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Soyasaponin Bb

CAS No.:51330-27-9

Soyasaponin Bb
Catalogue No.: BP1332
Formula: C48H78O18
Mol Weight: 943.134
Botanical Source: Glycine max
Contacts
+86-28-82633860  +86-18080483897
 
Email: sales@biopurify.com biopurify@gmail.com

Soyasaponin Bb

CAS No.:51330-27-9

Soyasaponin Bb
Catalogue No.: BP1332
Formula: C48H78O18
Mol Weight: 943.134
Botanical Source: Glycine max
Contacts
+86-28-82633860  +86-18080483897
 
Email: sales@biopurify.com biopurify@gmail.com
Over 15 years of industry experience in phytochemicals from R&D(reference substances) to Industrialization, please feel free to contact us!

Product name: Soyasaponin Bb
Synonym name: Soyasaponin I
Catalogue No.: BP1332
Cas No.: 51330-27-9
Formula: C48H78O18
Mol Weight: 943.134
Botanical Source: Glycine max
Physical Description:
Type of Compound: Triterpenoids

Purity: 95%~99%
Analysis Method: HPLC-DAD or/and HPLC-ELSD
Identification Method: Mass, NMR
Packing: Brown vial or HDPE plastic bottle

Storage: Store in a well closed container, protected from air and light. Put into refrigerate or freeze for long term storage.
Whenever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20℃. Generally, these will be useable for up to two weeks.

The product could be supplied from milligrams to grams
Inquire for bulk scale.




Description:

Soyasaponin Bb can suppress Eca-9706 cell growth, reverse effects on over expression of c-met, VEGF, and induce cell apoptosis through inhibiting HDAC1-NF-kappaB and activating PETEN and caspase-3 signaling pathways.

 

References:

Wei Sheng Yan Jiu. 2010 Jul;39(4):444-6.    

Apoptosis effects on human esophageal cancer cells by soyasaponin Bb and its machanism.   

To explore the effect and potential mechanism of apoptosis in the Eca-9706 cells induced by Soyasaponin Bb. 

METHODS AND RESULTS:

Different concentrations of Soyasaponin Bb were on the Eca-9706 cell. Cell growth suppression rate was detected by MTT. Apoptotic rate was detected by TUNEL. The expression changes of HDAC1, NF-kappaB, PTEN, cyclin D1, c-met, VEGF or caspase-3 in the SSBb were detected by immunohistochemistry and immunoblotting. Compared with the control group, the growth-inhibition rate and apoptotic rate were increased, the expressions of PTEN, caspase 3 were increased, the expressions of c-met, VEGF, HDAC1, NF-kappaB and cyclin D1 were decreased. 

CONCLUSIONS:

SSBb can suppress Eca-9706 cell growth. SSBb can exhibit reverse effects on over expression of c-met, VEGF in Eca-9706 cells. Eca-9706 cell apoptosis can be induced by SSBb through inhibiting HDAC1-NF-kappaB and activating PETEN and caspase-3 signaling pathways.    

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