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(−)-Τ-muurolol |
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CHEBI:132906 |
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(-)-Tau-muurolol |
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A cadinane sesquiterpenoid that consists of 4-isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalene having a hydroxy substituent at position 1 and (1S,4S,4aR,8aS)-configuration. |
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This entity has been manually annotated by the ChEBI Team.
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qingping liu
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Molfile
XML
SDF
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InChI=1S/C15H26O/c1- 10(2) 12- 7- 8- 15(4,16) 14- 6- 5- 11(3) 9- 13(12) 14/h9- 10,12- 14,16H,5- 8H2,1- 4H3/t12- ,13- ,14- ,15- /m0/s1 |
LHYHMMRYTDARSZ-AJNGGQMLSA-N |
O[C@@]1([C@@]2([C@]([C@@H](CC1)C(C)C)(C=C(CC2)C)[H])[H])C |
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Calocedrus macrolepis
(NCBI:txid103965)
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Found in
leaf
(BTO:0000713).
See:
PubMed
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Chamaecyparis obtusa
(NCBI:txid13415)
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Found in
heartwood
(PO:0004512).
See:
DOI
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Chiliadenus lopadusanus
(NCBI:txid1548557)
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Found in
flower
(BTO:0000469).
See:
PubMed
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Chiliadenus lopadusanus
(NCBI:txid1548557)
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Found in
leaf
(BTO:0000713).
See:
PubMed
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Homalomena aromatica
(NCBI:txid1804071)
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Found in
rhizome
(BTO:0001181).
See:
PubMed
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Streptomyces sp. M491
(NCBI:txid345410)
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See:
PubMed
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Cunninghamia konishii
(NCBI:txid66170)
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Found in
heartwood
(PO:0004512).
See:
PubMed
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plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
fungicide
A substance used to destroy fungal pests.
volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
marine metabolite
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
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fungicide
A substance used to destroy fungal pests.
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View more via ChEBI Ontology
(1S,4S,4aR,8aS)- 4- isopropyl- 1,6- dimethyl- 1,2,3,4,4a,7,8,8a- octahydronaphthalen- 1- ol
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(−)-τ-muurolol
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ChEBI
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10-epi-α-muurolol
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NIST Chemistry WebBook
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α-epi-muurolol
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NIST Chemistry WebBook
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epi-α-muurolol
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NIST Chemistry WebBook
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epi-alpha-Muurolol
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KNApSAcK
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T-Muurolol
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ChemIDplus
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19912-62-0
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CAS Registry Number
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NIST Chemistry WebBook
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19912-62-0
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CAS Registry Number
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ChemIDplus
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2210160
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Reaxys Registry Number
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Reaxys
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18206367
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PubMed citation
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Europe PMC
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19072130
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PubMed citation
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Europe PMC
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22129092
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PubMed citation
|
Europe PMC
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22888533
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PubMed citation
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Europe PMC
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23177818
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PubMed citation
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Europe PMC
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24079193
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PubMed citation
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Europe PMC
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IND500613940
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Agricola citation
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Europe PMC
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