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ChEBI
> Main
CHEBI:183228 - (
R
)-goitrin
Main
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ChEBI Name
(
R
)-goitrin
ChEBI ID
CHEBI:183228
ChEBI ASCII Name
(R)-goitrin
Definition
A 5-ethenyl-1,3-oxazolidine-2-thione that has
R
-configuration. It is a constituent of a traditional Chinese herbal medicine,
Radix isatidis
.
Stars
This entity has been manually annotated by the ChEBI Team.
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Molfile
Formula
C5H7NOS
Net Charge
0
Average Mass
129.180
Monoisotopic Mass
129.02484
InChI
InChI=1S/C5H7NOS/c1-2-4-3-6-5(8)7-4/h2,4H,1,3H2,(H,6,8)/t4-/m1/s1
InChIKey
UZQVYLOFLQICCT-SCSAIBSYSA-N
SMILES
[H][C@]1(CNC(=S)O1)C=C
Metabolite of Species
Details
Isatis tinctoria
(NCBI:txid161756)
Found in Root
(BTO:0001188)
. See:
PubMed
Orychophragmus violaceus
(NCBI:txid71234)
Found in seed
(BTO:0001226)
. See:
PubMed
Roles Classification
Biological Role
(s):
antiviral agent
A substance that destroys or inhibits replication of viruses.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(
R
)-goitrin (
CHEBI:183228
)
has role
antiviral agent (
CHEBI:22587
)
(
R
)-goitrin (
CHEBI:183228
)
has role
plant metabolite (
CHEBI:76924
)
(
R
)-goitrin (
CHEBI:183228
)
is a
5-ethenyl-1,3-oxazolidine-2-thione (
CHEBI:183227
)
(
R
)-goitrin (
CHEBI:183228
)
is enantiomer of
(
S
)-goitrin (
CHEBI:80751
)
Incoming
(
R
S
)-goitrin (
CHEBI:183226
)
has part
(
R
)-goitrin (
CHEBI:183228
)
(
S
)-goitrin (
CHEBI:80751
)
is enantiomer of
(
R
)-goitrin (
CHEBI:183228
)
IUPAC Name
(5
R
)-5-ethenyl-1,3-oxazolidine-2-thione
Synonyms
Sources
(5
R
)-5-vinyl-1,3-oxazolidine-2-thione
ChEBI
(
R
)-5-ethenyl-2-oxazolidinethione
ChemIDplus
(
R
)-5-vinyl-2-oxazolidinethione
ChemIDplus
BA 51-090278
ChemIDplus
D
-goitrin
ChemIDplus
epigoitrin
ChemIDplus
Manual Xref
Database
2297322
ChemSpider
View more database links
Registry Number
Type
Source
1072-93-1
CAS Registry Number
ChemIDplus
Citations
Types
Sources
11170613
PubMed citation
Europe PMC
17401984
PubMed citation
Europe PMC
19160787
PubMed citation
Europe PMC
23901642
PubMed citation
Europe PMC
25345127
PubMed citation
Europe PMC
26989425
PubMed citation
Europe PMC
27022502
PubMed citation
Europe PMC
27468553
PubMed citation
Europe PMC
28617329
PubMed citation
Europe PMC
28894621
PubMed citation
Europe PMC
30505662
PubMed citation
Europe PMC
30792656
PubMed citation
Europe PMC
31918015
PubMed citation
Europe PMC
32805551
PubMed citation
Europe PMC
33755912
PubMed citation
Europe PMC
34627086
PubMed citation
Europe PMC
7390339
PubMed citation
Europe PMC
Last Modified
02 November 2021