
https://www.proquest.com/docview/1460341425/abstract/
https://search.proquest.com/docview/76971517
Volume 49
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
ispartofPNX Chemical and Pharmaceutical Bulletin, 2001, Vol.49(3), pp.253-257
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLbK4AEJIe4UBlgCTSCW0sS5-bGig45pbMA6bU9RHCe0iF5E24fy6_lO7SYpA2nw4laxnTbn8vmcE59jxl4omAESmOcIpaXjKz9z0sgLHC3bGa2xcOYoDnn4Mez1_Q9nwVmjUdR2LS3mqpX9_GNeyf9wFdfAV8qS_QfOljfFBXwHf9GCw2gvxeNVOM8e9g2jrzukDVvL76u6APH-KXn83WE2oE12Ojch1y-TUQ6AoGA9TE06iXL4dZ3tW1YsWBcRILGYDjaC3qperpsYddTrHO51TdrPYDRZaMDEIMUa-7ozGNnMKYrg9I76B5_PV-Nsv_3ciDvUNl6VWCodT1h4yg18Cj-Ca2syiNf4akqSWjkSdbAMRG3d9Uyh6guQ7vmUppBNVcuXrXJKvW72b-tZucuQ_BvMTjA38WWCuVfYVS-SATnpB5_Kt02wAqPyxD16IlvGFnPfVL-7Ybhc-wbbnYoy3JimM1C_MKeg_N1NWZkrJ7fYTetn8I4RmtuskY_vsJ1jw8zlLj-p8u5mu3yHH1clzJd32fuaZPFJwWuS9XL_9BWvpIqTVHGSKr6WKl5J1T3Wf7d38rbn2CM3nAwqO3eiIANEx37qF4Eb6TBWnqulW2jAOnqyVIW5pIR7HYo0dt0ib0PbZRqodqTzoBD32dZ4Ms4fMg5DO4zTogi1Vr7QkWpD7bXSnhagsXSb7PmansnUVFZJLnKsyWJD6nKM1bb1GGEaDK16QDHAQ5NtbzCnvIMUAm4QdVteJVanZ-QIt2HXYSFrsmdlNxCXXqOl43yymCVRCHADdZrsgeFw9ffhLQjpikeXerTH7HqlV9tsa_5jkT-BhTtXT1fi-QtqjKZG
link.rule.ids 315,786,790,27957,27958
linkProvider Colorado Alliance of Research Libraries
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Interaction+of+Diphenyltin%28IV%29+Dichloride+with+Some+Selected+Bioligands&rft.jtitle=Chemical+%26+pharmaceutical+bulletin&rft.au=MOHAMED%2C+Mahmoud+Mohamed+Ahmed&rft.au=SHOUKRY%2C+Mohamed+Mohamed&rft.date=2001-03-01&rft.issn=0009-2363&rft.eissn=1347-5223&rft.volume=49&rft.issue=3&rft.spage=253&rft.epage=257&rft_id=info:doi/10.1248%2Fcpb.49.253&rft.externalDBID=n%2Fa&rft.externalDocID=10_1248_cpb_49_253
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0009-2363&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0009-2363&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0009-2363&client=summon