Ursolic acid, Pentacyclic triterpenoid (ab141113)
Key features and details
- Pentacyclic triterpenoid; antitumourigenic.
- CAS Number: 77-52-1
- Purity: > 99%
- Soluble in DMSO to 25 mM
- Form / State: Solid
Overview
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Product name
Ursolic acid, Pentacyclic triterpenoid -
Description
Pentacyclic triterpenoid; antitumourigenic. -
Biological description
Pentacyclic triterpenoid. Suppresses NF-κB activation in vitro. Antitumourigenic, antiangiogenic, anti-inflammatory and proapoptotic effects.
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Purity
> 99% -
CAS Number
77-52-1 -
Chemical structure
Properties
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Chemical name
(3β)-3-Hydroxyurs-12-en-28-oic acid -
Molecular weight
456.71 -
Molecular formula
C30H48O3 -
PubChem identifier
64945 -
Storage instructions
Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months. -
Solubility overview
Soluble in DMSO to 25 mM -
Handling
Wherever 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°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
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SMILES
O=C(O)[C@]45CC[C@]3(C)C(=CC[C@H]2[C@@]3(C)CC[C@@H]1[C@]2(C)CC[C@H](O)C1(C)C)[C@@H]5[C@@H](C)[C@H](C)CC4 -
Research areas
- Metabolism
- Pathways and Processes
- Metabolic signaling pathways
- Lipid and lipoprotein metabolism
- Lipid metabolism
- Metabolism
- Pathways and Processes
- Metabolic signaling pathways
- Energy transfer pathways
- Energy Metabolism
Images
Protocols
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
References (1)
ab141113 has been referenced in 1 publication.
- Mirza FJ & Zahid S Ursolic acid and rosmarinic acid ameliorate alterations in hippocampal neurogenesis and social memory induced by amyloid beta in mouse model of Alzheimer's disease. Front Pharmacol 13:1058358 (2022). PubMed: 36618920