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> Main
CHEBI:141968 - caracurine VII
Main
ChEBI Ontology
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ChEBI Name
caracurine VII
ChEBI ID
CHEBI:141968
Definition
A monoterpenoid indole alkaloid with formula C
19
H
22
N
2
O
2
, isolated from several species of
Strychnos
.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Mark Williams
Supplier Information
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Formula
C19H22N2O2
Net Charge
0
Average Mass
310.391
Monoisotopic Mass
310.16813
InChI
InChI=1S/C19H22N2O2/c22-
18-
16-
12-
9-
15-
19(6-
7-
21(15)
10-
11(12)
5-
8-
23-
18)
13-
3-
1-
2-
4-
14(13)
20-
17(16)
19/h1-
5,12,15-
18,20,22H,6-
10H2/t12-
,15-
,16+,17-
,18+,19+/m0/s1
InChIKey
UFUDXCDPABDFHK-SRCYXDNASA-N
SMILES
C1=CC=C2C(=C1)[C@]34CCN5CC6=CCO[C@H]([C@]([C@]6(C[C@@]35[H])[H])([C@@]4(N2)[H])[H])O
Metabolite of Species
Details
Strychnos dolichothyrsa
(IPNI:547167-1)
Found in bark
(BTO:0001301)
. See:
PubMed
Strychnos matopensis
(NCBI:txid1040897)
Found in root
(BTO:0001188)
. See: Massiot, G et al. Alkaloids from roots of Strychnos matopensis (1988). Phytochemistry, Vol 27(10), p 3293-3304.
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via
alkaloid
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
caracurine VII (
CHEBI:141968
)
has role
plant metabolite (
CHEBI:76924
)
caracurine VII (
CHEBI:141968
)
is a
monoterpenoid indole alkaloid (
CHEBI:65323
)
caracurine VII (
CHEBI:141968
)
is a
organic heterohexacyclic compound (
CHEBI:51914
)
caracurine VII (
CHEBI:141968
)
is a
primary alcohol (
CHEBI:15734
)
caracurine VII (
CHEBI:141968
)
is a
tertiary amino compound (
CHEBI:50996
)
IUPAC Name
(17
R
)-19,20-didehydro-17,18-epoxycuran-17-ol
Synonyms
Sources
1-deacetyldiaboline
ChemIDplus
caracurin VII
ChEBI
caracurine
ChemIDplus
caracurine VII
ChemIDplus
deacetyldiaboline
ChemIDplus
desacetyldiaboline
ChEBI
Wieland-Gumlich aldehyde
ChemIDplus
Manual Xref
Database
Wieland-Gumlich_aldehyde
Wikipedia
View more database links
Registry Numbers
Types
Sources
43170
Reaxys Registry Number
Reaxys
466-85-3
CAS Registry Number
ChemIDplus
Citations
Types
Sources
10807177
PubMed citation
Europe PMC
15647330
PubMed citation
Europe PMC
17402076
PubMed citation
Europe PMC
29711638
PubMed citation
Europe PMC
Last Modified
13 September 2018