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Cat. No.: HY-N1853

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3β-Acetoxy-12α-hydroxyoleanan-13β,28-olide

3β-Acetoxy-12α-hydroxyoleanan-13β,28-olide is a natural triterpene.

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

CAS No.: 62498-83-3
Formula: C₃₂H₅₀O₅
Molecular Weight:514.74

Storage:

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

Data Sheet (272 KB)

3β-Acetoxy-12α-hydroxyoleanan-13β,28-olide Chemical Structure

CAS No.: 62498-83-3

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Biological Activity
- Description
- Cellular Effect
Chemical Information
Purity & Documentation
References
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Classifications
Bioz

Biological Activity

Description

3β-Acetoxy-12α-hydroxyoleanan-13β,28-olide is a natural triterpene.

Cellular Effect

Cell Line	Type	Value	Description	References
8505C	IC₅₀	>90 μM Compound: 4	Cytotoxicity against human 8505C cells after 96 hrs by SRB assay Cytotoxicity against human 8505C cells after 96 hrs by SRB assay	[PMID: 24361521]
A2780	IC₅₀	63.2 μM Compound: 4	Cytotoxicity against human A2780 cells after 96 hrs by SRB assay Cytotoxicity against human A2780 cells after 96 hrs by SRB assay	[PMID: 24361521]
A549	IC₅₀	>90 μM Compound: 4	Cytotoxicity against human A549 cells after 96 hrs by SRB assay Cytotoxicity against human A549 cells after 96 hrs by SRB assay	[PMID: 24361521]
HT-29	IC₅₀	>90 μM Compound: 4	Cytotoxicity against human HT-29 cells after 96 hrs by SRB assay Cytotoxicity against human HT-29 cells after 96 hrs by SRB assay	[PMID: 24361521]
MCF7	IC₅₀	>90 μM Compound: 4	Cytotoxicity against human MCF7 cells after 96 hrs by SRB assay Cytotoxicity against human MCF7 cells after 96 hrs by SRB assay	[PMID: 24361521]
NIH3T3	IC₅₀	85.7 μM Compound: 4	Cytotoxicity against mouse NIH/3T3 cells after 96 hrs by SRB assay Cytotoxicity against mouse NIH/3T3 cells after 96 hrs by SRB assay	[PMID: 24361521]

Chemical Information

CAS No. 62498-83-3
Molecular Weight 514.74
Formula C₃₂H₅₀O₅
SMILES

C[C@]1([C@@]([C@]2([H])C3)(CC[C@]4([H])[C@@]2(CC[C@H](OC(C)=O)C4(C)C)C)C)[C@](OC5=O)([C@H]3O)[C@@](CC(C)(C)CC6)([H])[C@]56CC1
Structure Classification
- Terpenoids
- Triterpenes
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 (272 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]. Katai M, et al. Triterpenoids of the bark of Pieris japonica D. DON (Japanese Name: Asebi). II. 13C Nuclear magnetic resonance of the γ-lactones of ursane-and oleanane-type Triterpenes[J]. Chemical and pharmaceutical bulletin, 1983, 31(5): 1567-1571.

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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.

Keywords

3β-Acetoxy-12α-hydroxyoleanan-13β,28-olide

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Biological Activity
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3β-Acetoxy-12α-hydroxyoleanan-13β,28-olide

Biological Activity

Chemical Information

Purity & Documentation

References

Calculators

Help & FAQs

3β-Acetoxy-12α-hydroxyoleanan-13β,28-olide Related Classifications

HY-N1853 Related Classifications