≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Curdione inhibits CYP3A4 activity and the production of prostaglandin E2. Curdione inhibits proliferation of MCF-7 cells by inducing apoptosis. Curdione may be a candidate for anti-inflammatory and Y chemopreventive agents.
| ALogP | 3.351 |
|---|---|
| hba_count | 2 |
| Enlace rotable | 1 |
| Sonrisas canónicas | CC1CCC=C(CC(=O)C(CC1=O)C(C)C)C |
|---|---|
| IUPAC Name | (3S,6E,10S)-6,10-dimethyl-3-propan-2-ylcyclodec-6-ene-1,4-dione |
| InChIKey | KDPFMRXIVDLQKX-NHFJXKHHSA-N |
| INCHI | 1S/C15H24O2/c1-10(2)13-9-14(16)12(4)7-5-6-11(3)8-15(13)17/h6,10,12-13H,5,7-9H2,1-4H3/b11-6+/t12-,13-/m0/s1 |
| Isómeros SMILES | C[C@H]1CC/C=C(/CC(=O)[C@@H](CC1=O)C(C)C)\C |
| Peso molecular | 236.35 |
| Reaxy-Rn | 1967392 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1967392&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Clase | Prenol lipids |
| Subclass | Sesquiterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Germacrane sesquiterpenoids |
| Alternative Parents | Cyclic ketones Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Germacrane sesquiterpenoid - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as germacrane sesquiterpenoids. These are sesquiterpenoids having the germacrane skeleton, with a structure characterized by a cyclodecane ring substituted with an isopropyl and two methyl groups. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 E2619017 | Certificate of Analysis | Jun 01, 2022 | C418576 |
| G2203169 | Certificate of Analysis | Jun 01, 2022 | C418576 |
| G2203170 | Certificate of Analysis | Jun 01, 2022 | C418576 |
| G2203174 | Certificate of Analysis | Jun 01, 2022 | C418576 |
| Solubilidad | insoluble in H2O；≥104.6 mg/mL in EtOH |
|---|---|
| DMSO (mg/ml) Solubilidad máxima | 47 |
| DMSO (mM) Solubilidad máxima | 198.85774419329 |
| Peso molecular | 236.350 g/mol |
| XLogP3 | 2.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 236.178 Da |
| Monoisotopic Mass | 236.178 Da |
| Topological Polar Surface Area | 34.100 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 326.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
| 1. Jingwei Liu, Tong Shu, Yiheng Mu, Wanlin Zheng, Xiaohuan Lu, Hong Tao. (2025) Curdione combined with borneol treats bacterial mixed HPV infection by regulating the crosstalk among immune cells. Frontiers in Immunology, [PMID:39911394] [10.3389/fimmu.2025.1503355] |
