アビエタン
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- abietane diterpene
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/01/26 16:04:40」(JST)
[Wiki en表示]
Abietane |
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Identifiers |
CAS number |
19407-12-6 N |
PubChem |
6857485 |
ChemSpider |
5256821 Y |
ChEBI |
CHEBI:35673 Y |
Jmol-3D images |
Image 1 |
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[H][C@]12[C@@](C[C@@H](C(C)C)CC2)([H])CC[C@@]3([H])C(C)(C)CCC[C@@]31C
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InChI=1S/C20H36/c1-14(2)15-7-9-17-16(13-15)8-10-18-19(3,4)11-6-12-20(17,18)5/h14-18H,6-13H2,1-5H3/t15-,16-,17-,18-,20+/m0/s1 Y
Key: STIVVCHBLMGYSL-ZYNAIFEFSA-N Y
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Properties |
Molecular formula |
C20H36 |
Molar mass |
276.50 g mol−1 |
Density |
0.876 g/ml |
Melting point |
338 °C; 640 °F; 611 K |
N (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) |
Infobox references |
Abietane is a diterpene that forms the structural basis for a variety of natural chemical compounds such as abietic acid,[1] carnosic acid, and ferruginol which are collectively known as abietanes or abietane diterpenes.
See also[edit]
References[edit]
- ^ San Feliciano, Arturo; Gordaliza, Marina; Salinero, Miguel A.; Miguel del Corral, Jose M (1993). "Abietane acids: sources, biological activities, and therapeutic uses". Planta Medica 59 (6): 485–490. doi:10.1055/s-2006-959744. PMID 8302943.
English Journal
- Isolation, structure elucidation, and induction of hepatoma cell apoptosis of abietane diterpenoids from Abies faxoniana.
- Wang GW1, Lv C2,3, Shen YH2, Zhang WD2,3.
- Journal of Asian natural products research.J Asian Nat Prod Res.2017 May;19(5):448-456. doi: 10.1080/10286020.2016.1232714. Epub 2016 Oct 3.
- PMID 27690644
- Effect of rosmarinic acid and carnosic acid on AGEs formation in vitro.
- Ou J1, Huang J2, Wang M3, Ou S4.
- Food chemistry.Food Chem.2017 Apr 15;221:1057-1061. doi: 10.1016/j.foodchem.2016.11.056. Epub 2016 Nov 11.
- PMID 27979058
- Abietane diterpenoids from Cephalotaxus lanceolata.
- Chen XJ1,2, Ni L2, Bao MF2, Wang L1, Cai XH2.
- Natural product research.Nat Prod Res.2017 Apr 12:1-6. doi: 10.1080/14786419.2017.1314280. [Epub ahead of print]
- PMID 28399666
Japanese Journal
- Diterpene Para-Hydroquinone Compounds Derived from Cryptoquinone Inhibit Adipocyte Differentiation of Mouse 3T3-L1 Cells and Activate the Nrf2/ARE Pathway
- SASAKI Shunsuke,TOZAWA Terumasa,SUGAMOTO Kazuhiro [他],MATSUSHITA Yohichi,SATOH Takumi
- Bioscience, Biotechnology, and Biochemistry 77(10), 2131-2133, 2013
- … Cryptoquinone, an abietane-type diterpene para-quinone from the bark of Cryptomeria japonica has antifungal and cytotoxic activities, but its biological actions are largely unknown. …
- NAID 130003381875
- New ent-Abietane and ent-Kaurane Diterpenoids from Isodon rubescens
- Liu Xu,Zhan Rui,Wang Wei-Guang [他],Du Xue,Li Xiao-Nian,Yang Jian-Hong,Zhang Peng,Li Yan,Pu Jian-Xin,Wu Ji-Zhou,Sun Han-Dong
- Chemical and Pharmaceutical Bulletin 61(1), 90-95, 2013
- … Five new ent-abietane diterpenoids, ent-abierubesins A–E (1–5), and two new ent-kauranoids, hubeirubesins A and B (6, 7), together with three known diterpenoids (8–10), were isolated from the aerial parts of Isodon rubescens. …
- NAID 130003360716
- Terpenes isolated from Chamaecyparis pisifera and their affect to Seiridium canker
- 茨城大学教育学部紀要. 自然科学 (60), 79-89, 2011
- … Fourteen diterpenes (6 abietane-type, 1 pimarane-type, 2 pisifera-type, 3 labdane-type, and 1dinorlabdane-type) in the bark, 4 sesquiterpenes in the wood and 6 diterpenes (4 abietane-type and2 pisifera-type) in the leaf were isolated from Chamaecyparis pisifera. …
- NAID 80021849811
Related Links
- Structure, properties, spectra, suppliers and links for: Abietane. ... Predicted data is generated using the US Environmental Protection Agency’s EPISuite Log Octanol-Water Partition Coef (SRC): Log Kow (KOWWIN v1.67 ...
- Labelling experiments with [1-13C] glucose, [1-13C] sodium acetate and [1,2-13C2] sodium acetate proved that the fundamental isopentenyl diphosphate (IPP) unit, ... 1. Introduction Abietane diterpenoids are a class of natural ...
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