Structure-Activity Relationships of Synthetic Analogs of Jasmonic Acid and Coronatine on Induction of Benzophenanthridine Alkaloid Accumulation in Eschscholzia californica Cell Cultures (Record no. 40787)

MARC details
000 -LEADER
fixed length control field 02169nam a2200217Ia 4500
003 - CONTROL NUMBER IDENTIFIER
control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625124643.0
040 ## - CATALOGING SOURCE
Transcribing agency CICY
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-6443
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 250602s9999 xx |||||s2 |||| ||und|d
245 10 - TITLE STATEMENT
Title Structure-Activity Relationships of Synthetic Analogs of Jasmonic Acid and Coronatine on Induction of Benzophenanthridine Alkaloid Accumulation in Eschscholzia californica Cell Cultures
490 0# - SERIES STATEMENT
Volume/sequential designation Biological Chemistry, 381(8), p.741-748, 2000
520 3# - SUMMARY, ETC.
Summary, etc. A facile test system based on the accumulation of benzo[ c]phenanthridine alkaloids in Eschscholzia californica cell suspension culture (an indicator of defense gene activation)has been used to analyze a series of synthetic compounds for elicitorlike activity. Of the 200 jasmonic acid and coronatine analogs tested with this system, representative results obtained with 49 of them are presented here. The following can be summarized concerning structureactivity relationships: there is a large degree of plasticity allowed at the C-3 of jasmonic acid in the activation of defense genes. The carbonyl moiety is not strictly required, but exocyclic double bond character appears necessary. The pentenyl side chain at C-2 cannot tolerate bulky groups at the terminal carbon and still be biologically active. Substitutions to the C-1' position are tolerated if they can potentially undergo ßoxidation. Either an alkanoic acid or methyl ester is required at C-1, or a side chain that can be shortened by ßoxidation or by peptidase hydrolysis. Coronatine and various derivatives thereof are not as effective as jasmonic acid, and derivatives in inducing benzophenanthridine alkaloid accumulation. Jasmonic acid rather than the octadecanoic precursors is therefore considered to be a likely signal transducer of defense gene activation in planta.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Haider, G.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name von Schrader, T.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Füßlein, M.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Blechert, S.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Kutchan, T.M.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1nCA-y7BX7vrUd59U0BXAaTi2qQJxsPEs/view?usp=drivesdk">https://drive.google.com/file/d/1nCA-y7BX7vrUd59U0BXAaTi2qQJxsPEs/view?usp=drivesdk</a>
Public note Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Clasificación local
Koha item type Documentos solicitados
Holdings
Lost status Source of classification or shelving scheme Damaged status Not for loan Collection Home library Current library Shelving location Date acquired Total checkouts Full call number Date last seen Price effective from Koha item type
  Clasificación local     Ref1 CICY CICY Documento préstamo interbibliotecario 25.06.2025   B-6443 25.06.2025 25.06.2025 Documentos solicitados