ent-3β-Hydroxykaur-16-en-19-oic acid - Names and Identifiers
Name | ent-3β-Hydroxykaur-16-en-19-oic acid
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Synonyms | ENT-3Β-HYDROXYKAUR-16-EN-19-OIC ent-3β-Hydroxykaur-16-en-19-oic acid ent-3beta-Hydroxykaur-16-en-19-oic acid Kaur-16-en-18-oic acid, 3-hydroxy-, (3α,4α)- (3alpha,4alpha)-3-Hydroxykaur-16-en-18-oic acid (3R,4S,4aS,6aS,9R,11aR,11bS)-3-hydroxy-4,11b-dimethyl-8-methylenetetradecahydro-6a,9-methanocyclohepta[a]naphthalene-4-carboxylicaci
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CAS | 66556-91-0
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ent-3β-Hydroxykaur-16-en-19-oic acid - Physico-chemical Properties
Molecular Formula | C20H30O3
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Molar Mass | 318.45 |
Density | 1.16±0.1 g/cm3(Predicted) |
Melting Point | 207-210℃ |
Boling Point | 467.4±45.0 °C(Predicted) |
pKa | 4.50±0.60(Predicted) |
Storage Condition | 2-8℃ |
ent-3β-Hydroxykaur-16-en-19-oic acid - Introduction
Pill acid (ent-3β-hydroxykol-16-ene-19-acid) is a natural diterpenoid. The following is a description of its nature, use, formulation and safety information:
Nature:
-must acid is a structurally unique organic acid with anti-inflammatory and anti-tumor activities.
-It takes the form of a white crystalline solid.
-The compound has low solubility in non-polar solvents.
Use:
-or acid is often used as a drug lead compound to study its potential activity as an anti-inflammatory and anti-tumor agent.
-It can also be used as a precursor of natural plant-derived anti-cancer therapeutic drugs.
Method:
-or acid can be obtained by extraction from natural plants or chemical synthesis.
-Chemical synthesis usually includes the synthesis of intermediates with similar structures, and then reaction and conversion to produce the target compound.
Safety Information:
-Detailed information on the toxicity and safety of the acid is currently unclear because it is a relatively new compound.
-When using or handling it, you need to follow laboratory safety regulations and operating procedures, and use appropriate protective equipment.
-Before further development and application of this compound, further toxicity research and evaluation are required.
Last Update:2024-04-09 02:00:53