Atractylon (BioDeep_00000000463)

   


代谢物信息卡片


Naphtho(2,3-b)furan, 4,4a,5,6,7,8,8a,9-octahydro-3,8a-dimethyl-5-methylene-, (4aS-trans)-

化学式: C15H20O (216.1514)
中文名称: 苍术酮
谱图信息: 最多检出来源 Mentha canadensis(plant) 91.18%

分子结构信息

SMILES: C1(=C)[C@H]2[C@](CCC1)(Cc1c(C2)c(co1)C)C
InChI: InChI=1S/C15H20O/c1-10-5-4-6-15(3)8-14-12(7-13(10)15)11(2)9-16-14/h9,13H,1,4-8H2,2-3H3



数据库引用编号

16 个数据库交叉引用编号

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)

8 个相关的物种来源信息

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。

亚细胞结构定位 关联基因列表
Cytoplasm 7 BCL2, CDH1, CDH2, IL13, PIK3CA, PTGS2, TMPO
Peripheral membrane protein 2 CLTCL1, PTGS2
Endoplasmic reticulum membrane 2 BCL2, PTGS2
Nucleus 5 BCL2, CDH1, PRPF31, SIRT3, TMPO
cytosol 4 BCL2, CDH1, CLTCL1, PIK3CA
dendrite 1 DRD2
trans-Golgi network 2 CDH1, CLTCL1
nucleoplasm 3 CDH1, PRPF31, SIRT3
Cell membrane 3 CDH1, CDH2, DRD2
Cytoplasmic side 1 CLTCL1
lamellipodium 3 CDH1, CDH2, PIK3CA
Multi-pass membrane protein 1 DRD2
Golgi apparatus membrane 1 DRD2
Synapse 1 DRD2
cell junction 2 CDH1, CDH2
cell surface 1 CDH2
glutamatergic synapse 2 CDH1, DRD2
Golgi apparatus 1 CDH1
Golgi membrane 1 DRD2
postsynapse 1 CDH1
presynaptic membrane 1 DRD2
sarcolemma 1 CDH2
acrosomal vesicle 1 DRD2
endosome 1 CDH1
plasma membrane 6 CDH1, CDH2, DRD2, IFNLR1, IGHE, PIK3CA
synaptic vesicle membrane 1 DRD2
Membrane 6 BCL2, CDH1, CDH2, CLTCL1, IFNLR1, TMPO
apical plasma membrane 1 CDH2
axon 1 DRD2
basolateral plasma membrane 1 CDH2
caveola 1 PTGS2
extracellular exosome 2 CDH1, CLTCL1
endoplasmic reticulum 2 BCL2, PTGS2
extracellular space 5 IGHE, IL13, IL4, IL5, IL6
perinuclear region of cytoplasm 2 CDH1, PIK3CA
adherens junction 2 CDH1, CDH2
apicolateral plasma membrane 1 CDH2
intercalated disc 2 CDH2, PIK3CA
mitochondrion 2 BCL2, SIRT3
protein-containing complex 3 BCL2, PTGS2, SIRT3
Microsome membrane 1 PTGS2
postsynaptic density 1 CDH2
Single-pass type I membrane protein 4 CDH1, CDH2, IFNLR1, IGHE
Secreted 4 IL13, IL4, IL5, IL6
extracellular region 7 CDH1, DNAH9, IGHE, IL13, IL4, IL5, IL6
cytoplasmic side of plasma membrane 1 CDH1
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 1 BCL2
Mitochondrion matrix 1 SIRT3
mitochondrial matrix 1 SIRT3
ciliary membrane 1 DRD2
motile cilium 1 DNAH9
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 3 BCL2, CDH1, TMPO
external side of plasma membrane 1 IL13
actin cytoskeleton 1 CDH1
dendritic spine 1 DRD2
perikaryon 1 DRD2
apical part of cell 1 CDH2
cell-cell junction 1 CDH2
clathrin-coated pit 1 CLTCL1
postsynaptic membrane 1 DRD2
presynaptic active zone membrane 1 CDH2
Cell membrane, sarcolemma 1 CDH2
pore complex 1 BCL2
focal adhesion 1 CDH2
microtubule 1 DNAH9
spindle 1 CLTCL1
GABA-ergic synapse 1 DRD2
Cell junction, adherens junction 2 CDH1, CDH2
flotillin complex 1 CDH1
collagen-containing extracellular matrix 1 CDH2
fascia adherens 1 CDH2
lateral plasma membrane 2 CDH1, DRD2
axoneme 1 DNAH9
nuclear speck 1 PRPF31
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 2 PTGS2, TMPO
nuclear outer membrane 1 PTGS2
Late endosome 1 CLTCL1
neuron projection 2 CDH2, PTGS2
cilium 1 DRD2
chromatin 1 TMPO
IgE immunoglobulin complex 1 IGHE
Golgi apparatus, trans-Golgi network 1 CDH1
Cytoplasm, cytoskeleton, cilium axoneme 1 DNAH9
non-motile cilium 1 DRD2
spliceosomal complex 1 PRPF31
[Isoform 2]: Cell membrane 1 IGHE
sperm flagellum 1 DRD2
nuclear envelope 1 TMPO
Endomembrane system 1 CLTCL1
sorting endosome 1 CLTCL1
Cytoplasmic vesicle membrane 1 CLTCL1
Nucleus speckle 1 PRPF31
myelin sheath 1 BCL2
clathrin-coated vesicle 1 CLTCL1
plasma membrane raft 1 CDH2
endoplasmic reticulum lumen 3 CDH2, IL6, PTGS2
MLL1 complex 1 PRPF31
axon terminus 1 DRD2
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
endocytic vesicle 1 DRD2
anaphase-promoting complex 1 CDH1
clathrin-coated endocytic vesicle 1 CLTCL1
9+2 motile cilium 1 DNAH9
dynein complex 1 DNAH9
Cajal body 1 PRPF31
[Isoform 2]: Nucleus 1 CDH1
U2-type precatalytic spliceosome 1 PRPF31
U2-type spliceosomal complex 1 PRPF31
postsynaptic specialization membrane 1 CDH2
apical junction complex 1 CDH1
U4/U6 x U5 tri-snRNP complex 1 PRPF31
dopaminergic synapse 1 DRD2
clathrin coat of coated pit 1 CLTCL1
coated vesicle 1 CLTCL1
Cell junction, desmosome 2 CDH1, CDH2
desmosome 2 CDH1, CDH2
Membrane, coated pit 1 CLTCL1
catenin complex 2 CDH1, CDH2
Nucleus, Cajal body 1 PRPF31
precatalytic spliceosome 1 PRPF31
[Isoform 3]: Cell membrane 1 IGHE
clathrin coat of trans-Golgi network vesicle 1 CLTCL1
[Isoform 1]: Secreted 1 IGHE
IgE B cell receptor complex 1 IGHE
immunoglobulin complex, circulating 1 IGHE
interleukin-6 receptor complex 1 IL6
clathrin complex 1 CLTCL1
BAD-BCL-2 complex 1 BCL2
G protein-coupled receptor complex 1 DRD2
U4 snRNP 1 PRPF31
[Isoform Zeta]: Cytoplasm 1 TMPO
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA
U4atac snRNP 1 PRPF31
spliceosomal tri-snRNP complex 1 PRPF31
interleukin-28 receptor complex 1 IFNLR1
outer dynein arm 1 DNAH9
distal portion of axoneme 1 DNAH9


文献列表

  • Baohong Song, Wei Wang, Ruipeng Liu, Jinjin Cai, Yuanyuan Jiang, Xuemei Tang, Hongfei Wu, Hui Ao, Lu Chen. Geographic Differentiation of Essential Oil from Rhizome of Cultivated Atractylodes lancea by Using GC-MS and Chemical Pattern Recognition Analysis. Molecules (Basel, Switzerland). 2023 Feb; 28(5):. doi: 10.3390/molecules28052216. [PMID: 36903461]
  • Cholil Yun, Zhuowen Zhao, Lin Gu, Zhonghua Zhang, Shengfang Wang, Yutong Shi, Na Miao, Ilbong Ri, Wenjie Wang, Huimei Wang. In vitro production of atractylon and β-eudesmol from Atractylodes chinensis by adventitious root culture. Applied microbiology and biotechnology. 2022 Nov; 106(21):7027-7037. doi: 10.1007/s00253-022-12194-5. [PMID: 36171502]
  • Junjun Mao, Xinping Wang, Minghui Yu, Chenkun Sun. Effects of Atractylon on Proliferation and Apoptosis of Intestinal Cancer Cells Through PI3K/AKT/mTOR Signaling Pathway. Cellular and molecular biology (Noisy-le-Grand, France). 2022 May; 68(5):153-160. doi: 10.14715/cmb/2022.68.5.21. [PMID: 36029491]
  • Yang Cheng, Jian Ping, Jianjie Chen, Yifei Fu, Hui Zhao, Jiahua Xue. Molecular mechanism of atractylon in the invasion and migration of hepatic cancer cells based on high‑throughput sequencing. Molecular medicine reports. 2022 04; 25(4):. doi: 10.3892/mmr.2022.12628. [PMID: 35119084]
  • Hongli Li, Fei Wang, Zhenyu Zhou, Xi Jiang, Fei Li, Yaru Feng, Chuhe Liu, Yu Zhang, Shengjie Fan, Xiaojun Wu, Cheng Huang. Atractylon, a novel dopamine 2 receptor agonist, ameliorates Parkinsonian like motor dysfunctions in MPTP-induced mice. Neurotoxicology. 2022 03; 89(?):121-126. doi: 10.1016/j.neuro.2022.01.010. [PMID: 35104500]
  • Chunmei Zhai, Jianping Zhao, Amar G Chittiboyina, Yonghai Meng, Mei Wang, Ikhlas A Khan. Newly Generated Atractylon Derivatives in Processed Rhizomes of Atractylodes macrocephala Koidz. Molecules (Basel, Switzerland). 2020 Dec; 25(24):. doi: 10.3390/molecules25245904. [PMID: 33322214]
  • Yan Lin, Xiuxiu Liu, Dan Tan, Zhiyan Jiang. Atractylon treatment prevents sleep-disordered breathing-induced cognitive dysfunction by suppression of chronic intermittent hypoxia-induced M1 microglial activation. Bioscience reports. 2020 06; 40(6):. doi: 10.1042/bsr20192800. [PMID: 32490526]
  • Na-Ra Han, Phil-Dong Moon, Sun-Young Nam, Ka-Jung Ryu, Myoung-Schook Yoou, Jung-Hye Choi, Sung-Yeoun Hwang, Hyung-Min Kim, Hyun-Ja Jeong. Inhibitory effects of atractylone on mast cell-mediated allergic reactions. Chemico-biological interactions. 2016 Oct; 258(?):59-68. doi: 10.1016/j.cbi.2016.08.015. [PMID: 27553716]
  • Hee-Yun Kim, Sun-Young Nam, Sung-Yeoun Hwang, Hyung-Min Kim, Hyun-Ja Jeong. Atractylone, an active constituent of KMP6, attenuates allergic inflammation on allergic rhinitis in vitro and in vivo models. Molecular immunology. 2016 10; 78(?):121-132. doi: 10.1016/j.molimm.2016.09.007. [PMID: 27636508]
  • Yang Cheng, Jing-Yin Mai, Tian-Lu Hou, Jian Ping, Jian-Jie Chen. Antiviral activities of atractylon from Atractylodis Rhizoma. Molecular medicine reports. 2016 Oct; 14(4):3704-10. doi: 10.3892/mmr.2016.5713. [PMID: 27600871]
  • Lih-Geeng Chen, Yun-Sheng Jan, Po-Wei Tsai, Hisayoshi Norimoto, Seiwa Michihara, Chiaki Murayama, Ching-Chiung Wang. Anti-inflammatory and Antinociceptive Constituents of Atractylodes japonica Koidzumi. Journal of agricultural and food chemistry. 2016 Mar; 64(11):2254-62. doi: 10.1021/acs.jafc.5b05841. [PMID: 26919689]
  • Megumi Iwasa, Toshiki Iwasaki, Toshirou Ono, Mitsuo Miyazawa. Chemical composition and major odor-active compounds of essential oil from PINELLIA TUBER (dried rhizome of Pinellia ternata) as crude drug. Journal of oleo science. 2014; 63(2):127-35. doi: 10.5650/jos.ess13092. [PMID: 24500103]
  • Wen-Long Zhao, Hui Wiu, Guo-Shun Shan, Tian-Zhu Jia. [Verification of processing theory of "reducing ketone and dryness, and increasing ester and effect" for bran-fried atractylodes]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2013 Oct; 38(20):3493-7. doi: . [PMID: 24490560]
  • Suihar Rong, Hai Lin, Ni Gao. [Study on processing technology and processing principles of atractrylodis macrocephalae rhizoma]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2011 Apr; 36(8):1001-3. doi: ". [PMID: 21809571]
  • Keiko Hasada, Takamitsu Yoshida, Takeshi Yamazaki, Naoki Sugimoto, Tetsuji Nishimura, Akito Nagatsu, Hajime Mizukami. Quantitative determination of atractylon in Atractylodis Rhizoma and Atractylodis Lanceae Rhizoma by 1H-NMR spectroscopy. Journal of natural medicines. 2010 Apr; 64(2):161-6. doi: 10.1007/s11418-010-0393-x. [PMID: 20165926]
  • Dan Shou, Shiwen Dai, Jianmin Zhang, Hongyu Li, Zhongming Yu. [Simultaneous determination of atractylenolide III, atractylenolide I and atractylon in Artactylodis macrocephala using microbore liquid chromatography]. Se pu = Chinese journal of chromatography. 2008 Sep; 26(5):637-9. doi: . [PMID: 19160769]
  • Zhen Ouyang, Ling Yang, Shu-Lan Su, Xu Feng, Ming Wang. [Fingerprint of volatile oil of Atractylodes lancea by GC-MS]. Yao xue xue bao = Acta pharmaceutica Sinica. 2007 Sep; 42(9):968-72. doi: . [PMID: 18050740]
  • Mitsuo Miyazawa, Jyunichi Kawata. Composition of the essential oil of rootstock from Cimicifuga simplex. Natural product research. 2006 May; 20(6):542-7. doi: 10.1080/14786410500182037. [PMID: 16835085]
  • Ching-Chiung Wang, Lih-Geeng Chen, Ling-Ling Yang. Cytotoxic activity of sesquiterpenoids from Atractylodes ovata on leukemia cell lines. Planta medica. 2002 Mar; 68(3):204-8. doi: 10.1055/s-2002-23144. [PMID: 11914954]
  • M Resch, A Steigel, Z L Chen, R Bauer. 5-Lipoxygenase and cyclooxygenase-1 inhibitory active compounds from Atractylodes lancea. Journal of natural products. 1998 Mar; 61(3):347-50. doi: 10.1021/np970430b. [PMID: 9544564]
  • M Kohjyouma, S Nakajima, A Namera, R Shimizu, H Mizukami, H Kohda. Random amplified polymorphic DNA analysis and variation of essential oil components of Atractylodes plants. Biological & pharmaceutical bulletin. 1997 May; 20(5):502-6. doi: 10.1248/bpb.20.502. [PMID: 9178929]
  • H Mizukami, R Shimizu, H Kohda, M Kohjyouma, F Kawanishi, N Hiraoka. Restriction fragment length polymorphisms of rDNA and variation of essential oil composition in Atractylodes plants. Biological & pharmaceutical bulletin. 1996 Apr; 19(4):577-80. doi: 10.1248/bpb.19.577. [PMID: 8860962]
  • K Satoh, F Nagai, K Ushiyama, I Kano. Specific inhibition of Na+,K(+)-ATPase activity by atractylon, a major component of byaku-jutsu, by interaction with enzyme in the E2 state. Biochemical pharmacology. 1996 Feb; 51(3):339-43. doi: 10.1016/0006-2952(95)02188-4. [PMID: 8573201]
  • J M Hwang, T H Tseng, Y S Hsieh, F P Chou, C J Wang, C Y Chu. Inhibitory effect of atractylon on tert-butyl hydroperoxide induced DNA damage and hepatic toxicity in rat hepatocytes. Archives of toxicology. 1996; 70(10):640-4. doi: 10.1007/s002040050323. [PMID: 8870957]
  • Y Kiso, M Tohkin, H Hikino. Mechanism of antihepatotoxic activity of atractylon, I: Effect on free radical generation and lipid peroxidation. Planta medica. 1985 Apr; ?(2):97-100. doi: 10.1055/s-2007-969416. [PMID: 4034742]
  • Y Kiso, M Tohkin, H Hikino. Antihepatotoxic principles of Atractylodes rhizomes. Journal of natural products. 1983 Sep; 46(5):651-4. doi: 10.1021/np50029a010. [PMID: 6418860]