Pentacosane (BioDeep_00000382669)

Main id: BioDeep_00000017619

 

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


EINECS 211-123-6

化学式: C25H52 (352.4069)
中文名称: 二十五烷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCCCCCCCCCCCCCCCCCCCCCCCC
InChI: InChI=1S/C25H52/c1-3-5-7-9-11-13-15-17-19-21-23-25-24-22-20-18-16-14-12-10-8-6-4-2/h3-25H2,1-2H3

描述信息

Pentacosane is one of the major components in the acetone extract from Curcuma raktakanda and is also in the essential oil from the leaves of Malus domestica. Pentacosane exhibit anti-cancer activities[1].
Pentacosane is one of the major components in the acetone extract from Curcuma raktakanda and is also in the essential oil from the leaves of Malus domestica. Pentacosane exhibit anti-cancer activities[1].

同义名列表

14 个代谢物同义名

EINECS 211-123-6; CH3-[CH2]23-CH3; 286931_ALDRICH; 442699_SUPELCO; n-pentacosane; CHEBI:32938; 76495_FLUKA; 76493_FLUKA; Pentacosane; NSC 158663; AI3-36478; NSC158663; 629-99-2; Pentacosane



数据库引用编号

8 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)

396 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

  • Mayanka Walia, Tavleen S Mann, Dharmesh Kumar, Vijai K Agnihotri, Bikram Singh. Chemical Composition and In Vitro Cytotoxic Activity of Essential Oil of Leaves of Malus domestica Growing in Western Himalaya (India). Evidence-based complementary and alternative medicine : eCAM. 2012; 2012(?):649727. doi: 10.1155/2012/649727. [PMID: 22619691]
  • Ill-Min Chung, Hyung-In Moon. Immunotoxicity activity of 1,2,4-trimethoxybenzene from the Paulownia coreana Uyeki. against Aedes aegypti L. Immunopharmacology and immunotoxicology. 2011 Mar; 33(1):97-9. doi: 10.3109/08923973.2010.482591. [PMID: 20476845]
  • Vernard R Lewis, Lori J Nelson, Michael I Haverty, James A Baldwin. Quantitative changes in hydrocarbons over time in fecal pellets of Incisitermes minor may predict whether colonies are alive or dead. Journal of chemical ecology. 2010 Nov; 36(11):1199-206. doi: 10.1007/s10886-010-9864-5. [PMID: 20882326]
  • Ljuba Evstatieva, Milka Todorova, Daniela Antonova, Jordanka Staneva. Chemical composition of the essential oils of Rhodiola rosea L. of three different origins. Pharmacognosy magazine. 2010 Oct; 6(24):256-8. doi: 10.4103/0973-1296.71782. [PMID: 21120024]
  • Shahrokh Bagheri-Gavkosh, Mohsen Bigdeli, Masoomeh Shams-Ghahfarokhi, Mehdi Razzaghi-Abyaneh. Inhibitory effects of Ephedra major Host on Aspergillus parasiticus growth and aflatoxin production. Mycopathologia. 2009 Nov; 168(5):249-55. doi: 10.1007/s11046-009-9220-x. [PMID: 19557546]
  • Aysel Ugur, Nurdan Sarac, M Emin Duru, Yavuz Beyatli. In vitro study of antibacterial activity on multi-resistant bacteria and chemical composition of the chloroform extract of endemic Centaurea drabifolia subsp. cappadocica. Natural product communications. 2009 Sep; 4(9):1267-70. doi: ". [PMID: 19831042]
  • Ye-Gao Chen, Xiao-Ping Song, Li-Na Hai, Yu-Ping Lv, A Fang, F Halaweish, Xin-Rong Liao. Compounds with DNA cleaving activity from Kadsura ananosma. Die Pharmazie. 2006 Oct; 61(10):891-2. doi: . [PMID: 17069433]
  • Huaping Lei, Qinglong Shi, Fahuan Ge, Jianguo Pan. [Supercritical CO2 extraction of fatty oils from bee pollen and its GC-MS analysis]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2004 Mar; 27(3):177-80. doi: ". [PMID: 15272780]
  • Robert J Bartelt, Allard A Cossé, Richard J Petroski, David K Weaver. Cuticular hydrocarbons and novel alkenediol iacetates from wheat stem sawfly (Cephus cinctus): natural oxidation to pheromone components. Journal of chemical ecology. 2002 Feb; 28(2):385-405. doi: 10.1023/a:1017994410538. [PMID: 11925075]