agaric acid
agaric acid structure
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Common Name | agaric acid | ||
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| CAS Number | 666-99-9 | Molecular Weight | 416.54900 | |
| Density | 1.115g/cm3 | Boiling Point | 509.3ºC at 760 mmHg | |
| Molecular Formula | C22H40O7 | Melting Point | 142° (dec) | |
| MSDS | Chinese USA | Flash Point | 275.9ºC | |
Use of agaric acidAgaric acid (Agaricinic Acid) is obtained from various plants of the fungous tribe, i.e. Polyporus officinalis and Polyporus igniarius. Agaric acid induces mitochondrial permeability transition through its interaction with the adenine nucleotide translocase. Agaric acid promotes efflux of accumulated Ca2+, collapse of transmembrane potential, and mitochondrial swelling. Agaric acid is used to regulate lipid metabolism[1]. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | 2-hydroxynonadecane-1,2,3-tricarboxylic acid |
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| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | Agaric acid (Agaricinic Acid) is obtained from various plants of the fungous tribe, i.e. Polyporus officinalis and Polyporus igniarius. Agaric acid induces mitochondrial permeability transition through its interaction with the adenine nucleotide translocase. Agaric acid promotes efflux of accumulated Ca2+, collapse of transmembrane potential, and mitochondrial swelling. Agaric acid is used to regulate lipid metabolism[1]. |
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| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Density | 1.115g/cm3 |
|---|---|
| Boiling Point | 509.3ºC at 760 mmHg |
| Melting Point | 142° (dec) |
| Molecular Formula | C22H40O7 |
| Molecular Weight | 416.54900 |
| Flash Point | 275.9ºC |
| Exact Mass | 416.27700 |
| PSA | 132.13000 |
| LogP | 4.84900 |
| Index of Refraction | 1.501 |
| InChIKey | HZLCGUXUOFWCCN-UHFFFAOYSA-N |
| SMILES | CCCCCCCCCCCCCCCCC(C(=O)O)C(O)(CC(=O)O)C(=O)O |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| RIDADR | NONH for all modes of transport |
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| WGK Germany | 3 |
| RTECS | RA5365000 |
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 0 | |
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| DownStream 4 | |
CAS#:629-66-3
CAS#:71595-37-4
CAS#:64-19-7
CAS#:57-11-4This table lists relevant public references with title, journal and publication metadata for this compound.
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Agaric acid induces mitochondrial permeability transition through its interaction with the adenine nucleotide translocase. Its dependence on membrane fluidity.
Mitochondrion 5 , 272-281, (2005) The effect of agaric acid as inducer of mitochondrial permeability transition was studied. It was found that: (i) agaric acid (AA) promoted efflux of accumulated Ca2+, collapse of transmembrane potent... |
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The mechanisms of fatty acid-induced proton permeability of the inner mitochondrial membrane.
J. Bioenerg. Biomembr. 31 , 447-455, (1999) Nonesterified long-chain fatty acids have long been known as uncouplers of oxidative phosphorylation. They are efficient protonophores in the inner mitochondrial membrane but not so in artificial phos... |
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The effect of N-ethylmaleimide on permeability transition as induced by carboxyatractyloside, agaric acid, and oleate.
Cell Biochem. Biophys. 51 , 81-87, (2008) In this work, we studied the effect of N-ethylmaleimide on permeability transition. The findings indicate that the amine inhibited the effects of carboxyatractyloside and agaric acid. It is known that... |
This table contains target information, in‑vitro & in‑vivo assay data for this compound.
This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| Laricic acid |
| n-Hexadecylcitric acid |
| EINECS 211-566-5 |
| Agaricinic acid |
| (2S,3S)-2-Hydroxy-nonadecan-1,2,3-tricarbonsaeure |
| Lr-2-Hydroxy-nonadecan-1,2rF,3cF-tricarbonsaeure |
| Agaric acid |
| Agaricinsaeure |
| MFCD00002665 |
| Agaricin |
| (2S,3S)-2-Hydroxy-nonadecan-1,2,3-tricarbonsaeure (Agaricinsaeure) |
| Agaricic acid |
| (2S,3S)-2-hydroxy-nonadecane-1,2,3-tricarboxylic acid |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What is the melting point of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: Melting point of 2-hydroxynonadecane-1,2,3-tricarboxylic acid is 142° (dec). |
| Q: What is the boiling point of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: Boiling point of 2-hydroxynonadecane-1,2,3-tricarboxylic acid is 509.3ºC at 760 mmHg. |
| Q: What English synonyms does 2-hydroxynonadecane-1,2,3-tricarboxylic acid have? |
| A: English synonyms of 2-hydroxynonadecane-1,2,3-tricarboxylic acid: Laricic acid, n-Hexadecylcitric acid, EINECS 211-566-5, Agaricinic acid, (2S,3S)-2-Hydroxy-nonadecan-1,2,3-tricarbonsaeure, Lr-2-Hydroxy-nonadecan-1,2rF,3cF-tricarbonsaeure, Agaric acid, Agaricinsaeure, MFCD00002665, Agaricin, (2S,3S)-2-Hydroxy-nonadecan-1,2,3-tricarbonsaeure (Agaricinsaeure), Agaricic acid, (2S,3S)-2-hydroxy-nonadecane-1,2,3-tricarboxylic acid. |
| Q: What are the uses of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: Main uses of 2-hydroxynonadecane-1,2,3-tricarboxylic acid: Agaric acid (Agaricinic Acid) is obtained from various plants of the fungous tribe, i.e. Polyporus officinalis and Polyporus igniarius. Agaric acid induces mitochondrial permeability transition through its interaction with the adenine nucleotide translocase. Agaric acid promotes efflux of accumulated Ca2+, collapse of transmembrane potential, and mitochondrial swelling. Agaric acid is used to regulate lipid metabolism[1]. |
| Q: What are the downstream products of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: Related downstream products(CAS) of 2-hydroxynonadecane-1,2,3-tricarboxylic acid: 629-66-3;71595-37-4;64-19-7;57-11-4. |
| Q: What is the English name of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: The English name of 2-hydroxynonadecane-1,2,3-tricarboxylic acid is 2-hydroxynonadecane-1,2,3-tricarboxylic acid. |
| Q: What is the CAS number of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: CAS number of 2-hydroxynonadecane-1,2,3-tricarboxylic acid is 666-99-9. |
| Q: What is the molecular formula of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: Molecular formula of 2-hydroxynonadecane-1,2,3-tricarboxylic acid is C22H40O7. |
| Q: What is the molecular weight of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: Molecular weight of 2-hydroxynonadecane-1,2,3-tricarboxylic acid is 416.54900. |
| Q: What is the InChIKey of 2-hydroxynonadecane-1,2,3-tricarboxylic acid? |
| A: InChIKey of 2-hydroxynonadecane-1,2,3-tricarboxylic acid is HZLCGUXUOFWCCN-UHFFFAOYSA-N. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| Dayang Chem (Hangzhou) Co., Ltd. |