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Argyreia nervosa (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Argyreia nervosa" in English language version.

refsWebsite
Global rank English rank
12nih.gov
4th place
4th place
10doi.org
2nd place
2nd place
4worldcat.org
5th place
5th place
2web.archive.org
1st place
1st place
1ars-grin.gov
607th place
747th place
1ayurveda.hu
low place
low place
1semanticscholar.org
11th place
8th place
1elsevier.com
610th place
704th place
1entheology.org
low place
low place
1hawaii.edu
1,308th place
924th place
1books.google.com
3rd place
3rd place

ars-grin.gov

npgsweb.ars-grin.gov

  • "Argyreia nervosa". Germplasm Resources Information Network. Agricultural Research Service, United States Department of Agriculture. Retrieved 2010-11-10.

ayurveda.hu

  • The Ayurvedic Pharmacopoeia of India, part 1, vol. 5. Government of India, Ministry of Health and Family Welfare, Department of Ayush. http://www.ayurveda.hu/api/API-Vol-5.pdf
    A. nervosa entry: page 16
    “T.L.C. of methanolic extract of the roots on precoated silica gel G plate using methanol - chloroform (20 : 80) showed a blue fluorescent spot under UV (365nm) along with number of other spots of very weak intensity. Due to the presence of very negligible amount of alkaloids in the roots these could not be isolated.” (p. 17)

books.google.com

doi.org

  • E. Al-Assmar, Sami (1999). "The Seeds of the Hawaiian Baby Woodrose Are a Powerful Hallucinogen". Arch Intern Med. 159 (17): 2090. doi:10.1001/archinte.159.17.2090 (inactive 2024-11-13). PMID 10510998.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
  • Paulke, Alexander; et al. (2015). "Studies on the alkaloid composition of the Hawaiian Baby Woodrose Argyreia nervosa, a common legal high". Forensic Science International. 249: 281–293. doi:10.1016/j.forsciint.2015.02.011. PMID 25747328.
  • Halpern, J.H. (2004). "Hallucinogens and dissociative agents naturally growing in the United States". Pharmacology & Therapeutics. 102 (2): 131–138. doi:10.1016/j.pharmthera.2004.03.003. PMID 15163594. S2CID 30734515. Although LSD does not occur in nature, a close analogue, lysergic acid amide (LSA, ergine) is found in the seeds of Argyreia nervosa (Hawaiian baby woodrose)
  • Chao JM, Der Marderosian AH (1973). "Ergoline alkaloidal constituents of Hawaiian baby wood rose, Argyreia nervosa (Burmf) Bojer". J. Pharm. Sci. 62 (4): 588–91. doi:10.1002/jps.2600620409. PMID 4698977.
  • Paulke, Alexander; Kremer, Christian; Wunder, Cora; Wurglics, Mario; Schubert-Zsilavecz, Manfred; Toennes, Stefan W. (2014-09-01). "Identification of legal highs – Ergot alkaloid patterns in two Argyreia nervosa products". Forensic Science International. 242: 62–71. doi:10.1016/j.forsciint.2014.06.025. ISSN 0379-0738. PMID 25036782
    “Additionally the presence of the ergot alkaloid diastereomers chanoclavine I and II was assumed in DF (cf. Fig. 6) together with traces of lysergic acid and the isobars lysergol, isolysergol, elymoclavine, molliclavine, setoclavine, or isosetoclavine.” (3.1. Mass spectrometry data, p. 65)
    “Indications of traces of [M+H]+ = 255.15 0.01 corresponding to lysergol/isolysergol, elymoclavine, setoclavine/isosetoclavine or molliclavine as well as [M+H]+ = 269.13 0.01 corresponding to lysergic acid were only obtained in the DF extracts and the resolution and the quality of the EICs and product spectra was poor. Therefore, the presence of lysergol/isolysergol, elymoclavine, setoclavine/isosetoclavine, molliclavine or lysergic acid cannot be excluded, but proof cannot be provided and additional research will be necessary.” (3.1. Mass spectrometry data, pages 65 & 68)    {{cite journal}}: CS1 maint: postscript (link)
  • Paulke, Alexander; et al. (2015). "Studies on the alkaloid composition of the Hawaiian Baby Woodrose Argyreia nervosa, a common legal high". Forensic Science International. 249: 281–293. doi:10.1016/j.forsciint.2015.02.011. PMID 25747328
    “On the other hand, methylergometrine, methysergide, and lysergylalanine were detected, which have not yet been reported as compounds of Argyreia nervosa seeds. Furthermore, some high molecular weight ergot alkaloid derivatives and hydroxyalanine derived ergopeptide fragments could be observed at various retention times (c.f. chapter 3.1). Altogether, lysergylalanine, the high molecular weight ergot alkaloids and the hydroxyalanine derived ergopeptide fragments strongly suggest the presence of ergopeptides in Argyreia nervosa. However, due to the disadvantage of the applied APCI technique for peptide analysis (c.f. chapter 3.1) additional research (e.g. ESI-HRMS/MS) will be necessary to verify this assumption and to elucidate the structure of the ergopeptides.” (3. Results and discussion, p. 283)    {{cite journal}}: CS1 maint: postscript (link)
  • Nowak, Julia; Woźniakiewicz, Michał; Klepacki, Piotr; Sowa, Anna; Kościelniak, Paweł (May 2016). "Identification and determination of ergot alkaloids in Morning Glory cultivars". Analytical and Bioanalytical Chemistry. 408 (12): 3093–3102. doi:10.1007/s00216-016-9322-5. ISSN 1618-2642. PMC 4830885. PMID 26873205"ergine and ergometrine concentration is 12-fold lower in plant samples than in seeds." Analysis of IP-HB2 young plants{{cite journal}}: CS1 maint: postscript (link)
  • Rahman, A.; Ali, M.; Khan, N. Z. (2003). "Argyroside from Argyreia nervosa Seeds". ChemInform. 34 (21): 60–2. doi:10.1002/chin.200321168. ISSN 0931-7597. PMID 12622256.
  • Paulke, Alexander; Kremer, Christian; Wunder, Cora; Wurglics, Mario; Schubert-Zsilavecz, Manfred; Toennes, Stefan W. (2014). "Identification of legal highs--ergot alkaloid patterns in two Argyreia nervosa products". Forensic Science International. 242: 62–71. doi:10.1016/j.forsciint.2014.06.025. ISSN 1872-6283. PMID 25036782.
  • Bharati, A. J.; Bansal, Y. K. (2014). "Phytochemical investigation of natural and in vitro raised Vṛddhadāruka plants". Ancient Science of Life. 34 (2): 80–84. doi:10.4103/0257-7941.153463. PMC 4389397. PMID 25861141.

elsevier.com

linkinghub.elsevier.com

  • Paulke, Alexander; Kremer, Christian; Wunder, Cora; Wurglics, Mario; Schubert-Zsilavecz, Manfred; Toennes, Stefan W. (2014-09-01). "Identification of legal highs – Ergot alkaloid patterns in two Argyreia nervosa products". Forensic Science International. 242: 62–71. doi:10.1016/j.forsciint.2014.06.025. ISSN 0379-0738. PMID 25036782
    “Additionally the presence of the ergot alkaloid diastereomers chanoclavine I and II was assumed in DF (cf. Fig. 6) together with traces of lysergic acid and the isobars lysergol, isolysergol, elymoclavine, molliclavine, setoclavine, or isosetoclavine.” (3.1. Mass spectrometry data, p. 65)
    “Indications of traces of [M+H]+ = 255.15 0.01 corresponding to lysergol/isolysergol, elymoclavine, setoclavine/isosetoclavine or molliclavine as well as [M+H]+ = 269.13 0.01 corresponding to lysergic acid were only obtained in the DF extracts and the resolution and the quality of the EICs and product spectra was poor. Therefore, the presence of lysergol/isolysergol, elymoclavine, setoclavine/isosetoclavine, molliclavine or lysergic acid cannot be excluded, but proof cannot be provided and additional research will be necessary.” (3.1. Mass spectrometry data, pages 65 & 68)    {{cite journal}}: CS1 maint: postscript (link)

entheology.org

hawaii.edu

evols.library.manoa.hawaii.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

  • E. Al-Assmar, Sami (1999). "The Seeds of the Hawaiian Baby Woodrose Are a Powerful Hallucinogen". Arch Intern Med. 159 (17): 2090. doi:10.1001/archinte.159.17.2090 (inactive 2024-11-13). PMID 10510998.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
  • Paulke, Alexander; et al. (2015). "Studies on the alkaloid composition of the Hawaiian Baby Woodrose Argyreia nervosa, a common legal high". Forensic Science International. 249: 281–293. doi:10.1016/j.forsciint.2015.02.011. PMID 25747328.
  • Halpern, J.H. (2004). "Hallucinogens and dissociative agents naturally growing in the United States". Pharmacology & Therapeutics. 102 (2): 131–138. doi:10.1016/j.pharmthera.2004.03.003. PMID 15163594. S2CID 30734515. Although LSD does not occur in nature, a close analogue, lysergic acid amide (LSA, ergine) is found in the seeds of Argyreia nervosa (Hawaiian baby woodrose)
  • Chao JM, Der Marderosian AH (1973). "Ergoline alkaloidal constituents of Hawaiian baby wood rose, Argyreia nervosa (Burmf) Bojer". J. Pharm. Sci. 62 (4): 588–91. doi:10.1002/jps.2600620409. PMID 4698977.
  • Paulke, Alexander; Kremer, Christian; Wunder, Cora; Wurglics, Mario; Schubert-Zsilavecz, Manfred; Toennes, Stefan W. (2014-09-01). "Identification of legal highs – Ergot alkaloid patterns in two Argyreia nervosa products". Forensic Science International. 242: 62–71. doi:10.1016/j.forsciint.2014.06.025. ISSN 0379-0738. PMID 25036782
    “Additionally the presence of the ergot alkaloid diastereomers chanoclavine I and II was assumed in DF (cf. Fig. 6) together with traces of lysergic acid and the isobars lysergol, isolysergol, elymoclavine, molliclavine, setoclavine, or isosetoclavine.” (3.1. Mass spectrometry data, p. 65)
    “Indications of traces of [M+H]+ = 255.15 0.01 corresponding to lysergol/isolysergol, elymoclavine, setoclavine/isosetoclavine or molliclavine as well as [M+H]+ = 269.13 0.01 corresponding to lysergic acid were only obtained in the DF extracts and the resolution and the quality of the EICs and product spectra was poor. Therefore, the presence of lysergol/isolysergol, elymoclavine, setoclavine/isosetoclavine, molliclavine or lysergic acid cannot be excluded, but proof cannot be provided and additional research will be necessary.” (3.1. Mass spectrometry data, pages 65 & 68)    {{cite journal}}: CS1 maint: postscript (link)
  • Paulke, Alexander; et al. (2015). "Studies on the alkaloid composition of the Hawaiian Baby Woodrose Argyreia nervosa, a common legal high". Forensic Science International. 249: 281–293. doi:10.1016/j.forsciint.2015.02.011. PMID 25747328
    “On the other hand, methylergometrine, methysergide, and lysergylalanine were detected, which have not yet been reported as compounds of Argyreia nervosa seeds. Furthermore, some high molecular weight ergot alkaloid derivatives and hydroxyalanine derived ergopeptide fragments could be observed at various retention times (c.f. chapter 3.1). Altogether, lysergylalanine, the high molecular weight ergot alkaloids and the hydroxyalanine derived ergopeptide fragments strongly suggest the presence of ergopeptides in Argyreia nervosa. However, due to the disadvantage of the applied APCI technique for peptide analysis (c.f. chapter 3.1) additional research (e.g. ESI-HRMS/MS) will be necessary to verify this assumption and to elucidate the structure of the ergopeptides.” (3. Results and discussion, p. 283)    {{cite journal}}: CS1 maint: postscript (link)
  • Nowak, Julia; Woźniakiewicz, Michał; Klepacki, Piotr; Sowa, Anna; Kościelniak, Paweł (May 2016). "Identification and determination of ergot alkaloids in Morning Glory cultivars". Analytical and Bioanalytical Chemistry. 408 (12): 3093–3102. doi:10.1007/s00216-016-9322-5. ISSN 1618-2642. PMC 4830885. PMID 26873205"ergine and ergometrine concentration is 12-fold lower in plant samples than in seeds." Analysis of IP-HB2 young plants{{cite journal}}: CS1 maint: postscript (link)
  • Rahman, A.; Ali, M.; Khan, N. Z. (2003). "Argyroside from Argyreia nervosa Seeds". ChemInform. 34 (21): 60–2. doi:10.1002/chin.200321168. ISSN 0931-7597. PMID 12622256.
  • Paulke, Alexander; Kremer, Christian; Wunder, Cora; Wurglics, Mario; Schubert-Zsilavecz, Manfred; Toennes, Stefan W. (2014). "Identification of legal highs--ergot alkaloid patterns in two Argyreia nervosa products". Forensic Science International. 242: 62–71. doi:10.1016/j.forsciint.2014.06.025. ISSN 1872-6283. PMID 25036782.
  • Bharati, A. J.; Bansal, Y. K. (2014). "Phytochemical investigation of natural and in vitro raised Vṛddhadāruka plants". Ancient Science of Life. 34 (2): 80–84. doi:10.4103/0257-7941.153463. PMC 4389397. PMID 25861141.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

  • Halpern, J.H. (2004). "Hallucinogens and dissociative agents naturally growing in the United States". Pharmacology & Therapeutics. 102 (2): 131–138. doi:10.1016/j.pharmthera.2004.03.003. PMID 15163594. S2CID 30734515. Although LSD does not occur in nature, a close analogue, lysergic acid amide (LSA, ergine) is found in the seeds of Argyreia nervosa (Hawaiian baby woodrose)

web.archive.org

worldcat.org

search.worldcat.org

  • Paulke, Alexander; Kremer, Christian; Wunder, Cora; Wurglics, Mario; Schubert-Zsilavecz, Manfred; Toennes, Stefan W. (2014-09-01). "Identification of legal highs – Ergot alkaloid patterns in two Argyreia nervosa products". Forensic Science International. 242: 62–71. doi:10.1016/j.forsciint.2014.06.025. ISSN 0379-0738. PMID 25036782
    “Additionally the presence of the ergot alkaloid diastereomers chanoclavine I and II was assumed in DF (cf. Fig. 6) together with traces of lysergic acid and the isobars lysergol, isolysergol, elymoclavine, molliclavine, setoclavine, or isosetoclavine.” (3.1. Mass spectrometry data, p. 65)
    “Indications of traces of [M+H]+ = 255.15 0.01 corresponding to lysergol/isolysergol, elymoclavine, setoclavine/isosetoclavine or molliclavine as well as [M+H]+ = 269.13 0.01 corresponding to lysergic acid were only obtained in the DF extracts and the resolution and the quality of the EICs and product spectra was poor. Therefore, the presence of lysergol/isolysergol, elymoclavine, setoclavine/isosetoclavine, molliclavine or lysergic acid cannot be excluded, but proof cannot be provided and additional research will be necessary.” (3.1. Mass spectrometry data, pages 65 & 68)    {{cite journal}}: CS1 maint: postscript (link)
  • Nowak, Julia; Woźniakiewicz, Michał; Klepacki, Piotr; Sowa, Anna; Kościelniak, Paweł (May 2016). "Identification and determination of ergot alkaloids in Morning Glory cultivars". Analytical and Bioanalytical Chemistry. 408 (12): 3093–3102. doi:10.1007/s00216-016-9322-5. ISSN 1618-2642. PMC 4830885. PMID 26873205"ergine and ergometrine concentration is 12-fold lower in plant samples than in seeds." Analysis of IP-HB2 young plants{{cite journal}}: CS1 maint: postscript (link)
  • Rahman, A.; Ali, M.; Khan, N. Z. (2003). "Argyroside from Argyreia nervosa Seeds". ChemInform. 34 (21): 60–2. doi:10.1002/chin.200321168. ISSN 0931-7597. PMID 12622256.
  • Paulke, Alexander; Kremer, Christian; Wunder, Cora; Wurglics, Mario; Schubert-Zsilavecz, Manfred; Toennes, Stefan W. (2014). "Identification of legal highs--ergot alkaloid patterns in two Argyreia nervosa products". Forensic Science International. 242: 62–71. doi:10.1016/j.forsciint.2014.06.025. ISSN 1872-6283. PMID 25036782.