Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 10 of 10 entries
Sorted by: Best Match Show Resources per page
Isolation and identification of oviposition deterrents to cabbage butterfly,Pieris rapae, fromErysimum cheiranthoides.

Journal of chemical ecology

Sachdev-Gupta K, Renwick JA, Radke CD.
PMID: 24263711
J Chem Ecol. 1990 Apr;16(4):1059-67. doi: 10.1007/BF01021010.

Avoidance of some crucifer species by the crucifer specialist,Pieris rapae, has been attributed to the presence of oviposition deterrents in these plants. Studies on one such unacceptable plant,Erysimum cheiranthoides, have resulted in the isolation ofn-butanol-soluble deterrents from the alcoholic...

Cite
Sachdev-Gupta K, Renwick JA, Radke CD. Isolation and identification of oviposition deterrents to cabbage butterfly,Pieris rapae, fromErysimum cheiranthoides. J Chem Ecol. 1990;16(4):1059-67doi: 10.1007/BF01021010.
Sachdev-Gupta, K., Renwick, J. A., & Radke, C. D. (1990). Isolation and identification of oviposition deterrents to cabbage butterfly,Pieris rapae, fromErysimum cheiranthoides. Journal of chemical ecology, 16(4), 1059-67. https://doi.org/10.1007/BF01021010
Sachdev-Gupta, K, et al. "Isolation and identification of oviposition deterrents to cabbage butterfly,Pieris rapae, fromErysimum cheiranthoides." Journal of chemical ecology vol. 16,4 (1990): 1059-67. doi: https://doi.org/10.1007/BF01021010
Sachdev-Gupta K, Renwick JA, Radke CD. Isolation and identification of oviposition deterrents to cabbage butterfly,Pieris rapae, fromErysimum cheiranthoides. J Chem Ecol. 1990 Apr;16(4):1059-67. doi: 10.1007/BF01021010. PMID: 24263711.
Copy Download .nbib Format: NLM
Cardiac glycosides from erysimum cheiranthoides.

Phytochemistry

Lei ZH, Jin ZX, Ma YL, Tai BS, Kong Q, Yahara S, Nohara T.
PMID: 11711105
Phytochemistry. 1998 Nov 20;49(6):1801-1803. doi: 10.1016/s0031-9422(98)00264-7.

Two new cardiac glycosides were isolated from the seeds of Erysimum cheiranthoides. Their structures were characterized as strophanthidin glycosides of 3-O-alpha-L-rhamnopyranosyl-(1-->4)-3-O-acetyl-beta-D-digitoxopyranosyl and 3-O-beta-D-glucpyranosyl-(1-->4)-alpha-L-rhamnopyranosyl-(1-->4)-3-O-acetyl-beta-D-digitoxopyranosyl.

Cite
Lei ZH, Jin ZX, Ma YL, et al. Cardiac glycosides from erysimum cheiranthoides. Phytochemistry. 1998;49(6):1801-1803doi: 10.1016/s0031-9422(98)00264-7.
Lei, Z. H., Jin, Z. X., Ma, Y. L., Tai, B. S., Kong, Q., Yahara, S., & Nohara, T. (1998). Cardiac glycosides from erysimum cheiranthoides. Phytochemistry, 49(6), 1801-1803. https://doi.org/10.1016/s0031-9422(98)00264-7
Lei, Zhen Huan, et al. "Cardiac glycosides from erysimum cheiranthoides." Phytochemistry vol. 49,6 (1998): 1801-1803. doi: https://doi.org/10.1016/s0031-9422(98)00264-7
Lei ZH, Jin ZX, Ma YL, Tai BS, Kong Q, Yahara S, Nohara T. Cardiac glycosides from erysimum cheiranthoides. Phytochemistry. 1998 Nov 20;49(6):1801-1803. doi: 10.1016/s0031-9422(98)00264-7. PMID: 11711105.
Copy Download .nbib Format: NLM
Role of Intracellular Sodium Activity in the Control of Contraction in Cardiac Purkinje Fibers.

Journal of biomedical science

Abete P, Vassalle M.
PMID: 11725004
J Biomed Sci. 1994 Dec;1(1):28-42. doi: 10.1007/BF02258337.

The role of intracellular sodium activity (a(i)(Na)) in the control of force was studied in sheep cardiac Purkinje fibers exposed to norepinephrine (NE) and high [Ca](o) in the absence and presence of overdrive or of a low concentration of...

Cite
Abete P, Vassalle M. Role of Intracellular Sodium Activity in the Control of Contraction in Cardiac Purkinje Fibers. J Biomed Sci. 1994;1(1):28-42doi: 10.1007/BF02258337.
Abete, P., & Vassalle, M. (1994). Role of Intracellular Sodium Activity in the Control of Contraction in Cardiac Purkinje Fibers. Journal of biomedical science, 1(1), 28-42. https://doi.org/10.1007/BF02258337
Abete, P., and Vassalle, M.. "Role of Intracellular Sodium Activity in the Control of Contraction in Cardiac Purkinje Fibers." Journal of biomedical science vol. 1,1 (1994): 28-42. doi: https://doi.org/10.1007/BF02258337
Abete P, Vassalle M. Role of Intracellular Sodium Activity in the Control of Contraction in Cardiac Purkinje Fibers. J Biomed Sci. 1994 Dec;1(1):28-42. doi: 10.1007/BF02258337. PMID: 11725004.
Copy Download .nbib Format: NLM
Cesium, Na(+)-K(+) Pump and Pacemaker Potential in Cardiac Purkinje Fibers.

Journal of biomedical science

Sternlicht JP, Vassalle M.
PMID: 11725074
J Biomed Sci. 1995 Oct;2(4):366-378. doi: 10.1007/BF02255224.

The mechanisms of the hyperpolarizing and depolarizing actions of cesium were studied in cardiac Purkinje fibers perfused in vitro by means of a microelectrode technique under conditions that modify either the Na(+)-K(+) pump activity or I(f). Cs(+) (2 mM)...

Cite
Sternlicht JP, Vassalle M. Cesium, Na(+)-K(+) Pump and Pacemaker Potential in Cardiac Purkinje Fibers. J Biomed Sci. 1995;2(4):366-378doi: 10.1007/BF02255224.
Sternlicht, J. P., & Vassalle, M. (1995). Cesium, Na(+)-K(+) Pump and Pacemaker Potential in Cardiac Purkinje Fibers. Journal of biomedical science, 2(4), 366-378. https://doi.org/10.1007/BF02255224
Sternlicht, J.P., and Vassalle, M.. "Cesium, Na(+)-K(+) Pump and Pacemaker Potential in Cardiac Purkinje Fibers." Journal of biomedical science vol. 2,4 (1995): 366-378. doi: https://doi.org/10.1007/BF02255224
Sternlicht JP, Vassalle M. Cesium, Na(+)-K(+) Pump and Pacemaker Potential in Cardiac Purkinje Fibers. J Biomed Sci. 1995 Oct;2(4):366-378. doi: 10.1007/BF02255224. PMID: 11725074.
Copy Download .nbib Format: NLM
The two available through degradation of strophanthidine, 3 beta, 5,14-trioxy-14-iso-21-norpregnan-19,20-diacids, isomeric at C-17; Glycosides and aglycons.

Helvetica chimica acta

BUZAS A, REICHSTEIN T.
PMID: 18912370
Helv Chim Acta. 1948;31(1):84-90. doi: 10.1002/hlca.19480310117.

No abstract available.

Cite
BUZAS A, REICHSTEIN T. Die zwei durch Abbau von Strophanthidin erhältlichen, an C-17 raumisomeren 3 beta,5,14-Trioxy-14-iso-21-norpregnan-19,20-disäuren; Glykoside und Aglykone. The two available through degradation of strophanthidine, 3 beta, 5,14-trioxy-14-iso-21-norpregnan-19,20-diacids, isomeric at C-17; Glycosides and aglycons. Helv Chim Acta. 1948;31(1):84-90doi: 10.1002/hlca.19480310117.
BUZAS, A., & REICHSTEIN, T. (1948). Die zwei durch Abbau von Strophanthidin erhältlichen, an C-17 raumisomeren 3 beta,5,14-Trioxy-14-iso-21-norpregnan-19,20-disäuren; Glykoside und Aglykone. The two available through degradation of strophanthidine, 3 beta, 5,14-trioxy-14-iso-21-norpregnan-19,20-diacids, isomeric at C-17; Glycosides and aglycons. Helvetica chimica acta, 31(1), 84-90. https://doi.org/10.1002/hlca.19480310117
BUZAS, A, and REICHSTEIN, T. "Die zwei durch Abbau von Strophanthidin erhältlichen, an C-17 raumisomeren 3 beta,5,14-Trioxy-14-iso-21-norpregnan-19,20-disäuren; Glykoside und Aglykone." The two available through degradation of strophanthidine, 3 beta, 5,14-trioxy-14-iso-21-norpregnan-19,20-diacids, isomeric at C-17; Glycosides and aglycons. Helvetica chimica acta vol. 31,1 (1948): 84-90. doi: https://doi.org/10.1002/hlca.19480310117
BUZAS A, REICHSTEIN T. Die zwei durch Abbau von Strophanthidin erhältlichen, an C-17 raumisomeren 3 beta,5,14-Trioxy-14-iso-21-norpregnan-19,20-disäuren; Glykoside und Aglykone. The two available through degradation of strophanthidine, 3 beta, 5,14-trioxy-14-iso-21-norpregnan-19,20-diacids, isomeric at C-17; Glycosides and aglycons. Helv Chim Acta. 1948;31(1):84-90. doi: 10.1002/hlca.19480310117. German. PMID: 18912370.
Copy Download .nbib Format: NLM
STROPHANTHIN. XXIX. THE DEHYDROGENATION OF STROPHANTHIDIN.

Science (New York, N.Y.)

Elderfield RC, Jacobs WA.
PMID: 17837452
Science. 1934 Mar 23;79(2047):279-80. doi: 10.1126/science.79.2047.279.

No abstract available.

Cite
Elderfield RC, Jacobs WA. STROPHANTHIN. XXIX. THE DEHYDROGENATION OF STROPHANTHIDIN. Science. 1934;79(2047):279-80doi: 10.1126/science.79.2047.279.
Elderfield, R. C., & Jacobs, W. A. (1934). STROPHANTHIN. XXIX. THE DEHYDROGENATION OF STROPHANTHIDIN. Science (New York, N.Y.), 79(2047), 279-80. https://doi.org/10.1126/science.79.2047.279
Elderfield, R C, and Jacobs, W A. "STROPHANTHIN. XXIX. THE DEHYDROGENATION OF STROPHANTHIDIN." Science (New York, N.Y.) vol. 79,2047 (1934): 279-80. doi: https://doi.org/10.1126/science.79.2047.279
Elderfield RC, Jacobs WA. STROPHANTHIN. XXIX. THE DEHYDROGENATION OF STROPHANTHIDIN. Science. 1934 Mar 23;79(2047):279-80. doi: 10.1126/science.79.2047.279. PMID: 17837452.
Copy Download .nbib Format: NLM
Cardenolides as oviposition deterrents to twoPieris species: Structure-activity relationships.

Journal of chemical ecology

Huang X, Renwick JA.
PMID: 24242301
J Chem Ecol. 1994 May;20(5):1039-51. doi: 10.1007/BF02059740.

Oviposition responses ofPieris rapae andP. napi oleracea to 18 cardenolides were compared under the same conditions. Effects of different concentrations of selected cardenolides were also tested. Most of the compounds were deterrent to oviposition by both insects, but to...

Cite
Huang X, Renwick JA. Cardenolides as oviposition deterrents to twoPieris species: Structure-activity relationships. J Chem Ecol. 1994;20(5):1039-51doi: 10.1007/BF02059740.
Huang, X., & Renwick, J. A. (1994). Cardenolides as oviposition deterrents to twoPieris species: Structure-activity relationships. Journal of chemical ecology, 20(5), 1039-51. https://doi.org/10.1007/BF02059740
Huang, X, and Renwick, J A. "Cardenolides as oviposition deterrents to twoPieris species: Structure-activity relationships." Journal of chemical ecology vol. 20,5 (1994): 1039-51. doi: https://doi.org/10.1007/BF02059740
Huang X, Renwick JA. Cardenolides as oviposition deterrents to twoPieris species: Structure-activity relationships. J Chem Ecol. 1994 May;20(5):1039-51. doi: 10.1007/BF02059740. PMID: 24242301.
Copy Download .nbib Format: NLM
STROPHANTHIN. XIX. THE DEHYDROGENATION OF STROPHANTHIDIN AND GITOXIGENIN.

Science (New York, N.Y.)

Jacobs WA, Fleck EE.
PMID: 17802370
Science. 1931 Jan 30;73(1883):133-4. doi: 10.1126/science.73.1883.133.

No abstract available.

Cite
Jacobs WA, Fleck EE. STROPHANTHIN. XIX. THE DEHYDROGENATION OF STROPHANTHIDIN AND GITOXIGENIN. Science. 1931;73(1883):133-4doi: 10.1126/science.73.1883.133.
Jacobs, W. A., & Fleck, E. E. (1931). STROPHANTHIN. XIX. THE DEHYDROGENATION OF STROPHANTHIDIN AND GITOXIGENIN. Science (New York, N.Y.), 73(1883), 133-4. https://doi.org/10.1126/science.73.1883.133
Jacobs, W A, and Fleck, E E. "STROPHANTHIN. XIX. THE DEHYDROGENATION OF STROPHANTHIDIN AND GITOXIGENIN." Science (New York, N.Y.) vol. 73,1883 (1931): 133-4. doi: https://doi.org/10.1126/science.73.1883.133
Jacobs WA, Fleck EE. STROPHANTHIN. XIX. THE DEHYDROGENATION OF STROPHANTHIDIN AND GITOXIGENIN. Science. 1931 Jan 30;73(1883):133-4. doi: 10.1126/science.73.1883.133. PMID: 17802370.
Copy Download .nbib Format: NLM
[New cardenolides from Convallaria majalis].

Planta medica

Kopp B, Kubelka W.
PMID: 17396911
Planta Med. 1982 Aug;45(4):195-202. doi: 10.1055/s-2007-971372.

From the leaves of Convallaria majalis L. eight glycosides of strophanthidin, cannogenol, sarmentogenin and 19-hydroxysarmentogenin, resp., were isolated and structurally elucidated as strophanthidin-3-O-6'-deoxy-beta-D-allosido-alpha-L-rhamnoside, strophanthidin-3-O-6'-deoxy-beta-D-allosido-alpha-L-arabinoside, strophanthidin-3-O-alpha-L-rhamnosido-2'-beta-D-glucoside, cannogenol-3-O-6'-deoxy-beta-D-allosido-beta-D-glucoside, cannogenol-3-O-6'-deoxy-beta-D-allosido-alpha-L-rhamnoside, 19-hydroxy-sarmentogenin-3-O-alpha-L-rhamnoside, sarmentogenin-3-O-6'-deoxy-beta-D-allosido-alpha-L-rhamnoside and sarmentogenin-3-O-6'-deoxy-beta-D-guloside, mainly by means of their H-NMR-spectra, by EI-MS...

Cite
Kopp B, Kubelka W. Neue Cardenolide aus Convallaria majalis. [New cardenolides from Convallaria majalis]. Planta Med. 1982;45(4):195-202doi: 10.1055/s-2007-971372.
Kopp, B., & Kubelka, W. (1982). Neue Cardenolide aus Convallaria majalis. [New cardenolides from Convallaria majalis]. Planta medica, 45(4), 195-202. https://doi.org/10.1055/s-2007-971372
Kopp, B, and Kubelka, W. "Neue Cardenolide aus Convallaria majalis." [New cardenolides from Convallaria majalis]. Planta medica vol. 45,4 (1982): 195-202. doi: https://doi.org/10.1055/s-2007-971372
Kopp B, Kubelka W. Neue Cardenolide aus Convallaria majalis. [New cardenolides from Convallaria majalis]. Planta Med. 1982 Aug;45(4):195-202. doi: 10.1055/s-2007-971372. German. PMID: 17396911.
Copy Download .nbib Format: NLM
Strophanthidin Attenuates MAPK, PI3K/AKT/mTOR, and Wnt/β-Catenin Signaling Pathways in Human Cancers.

Frontiers in oncology

Reddy D, Ghosh P, Kumavath R.
PMID: 32010609
Front Oncol. 2020 Jan 17;9:1469. doi: 10.3389/fonc.2019.01469. eCollection 2019.

Lung cancer is the most prevalent in cancer-related deaths, while breast carcinoma is the second most dominant cancer in women, accounting for the most number of deaths worldwide. Cancers are heterogeneous diseases that consist of several subtypes based on...

Cite
Reddy D, Ghosh P, Kumavath R. Strophanthidin Attenuates MAPK, PI3K/AKT/mTOR, and Wnt/β-Catenin Signaling Pathways in Human Cancers. Front Oncol. 2020;9:1469doi: 10.3389/fonc.2019.01469.
Reddy, D., Ghosh, P., & Kumavath, R. (2019). Strophanthidin Attenuates MAPK, PI3K/AKT/mTOR, and Wnt/β-Catenin Signaling Pathways in Human Cancers. Frontiers in oncology, 91469. https://doi.org/10.3389/fonc.2019.01469
Reddy, Dhanasekhar, et al. "Strophanthidin Attenuates MAPK, PI3K/AKT/mTOR, and Wnt/β-Catenin Signaling Pathways in Human Cancers." Frontiers in oncology vol. 9 (2019): 1469. doi: https://doi.org/10.3389/fonc.2019.01469
Reddy D, Ghosh P, Kumavath R. Strophanthidin Attenuates MAPK, PI3K/AKT/mTOR, and Wnt/β-Catenin Signaling Pathways in Human Cancers. Front Oncol. 2020 Jan 17;9:1469. doi: 10.3389/fonc.2019.01469. eCollection 2019. PMID: 32010609; PMCID: PMC6978703.
Copy Download .nbib Format: NLM
Showing 1 to 10 of 10 entries