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Cinnamates
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Cinnamates
Tree Number(s)
D02.241.223.200
Unique ID
D002934
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D002934
Scope Note
Derivatives of cinnamic acid (the structural formula: phenyl-HC=CH-COO-), including its salts and esters.
Entry Term(s)
Cinnamate
Registry Numbers
0
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2020/05/27
Allowable Qualifiers
administration & dosage (AD)
adverse effects (AE)
agonists (AG)
analysis (AN)
antagonists & inhibitors (AI)
blood (BL)
cerebrospinal fluid (CF)
chemical synthesis (CS)
chemistry (CH)
classification (CL)
economics (EC)
history (HI)
immunology (IM)
isolation & purification (IP)
metabolism (ME)
pharmacokinetics (PK)
pharmacology (PD)
poisoning (PO)
radiation effects (RE)
standards (ST)
supply & distribution (SD)
therapeutic use (TU)
toxicity (TO)
urine (UR)
Organic Chemicals [D02]
Carboxylic Acids [D02.241]
Acids, Carbocyclic [D02.241.223]
Benzoates [D02.241.223.100]
Cinnamates [D02.241.223.200]
Caffeic Acids [D02.241.223.200.054]
Chlorogenic Acid [D02.241.223.200.185]
Cinanserin [D02.241.223.200.200]
Coumaric Acids [D02.241.223.200.210]
Puromycin [D02.241.223.200.380]
Rosmarinic Acid [D02.241.223.200.690]
Cyclohexanecarboxylic Acids [D02.241.223.268]
Mandelic Acids [D02.241.223.475]
Phenylacetates [D02.241.223.601]
Phenylbutyrates [D02.241.223.651]
Phenylpropionates [D02.241.223.701]
Phenylpyruvic Acids [D02.241.223.751]
Phthalic Acids [D02.241.223.805]
Expand All
Collapse All
Cinnamates
Preferred
Concept UI
M0004490
Registry Numbers
0
Scope Note
Derivatives of cinnamic acid (the structural formula: phenyl-HC=CH-COO-), including its salts and esters.
Terms
Cinnamates
Preferred Term
Term UI
T008490
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1966)
Cinnamate
Term UI
T001008800
Date
02/27/2020
LexicalTag
NON
ThesaurusID
NLM (2021)
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