메뉴 건너뛰기




Volumn 72, Issue 6-7, 2007, Pages 524-534

New oxypregnane glycosides from appetite suppressant herbal supplement Hoodia gordonii

Author keywords

Asclepiadaceae; Hoodia gordonii; Hoodigosides A K; Oxypregnane; P57AS3

Indexed keywords

12 O BETA TIGLOYL 3BETA, 14BETA DIHYDROXY PREGN 5 EN 20 ONE; ANOREXIGENIC AGENT; BETA DEXTRO CYMAROPYRANOSE; BETA DEXTRO DIGITOXOYRANOSE; BETA DEXTRO GLUCOPYRANOSE; BETA DEXTRO OLEANDROPYRANOSE; BETA DEXTRO THEVETOPYRANOSE; DEOXYSUGAR; GLUCOSE; GLYCOSIDE; HERBACEOUS AGENT; OXYPREGNANE GLYCOSIDE DERIVATIVE; P 57AS3; PLANT EXTRACT; UNCLASSIFIED DRUG;

EID: 34248554412     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2007.03.003     Document Type: Article
Times cited : (56)

References (19)
  • 2
    • 34248538895 scopus 로고    scopus 로고
    • Van Heerden FR, Vleggaar R, Horak RM, Learmonth RA, Maharaj V, Whittal RD, inventor; (CSIR, South Africa) assignee. Steroidal glycosides, methods for their production and preparation, pharmaceutical compositions containing them, and their use as appetite suppressants. WO 98/46243 (1998).
  • 3
    • 4143129845 scopus 로고    scopus 로고
    • Increased ATP content/production in the hypothalamus may be a signal for energy-sensing of satiety: studies of the anorectic mechanism of a plant steroidal glycoside
    • MacLean D.B., and Luo L.-G. Increased ATP content/production in the hypothalamus may be a signal for energy-sensing of satiety: studies of the anorectic mechanism of a plant steroidal glycoside. Brain Res 1020 (2004) 1-11
    • (2004) Brain Res , vol.1020 , pp. 1-11
    • MacLean, D.B.1    Luo, L.-G.2
  • 4
    • 34248509606 scopus 로고    scopus 로고
    • Rubin ID, Cawthorne MA, Bindra JS, inventor; (Phytopharm PLC, UK) assignee. Extracts, compounds & pharmaceutical compositions having anti-diabetic activity and their use. EP 1 166 792 A2 (2001).
  • 5
    • 34248521375 scopus 로고    scopus 로고
    • Horak RM, Maharaj V, Hakkinen J, inventor; (Phytopharm Plc, UK) assignee. Steroidal glycosides or plant extracts for treatment of gastric acid secretion damage. EP 1 099 444 A1 (2000).
  • 6
    • 33750711741 scopus 로고    scopus 로고
    • Determination of the appetite suppressant P57 in Hoodia gordonii plant extracts and dietary supplements by liquid chromatography/electrospray ionization mass spectrometry (LC-MSD-TOF) and LC-UV methods
    • Avula B., Wang Y.-H., Pawar R.S., Shukla Y.J., Schaneberg B., and Khan I.A. Determination of the appetite suppressant P57 in Hoodia gordonii plant extracts and dietary supplements by liquid chromatography/electrospray ionization mass spectrometry (LC-MSD-TOF) and LC-UV methods. J AOAC Int 89 (2006) 606-611
    • (2006) J AOAC Int , vol.89 , pp. 606-611
    • Avula, B.1    Wang, Y.-H.2    Pawar, R.S.3    Shukla, Y.J.4    Schaneberg, B.5    Khan, I.A.6
  • 7
    • 33947488027 scopus 로고
    • Quantitative determination of monosaccharides as their alditol acetates by gas liquid chromatography
    • Sawardekar J.S., Sloneker J.H., and Jeanes A. Quantitative determination of monosaccharides as their alditol acetates by gas liquid chromatography. Anal Chem 37 (1965) 1602-1604
    • (1965) Anal Chem , vol.37 , pp. 1602-1604
    • Sawardekar, J.S.1    Sloneker, J.H.2    Jeanes, A.3
  • 8
    • 85008120457 scopus 로고
    • Gas-liquid chromatographic separations of aldose enantiomers as trimethylsilyl ethers of methyl 2-(polyhydroxyalkyl)-thiazolidine-4(R)-carboxylates
    • Hara S., Okabe H., and Mihashi K. Gas-liquid chromatographic separations of aldose enantiomers as trimethylsilyl ethers of methyl 2-(polyhydroxyalkyl)-thiazolidine-4(R)-carboxylates. Chem Pharm Bull 35 (1987) 501-506
    • (1987) Chem Pharm Bull , vol.35 , pp. 501-506
    • Hara, S.1    Okabe, H.2    Mihashi, K.3
  • 9
    • 20444506015 scopus 로고    scopus 로고
    • Synthesis, antimalarial, antileishmanial, and antimicrobial activities of some 8-quinolinamine analogues
    • Jain M., Khan S.I., Tekwani B.L., Jacob M.R., Singh S., Singh P.P., et al. Synthesis, antimalarial, antileishmanial, and antimicrobial activities of some 8-quinolinamine analogues. Bioorg Med Chem 13 (2005) 4458-4466
    • (2005) Bioorg Med Chem , vol.13 , pp. 4458-4466
    • Jain, M.1    Khan, S.I.2    Tekwani, B.L.3    Jacob, M.R.4    Singh, S.5    Singh, P.P.6
  • 11
    • 0013818648 scopus 로고
    • Studies on the constituents of asclepiadaceae plants. XVI. On the components of Metaplexis japonica MAKINO. III. The structure of benzoylramanone
    • Mitsuhashi H., and Nomura T. Studies on the constituents of asclepiadaceae plants. XVI. On the components of Metaplexis japonica MAKINO. III. The structure of benzoylramanone. Chem Pharm Bull 13 (1965) 1332-1340
    • (1965) Chem Pharm Bull , vol.13 , pp. 1332-1340
    • Mitsuhashi, H.1    Nomura, T.2
  • 12
    • 0034624465 scopus 로고    scopus 로고
    • Steroidal glycosides from the aerial part of Asclepias incarnata
    • Warashina T., and Noro T. Steroidal glycosides from the aerial part of Asclepias incarnata. Phytochemistry 53 (2000) 485-498
    • (2000) Phytochemistry , vol.53 , pp. 485-498
    • Warashina, T.1    Noro, T.2
  • 14
    • 18444381437 scopus 로고    scopus 로고
    • NMR spectroscopy in the study of carbohydrates: characterizing the structural complexity
    • Bubb W.A. NMR spectroscopy in the study of carbohydrates: characterizing the structural complexity. Concepts Magn Reson Part A 19A (2003) 1-19
    • (2003) Concepts Magn Reson Part A , vol.19 A , pp. 1-19
    • Bubb, W.A.1
  • 15
    • 9644301102 scopus 로고    scopus 로고
    • Stemmosides C and D, two novel unusual pregnane glycosides from Solenostemma argel: structural elucidation and configurational study by a combined NMR-quantum mechanical strategy
    • Plaza A., Piacente S., Perrone A., Hamed A., Pizza C., and Bifulco G. Stemmosides C and D, two novel unusual pregnane glycosides from Solenostemma argel: structural elucidation and configurational study by a combined NMR-quantum mechanical strategy. Tetrahedron 60 (2004) 12201-12209
    • (2004) Tetrahedron , vol.60 , pp. 12201-12209
    • Plaza, A.1    Piacente, S.2    Perrone, A.3    Hamed, A.4    Pizza, C.5    Bifulco, G.6
  • 17
    • 0001425971 scopus 로고
    • Four pregnane glycosides, boucerosides AI, AII, BI and BII, from Boucerosia aucheriana
    • Hayashi K., Iida I., Nakao Y., Nakao Y., and Kaneko K. Four pregnane glycosides, boucerosides AI, AII, BI and BII, from Boucerosia aucheriana. Phytochemistry 27 (1988) 3919-3924
    • (1988) Phytochemistry , vol.27 , pp. 3919-3924
    • Hayashi, K.1    Iida, I.2    Nakao, Y.3    Nakao, Y.4    Kaneko, K.5
  • 18
    • 0034097316 scopus 로고    scopus 로고
    • Cardenolide and oxypregnane glycosides from the root of Asclepias incarnata L
    • Warashina T., and Noro T. Cardenolide and oxypregnane glycosides from the root of Asclepias incarnata L. Chem Pharm Bull 48 (2000) 516-524
    • (2000) Chem Pharm Bull , vol.48 , pp. 516-524
    • Warashina, T.1    Noro, T.2
  • 19
    • 0025059062 scopus 로고
    • Cardiac glycosides of Beaumontia brevituba and B. Murtonii
    • Yamauchi T., Abe F., and Santisuk T. Cardiac glycosides of Beaumontia brevituba and B. Murtonii. Phytochemistry 29 (1990) 1961-1965
    • (1990) Phytochemistry , vol.29 , pp. 1961-1965
    • Yamauchi, T.1    Abe, F.2    Santisuk, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.