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Cat. No.: HY-N17752

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Phaseoloideside C

Phaseoloideside C is an oleanane-type triterpenoid saponin. Phaseoloideside C can be isolated from the seeds of *Entada phaseoloides*. Phaseoloideside C exhibits no cytotoxicity against hepatocellular carcinoma cells, esophageal carcinoma cells, cervical carcinoma cells, and colon carcinoma cells .

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

CAS No.: 1453187-72-8
Formula: C₇₀H₁₁₃NO₃₆
Molecular Weight:1544.63

Storage:

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

Data Sheet (269 KB)

Phaseoloideside C Chemical Structure

CAS No.: 1453187-72-8

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Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- In Vitro
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

In Vitro

Phaseoloideside C (48 h) exhibits no cytotoxicity against HepG-2, Eca-109, SW480, and HeLa cell lines^[1].

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

Cell Cytotoxicity Assay^[1]

Cell Line:

HepG-2 (human hepatocellular carcinoma cell line), Eca-109 (human esophageal carcinoma cell line), SW480 (human colon carcinoma cell line), HeLa (human epithelial carcinoma cell line)
Concentration:

unspecified
Incubation Time:

48 h (incubation after compound addition)
Result:

Exhibited no in vitro cytotoxicity against HepG-2, Eca-109, SW480, and HeLa cell lines.

Chemical Information

CAS No. 1453187-72-8
Molecular Weight 1544.63
Formula C₇₀H₁₁₃NO₃₆
SMILES

O[C@H]([C@](O)(CO1)CO[C@H]2[C@@H]([C@](O)(CO2)CO)O)[C@@H]1O[C@H]([C@H]([C@@H]([C@H](O3)CO)O)O)[C@@H]3OC([C@]45[C@](CC(C)(CC5)C)([H])C6=CC[C@@]([C@@]7([C@@](C(C)([C@H](CC7)O[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO[C@H]9[C@@H]([C@H]([C@H](CO9)O)O[C@H]%10[C@@H]([C@H]([C@@H](CO%10)O)O)O)O)O[C@@H]%11O[C@@H]([C@H]([C@@H]([C@H]%11O)O)O)CO)O)NC(C)=O)C)([H])CC%12)C)([H])[C@]%12(C)[C@@]6([C@H]([C@H]4O)O)C)=O
Structure Classification
- Terpenoids
- Pentacyclic Triterpenoids
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

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

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (269 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Xiong, et al. Triterpene Saponins from Entada phaseoloides. HCA, 2013;96: 1579-1589.

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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