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ChEBI
> Main
CHEBI:134301 - salvianolic acid B
Main
ChEBI Ontology
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ChEBI Name
salvianolic acid B
ChEBI ID
CHEBI:134301
Definition
A member of the class of 1-benzofurans that is an antioxidant and free radical scavenging compound extracted from
S. miltiorrhiza
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Sabrina Toro
Supplier Information
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Molfile
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Formula
C36H30O16
Net Charge
0
Average Mass
718.620
Monoisotopic Mass
718.15338
InChI
InChI=1S/C36H30O16/c37-
20-
6-
1-
16(11-
24(20)
41)
13-
27(34(45)
46)
50-
29(44)
10-
5-
18-
3-
9-
23(40)
33-
30(18)
31(32(52-
33)
19-
4-
8-
22(39)
26(43)
15-
19)
36(49)
51-
28(35(47)
48)
14-
17-
2-
7-
21(38)
25(42)
12-
17/h1-
12,15,27-
28,31-
32,37-
43H,13-
14H2,(H,45,46)
(H,47,48)
/b10-
5+/t27-
,28-
,31+,32-
/m1/s1
InChIKey
SNKFFCBZYFGCQN-VWUOOIFGSA-N
SMILES
OC(=O)
[C@@H]
(CC1=CC(O)
=C(O)
C=C1)
OC(=O)
\C=C\C1=C2[C@@H]
([C@H]
(OC2=C(O)
C=C1)
C1=CC(O)
=C(O)
C=C1)
C(=O)
O[C@H]
(CC1=CC(O)
=C(O)
C=C1)
C(O)
=O
Metabolite of Species
Details
Salvia miltiorrhiza
(NCBI:txid226208)
See:
PubMed
Roles Classification
Chemical Role
(s):
antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
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.
osteogenesis regulator
Any compound that induces or regulates osteogenesis.
apoptosis inducer
Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
autophagy inhibitor
Any compound that inhibits the process of autophagy (the self-digestion of one or more components of a cell through the action of enzymes originating within the same cell).
Application
(s):
anti-inflammatory agent
Any compound that has anti-inflammatory effects.
hypoglycemic agent
A drug which lowers the blood glucose level.
hepatoprotective agent
Any compound that is able to prevent damage to the liver.
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
cardioprotective agent
Any protective agent that is able to prevent damage to the heart.
antidepressant
Antidepressants are mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions.
antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
salvianolic acid B (
CHEBI:134301
)
has role
anti-inflammatory agent (
CHEBI:67079
)
salvianolic acid B (
CHEBI:134301
)
has role
antidepressant (
CHEBI:35469
)
salvianolic acid B (
CHEBI:134301
)
has role
antineoplastic agent (
CHEBI:35610
)
salvianolic acid B (
CHEBI:134301
)
has role
antioxidant (
CHEBI:22586
)
salvianolic acid B (
CHEBI:134301
)
has role
apoptosis inducer (
CHEBI:68495
)
salvianolic acid B (
CHEBI:134301
)
has role
autophagy inhibitor (
CHEBI:88230
)
salvianolic acid B (
CHEBI:134301
)
has role
cardioprotective agent (
CHEBI:77307
)
salvianolic acid B (
CHEBI:134301
)
has role
hepatoprotective agent (
CHEBI:62868
)
salvianolic acid B (
CHEBI:134301
)
has role
hypoglycemic agent (
CHEBI:35526
)
salvianolic acid B (
CHEBI:134301
)
has role
neuroprotective agent (
CHEBI:63726
)
salvianolic acid B (
CHEBI:134301
)
has role
osteogenesis regulator (
CHEBI:63054
)
salvianolic acid B (
CHEBI:134301
)
has role
plant metabolite (
CHEBI:76924
)
salvianolic acid B (
CHEBI:134301
)
is a
1-benzofurans (
CHEBI:38830
)
salvianolic acid B (
CHEBI:134301
)
is a
catechols (
CHEBI:33566
)
salvianolic acid B (
CHEBI:134301
)
is a
dicarboxylic acid (
CHEBI:35692
)
salvianolic acid B (
CHEBI:134301
)
is a
enoate ester (
CHEBI:51702
)
salvianolic acid B (
CHEBI:134301
)
is a
polyphenol (
CHEBI:26195
)
IUPAC Name
(2
R
)-
2-
({(2
E
)-
3-
[(2
S
,3
S
)-
3-
{[(1
R
)-
1-
carboxy-
2-
(3,4-
dihydroxyphenyl)ethoxy]carbonyl}-
2-
(3,4-
dihydroxyphenyl)-
7-
hydroxy-
2,3-
dihydro-
1-
benzofuran-
4-
yl]prop-
2-
enoyl}oxy)-
3-
(3,4-
dihydroxyphenyl)propanoic acid
Synonyms
Sources
Dan Shen Suan B
ChemIDplus
Danfensuan B
ChEBI
Lithospermate B
SUBMITTER
Lithospermic acid B
KNApSAcK
Manual Xrefs
Databases
6441188
Pubchem accession
C00031982
KNApSAcK
FDB030001
FooDB
View more database links
Registry Numbers
Types
Sources
121521-90-2
CAS Registry Number
ChemIDplus
8182741
Reaxys Registry Number
Reaxys
Citations
Types
Sources
1414377
PubMed citation
Europe PMC
16933885
PubMed citation
Europe PMC
27278104
PubMed citation
Europe PMC
27424655
PubMed citation
Europe PMC
27442887
PubMed citation
Europe PMC
27484287
PubMed citation
Europe PMC
27490455
PubMed citation
Europe PMC
27497919
PubMed citation
Europe PMC
27507327
PubMed citation
Europe PMC
27513569
PubMed citation
Europe PMC
27557491
PubMed citation
Europe PMC
27569393
PubMed citation
Europe PMC
27586425
PubMed citation
Europe PMC
27592492
PubMed citation
Europe PMC
27614127
PubMed citation
Europe PMC
27670752
PubMed citation
Europe PMC
27716647
PubMed citation
Europe PMC
27779641
PubMed citation
Europe PMC
27827892
PubMed citation
Europe PMC
27843313
PubMed citation
Europe PMC
27852325
PubMed citation
Europe PMC
27893819
PubMed citation
Europe PMC
27941340
PubMed citation
Europe PMC
27973422
PubMed citation
Europe PMC
27989594
PubMed citation
Europe PMC
28000873
PubMed citation
Europe PMC
28072989
PubMed citation
Europe PMC
28116660
PubMed citation
Europe PMC
28178753
PubMed citation
Europe PMC
28211114
PubMed citation
Europe PMC
28214521
PubMed citation
Europe PMC
28244648
PubMed citation
Europe PMC
28251987
PubMed citation
Europe PMC
28254683
PubMed citation
Europe PMC
Last Modified
25 September 2020
General Comment
2020-09-25
Structure updated due to evidence found in PMID:16933885.