myrtenal (BioDeep_00000395552)

   

PANOMIX_OTCML-2023 natural product


代谢物信息卡片


BICYCLO(3.1.1)HEPT-2-ENE-2-CARBOXALDEHYDE, 6,6-DIMETHYL-, (1R,5S)-REL-

  化学式: C10H14O (150.1045)
中文名称: （-）-Myrtenal, 桃金娘烯醛, (1R)-(-)-桃金娘烯醛
  谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 88.1%

分子结构信息

SMILES: CC1(C)C2CC=C(C=O)C1C2
InChI: InChI=1S/C10H14O/c1-10(2)8-4-3-7(6-11)9(10)5-8/h3,6,8-9H,4-5H2,1-2H3/t8-,9-/m0/s1


描述信息

(-)-Myrtenal is a natural product found in Cyperus articulatus, Forsythia viridissima, and other organisms with data available.
(?)-Myrtenal ((1R)-(?)-Myrtenal) is an orally active terpene with antitumour activity. (?)-Myrtenal ameliorates hyperglycemia by enhancing GLUT2 through Akt in the skeletal muscle and liver of diabetic rats[1][2].
(?)-Myrtenal ((1R)-(?)-Myrtenal) is an orally active terpene with antitumour activity. (?)-Myrtenal ameliorates hyperglycemia by enhancing GLUT2 through Akt in the skeletal muscle and liver of diabetic rats[1][2].
(?)-Myrtenal ((1R)-(?)-Myrtenal) is an orally active terpene with antitumour activity. (?)-Myrtenal ameliorates hyperglycemia by enhancing GLUT2 through Akt in the skeletal muscle and liver of diabetic rats[1][2].
(?)-Myrtenal ((1R)-(?)-Myrtenal) is an orally active terpene with antitumour activity. (?)-Myrtenal ameliorates hyperglycemia by enhancing GLUT2 through Akt in the skeletal muscle and liver of diabetic rats[1][2].
(?)-Myrtenal ((1R)-(?)-Myrtenal) is an orally active terpene with antitumour activity. (?)-Myrtenal ameliorates hyperglycemia by enhancing GLUT2 through Akt in the skeletal muscle and liver of diabetic rats[1][2].
(?)-Myrtenal ((1R)-(?)-Myrtenal) is an orally active terpene with antitumour activity. (?)-Myrtenal ameliorates hyperglycemia by enhancing GLUT2 through Akt in the skeletal muscle and liver of diabetic rats[1][2].

同义名列表

42 个代谢物同义名

BICYCLO(3.1.1)HEPT-2-ENE-2-CARBOXALDEHYDE, 6,6-DIMETHYL-, (1R,5S)-REL-; BICYCLO(3.1.1)HEPT-2-ENE-2-CARBOXALDEHYDE, 6,6-DIMETHYL-, (1R,5S)-; Bicyclo(3.1.1)hept-2-ene-2-carboxaldehyde, 6,6-dimethyl-, (1R)-; Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde, 6,6-dimethyl-, (1S)-; (1R,5S)-6,6-DIMETHYLBICYCLO(3.1.1)HEPT-2-ENE-2-CARBOXALDEHYDE; (1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde; 6,6-Dimethylbicyclo(3.1.1)hept-2-ene-2-carboxaldehyde; 6,6-dimethyl-bicyclo[3.1.1]hept-2-ene-2-carbaldehyde; 2-FORMYL-6,6-DIMETHYLBICYCLO(3.1.1)HEPT-2-ENE [FHFI]; (-)-Myrtenal, >=97.0\\% (sum of enantiomers, GC); 2-Formyl-6,6-dimethylbicyclo(3.1.1)hept-2-ene; 2-Norpinene-2-carboxaldehyde, 6,6-dimethyl-; 6,6-Dimethyl-2-norpinene-2-carboxaldehyde; (1R)-(-)-Myrtenal, analytical standard; KMRMUZKLFIEVAO-IUCAKERBSA-N; (1R)-(-)-Myrtenal, >=97\\%; Pin-2-ene-1-carbaldehyde; (1R)-(-)-Myrtenal, 98\\%; (-)-(1r,5s)-myrtenal; (1R)-(?)-Myrtenal; MYRTENAL, (+/-)-; UNII-EH2E303QRY; UNII-8J97443QRZ; (+/-)-MYRTENAL; Myrtenal, (-)-; ( )-Myrtenal; (−)-Myrtenal; (-)-Myrtenal; (?)-Myrtenal; EH2E303QRY; 8J97443QRZ; AI3-37785; Benihinal; myrtenal; (-)-Myrtenal; (?)-(1R,5S)-Myrtenal; Myrtenal; (1R)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-carboxaldehyde; (?)-Myrtenal, (1R)-2-Pinen-10-al, (1R)-6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-carbaldehyd; (1R)-(-)-Myrtenal, >=97%; (1R)-(-)-Myrtenal, 98%; (1R)-2-Pinen-10-al



数据库引用编号

9 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)

315 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

  • Liyan Yu, Hongguang Liu, Xiaoxia Ma, Vidya Devanathadesikan Seshadri, Xuan Gao. Anti-atherosclerotic Effects of Myrtenal in High-Fat Diet-Induced Atherosclerosis in Rats. Applied biochemistry and biotechnology. 2022 Dec; 194(12):5717-5733. doi: 10.1007/s12010-022-04044-x. [PMID: 35804285]
  • Ayyasamy Rathinam, Leelavinothan Pari, Manigandan Venkatesan, Shankar Munusamy. Myrtenal attenuates oxidative stress and inflammation in a rat model of streptozotocin-induced diabetes. Archives of physiology and biochemistry. 2022 Feb; 128(1):175-183. doi: 10.1080/13813455.2019.1670212. [PMID: 31564173]
  • Baoyu Li, Guishan Lin, Wengui Duan, Xiaoyu Wang, Bo Cen. Synthesis of Myrtenal-Based Nanocellulose/Diacylhydrazine Complexes with Antifungal Activity for Plant Protection. Journal of agricultural and food chemistry. 2021 Nov; 69(44):12956-12965. doi: 10.1021/acs.jafc.1c02694. [PMID: 34714664]
  • Wen-Xuan Li, Ping Qian, Yi-Tong Guo, Li Gu, Jessore Jurat, Yang Bai, Dong-Fang Zhang. Myrtenal and β-caryophyllene oxide screened from Liquidambaris Fructus suppress NLRP3 inflammasome components in rheumatoid arthritis. BMC complementary medicine and therapies. 2021 Sep; 21(1):242. doi: 10.1186/s12906-021-03410-2. [PMID: 34583676]
  • Mingzhen Zhao, Bin Liu, Yaya Sun, Yuanyuan Wang, Lulu Dai, Hui Chen. Presence and roles of myrtenol, myrtanol and myrtenal in Dendroctonus armandi (Coleoptera: Curculionidae: Scolytinae) and Pinus armandi (Pinales: Pinaceae: Pinoideae). Pest management science. 2020 Jan; 76(1):188-197. doi: 10.1002/ps.5492. [PMID: 31106502]
  • Brunna Xavier Martins, Raul Ferraz Arruda, Gildeíde Aparecida Costa, Hassan Jerdy, Sávio Bastos de Souza, Julianna Maria Santos, William Rodrigues de Freitas, Milton Masahiko Kanashiro, Eulógio Carlos Queiroz de Carvalho, Nadir Francisca Sant'Anna, Fernanda Antunes, Raul Martinez-Zaguilan, Sennoune Souad, Anna Lvovna Okorokova-Façanha, Arnoldo Rocha Façanha. Myrtenal-induced V-ATPase inhibition - A toxicity mechanism behind tumor cell death and suppressed migration and invasion in melanoma. Biochimica et biophysica acta. General subjects. 2019 01; 1863(1):1-12. doi: 10.1016/j.bbagen.2018.09.006. [PMID: 30279148]
  • D Andrys, M Adaszyńska-Skwirzyńska, D Kulpa. Jasmonic acid changes the composition of essential oil isolated from narrow-leaved lavender propagated in in vitro cultures. Natural product research. 2018 Apr; 32(7):834-839. doi: 10.1080/14786419.2017.1309533. [PMID: 28421828]
  • Rathinam Ayyasamy, Pari Leelavinothan. Myrtenal alleviates hyperglycaemia, hyperlipidaemia and improves pancreatic insulin level in STZ-induced diabetic rats. Pharmaceutical biology. 2016 Nov; 54(11):2521-2527. doi: 10.3109/13880209.2016.1168852. [PMID: 27158912]
  • Sungeun Cho, Edwin Nuijten, Robert L Shewfelt, Stanley J Kays. Aroma chemistry of African Oryza glaberrima and Oryza sativa rice and their interspecific hybrids. Journal of the science of food and agriculture. 2014 Mar; 94(4):727-35. doi: 10.1002/jsfa.6329. [PMID: 23907855]
  • Ana T Rufino, Madalena Ribeiro, Fernando Judas, Lígia Salgueiro, Maria C Lopes, Carlos Cavaleiro, Alexandrina F Mendes. Anti-inflammatory and chondroprotective activity of (+)-α-pinene: structural and enantiomeric selectivity. Journal of natural products. 2014 Feb; 77(2):264-9. doi: 10.1021/np400828x. [PMID: 24455984]
  • Lingaiah Hari Babu, Srinivasan Perumal, Maruthaiveeran Periyasamy Balasubramanian. Myrtenal, a natural monoterpene, down-regulates TNF-α expression and suppresses carcinogen-induced hepatocellular carcinoma in rats. Molecular and cellular biochemistry. 2012 Oct; 369(1-2):183-93. doi: 10.1007/s11010-012-1381-0. [PMID: 22763672]
  • Lingaiah Hari Babu, Srinivasan Perumal, Maruthaiveeran Periyasamy Balasubramanian. Myrtenal attenuates diethylnitrosamine-induced hepatocellular carcinoma in rats by stabilizing intrinsic antioxidants and modulating apoptotic and anti-apoptotic cascades. Cellular oncology (Dordrecht). 2012 Aug; 35(4):269-83. doi: 10.1007/s13402-012-0086-4. [PMID: 22722977]
  • Dorothea Kaufmann, Anudeep Kaur Dogra, Michael Wink. Myrtenal inhibits acetylcholinesterase, a known Alzheimer target. The Journal of pharmacy and pharmacology. 2011 Oct; 63(10):1368-71. doi: 10.1111/j.2042-7158.2011.01344.x. [PMID: 21899553]
  • Ping Yan, Zhe-zhi Wang. [Analysis of essential oil from different organs of Caryopteris tangutica]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2009 Jan; 32(1):61-5. doi: ". [PMID: 19445123]