Тетродотоксин (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Тетродотоксин" in Serbian language version.

refsWebsite

Global rank Serbian rank

9doi.org

2^nd place

4^th place

7nih.gov

4^th place

8^th place

2acs.org

1,248^th place

389^th place

1wiley.com

222^nd place

155^th place

1sciencedirect.com

149^th place

283^rd place

1wikipedia.org

low place

1web.archive.org

1^st place

1rubicon-foundation.org

low place

4,389^th place

1citeulike.org

low place

211^th place

acs.org

pubs.acs.org

Tetko IV, Tanchuk VY, Kasheva TN, Villa AE (2001). „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Chem Inf. Comput. Sci. 41: 1488—1493. PMID 11749573. doi:10.1021/ci000392t.
Ertl P.; Rohde B.; Selzer P. (2000). „Fast calculation of molecular polar surface area as a sum of fragment based contributions and its application to the prediction of drug transport properties”. J. Med. Chem. 43: 3714—3717. PMID 11020286. doi:10.1021/jm000942e.

citeulike.org

Ghose, A.K.; Viswanadhan V.N. & Wendoloski, J.J. (1998). „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragment Methods: An Analysis of AlogP and CLogP Methods”. J. Phys. Chem. A. 102: 3762—3772. doi:10.1021/jp980230o.

doi.org

Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
Kishi Y, Aratani M, Fukuyama T, Nakatsubo F, Goto T, Inoue S, Tanino H, Sugiura S, Kakoi H (1972). „Synthetic studies on tetrodotoxin and related compounds. 3. A stereospecific synthesis of an equivalent of acetylated tetrodamine”. J. Am. Chem. Soc. 94 (26): 9217—9. PMID 4642370. doi:10.1021/ja00781a038.
Kishi Y, Fukuyama T, Aratani M, Nakatsubo F, Goto T, Inoue S, Tanino H, Sugiura S, Kakoi H (1972). „Synthetic studies on tetrodotoxin and related compounds. IV. Stereospecific total syntheses of DL-tetrodotoxin”. J. Am. Chem. Soc. 94 (26): 9219—9221. PMID 4642371. doi:10.1021/ja00781a039.
Ghose, A.K.; Viswanadhan V.N. & Wendoloski, J.J. (1998). „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragment Methods: An Analysis of AlogP and CLogP Methods”. J. Phys. Chem. A. 102: 3762—3772. doi:10.1021/jp980230o.
Tetko IV, Tanchuk VY, Kasheva TN, Villa AE (2001). „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Chem Inf. Comput. Sci. 41: 1488—1493. PMID 11749573. doi:10.1021/ci000392t.
Ertl P.; Rohde B.; Selzer P. (2000). „Fast calculation of molecular polar surface area as a sum of fragment based contributions and its application to the prediction of drug transport properties”. J. Med. Chem. 43: 3714—3717. PMID 11020286. doi:10.1021/jm000942e.
Anderson WH (1988). „Tetrodotoxin and the zombi phenomenon”. Journal of Ethnopharmacology. 23 (1): 121—6. PMID 3419200. doi:10.1016/0378-8741(88)90122-5.

nih.gov

ncbi.nlm.nih.gov

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
Clark RF, Williams SR, Nordt SP, Manoguerra AS (1999). „A review of selected seafood poisonings”. Undersea Hyperb Med. 26 (3): 175—84. PMID 10485519. Архивирано из оригинала 11. 08. 2011. г. Приступљено 12. 8. 2008.
Kishi Y, Aratani M, Fukuyama T, Nakatsubo F, Goto T, Inoue S, Tanino H, Sugiura S, Kakoi H (1972). „Synthetic studies on tetrodotoxin and related compounds. 3. A stereospecific synthesis of an equivalent of acetylated tetrodamine”. J. Am. Chem. Soc. 94 (26): 9217—9. PMID 4642370. doi:10.1021/ja00781a038.
Kishi Y, Fukuyama T, Aratani M, Nakatsubo F, Goto T, Inoue S, Tanino H, Sugiura S, Kakoi H (1972). „Synthetic studies on tetrodotoxin and related compounds. IV. Stereospecific total syntheses of DL-tetrodotoxin”. J. Am. Chem. Soc. 94 (26): 9219—9221. PMID 4642371. doi:10.1021/ja00781a039.
Tetko IV, Tanchuk VY, Kasheva TN, Villa AE (2001). „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Chem Inf. Comput. Sci. 41: 1488—1493. PMID 11749573. doi:10.1021/ci000392t.
Ertl P.; Rohde B.; Selzer P. (2000). „Fast calculation of molecular polar surface area as a sum of fragment based contributions and its application to the prediction of drug transport properties”. J. Med. Chem. 43: 3714—3717. PMID 11020286. doi:10.1021/jm000942e.
Anderson WH (1988). „Tetrodotoxin and the zombi phenomenon”. Journal of Ethnopharmacology. 23 (1): 121—6. PMID 3419200. doi:10.1016/0378-8741(88)90122-5.

rubicon-foundation.org

archive.rubicon-foundation.org

Clark RF, Williams SR, Nordt SP, Manoguerra AS (1999). „A review of selected seafood poisonings”. Undersea Hyperb Med. 26 (3): 175—84. PMID 10485519. Архивирано из оригинала 11. 08. 2011. г. Приступљено 12. 8. 2008.

sciencedirect.com

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

web.archive.org

Clark RF, Williams SR, Nordt SP, Manoguerra AS (1999). „A review of selected seafood poisonings”. Undersea Hyperb Med. 26 (3): 175—84. PMID 10485519. Архивирано из оригинала 11. 08. 2011. г. Приступљено 12. 8. 2008.

wikipedia.org

sr.wikipedia.org

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

wiley.com

onlinelibrary.wiley.com

Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.