Lanosta-8,24-dien-21-oic acid, 3,16-dihydroxy-, (3β,16α)-
16α-Hydroxytrametenolic acid
CAS: 176390-68-4
Molecular Formula: C30H48O4
Lanosta-8,24-dien-21-oic acid, 3,16-dihydroxy-, (3β,16α)- - Names and Identifiers
| Name | 16α-Hydroxytrametenolic acid |
| Synonyms | 16α-Hydroxytrametenolic acid 16 alpha-Hydroxytrametenolic acid Lanosta-8,24-dien-21-oic acid, 3,16-dihydroxy-, (3β,16α)- |
| CAS | 176390-68-4 |
Lanosta-8,24-dien-21-oic acid, 3,16-dihydroxy-, (3β,16α)- - Physico-chemical Properties
| Molecular Formula | C30H48O4 |
| Molar Mass | 472.71 |
| Density | 1.11±0.1 g/cm3(Predicted) |
| Boling Point | 598.3±50.0 °C(Predicted) |
| pKa | 4.65±0.10(Predicted) |
| Storage Condition | -20℃ |
Lanosta-8,24-dien-21-oic acid, 3,16-dihydroxy-, (3β,16α)- - Introduction
16α-Hydroxytrametenolic acid is a natural triterpenoid. It is often extracted from fungi such as Tremella (Auricularia auricula-judae).
Its chemical formula is C32H52O4 and has a molecular weight of 524.76g/mol. Its structure contains a hydroxyl group (-OH) and four ring structures.
16α-Hydroxytrametenolic acid has a variety of biological activities, including anti-inflammatory, anti-tumor, antioxidant and immunomodulatory effects. It is widely studied and applied in the field of traditional Chinese medicine, which helps to improve immune function, anti-tumor treatment and reduce chronic inflammatory reaction.
The method for preparing 16α-Hydroxytrametenolic acid is usually obtained through the fermentation and extraction process of fungi. First, the fungus such as Tremella fuciformis is cultured, then it is subjected to enzymatic hydrolysis or acid-base treatment, and finally the target product is obtained by solvent extraction and purification.
Regarding safety information, 16α-Hydroxytrametenolic acid is a natural product and has been used in many experimental and clinical studies, and is considered to have good safety. However, sufficient toxicological data are not yet available, so appropriate safety considerations need to be taken in use. In the use of the process should follow the laboratory's safety procedures, and follow the relevant regulations and guidelines.
Its chemical formula is C32H52O4 and has a molecular weight of 524.76g/mol. Its structure contains a hydroxyl group (-OH) and four ring structures.
16α-Hydroxytrametenolic acid has a variety of biological activities, including anti-inflammatory, anti-tumor, antioxidant and immunomodulatory effects. It is widely studied and applied in the field of traditional Chinese medicine, which helps to improve immune function, anti-tumor treatment and reduce chronic inflammatory reaction.
The method for preparing 16α-Hydroxytrametenolic acid is usually obtained through the fermentation and extraction process of fungi. First, the fungus such as Tremella fuciformis is cultured, then it is subjected to enzymatic hydrolysis or acid-base treatment, and finally the target product is obtained by solvent extraction and purification.
Regarding safety information, 16α-Hydroxytrametenolic acid is a natural product and has been used in many experimental and clinical studies, and is considered to have good safety. However, sufficient toxicological data are not yet available, so appropriate safety considerations need to be taken in use. In the use of the process should follow the laboratory's safety procedures, and follow the relevant regulations and guidelines.
Last Update：2024-04-10 22:29:15
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