Synthesis of Dihydrohelminthosporic Acids and their Plant Growth-promoting Activity

1965 ◽  
Vol 29 (6) ◽  
pp. 595-596 ◽  
Author(s):  
Saburo TAMURA ◽  
Akira SAKURAI
PLoS ONE ◽  
2019 ◽  
Vol 14 (4) ◽  
pp. e0207968 ◽  
Author(s):  
Yong-Hak Kim ◽  
Yunhee Choi ◽  
Yu Yeong Oh ◽  
Nam-Chul Ha ◽  
Jaekyeong Song

2000 ◽  
Vol 41 (18) ◽  
pp. 3453-3457 ◽  
Author(s):  
Jun-ichi Furukawa ◽  
Shigeru Kobayashi ◽  
Motoyoshi Nomizu ◽  
Norio Nishi ◽  
Nobuo Sakairi

2007 ◽  
Vol 2 (8) ◽  
pp. 1934578X0700200 ◽  
Author(s):  
Manoj K Goel ◽  
Arun K Kukreja ◽  
Anil K Singh ◽  
Suman Preet S Khanuja

Phyllocladane diterpenoids, particularly calliterpenone (1) and calliterpenone monoacetate (2), isolated from leaves of Callicarpa macrophylla, produced significantly higher growth and multiplication of in vitro shoot cultures of Rauwolfia serpentina at 0.25 and 0.5 mg/L concentrations, respectively, compared to certain other plant growth regulators (0.1-5.0 mg/L) tested under in vitro conditions. This is the first report of the plant growth promoting activities of 1 and 2 in plant tissue cultures.


2005 ◽  
Vol 83 (8) ◽  
pp. 1084-1092 ◽  
Author(s):  
Daniel G Rivera ◽  
Francisco Coll

Seven new pregnane compounds bearing some representative A- and B-ring brassinosteroid functions, as well as hydrogen bond donor and acceptor ones on the D ring, were efficiently synthesized. The obtained compounds did not show remarkable plant growth-promoting activity in the radish hypocotyl elongation and cotyledon expansion bioassays, however, introducing oxygen and amino functions on the D ring led to an enhancement of the bioactivity. The 16β-functionalized pregnane brassinosteroid-like compounds were slightly more active than the 16α-functionalized ones.Key words: steroids, brassinosteroids, pregnane analogues.


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