Introduction:Basic information about CAS 134418-28-3|Dehydroandrographolide, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Dehydroandrographolide |
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| CAS Number | 134418-28-3 | Molecular Weight | 332.43 |
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| Density | 1.2±0.1 g/cm3 | Boiling Point | 512.8±50.0 °C at 760 mmHg |
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| Molecular Formula | C20H28O4 | Melting Point | / |
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| MSDS | ChineseUSA | Flash Point | 178.3±23.6 °C |
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Names
| Name | Dehydroandrographolide |
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| Synonym | More Synonyms |
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Dehydroandrographolide BiologicalActivity
| Description | Dehydroandrographolide is extracted from herbal medicine Andrographis paniculata (Burm f) Nees; alleviate oxidative stress in LPS-induced acute lung injury possibly by inactivating iNOS. |
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| Related Catalog | Signaling Pathways >>Anti-infection >>Influenza VirusNatural Products >>Terpenoids and GlycosidesResearch Areas >>Infection |
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| References | [1]. Chen Q, et al. Pharmacokinetics and tolerance of dehydroandrographolide succinate injection after intravenous administration in healthy Chinese volunteers. Acta Pharmacol Sin. 2012 Oct;33(10):1332-6. [2]. Chao WW, et al. Isolation and identification of bioactive compounds in Andrographis paniculata (Chuanxinlian). Chin Med. 2010 May 13;5:17. [3]. Basak A, et al. Inhibition of proprotein convertases-1, -7 and furin by diterpines of Andrographis paniculata and their succinoyl esters. Biochem J. 1999 Feb 15;338 ( Pt 1):107-13. [4]. Zhu T, et al. Dehydroandrographolide succinate inhibits oxidative stress in mice with lipopolysaccharide-induced acute lung injury by inactivating iNOS. Nan Fang Yi Ke Da Xue Xue Bao. 2012 Sep;32(9):1238-41. [5]. Chen H, et al. Synthesis, structure-activity relationships and biological evaluation of dehydroandrographolide and andrographolide derivatives as novel anti-hepatitis B virus agents. Bioorg Med Chem Lett. 2014 May 15;24(10):2353-9. |
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Chemical & Physical Properties
| Density | 1.2±0.1 g/cm3 |
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| Boiling Point | 512.8±50.0 °C at 760 mmHg |
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| Molecular Formula | C20H28O4 |
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| Molecular Weight | 332.43 |
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| Flash Point | 178.3±23.6 °C |
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| PSA | 86.99000 |
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| LogP | 2.97 |
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| Vapour Pressure | 0.0±3.0 mmHg at 25°C |
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| Index of Refraction | 1.584 |
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| InChIKey | YIIRVUDGRKEWBV-LHHJGKSTSA-N |
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| SMILES | C=C1CCC2C(C)(CO)C(O)CCC2(C)C1CC=C1C=COC1=O |
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Safety Information
| Hazard Codes | Xi |
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| Safety Phrases | 24/25 |
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| RIDADR | NONH for all modes of transport |
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| RTECS | LU3490300 |
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Synonyms
| (3E)-4-Hydroxy-3-{2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylenedecahydronaphthalen-1-yl]ethylidene}furan-2(3H)-one |
| Dehydroanddrographolide |
| 2(3H)-Furanone,3-[2-[(1S,4aS,5R,6R,8aS)-decahydro |
| DEOXY-11,12-DIDEHYDROANDROGRAPHOLIDE |
| (3E)-4-Hydroxy-3-{2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylenedecahydro-1-naphthalenyl]ethylidene}-2(3H)-furanone |
| Dehydroandrographoline |
| 6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-1-naphthalenyl]ethylidene]-,(3E) |
| ANDROGRAPHOLIDE,DEHYDRO |
| 2(3H)-Furanone, 3-[2-[(1R,4aS,5R,6R,8aS)-decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-1-naphthalenyl]ethylidene]-4-hydroxy-, (3E)- |
| 14-Deoxy-11-dehydroandrographolide |
| Dehydrographkide |