Source:http://linkedlifedata.com/resource/pubmed/id/10915053
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
14
|
| pubmed:dateCreated |
2000-11-28
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| pubmed:abstractText |
Replacing the 4'-carbonyl group of abscisic acid with a methoxy group does not affect the abscisic acid (ABA)-like activities of the product in barley aleurone protoplasts, although the reduction of ABA to 4'-hydroxyl derivatives significantly reduces the ABA-like activity of the products. This suggests that methoxy derivatives of abscisic acid might be used to produce probes for ABA binding proteins.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
0960-894X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
17
|
| pubmed:volume |
10
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
1571-4
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| pubmed:dateRevised |
2008-11-21
|
| pubmed:meshHeading |
pubmed-meshheading:10915053-Abscisic Acid,
pubmed-meshheading:10915053-Drug Design,
pubmed-meshheading:10915053-Enzyme Induction,
pubmed-meshheading:10915053-Hordeum,
pubmed-meshheading:10915053-Molecular Structure,
pubmed-meshheading:10915053-Plant Growth Regulators,
pubmed-meshheading:10915053-Protoplasts,
pubmed-meshheading:10915053-Structure-Activity Relationship,
pubmed-meshheading:10915053-alpha-Amylases
|
| pubmed:year |
2000
|
| pubmed:articleTitle |
Synthesis and biological activity of 4'-methoxy derivatives of abscisic acid.
|
| pubmed:affiliation |
RIKEN (The Institute of Physical and Chemical Research), Wako, Saitama, Japan. tasami@postman.riken.gp.jp
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| pubmed:publicationType |
Journal Article
|