Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C27H30O15.2H2O |
Molecular Weight | 630.5487 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 10 / 10 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.OC[C@H]1O[C@@H](OC2=C([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(O)=C4C(=O)C=C(OC4=C2)C5=CC=C(O)C=C5)[C@H](O)[C@@H](O)[C@@H]1O
InChI
InChIKey=ZAFQLXXCXLWNGI-IKKNXKRYSA-N
InChI=1S/C27H30O15.2H2O/c28-7-15-19(32)22(35)24(37)26(40-15)18-14(41-27-25(38)23(36)20(33)16(8-29)42-27)6-13-17(21(18)34)11(31)5-12(39-13)9-1-3-10(30)4-2-9;;/h1-6,15-16,19-20,22-30,32-38H,7-8H2;2*1H2/t15-,16-,19-,20-,22+,23+,24-,25-,26+,27-;;/m1../s1
Molecular Formula | C27H30O15 |
Molecular Weight | 594.5181 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 10 / 10 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | H2O |
Molecular Weight | 18.0153 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Saponarin (SA), a natural flavonoid, is known for its antioxidant and hepatoprotective activities. Saponarin
is found in diverse plants, including Tinospora cordifolia, which is used in an anti-diabetic drug, Aloe barbadensis, and barley leaves.Saponarin, isolated from Gypsophila trichotoma Wend., showed in vitro and in vivo hepatoprotective and antioxidant activity against CCl₄-induced liver damage. Saponarin pretreatment also decreased cocaine toxicity both by increasing GSH levels and antioxidant enzyme activities. SA isolated from barley sprouts exerts anti-inflammatory effects in LPS-induced RAW 264.7 macrophages via inhibition of NF-κB, ERK and p38 signaling. Thus, SA may be a promising natural anti-inflammatory agent. Saponarin improves gluconeogenesis and glucose uptake. Saponarin regulates AMPK through induction of intracellular calcium levels. Saponarin has a hypoglycemic effect through the activation of the AMMKb–AMPK–CREB signaling axis in hepatocytes.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0004364 |
|||
Target ID: map04064 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25238253 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Hepatoprotective effects of saponarin, isolated from Gypsophila trichotoma Wend. on cocaine-induced oxidative stress in rats. | 2011 |
|
Hepatoprotective and antioxidant effects of saponarin, isolated from Gypsophila trichotoma Wend. on paracetamol-induced liver damage in rats. | 2013 |
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Protective effects of the apigenin-O/C-diglucoside saponarin from Gypsophila trichotoma on carbone tetrachloride-induced hepatotoxicity in vitro/in vivo in rats. | 2014 Jan 15 |
|
Saponarin from barley sprouts inhibits NF-κB and MAPK on LPS-induced RAW 264.7 cells. | 2014 Nov |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23878818
Rats were challenged with paracetamol alone (600 mg/kg, i.p.) and after 7-day pretreatment with saponarin (80 mg/kg, oral gavage). Saponarin pretreatment resulted in significant increase in cell antioxidant defence system and GSH levels and decrease in lipid peroxidation.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23878818
In freshly isolated rat hepatocytes, paracetamol (100 umol) led to a significant decrease in cell viability, increased LDH leakage, decreased levels of cellular GSH, and elevated MDA quantity. Saponarin (60-0.006 ug/mL) preincubation, however, significantly ameliorated paracetamol-induced hepatotoxicity in a concentration-dependent manner.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 00:59:56 GMT 2023
by
admin
on
Sat Dec 16 00:59:56 GMT 2023
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Record UNII |
B3LI1S3ZJV
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Record Status |
Validated (UNII)
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Record Version |
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE | |||
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ANHYDROUS->SOLVATE |