[10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] (5E,8E,11E,14E)-icosa-5,8,11,14-tetraenoate (BioDeep_00000912165)

Main id: BioDeep_00000023991

 

PANOMIX_OTCML-2023


代谢物信息卡片


[10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] (5E,8E,11E,14E)-icosa-5,8,11,14-tetraenoate

化学式: C47H76O2 (672.5844996)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(C)CCC[C@@H](C)[C@H]1CC[C@@]2([H])[C@]3([H])CC=C4C[C@@H](OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)CC[C@]4(C)[C@@]3([H])CC[C@]12C
InChI: InChI=1S/C47H76O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-27-45(48)49-40-32-34-46(5)39(36-40)28-29-41-43-31-30-42(38(4)26-24-25-37(2)3)47(43,6)35-33-44(41)46/h11-12,14-15,17-18,20-21,28,37-38,40-44H,7-10,13,16,19,22-27,29-36H2,1-6H3/b12-11+,15-14+,18-17+,21-20+

描述信息

Cholesteryl arachidonate is an endogenous metabolite.

同义名列表

2 个代谢物同义名

[10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] (5E,8E,11E,14E)-icosa-5,8,11,14-tetraenoate; Cholesteryl arachidonate



数据库引用编号

3 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)

0 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。



文献列表

  • Shanshan Zhong, Luxiao Li, Xia Shen, Qiujing Li, Wenxin Xu, Xiaoping Wang, Yongzhen Tao, Huiyong Yin. An update on lipid oxidation and inflammation in cardiovascular diseases. Free radical biology & medicine. 2019 11; 144(?):266-278. doi: 10.1016/j.freeradbiomed.2019.03.036. [PMID: 30946962]
  • Thai Q Do, Safiehkhatoon Moshkani, Patricia Castillo, Suda Anunta, Adelina Pogosyan, Annie Cheung, Beth Marbois, Kym F Faull, William Ernst, Su Ming Chiang, Gary Fujii, Catherine F Clarke, Krishna Foster, Edith Porter. Lipids including cholesteryl linoleate and cholesteryl arachidonate contribute to the inherent antibacterial activity of human nasal fluid. Journal of immunology (Baltimore, Md. : 1950). 2008 Sep; 181(6):4177-87. doi: 10.4049/jimmunol.181.6.4177. [PMID: 18768875]
  • Richard Harkewicz, Karsten Hartvigsen, Felicidad Almazan, Edward A Dennis, Joseph L Witztum, Yury I Miller. Cholesteryl ester hydroperoxides are biologically active components of minimally oxidized low density lipoprotein. The Journal of biological chemistry. 2008 Apr; 283(16):10241-51. doi: 10.1074/jbc.m709006200. [PMID: 18263582]
  • Huiyong Yin, Jason D Morrow, Ned A Porter. Identification of a novel class of endoperoxides from arachidonate autoxidation. The Journal of biological chemistry. 2004 Jan; 279(5):3766-76. doi: 10.1074/jbc.m307137200. [PMID: 14594817]
  • Huiyong Yin, Christine M Havrilla, Jason D Morrow, Ned A Porter. Formation of isoprostane bicyclic endoperoxides from the autoxidation of cholesteryl arachidonate. Journal of the American Chemical Society. 2002 Jul; 124(26):7745-54. doi: 10.1021/ja0201092. [PMID: 12083928]
  • V Schlotte, A Sevanian, P Hochstein, K U Weithmann. Effect of uric acid and chemical analogues on oxidation of human low density lipoprotein in vitro. Free radical biology & medicine. 1998 Nov; 25(7):839-47. doi: 10.1016/s0891-5849(98)00160-9. [PMID: 9823550]
  • B Cheng, J Kowal. Analysis of adrenal cholesteryl esters by reversed phase high performance liquid chromatography. Journal of lipid research. 1994 Jun; 35(6):1115-21. doi: . [PMID: 8077850]
  • J V Hunt, K L Carpenter, M A Bottoms, N P Carter, C E Marchant, M J Mitchinson. Flow cytometric measurement of ceroid accumulation in macrophages. Atherosclerosis. 1993 Jan; 98(2):229-39. doi: 10.1016/0021-9150(93)90132-e. [PMID: 8457262]
  • N Araki, S Horiuchi, A T Rahim, K Takata, Y Morino. Microquantification of cholesterol and cholesteryl esters in rat peritoneal macrophages by reverse-phase high-performance liquid chromatography. Analytical biochemistry. 1990 Mar; 185(2):339-45. doi: 10.1016/0003-2697(90)90305-s. [PMID: 2339790]
  • Y Yamamoto, E Niki. Presence of cholesteryl ester hydroperoxide in human blood plasma. Biochemical and biophysical research communications. 1989 Dec; 165(3):988-93. doi: 10.1016/0006-291x(89)92700-9. [PMID: 2610703]
  • R Y Ball, K L Carpenter, M J Mitchinson. Ceroid accumulation by murine peritoneal macrophages exposed to artificial lipoproteins: ultrastructural observations. British journal of experimental pathology. 1988 Feb; 69(1):43-56. doi: . [PMID: 3348959]
  • N P Odushko, N F Muliar. [Serum cholesterol ester level in patients with ischemic heart disease and liver disease]. Kardiologiia. 1984 Oct; 24(10):90-3. doi: NULL. [PMID: 6521191]
  • D A Wiebe, J T Bernert. Influence of incomplete cholesteryl ester hydrolysis on enzymic measurements of cholesterol. Clinical chemistry. 1984 Mar; 30(3):352-6. doi: 10.1093/clinchem/30.3.352. [PMID: 6697478]
  • J M Smaby, H L Brockman. Novel surface phase containing cholesteryl esters. 2. Nonequivalence of cholesteryl arachidonate and those with 18-carbon, cis-unsaturated acyl groups. Biochemistry. 1981 Feb; 20(4):724-30. doi: 10.1021/bi00507a009. [PMID: 7213606]