アルカロイド (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "アルカロイド" in Japanese language version.

refsWebsite

Global rank Japanese rank

10doi.org

2^nd place

6^th place

10xumuk.ru

low place

8google.co.jp

934^th place

57^th place

7nih.gov

4^th place

24^th place

3rsc.org

2,020^th place

2,834^th place

2yandex.ru

878^th place

3,658^th place

1iupac.org

538^th place

512^th place

1yale.edu

565^th place

1,647^th place

1plantcyc.org

low place

1qmul.ac.uk

1,735^th place

2,576^th place

doi.org

IUPAC. Compendium of Chemical Terminology, 2nd ed. (The "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997) ISBN 0-9678550-9-8 doi:10.1351/goldbook
Dimitris C. Gournelif, Gregory G. Laskarisb and Robert Verpoorte (1997). “Cyclopeptide alkaloids”. Nat. Prod. Rep. 14 (1): 75–82. doi:10.1039/NP9971400075. PMID 9121730.
Blankenship JD, Houseknecht JB, Pal S, Bush LP, Grossman RB, Schardl CL (2005). “Biosynthetic precursors of fungal pyrrolizidines, the loline alkaloids”. Chembiochem 6 (6): 1016–1022. doi:10.1002/cbic.200400327. PMID 15861432.
Faulkner JR, Hussaini SR, Blankenship JD, Pal S, Branan BM, Grossman RB, Schardl CL (2006). “On the sequence of bond formation in loline alkaloid biosynthesis”. Chembiochem 7 (7): 1078–1088. doi:10.1002/cbic.200600066. PMID 16755627.
Schardl CL, Grossman RB, Nagabhyru P, Faulkner JR, Mallik UP (2007). “Loline alkaloids: currencies of mutualism”. Phytochemistry 68 (7): 980–996. doi:10.1016/j.phytochem.2007.01.010. PMID 17346759.
Joseph P. Michael (2002). “Indolizidine and quinolizidine alkaloids”. Nat. Prod. Rep 19: 458–475. doi:10.1039/b208137g.
Kenneth W. Bentley (1997). “β-Phenylethylamines and the isoquinoline alkaloids”. Nat. Prod. Rep 14 (4): 387–411. doi:10.1039/NP9971400387. PMID 9281839.
John R. Lewis (2000). “Amaryllidaceae, muscarine, imidazole, oxazole, thiazole and peptide alkaloids, and other miscellaneous alkaloids”. Nat. Prod. Rep 17 (1): 57–84. doi:10.1039/a809403i. PMID 10714899.
Richard B. Herbert; Herbert, Richard B.; Herbert, Richard B. (1999). “The biosynthesis of plant alkaloids and nitrogenous microbial metabolites”. Nat. Prod. Rep 16: 199–208. doi:10.1039/a705734b.
Atta-ur-Rahman and M. Iqbal Choudhary (1997). “Diterpenoid and steroidal alkaloids”. Nat. Prod. Rep 14 (2): 191–203. doi:10.1039/np9971400191. PMID 9149410.

google.co.jp

books.google.co.jp

Andreas Luch (2009). Molecular, clinical and environmental toxicology. Springer. p. 20. ISBN 3-7643-8335-6
Robert Alan Lewis. Lewis' dictionary of toxicology. CRC Press, 1998, p. 51 ISBN 1-56670-223-2
Leland J. Cseke Natural Products from Plants Second Edition. – CRC, 2006, p. 30 ISBN 0-8493-2976-0
A. William Johnson Invitation to Organic Chemistry, Jones and Bartlett, 1999, p. 433 ISBN 0-7637-0432-6
Raj K Bansal A Text Book of Organic Chemistry. 4th Edition, New Age International, 2004, p. 644 ISBN 81-224-1459-1
G. A. Spiller Caffeine, CRC Press, 1997 ISBN 0-8493-2647-8
Thomas Acamovic, Colin S. Stewart, T. W. Pennycott (2004). Poisonous plants and related toxins, Volume 2001. CABI. p. 362. ISBN 0-85199-614-0
György Matolcsy, Miklós Nádasy, Viktor Andriska Pesticide chemistry, Elsevier, 2002, pp. 21–22 ISBN 0-444-98903-X

iupac.org

goldbook.iupac.org

IUPAC. Compendium of Chemical Terminology, 2nd ed. (The "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997) ISBN 0-9678550-9-8 doi:10.1351/goldbook

nih.gov

pubmed.ncbi.nlm.nih.gov

Dimitris C. Gournelif, Gregory G. Laskarisb and Robert Verpoorte (1997). “Cyclopeptide alkaloids”. Nat. Prod. Rep. 14 (1): 75–82. doi:10.1039/NP9971400075. PMID 9121730.
Blankenship JD, Houseknecht JB, Pal S, Bush LP, Grossman RB, Schardl CL (2005). “Biosynthetic precursors of fungal pyrrolizidines, the loline alkaloids”. Chembiochem 6 (6): 1016–1022. doi:10.1002/cbic.200400327. PMID 15861432.
Faulkner JR, Hussaini SR, Blankenship JD, Pal S, Branan BM, Grossman RB, Schardl CL (2006). “On the sequence of bond formation in loline alkaloid biosynthesis”. Chembiochem 7 (7): 1078–1088. doi:10.1002/cbic.200600066. PMID 16755627.
Schardl CL, Grossman RB, Nagabhyru P, Faulkner JR, Mallik UP (2007). “Loline alkaloids: currencies of mutualism”. Phytochemistry 68 (7): 980–996. doi:10.1016/j.phytochem.2007.01.010. PMID 17346759.
Kenneth W. Bentley (1997). “β-Phenylethylamines and the isoquinoline alkaloids”. Nat. Prod. Rep 14 (4): 387–411. doi:10.1039/NP9971400387. PMID 9281839.
John R. Lewis (2000). “Amaryllidaceae, muscarine, imidazole, oxazole, thiazole and peptide alkaloids, and other miscellaneous alkaloids”. Nat. Prod. Rep 17 (1): 57–84. doi:10.1039/a809403i. PMID 10714899.
Atta-ur-Rahman and M. Iqbal Choudhary (1997). “Diterpenoid and steroidal alkaloids”. Nat. Prod. Rep 14 (2): 191–203. doi:10.1039/np9971400191. PMID 9149410.

plantcyc.org

PlantCyc Pathway: ephedrine biosynthesis

qmul.ac.uk

iubmb.qmul.ac.uk

Spermine Biosynthesis

rsc.org

xumuk.ru

yale.edu

webspace.yale.edu

接尾辞 "ine" はギリシャ語の女性父称を作る接尾辞であり、「〜の娘」を意味する。すなわち、アトロピンは「Atropa（ベラドンナ）の娘」を意味する。[1]