| Name | 1,7-Dioxadispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione |
|---|---|
| Synonyms |
Anemone camphor
ANEMONIN(P) rel-(5R,6R)-1,7-Dioxadispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione Pulsatilla camphor 1,7-Dioxa-dispiro[4.0.4.2]dodeca-3,9-dien-2,8-dion Anemonin (6CI) 1,7-dioxa-dispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione Anemonin/Pulsatilla camphor 1,7-dioxadispiro[4.0.4^.2^]dodeca-3,9-diene-2,8-quinone (5R,6R)-rel-1,7-Dioxadispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione (5R,6R)-4,7-dioxadispiro[4.0.4^.2^]dodeca-1,9-diene-3,8-dione 1,7-dioxadispiro[4.0.4^.2^]dodeca-3,9-diene-2,8-dione 1,7-dinitro-naphthalene Naphthalene,1,7-dinitro (5S,6S)-1,7-dioxadispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione 1,7-Dinitro-naphthalin 1,7-Dioxadispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione, (5R,6R)-rel |
| Description | Anemonin (Pulsatilla camphor), a selective iNOS inhibitor, is also a PKC-θ inhibitor. Anemonin can significantly inhibit the translation or protein stability of PKC-θ protein. Anemonin also ameliorates dextran sodium sulfate-induced acute ulcerative colitis (UC) in mice. Anemonin can be used in the research of inflammation-related diseases[1][2]. |
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| Related Catalog | |
| References |
| Density | 1.45 |
|---|---|
| Boiling Point | 535.7ºC at 760 mmHg |
| Melting Point | 157-158ºC |
| Molecular Formula | C10H8O4 |
| Molecular Weight | 192.17 |
| Flash Point | 300.7ºC |
| Exact Mass | 192.04200 |
| PSA | 52.60000 |
| LogP | 0.48380 |
| Index of Refraction | 1.61 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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