(+)-iridodial lactol (BioDeep_00000840435)

Main id: BioDeep_00000007608

 

natural product


代谢物信息卡片


(+)-iridodial lactol

化学式: C10H16O2 (168.115)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1=CO[C@@H](O)[C@@H]2[C@@H](C)CC[C@H]12
InChI: InChI=1S/C10H16O2/c1-6-3-4-8-7(2)5-12-10(11)9(6)8/h5-6,8-11H,3-4H2,1-2H3/t6-,8+,9+,10+/m0/s1

描述信息

An iridoid monoterpenoid that is 1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran substituted by methyl groups at positions 4 and 7 and a hydroxy group at position 1 (the 1R,4aS,7S,7aR-stereoisomer).

同义名列表

1 个代谢物同义名

(+)-iridodial lactol



数据库引用编号

5 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

2 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(2)

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


文献列表

  • Hui Liu, Shuangcheng Liang, Meixian Zhu, Wenjing Shi, Chong Xu, Wuke Wei, Ruoting Zhan, Dongming Ma. A fused hybrid enzyme of 8-hydroxygeraniol oxidoreductase (8HGO) from Gardenia jasminoides and iridoid synthase (ISY) from Catharanthus roseus significantly enhances nepetalactol and iridoid production. Planta. 2024 Feb; 259(3):62. doi: 10.1007/s00425-023-04287-w. [PMID: 38319463]
  • Annoor Awadasseid, Wei Li, Zhan Liu, Chong Qiao, Jing Pang, Guolin Zhang, Yinggang Luo. Characterization of Camptotheca acuminata 10-hydroxygeraniol oxidoreductase and iridoid synthase and their application in biological preparation of nepetalactol in Escherichia coli featuring NADP+ - NADPH cofactors recycling. International journal of biological macromolecules. 2020 Nov; 162(?):1076-1085. doi: 10.1016/j.ijbiomac.2020.06.223. [PMID: 32599240]
  • Benjamin R Lichman, Mohamed O Kamileen, Gabriel R Titchiner, Gerhard Saalbach, Clare E M Stevenson, David M Lawson, Sarah E O'Connor. Uncoupled activation and cyclization in catmint reductive terpenoid biosynthesis. Nature chemical biology. 2019 01; 15(1):71-79. doi: 10.1038/s41589-018-0185-2. [PMID: 30531909]
  • Sándor Koczor, Ferenc Szentkirályi, József Vuts, John C Caulfield, David M Withall, John A Pickett, Michael A Birkett, Miklós Tóth. Conspecific and Heterogeneric Lacewings Respond to (Z)-4-Tridecene Identified from Chrysopa formosa (Neuroptera: Chrysopidae). Journal of chemical ecology. 2018 Feb; 44(2):137-146. doi: 10.1007/s10886-017-0920-2. [PMID: 29374366]
  • Alex Campbell, Philippe Bauchart, Nicholas D Gold, Yun Zhu, Vincenzo De Luca, Vincent J J Martin. Engineering of a Nepetalactol-Producing Platform Strain of Saccharomyces cerevisiae for the Production of Plant Seco-Iridoids. ACS synthetic biology. 2016 05; 5(5):405-14. doi: 10.1021/acssynbio.5b00289. [PMID: 26981892]
  • Sándor Koczor, Ferenc Szentkirályi, John A Pickett, Michael A Birkett, Miklós Tóth. Aphid Sex Pheromone Compounds Interfere with Attraction of Common Green Lacewings to Floral Bait. Journal of chemical ecology. 2015 Jun; 41(6):550-6. doi: 10.1007/s10886-015-0585-7. [PMID: 25956798]
  • Sándor Koczor, Ferenc Szentkirályi, Michael A Birkett, John A Pickett, Erzsébet Voigt, Miklós Tóth. Attraction of Chrysoperla carnea complex and Chrysopa spp. lacewings (Neuroptera: Chrysopidae) to aphid sex pheromone components and a synthetic blend of floral compounds in Hungary. Pest management science. 2010 Dec; 66(12):1374-9. doi: 10.1002/ps.2030. [PMID: 20949547]