Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C7H14O6 |
Molecular Weight | 194.1825 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CO[C@@H]1[C@@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@H]1O
InChI
InChIKey=DSCFFEYYQKSRSV-GESKJZQWSA-N
InChI=1S/C7H14O6/c1-13-7-5(11)3(9)2(8)4(10)6(7)12/h2-12H,1H3/t2-,3-,4-,5+,6-,7-/m0/s1
Molecular Formula | C7H14O6 |
Molecular Weight | 194.1825 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Natural O-methyl ether of myo-inositol, ononitol, (+)- is present, albeit in small amounts, in many plant families. For example, it was identified in pea (Pisum sativum L.) root nodules, in Cassia tora L. leaves, in leaves of Sesbania aculeate, Medicago sativa and others. In in vivo study, ononitol monohydrate decreased the levels of serum transaminase, lipid peroxidation and TNF-alpha but increased the levels of antioxidant and hepatic glutathione enzyme activities. Histopathological results also suggested the hepatoprotective activity of ononitol monohydrate with no adverse effect. Hence it was concluded that ononitol monohydrate is a potent hepatoprotective agent. Also, ononitol could be used as an agent to prepare botanical new pesticidal formulations.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19345078
Curator's Comment: Ononitol monohydrate
Rat: 20 mg/kg body weight for 8 days
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:21:06 UTC 2023
by
admin
on
Sat Dec 16 11:21:06 UTC 2023
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Record UNII |
A998ME07KR
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Record Status |
Validated (UNII)
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Record Version |
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-
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18266
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164619
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DTXSID601029635
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6090-97-7
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A998ME07KR
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ONONITOL
Created by
admin on Sat Dec 16 11:21:06 UTC 2023 , Edited by admin on Sat Dec 16 11:21:06 UTC 2023
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PARENT -> CONSTITUENT ALWAYS PRESENT |