1. Saccharides and Glycosides
    Terpenoids and Glycosides
  2. Siamenoside I

Siamenoside I 

Cat. No.: HY-N0612
Handling Instructions

Siamenoside I is one of the mogrosides that has several kinds of bioactivities.

For research use only. We do not sell to patients.

Siamenoside I Chemical Structure

Siamenoside I Chemical Structure

CAS No. : 126105-12-2

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Siamenoside I is one of the mogrosides that has several kinds of bioactivities.

In Vivo

In rat, the metabolic reactions of siamenoside I include deglycosylation, hydroxylation, dehydrogenation, deoxygenation, isomerization, and glycosylation. Siamenoside I and its metabolites are mainly distributed to the intestines, stomach, kidneys, and brain[1].

Molecular Weight







Room temperature in continental US; may vary elsewhere.


Please store the product under the recommended conditions in the Certificate of Analysis.

Animal Administration

The animal experiment lasts six days. The whole urine and feces of days 1-2 are collected as blank urine and feces samples, respectively. On days 3-5, the rats of test group are orally administrated with siamenoside I [50 mg/kg body weight, in normal saline (NS) solution] at 9:00, and all 72-h urine and feces are collected as drug-containing urine and feces samples, respectively. The rats of blank group are orally administrated with the same volume of NS. On day 6 at 9:00, the test and the blank group are treated with siamenoside I and NS again, respectively. After 1 h, blood sample is collected into a vacuum tube with sodium citrate as anticoagulant from rat heart under anesthesia. Then, the organs (heart, liver, spleen, lung, kidneys, stomach, small intestine, brain) and skeletal muscles of rats are collected and washed with NS, separately. All samples are kept at −80°C before further pretreatment.

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

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