Link to this page
Biological and Environmental Research Ontology
Preferred Name | Limonene, (+)- | |
Synonyms |
|
|
Definitions |
An oral dietary supplement containing a natural cyclic monoterpene, and a major component of the oil extracted from citrus peels, with potential chemopreventive and antineoplastic activities. Upon oral administration, D-limonene activates aldehyde dehydrogenase 3A1 (ALDH3A1), thereby decreasing aldehyde level. This may protect salivary stem/progenitor cells (SSPCs) from toxic aldehydes and prevent or improve radiation-induced xerostomia. Limonene and its metabolites perillic acid, dihydroperillic acid, uroterpenol and limonene 1,2-diol may also inhibit tumor growth through inhibition of p21-dependent signaling and may induce apoptosis via the induction of the transforming growth factor beta-signaling pathway. In addition, they inhibit post-translational modification of signal transduction proteins, resulting in G1 cell cycle arrest as well as differential expression of cell cycle- and apoptosis-related genes. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C61714 |
|
ALT_DEFINITION |
A terpene with two isoprene units forming a ring. The chemical structure is CC1=CCC(CC1)C(=C)C.
|
|
CAS_Registry |
5989-27-5 7705-13-7
|
|
CHEBI_ID |
CHEBI:15382
|
|
Chemical_Formula |
C10H16
|
|
code |
C61714
|
|
Contributing_Source |
CRCH CTRP FDA
|
|
definition |
An oral dietary supplement containing a natural cyclic monoterpene, and a major component of the oil extracted from citrus peels, with potential chemopreventive and antineoplastic activities. Upon oral administration, D-limonene activates aldehyde dehydrogenase 3A1 (ALDH3A1), thereby decreasing aldehyde level. This may protect salivary stem/progenitor cells (SSPCs) from toxic aldehydes and prevent or improve radiation-induced xerostomia. Limonene and its metabolites perillic acid, dihydroperillic acid, uroterpenol and limonene 1,2-diol may also inhibit tumor growth through inhibition of p21-dependent signaling and may induce apoptosis via the induction of the transforming growth factor beta-signaling pathway. In addition, they inhibit post-translational modification of signal transduction proteins, resulting in G1 cell cycle arrest as well as differential expression of cell cycle- and apoptosis-related genes.
|
|
Display_Name |
Limonene, (+)-
|
|
FDA_UNII_Code |
GFD7C86Q1W
|
|
in_subset |
http://purl.obolibrary.org/obo/NCIT_C63923 http://purl.obolibrary.org/obo/NCIT_C177537 http://purl.obolibrary.org/obo/NCIT_C116977 http://purl.obolibrary.org/obo/NCIT_C116978 http://purl.obolibrary.org/obo/NCIT_C128784 |
|
Is_Value_For_GDC_Property | ||
label |
Limonene, (+)-
|
|
Legacy Concept Name |
D-Limonene
|
|
Maps_To |
Limonene, (+)-
|
|
NCI_Drug_Dictionary_ID |
664042
|
|
PDQ_Closed_Trial_Search_ID |
664042
|
|
PDQ_Open_Trial_Search_ID |
664042
|
|
Preferred_Name |
Limonene, (+)-
|
|
prefixIRI |
NCIT:C61714
|
|
prefLabel |
Limonene, (+)-
|
|
Semantic_Type |
Pharmacologic Substance
|
|
UMLS_CUI |
C0950252
|
|
subClassOf |
Delete | Subject | Author | Type | Created |
---|---|---|---|---|
No notes to display |