InChI=1S/C37H40O9/c1- 21(2) 35- 17- 23(4) 37- 27(33(35) 44- 36(45- 35,46- 37) 19- 24- 9- 7- 6- 8- 10- 24) 14- 26(18- 34(41) 30(37) 13- 22(3) 32(34) 40) 20- 43- 31(39) 16- 25- 11- 12- 28(38) 29(15- 25) 42- 5/h6- 15,23,27,30,33,38,41H,1,16- 20H2,2- 5H3/t23- ,27+,30- ,33- ,34- ,35- ,36- ,37- /m1/s1 |
DSDNAKHZNJAGHN-MXTYGGKSSA-N |
C=1(C=C(C(=CC1) O) OC) CC(OCC2=C[C@@] 3([C@] 4([C@] 5([C@] (C2) (C(=O) C(=C5) C) O) [H] ) O[C@] 6(O[C@@] ([C@@] 3(O6) [H] ) (C(=C) C) C[C@H] 4C) CC=7C=CC=CC7) [H] ) =O |
|
Euphorbia poissonii
(NCBI:txid212962)
|
See:
Book: Harborne, Phytochemical Dictionary Second Edition, Taylor and Francis (1999), Chapter 52.
|
Euphorbia resinifera
(NCBI:txid457265)
|
See:
Book: Harborne, Phytochemical Dictionary Second Edition, Taylor and Francis (1999), Chapter 52.
|
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
neurotoxin
A poison that interferes with the functions of the nervous system.
analgesic
An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
TRPV1 agonist
An agonist at the transient receptor potential vanilloid 1 (TRPV1).
|
|
analgesic
An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
|
|
View more via ChEBI Ontology
[(2S,3aR,3bS,6aR,9aR,9bR,10R,11aR)- 2- benzyl- 6a- hydroxy- 8,10- dimethyl- 7- oxo- 11a- (prop- 1- en- 2- yl)- 3a,6,6a,7,9a,10,11,11a- octahydro- 3bH- 2,9b- epoxyazuleno[4',5':5,6]benzo[1,2- d][1,3]dioxol- 5- yl]methyl (4- hydroxy- 3- methoxyphenyl)acetate
|
(+)-resiniferatoxin
|
ChEBI
|
resiniferatoxin
|
KEGG COMPOUND
|
resiniferatoxin
|
UniProt
|
RTX
|
ChemIDplus
|
5371150
|
Reaxys Registry Number
|
Reaxys
|
57444-62-9
|
CAS Registry Number
|
ChemIDplus
|
26779292
|
PubMed citation
|
Europe PMC
|
27281200
|
PubMed citation
|
Europe PMC
|
2747924
|
PubMed citation
|
Europe PMC
|
27529257
|
PubMed citation
|
Europe PMC
|
29041773
|
PubMed citation
|
Europe PMC
|
29271803
|
PubMed citation
|
Europe PMC
|
29320813
|
PubMed citation
|
Europe PMC
|
29361418
|
PubMed citation
|
Europe PMC
|
29672450
|
PubMed citation
|
Europe PMC
|
29728656
|
PubMed citation
|
Europe PMC
|
30015705
|
PubMed citation
|
Europe PMC
|
30399572
|
PubMed citation
|
Europe PMC
|
30590777
|
PubMed citation
|
Europe PMC
|
31090543
|
PubMed citation
|
Europe PMC
|
31124075
|
PubMed citation
|
Europe PMC
|
31180583
|
PubMed citation
|
Europe PMC
|
31503071
|
PubMed citation
|
Europe PMC
|
31811858
|
PubMed citation
|
Europe PMC
|
32064609
|
PubMed citation
|
Europe PMC
|
32292906
|
PubMed citation
|
Europe PMC
|
7189445
|
PubMed citation
|
Europe PMC
|
|