Cedarwood oil terpenes (BioDeep_00000228021)
Main id: BioDeep_00000007506
human metabolite PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C15H24 (204.1878)
中文名称: 柏木油萜烯, α-柏木烯
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1=CCC23CC1C(C)(C)C2CCC3C
InChI: InChI=1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7,11-13H,5-6,8-9H2,1-4H3
描述信息
It is used as a food additive .
(-)-Cedrene (α-cedrene) is a sesquiterpene constituent of cedarwood oils, with anti-leukemic, antimicrobial and anti-obesity activities[1].
(-)-Cedrene (α-cedrene) is a sesquiterpene constituent of cedarwood oils, with anti-leukemic, antimicrobial and anti-obesity activities[1].
(-)-Cedrene (α-cedrene) is a sesquiterpene constituent of cedarwood oils, with anti-leukemic, antimicrobial and anti-obesity activities[1].
(-)-Cedrene (α-cedrene) is a sesquiterpene constituent of cedarwood oils, with anti-leukemic, antimicrobial and anti-obesity activities[1].
同义名列表
数据库引用编号
13 个数据库交叉引用编号
- ChEBI: CHEBI:167345
- PubChem: 521207
- HMDB: HMDB0303210
- foodb: FDB009128
- chemspider: 454638
- CAS: 68608-32-2
- CAS: 19069-48-8
- CAS: 469-61-4
- medchemexpress: HY-135190
- LOTUS: LTS0023956
- KEGG: C09630
- PubChem: 11820
- KNApSAcK: 10216
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
51 个相关的物种来源信息
- 42228 - Acoraceae: LTS0023956
- 4464 - Acorus: LTS0023956
- 4465 - Acorus calamus: 10.1016/J.PHYTOCHEM.2005.01.007
- 4465 - Acorus calamus: LTS0023956
- 165353 - Angelica sinensis (Oliv.)Diels: -
- 16727 - Aristolochiaceae: 10.1515/ZNC-1984-7-803
- 4219 - Artemisia: LTS0023956
- 72329 - Artemisia herba-alba: 10.1016/0031-9422(88)83114-5
- 72329 - Artemisia herba-alba: LTS0023956
- 4210 - Asteraceae: LTS0023956
- 74301 - Callitropsis funebris: 10.1135/CCCC19681939
- 13414 - Chamaecyparis: LTS0023956
- 13422 - Chrysanthemum: LTS0023956
- 146995 - Chrysanthemum indicum: 10.1002/CBDV.201000034
- 146995 - Chrysanthemum indicum: LTS0023956
- 3367 - Cupressaceae: LTS0023956
- 13468 - Cupressus: 10.1135/CCCC19681939
- 13468 - Cupressus: LTS0023956
- 329083 - Cupressus dupreziana: LTS0023956
- 13469 - Cupressus sempervirens: LTS0023956
- 2759 - Eukaryota: LTS0023956
- 9606 - Homo sapiens: -
- 13100 - Juniperus: LTS0023956
- 114268 - Juniperus californica: 10.3891/ACTA.CHEM.SCAND.15-0713
- 114268 - Juniperus californica: 10.3891/ACTA.CHEM.SCAND.15-0721
- 114268 - Juniperus californica: LTS0023956
- 1719643 - Juniperus foetidissima: 10.3891/ACTA.CHEM.SCAND.15-0721
- 1719643 - Juniperus foetidissima: LTS0023956
- 669713 - Juniperus horizontalis: 10.1139/V61-339
- 669713 - Juniperus horizontalis: LTS0023956
- 62753 - Juniperus procera: 10.3891/ACTA.CHEM.SCAND.15-0713
- 62753 - Juniperus procera: 10.3891/ACTA.CHEM.SCAND.15-0721
- 62753 - Juniperus procera: LTS0023956
- 177241 - Juniperus thurifera: 10.1016/S0040-4020(00)00292-1
- 177241 - Juniperus thurifera: 10.1055/S-2005-837753
- 177241 - Juniperus thurifera: LTS0023956
- 4136 - Lamiaceae: LTS0023956
- 4447 - Liliopsida: LTS0023956
- 105884 - Lonicera japonica: 10.3390/MOLECULES18021368
- 3398 - Magnoliopsida: LTS0023956
- 58019 - Pinopsida: LTS0023956
- 33090 - Plants: -
- 99101 - Seriphidium: LTS0023956
- 155231 - Sideritis: LTS0023956
- 155234 - Sideritis athoa: 10.1080/10412905.1993.9698303
- 155234 - Sideritis athoa: LTS0023956
- 155256 - Sideritis perfoliata: LTS0023956
- 35493 - Streptophyta: LTS0023956
- 58023 - Tracheophyta: LTS0023956
- 33090 - Viridiplantae: LTS0023956
- 94328 - Zingiber officinale: 10.1016/J.PHYTOCHEM.2005.08.001
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Yucong Li, Jiahui Shao, Yansong Fu, Yu Chen, Hongzhe Wang, Zhihui Xu, Haichao Feng, Weibing Xun, Yunpeng Liu, Nan Zhang, Qirong Shen, Wei Xuan, Ruifu Zhang. The volatile cedrene from Trichoderma guizhouense modulates Arabidopsis root development through auxin transport and signalling.
Plant, cell & environment.
2022 03; 45(3):969-984. doi:
10.1111/pce.14230
. [PMID: 34800291] - Anhye Kim, Stephen R Dueker, Jun Gi Hwang, Jangsoo Yoon, Sang-Won Lee, Hye Suk Lee, Byung-Yong Yu, Kyung-Sang Yu, Howard Lee. An Investigation of the Metabolism and Excretion of KD101 and Its Interindividual Differences: A Microtracing Mass Balance Study in Humans.
Clinical and translational science.
2021 01; 14(1):231-238. doi:
10.1111/cts.12848
. [PMID: 33460293] - Li Bai, Mei-Ling Jiao, Hong-Yuan Zang, Shan-Shan Guo, Yang Wang, Yu-Li Sang, Shu-Shan Du. Chemical composition of essential oils from four Rhododendron species and their repellent activity against three stored-product insects.
Environmental science and pollution research international.
2019 Aug; 26(22):23198-23205. doi:
10.1007/s11356-019-05577-1
. [PMID: 31201707] - Yuan Yuan, Ye Sun, Yanchun Zhao, Chungui Liu, Xiulan Chen, Fengtong Li, Jianzhong Bao. Identification of Floral Scent Profiles in Bearded Irises.
Molecules (Basel, Switzerland).
2019 May; 24(9):. doi:
10.3390/molecules24091773
. [PMID: 31067789] - Tao Tong, Rina Yu, Taesun Park. α-Cedrene protects rodents from high-fat diet-induced adiposity via adenylyl cyclase 3.
International journal of obesity (2005).
2019 01; 43(1):202-216. doi:
10.1038/s41366-018-0176-0
. [PMID: 30568259] - Tao Tong, Jinju Park, Cheil Moon, Taesun Park. Regulation of Adipogenesis and Thermogenesis through Mouse Olfactory Receptor 23 Stimulated by α-Cedrene in 3T3-L1 Cells.
Nutrients.
2018 Nov; 10(11):. doi:
10.3390/nu10111781
. [PMID: 30453511] - Tao Tong, Sang Eun Ryu, Yeojin Min, Claire A de March, Caroline Bushdid, Jérôme Golebiowski, Cheil Moon, Taesun Park. Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP-PKA pathway.
Scientific reports.
2017 08; 7(1):9471. doi:
10.1038/s41598-017-10379-x
. [PMID: 28842679] - Tae Hwan Kim, Sun Dong Yoo, Hye Suk Lee, Kyoung Mee Lee, Su Hyun Seok, Min Gi Kim, Byung Hwa Jung, Min Gyu Kim, Beom Soo Shin. In vivo absorption and disposition of α-cedrene, a sesquiterpene constituent of cedarwood oil, in female and male rats.
Drug metabolism and pharmacokinetics.
2015 Apr; 30(2):168-73. doi:
10.1016/j.dmpk.2014.12.003
. [PMID: 25857232] - Hong-bing Zhao, Zhi-hui Wang, Fang He, Han Meng, Jian-hua Peng, Ji-lian Shi. [Analysis of Volatile Oils from Different Processed Products of Zingiber officinale Rhizome by GC-MS].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2015 Apr; 38(4):723-6. doi:
. [PMID: 26672336]
- Pankaj Sharma, G C Shah. Composition and antioxidant activity of Senecio nudicaulis Wall. ex DC. (Asteraceae): a medicinal plant growing wild in Himachal Pradesh, India.
Natural product research.
2015; 29(9):883-6. doi:
10.1080/14786419.2014.990904
. [PMID: 25515495] - Oladipupo A Lawal, Isiaka A Ogunwande, Andy R Opoku. Constituents of essential oils from the leaf and flower of Plumeria alba grown in Nigeria.
Natural product communications.
2014 Nov; 9(11):1613-4. doi:
. [PMID: 25532294]
- Joo Yeon Hong, Byung Ho Lee, Tae Hwan Kim, Jongki Hong, Kyoung Mee Lee, Sun Dong Yoo, Hye Suk Lee. GC-MS/MS method for the quantification of α-cedrene in rat plasma and its pharmacokinetic application.
Journal of separation science.
2013 Nov; 36(21-22):3558-62. doi:
10.1002/jssc.201300828
. [PMID: 23996797] - N Böke Sarıkahya, P Kayce, E Halay, R S Göktürk, H Sümbül, S Kırmızıgül. Phytochemical analysis of the essential oils of 10 endemic Cephalaria species from Turkey.
Natural product research.
2013; 27(9):830-3. doi:
10.1080/14786419.2012.701216
. [PMID: 22757667] - Nasser M Al-Daghri, Majed S Alokail, Khalid M Alkharfy, Abdul Khader Mohammed, Sherif H Abd-Alrahman, Sobhy M Yakout, Osama E Amer, Soundararajan Krishnaswamy. Fenugreek extract as an inducer of cellular death via autophagy in human T lymphoma Jurkat cells.
BMC complementary and alternative medicine.
2012 Oct; 12(?):202. doi:
10.1186/1472-6882-12-202
. [PMID: 23110539] - Abha Chaudhary, Prabha Sharma, Gireesh Nadda, Dhananjay Kumar Tewary, Bikram Singh. Chemical composition and larvicidal activities of the Himalayan cedar, Cedrus deodara essential oil and its fractions against the diamondback moth, Plutella xylostella.
Journal of insect science (Online).
2011; 11(?):157. doi:
10.1673/031.011.15701
. [PMID: 22239128] - Héctor Isaac Rocha-González, Everardo Blaisdell-López, Vinicio Granados-Soto, Andrés Navarrete. Antinociceptive effect of 7-hydroxy-3,4-dihydrocadalin isolated from Heterotheca inuloides: role of peripheral 5-HT₁ serotonergic receptors.
European journal of pharmacology.
2010 Dec; 649(1-3):154-60. doi:
10.1016/j.ejphar.2010.09.022
. [PMID: 20863828] - E Nibret, M Wink. Trypanocidal and antileukaemic effects of the essential oils of Hagenia abyssinica, Leonotis ocymifolia, Moringa stenopetala, and their main individual constituents.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2010 Oct; 17(12):911-20. doi:
10.1016/j.phymed.2010.02.009
. [PMID: 20359874] - Ya-qin Wang, Jian-ping Ma, Sheng-li Pan, Ai-jun Hou, Jian-ming Huang. [Studies on the chemical constituents of Coleus forskohlii].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2009 Sep; 32(9):1381-5. doi:
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. [PMID: 20034210] - Xia Wang, Jing Xu, You-Lian Shen, Feng-Ying Liu, Yong-Jun Du. [Electroantennogram responses of Maruca testulalis (Lepidoptera: Pyralidae) to plant volatiles and sex pheromone].
Ying yong sheng tai xue bao = The journal of applied ecology.
2009 Aug; 20(8):1973-9. doi:
. [PMID: 19947220]
- Ping Yan, Zhe-zhi Wang. [Analysis of essential oil from different organs of Caryopteris tangutica].
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials.
2009 Jan; 32(1):61-5. doi:
"
. [PMID: 19445123] - Fangqiu Guo, Lanfang Huang, Shaoyun Zhou. [Headspace solid-phase microextraction-gas chromatography-mass spectrometry for analysis of volatile components from Atractlodes macrocephala Koidz].
Se pu = Chinese journal of chromatography.
2007 Jan; 25(1):43-7. doi:
. [PMID: 17432574]
- David Chappell, Andrew T Russell. From alpha-cedrene to crinipellin B and onward: 25 years of the alkene-arene meta-photocycloaddition reaction in natural product synthesis.
Organic & biomolecular chemistry.
2006 Dec; 4(24):4409-30. doi:
10.1039/b614011b
. [PMID: 17268633] - Johannes Panten, Heinz-Jürgen Bertram, Horst Surburg. New woody and ambery notes from cedarwood and turpentine oil.
Chemistry & biodiversity.
2004 Dec; 1(12):1936-48. doi:
10.1002/cbdv.200490148
. [PMID: 17191830] - Fred J Eller, Scott L Taylor. Pressurized fluids for extraction of cedarwood oil from Juniperus virginianna.
Journal of agricultural and food chemistry.
2004 Apr; 52(8):2335-8. doi:
10.1021/jf030783i
. [PMID: 15080642] - L Maistrello, G Henderson, R A Laine. Efficacy of vetiver oil and nootkatone as soil barriers against Formosan subterranean termite (Isoptera: Rhinotermitidae).
Journal of economic entomology.
2001 Dec; 94(6):1532-7. doi:
10.1603/0022-0493-94.6.1532
. [PMID: 11777060] - W J Kerr, M McLaughlin, A J Morrison, P L Pauson. Formal total synthesis of (+/-)-alpha- and beta-cedrene by preparation of cedrone. Construction of the tricyclic carbon skeleton by the use of a highly efficient intramolecular Khand annulation.
Organic letters.
2001 Sep; 3(19):2945-8. doi:
10.1021/ol016054a
. [PMID: 11554814] - T A Akeng'a, S C Chhabra. Analysis of the essential oil of Juniperus procera Endl. growing in Kenya.
African journal of medicine and medical sciences.
1997 Mar; 26(1-2):79-81. doi:
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. [PMID: 10895238] - A M Malkinson, B E Haley, B E Macintyre, M S Butley. Changes in pulmonary adenosine triphosphate-binding proteins detected by nucleotide photoaffinity labeling following treatment of mice with the tumor-modulatory agent butylated hydroxytoluene.
Cancer research.
1986 Sep; 46(9):4626-30. doi:
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. [PMID: 3731115] - A M Malkinson, D S Beer. Pharmacologic and genetic studies on the modulatory effects of butylated hydroxytoluene on mouse lung adenoma formation.
Journal of the National Cancer Institute.
1984 Oct; 73(4):925-33. doi:
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- A M Malkinson. Modulation of the incidence of urethane induced mouse lung adenomas by butylated hydroxytoluene (BHT).
Proceedings of the Western Pharmacology Society.
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