메뉴 건너뛰기




Volumn 117, Issue , 2015, Pages 194-199

Minor oxygenated cannabinoids from high potency Cannabis sativa L.

Author keywords

Anti bacterial; Anti leishmanial; Anti malarial; Cananbis; Cannabaceae; Cannabis sativa; High potency; Oxygenated cannabinoids

Indexed keywords

BACTERIA (MICROORGANISMS); CANNABACEAE; CANNABIS SATIVA; PLASMODIUM FALCIPARUM;

EID: 84935873694     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2015.04.007     Document Type: Article
Times cited : (71)

References (18)
  • 2
    • 50549083095 scopus 로고    scopus 로고
    • Structure determination and absolute configuration of cannabichromanone derivatives from high potency Cannabis sativa
    • S.A. Ahmed, S.A. Ross, D. Slade, M.M. Radwan, A.K. Ikhlas, and M.A. ElSohly Structure determination and absolute configuration of cannabichromanone derivatives from high potency Cannabis sativa Tetrahedron Lett. 49 2008 6050 6053
    • (2008) Tetrahedron Lett. , vol.49 , pp. 6050-6053
    • Ahmed, S.A.1    Ross, S.A.2    Slade, D.3    Radwan, M.M.4    Ikhlas, A.K.5    Elsohly, M.A.6
  • 4
    • 33947085552 scopus 로고
    • Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and.alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters
    • J.A. Dale, and H.S.J. Mosher Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and.alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters J. Am. Chem. Soc. 95 1973 512
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 512
    • Dale, J.A.1    Mosher, H.S.J.2
  • 5
    • 84933058635 scopus 로고    scopus 로고
    • Constituents of Cannabis Sativa
    • R.G. Pertwee, Oxford University Press
    • M.A. ElSohly, and W. Gul Constituents of Cannabis Sativa R.G. Pertwee, Handbook of Cannabis 2014 Oxford University Press 3 22
    • (2014) Handbook of Cannabis , pp. 3-22
    • Elsohly, M.A.1    Gul, W.2
  • 6
    • 27844525479 scopus 로고    scopus 로고
    • Chemical constituents of marijuana: The complex mixture of natural cannabinoids
    • M.A. ElSohly, and D. Slade Chemical constituents of marijuana: the complex mixture of natural cannabinoids Life Sci. 78 2005 539 548
    • (2005) Life Sci. , vol.78 , pp. 539-548
    • Elsohly, M.A.1    Slade, D.2
  • 7
    • 33644945013 scopus 로고    scopus 로고
    • New one-carbon degradative transformation of β-alkyl-β-azido alcohols
    • Q. Fan, N. Ni, Q. Li, L. Zhang, and Xin.-Shan. Ye New one-carbon degradative transformation of β-alkyl-β-azido alcohols Org. Lett. 8 2006 1007 1009
    • (2006) Org. Lett. , vol.8 , pp. 1007-1009
    • Fan, Q.1    Ni, N.2    Li, Q.3    Zhang, L.4    Ye Xin.-Shan.5
  • 8
    • 0015430982 scopus 로고
    • Metabolism of (-)-DELTA.9- and (-)-.DELTA.8-tetrahydrocannabinol by monkey liver
    • O. Gurny, D.E. Maynard, R.G. Pitcher, and R.W. Kieerstead Metabolism of (-)-DELTA.9- and (-)-.DELTA.8-tetrahydrocannabinol by monkey liver J. Am. Chem. Soc. 94 22 1972 7928 7935
    • (1972) J. Am. Chem. Soc. , vol.94 , Issue.22 , pp. 7928-7935
    • Gurny, O.1    Maynard, D.E.2    Pitcher, R.G.3    Kieerstead, R.W.4
  • 9
    • 38449102399 scopus 로고    scopus 로고
    • Mosher ester analysis for the determination of absolute configuration of stereogenic (A.K.A. Chiral) carbinol carbons
    • T.R. Hoye, C.S. Jeffrey, and F. Shao Mosher ester analysis for the determination of absolute configuration of stereogenic (a.k.a. Chiral) carbinol carbons Nat. Protoc. 2 2007 2451 2458
    • (2007) Nat. Protoc. , vol.2 , pp. 2451-2458
    • Hoye, T.R.1    Jeffrey, C.S.2    Shao, F.3
  • 11
    • 0014061503 scopus 로고
    • The absolute configuration of Δ1-tetra-hydrocannabinol, the major active constituent of hashish
    • R. Mechoulam, and Y. Gaoni The absolute configuration of Δ1-tetra-hydrocannabinol, the major active constituent of hashish Tetrahedron Lett. 8 12 1967 1109 1111
    • (1967) Tetrahedron Lett. , vol.8 , Issue.12 , pp. 1109-1111
    • Mechoulam, R.1    Gaoni, Y.2
  • 13
    • 41349085587 scopus 로고    scopus 로고
    • Isolation and characterization of new cannabis constituents from a high potency variety
    • M.M. Radwan, S.A. Ross, S.A. Ahmed, D. Slade, F. Zulfiqar, and M.A. ElSohly Isolation and characterization of new cannabis constituents from a high potency variety Planta Med. 74 2008 267 272
    • (2008) Planta Med. , vol.74 , pp. 267-272
    • Radwan, M.M.1    Ross, S.A.2    Ahmed, S.A.3    Slade, D.4    Zulfiqar, F.5    Elsohly, M.A.6
  • 15
    • 0002720261 scopus 로고
    • Constituents of Cannabis sativa L. XXVII. A review of the natural constituents: 1980-1994
    • S.A. Ross, and M.A. ElSohly Constituents of Cannabis sativa L. XXVII. A review of the natural constituents: 1980-1994 Zagazig J. Pharm. Sci. 4 1995 1 10
    • (1995) Zagazig J. Pharm. Sci. , vol.4 , pp. 1-10
    • Ross, S.A.1    Elsohly, M.A.2
  • 16
    • 0942277395 scopus 로고    scopus 로고
    • The assignment of absolute configuration by NMR
    • J.M. Seco, E. Quinoa, and R. Riguera The assignment of absolute configuration by NMR Chem. Rev. 104 2004 17 117
    • (2004) Chem. Rev. , vol.104 , pp. 17-117
    • Seco, J.M.1    Quinoa, E.2    Riguera, R.3
  • 17
    • 33947086629 scopus 로고
    • Selectivity, strategy, and efficiency in modem organic chemistry
    • G.R. Sullivan, J.A. Dale, and H.S.J. Mosher Selectivity, strategy, and efficiency in modem organic chemistry J. Org. Chem. 38 1973 2143
    • (1973) J. Org. Chem. , vol.38 , pp. 2143
    • Sullivan, G.R.1    Dale, J.A.2    Mosher, H.S.J.3
  • 18
    • 0017318105 scopus 로고
    • Transformations of 9α,10α-epoxy-hexahydrocannabinol acetate helv
    • P. Theodor, K. Kapa, and S. Gerard Transformations of 9α,10α-epoxy-hexahydrocannabinol acetate helv Chim. Acta 59 6 1976 1963
    • (1976) Chim. Acta , vol.59 , Issue.6 , pp. 1963
    • Theodor, P.1    Kapa, K.2    Gerard, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.