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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
Structure of SAPONARIN DIHYDRATE

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

HIDE SMILES / InChI

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

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
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
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

Patents

Sample Use Guides

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 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 Sat Dec 16 00:59:56 GMT 2023
Edited
by admin
on Sat Dec 16 00:59:56 GMT 2023
Record UNII
B3LI1S3ZJV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SAPONARIN DIHYDRATE
Common Name English
4H-1-BENZOPYRAN-4-ONE, 6-.BETA.-D-GLUCOPYRANOSYL-7-(.BETA.-D-GLUCOPYRANOSYLOXY)-5-HYDROXY-2-(4-HYDROXYPHENYL)-, DIHYDRATE
Common Name English
Code System Code Type Description
FDA UNII
B3LI1S3ZJV
Created by admin on Sat Dec 16 00:59:56 GMT 2023 , Edited by admin on Sat Dec 16 00:59:56 GMT 2023
PRIMARY
PUBCHEM
71586942
Created by admin on Sat Dec 16 00:59:56 GMT 2023 , Edited by admin on Sat Dec 16 00:59:56 GMT 2023
PRIMARY
CAS
11019-01-5
Created by admin on Sat Dec 16 00:59:56 GMT 2023 , Edited by admin on Sat Dec 16 00:59:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID00149165
Created by admin on Sat Dec 16 00:59:56 GMT 2023 , Edited by admin on Sat Dec 16 00:59:56 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE