738-87-4 (BioDeep_00000864938)

Main id: BioDeep_00000000694

 

PANOMIX_OTCML-2023


代谢物信息卡片


1-Cyclopropene-1-octanoic acid, 2-octyl-, homopolymer

化学式: C19H34O2 (294.2559)
中文名称: 苹婆酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCCCCCCCC1=C(C1)CCCCCCCC(=O)O
InChI: InChI=1S/C19H34O2/c1-2-3-4-5-7-10-13-17-16-18(17)14-11-8-6-9-12-15-19(20)21/h2-16H2,1H3,(H,20,21)

描述信息

同义名列表

16 个代谢物同义名

1-Cyclopropene-1-octanoic acid, 2-octyl-, homopolymer; 2-Octyl-1-cyclopropene-1-octanoic acid homopolymer; omega-(2-n-octylcycloprop-1-enyl)octanoic acid; 8-(2-Octyl-1-cyclopropen-1-yl)octanoic acid; 8-(2-octyl-1-cyclopropenyl)caprylic acid; 8-(2-octyl-1-cyclopropenyl)octanoic acid; 1-Cyclopropene-1-octanoic acid, 2-octyl-; 9,10-methylene-9-octadecenoic acid; Sterculinic acid; Sterculic acid; LMFA01030190; 55088-60-3; HSDB 3904; 738-87-4; C08366; Sterculic acid



数据库引用编号

12 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)

31 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 8 AIMP2, CASP3, DDIT3, FASN, GSDME, MDM2, P2RX7, XDH
Endoplasmic reticulum membrane 5 FADS1, FADS2, HMOX1, HSP90B1, SCD
Nucleus 7 AIMP2, ATF3, CASP3, DDIT3, HMOX1, HSP90B1, MDM2
cytosol 11 AIMP2, CASP3, DDIT3, FASN, GSDME, HMOX1, HSP90B1, LIPE, MDM2, RPE, XDH
nucleoplasm 4 ATF3, CASP3, HMOX1, MDM2
RNA polymerase II transcription regulator complex 2 ATF3, DDIT3
Cell membrane 3 GSDME, LIPE, P2RX7
Cytoplasmic side 1 HMOX1
Multi-pass membrane protein 5 FADS1, FADS2, GSDME, P2RX7, SCD
glutamatergic synapse 2 CASP3, MDM2
Golgi apparatus 1 FASN
Golgi membrane 1 INS
lysosomal membrane 1 GAA
neuromuscular junction 1 P2RX7
neuronal cell body 2 CASP3, P2RX7
postsynapse 1 P2RX7
smooth endoplasmic reticulum 1 HSP90B1
Cytoplasm, cytosol 2 AIMP2, LIPE
Lysosome 1 GAA
Presynapse 1 P2RX7
plasma membrane 6 FADS2, FASN, GAA, GSDME, MDM2, P2RX7
Membrane 11 AIMP2, FADS1, FADS2, FASN, GAA, GSDME, HMOX1, HSP90B1, LIPE, P2RX7, SCD
caveola 1 LIPE
extracellular exosome 5 FASN, GAA, HSP90B1, RPE, SOD2
Lysosome membrane 1 GAA
endoplasmic reticulum 3 HMOX1, HSP90B1, SCD
extracellular space 3 HMOX1, INS, XDH
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 2 HMOX1, HSP90B1
mitochondrion 3 FADS1, P2RX7, SOD2
protein-containing complex 2 HSP90B1, MDM2
intracellular membrane-bounded organelle 2 FADS1, GAA
postsynaptic density 2 CASP3, MDM2
Secreted 2 GAA, INS
extracellular region 3 GAA, HSP90B1, INS
mitochondrial outer membrane 1 HMOX1
Mitochondrion matrix 1 SOD2
mitochondrial matrix 1 SOD2
transcription regulator complex 1 DDIT3
external side of plasma membrane 1 P2RX7
nucleolus 3 ATF3, MDM2, SCD
midbody 1 HSP90B1
cell-cell junction 1 P2RX7
focal adhesion 1 HSP90B1
mitochondrial nucleoid 1 SOD2
Peroxisome 1 XDH
sarcoplasmic reticulum 1 XDH
collagen-containing extracellular matrix 1 HSP90B1
Late endosome 1 DDIT3
chromatin 2 ATF3, DDIT3
Nucleus, nucleolus 1 MDM2
endosome lumen 1 INS
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
[Isoform 1]: Endoplasmic reticulum membrane 1 FADS1
Nucleus, nucleoplasm 1 MDM2
tertiary granule membrane 1 GAA
Melanosome 2 FASN, HSP90B1
sperm plasma membrane 1 HSP90B1
secretory granule lumen 1 INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 HSP90B1, INS
transcription repressor complex 1 MDM2
endocytic vesicle membrane 1 MDM2
transport vesicle 1 INS
azurophil granule membrane 1 GAA
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
Single-pass type IV membrane protein 1 HMOX1
Sarcoplasmic reticulum lumen 1 HSP90B1
protein-DNA complex 1 DDIT3
ficolin-1-rich granule membrane 1 GAA
death-inducing signaling complex 1 CASP3
aminoacyl-tRNA synthetase multienzyme complex 1 AIMP2
[Isoform 2]: Endoplasmic reticulum membrane 1 FADS1
[Gasdermin-E, N-terminal]: Cell membrane 1 GSDME
[Gasdermin-E]: Cytoplasm, cytosol 1 GSDME
bleb 1 P2RX7
endocytic vesicle lumen 1 HSP90B1
endoplasmic reticulum chaperone complex 1 HSP90B1
autolysosome lumen 1 GAA
CHOP-C/EBP complex 1 DDIT3
CHOP-ATF3 complex 2 ATF3, DDIT3
CHOP-ATF4 complex 1 DDIT3
glycogen granule 1 FASN


文献列表

  • Ana Pariente, Álvaro Pérez-Sala, Rodrigo Ochoa, Miriam Bobadilla, Ángela Villanueva-Martínez, Rafael Peláez, Ignacio M Larráyoz. Identification of 7-Ketocholesterol-Modulated Pathways and Sterculic Acid Protective Effect in Retinal Pigmented Epithelium Cells by Using Genome-Wide Transcriptomic Analysis. International journal of molecular sciences. 2023 Apr; 24(8):. doi: 10.3390/ijms24087459. [PMID: 37108627]
  • Kristine Bertheussen, Merel van de Plassche, Thomas Bakkum, Berend Gagestein, Iakovia Ttofi, Alexi J C Sarris, Herman S Overkleeft, Mario van der Stelt, Sander I van Kasteren. Live-Cell Imaging of Sterculic Acid-a Naturally Occurring 1,2-Cyclopropene Fatty Acid-by Bioorthogonal Reaction with Turn-On Tetrazine-Fluorophore Conjugates. Angewandte Chemie (International ed. in English). 2022 09; 61(38):e202207640. doi: 10.1002/anie.202207640. [PMID: 35838324]
  • Andrea Palyzová, Tomáš Řezanka. Enantiomeric separation of triacylglycerols containing fatty acids with a ring (cyclofatty acids). Journal of chromatography. A. 2020 Jul; 1622(?):461103. doi: 10.1016/j.chroma.2020.461103. [PMID: 32317104]
  • Ana Pariente, Álvaro Pérez-Sala, Rodrigo Ochoa, Rafael Peláez, Ignacio M Larráyoz. Genome-Wide Transcriptomic Analysis Identifies Pathways Regulated by Sterculic Acid in Retinal Pigmented Epithelium Cells. Cells. 2020 05; 9(5):. doi: 10.3390/cells9051187. [PMID: 32403229]
  • Rafael Peláez, Ana Pariente, Álvaro Pérez-Sala, Ignacio M Larráyoz. Sterculic Acid: The Mechanisms of Action beyond Stearoyl-CoA Desaturase Inhibition and Therapeutic Opportunities in Human Diseases. Cells. 2020 01; 9(1):. doi: 10.3390/cells9010140. [PMID: 31936134]
  • Pan Hao, Intisar Q M Alaraj, Juma'a R Al Dulayymi, Mark S Baird, Jing Liu, Qun Liu. Sterculic Acid and Its Analogues Are Potent Inhibitors of Toxoplasma gondii. The Korean journal of parasitology. 2016 Apr; 54(2):139-45. doi: 10.3347/kjp.2016.54.2.139. [PMID: 27180571]
  • A K G Kadegowda, T A Burns, S L Pratt, S K Duckett. Inhibition of stearoyl-CoA desaturase 1 reduces lipogenesis in primary bovine adipocytes. Lipids. 2013 Oct; 48(10):967-76. doi: 10.1007/s11745-013-3823-1. [PMID: 23929455]
  • M S Herrera-Meza, M R Mendoza-López, O García-Barradas, M G Sanchez-Otero, E R Silva-Hernández, J O Angulo, R M Oliart-Ros. Dietary anhydrous milk fat naturally enriched with conjugated linoleic acid and vaccenic acid modify cardiovascular risk biomarkers in spontaneously hypertensive rats. International journal of food sciences and nutrition. 2013 Aug; 64(5):575-86. doi: 10.3109/09637486.2013.763908. [PMID: 23360131]
  • Anne-Catherine Schneider, Pauline Beguin, Sophie Bourez, James W Perfield, Eric Mignolet, Cathy Debier, Yves-Jacques Schneider, Yvan Larondelle. Conversion of t11t13 CLA into c9t11 CLA in Caco-2 cells and inhibition by sterculic oil. PloS one. 2012; 7(3):e32824. doi: 10.1371/journal.pone.0032824. [PMID: 22427892]
  • Massimo Bionaz, Kathiravan Periasamy, Sandra L Rodriguez-Zas, Walter L Hurley, Juan J Loor. A novel dynamic impact approach (DIA) for functional analysis of time-course omics studies: validation using the bovine mammary transcriptome. PloS one. 2012; 7(3):e32455. doi: 10.1371/journal.pone.0032455. [PMID: 22438877]
  • Xiao-Hong Yu, Richa Rawat, John Shanklin. Characterization and analysis of the cotton cyclopropane fatty acid synthase family and their contribution to cyclopropane fatty acid synthesis. BMC plant biology. 2011 May; 11(?):97. doi: 10.1186/1471-2229-11-97. [PMID: 21612656]
  • Shanmugam M Jeyakumar, Pratti Lopamudra, Suryaprakash Padmini, Nagalla Balakrishna, Nappan V Giridharan, Ayyalasomayajula Vajreswari. Fatty acid desaturation index correlates with body mass and adiposity indices of obesity in Wistar NIN obese mutant rat strains WNIN/Ob and WNIN/GR-Ob. Nutrition & metabolism. 2009 Jun; 6(?):27. doi: 10.1186/1743-7075-6-27. [PMID: 19519902]
  • Patricia Soulard, Meg McLaughlin, Jessica Stevens, Brendan Connolly, Rocco Coli, Leyu Wang, Jennifer Moore, Ming-Shang T Kuo, William A LaMarr, Can C Ozbal, B Ganesh Bhat. Development of a high-throughput screening assay for stearoyl-CoA desaturase using rat liver microsomes, deuterium labeled stearoyl-CoA and mass spectrometry. Analytica chimica acta. 2008 Oct; 627(1):105-11. doi: 10.1016/j.aca.2008.04.017. [PMID: 18790133]
  • Massimo Bionaz, Juan J Loor. Gene networks driving bovine milk fat synthesis during the lactation cycle. BMC genomics. 2008 Jul; 9(?):366. doi: 10.1186/1471-2164-9-366. [PMID: 18671863]
  • J Cao, J P Blond, J Bézard. Inhibition of fatty acid delta 6- and delta 5-desaturation by cyclopropene fatty acids in rat liver microsomes. Biochimica et biophysica acta. 1993 Dec; 1210(1):27-34. doi: 10.1016/0005-2760(93)90045-b. [PMID: 7903050]
  • D E Khoo, B Fermor, J Miller, C B Wood, K Apostolov, W Barker, R C Williamson, N A Habib. Manipulation of body fat composition with sterculic acid can inhibit mammary carcinomas in vivo. British journal of cancer. 1991 Jan; 63(1):97-101. doi: 10.1038/bjc.1991.20. [PMID: 1989672]
  • O Slayden, F Stormshak. In vivo and in vitro effects of a cyclopropenoid fatty acid on ovine corpus luteum function. Endocrinology. 1990 Dec; 127(6):3166-71. doi: 10.1210/endo-127-6-3166. [PMID: 2249645]
  • R A Zoeller, R Wood. Effects of cyclopropene fatty acids on the lipid composition of the Morris hepatoma 7288C. Lipids. 1984 Jul; 19(7):529-38. doi: 10.1007/bf02534486. [PMID: 6431218]
  • E Marciniak, J P Gockerman. Heparin-induced decrease in circulating antithrombin-III. Lancet (London, England). 1977 Sep; 2(8038):581-4. doi: 10.1016/s0140-6736(77)91429-5. [PMID: 71399]
  • T A Eisele, J K Yoss, J E Nixon, N E PAwlowski, L M Libbey, R O Sinnhuber. Rat urinary metabolites of [9,10-methylene-14C] sterculic acid. Biochimica et biophysica acta. 1977 Jul; 488(1):76-87. doi: 10.1016/0005-2760(77)90124-2. [PMID: 889861]