Ejibil (BioDeep_00000617099)
PANOMIX_OTCML-2023 Volatile Flavor Compounds
代谢物信息卡片
化学式: C9H12O (136.08881019999998)
中文名称: 1-苯基-1-丙醇
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCC(C1=CC=CC=C1)O
InChI: InChI=1S/C9H12O/c1-2-9(10)8-6-4-3-5-7-8/h3-7,9-10H,2H2,1H3
描述信息
1-Phenyl-1-propanol is used as a chiral building block and synthetic intermediate in the pharmaceutical industries. 1-Phenyl-1-propanol is an intermediate of anti-depressant agent Fluoxetine[1][2].
同义名列表
数据库引用编号
6 个数据库交叉引用编号
- ChEBI: CHEBI:31995
- PubChem: 7147
- Metlin: METLIN87821
- ChEMBL: CHEMBL1397202
- CAS: 93-54-9
- medchemexpress: HY-W012618
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
- Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Molecular pharmacology.
2019 11; 96(5):629-640. doi:
10.1124/mol.119.115964
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Biochemical and biophysical research communications.
2015 Feb; 457(2):194-9. doi:
10.1016/j.bbrc.2014.12.087
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BMC genomics.
2012 Jul; 13(?):295. doi:
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The New phytologist.
2012 Jul; 195(2):335-345. doi:
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Physiologia plantarum.
2012 Jun; 145(2):260-74. doi:
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Plant science : an international journal of experimental plant biology.
2012 Jan; 182(?):71-8. doi:
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The Plant journal : for cell and molecular biology.
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Plant physiology.
2011 Nov; 157(3):1056-66. doi:
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Plant cell reports.
2011 Nov; 30(11):2075-83. doi:
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Phytomedicine : international journal of phytotherapy and phytopharmacology.
2011 Jan; 18(2-3):134-42. doi:
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Plant, cell & environment.
2011 Jan; 34(1):149-61. doi:
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Molecules (Basel, Switzerland).
2010 Nov; 15(12):8641-88. doi:
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Proteomics.
2010 Jul; 10(13):2418-28. doi:
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Planta.
2010 Apr; 231(5):1061-76. doi:
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Phytochemistry.
2010 Apr; 71(5-6):605-13. doi:
10.1016/j.phytochem.2009.12.014
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Bioorganic & medicinal chemistry letters.
2010 Mar; 20(5):1520-3. doi:
10.1016/j.bmcl.2010.01.095
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Fitoterapia.
2010 Mar; 81(2):124-31. doi:
10.1016/j.fitote.2009.08.019
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Plant physiology.
2009 Dec; 151(4):1703-28. doi:
10.1104/pp.109.136804
. [PMID: 19926802] - Jin-shan Tang, Hao Gao, Chuan-xi Wang, Yi Dai, Li Bao, Wen-cai Ye, Xin-sheng Yao. Antioxidative phenylpropanoid-substituted epicatechin glycosides from Parabarium huaitingii.
Planta medica.
2009 Dec; 75(15):1586-90. doi:
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Langmuir : the ACS journal of surfaces and colloids.
2009 Oct; 25(19):11322-7. doi:
10.1021/la9005295
. [PMID: 19722601] - Taketo Uchiyama, Keiichi Tabata, Sawako Nomura, Yasuhisa Kaneko, Yasuo Fujimoto, Takashi Suzuki. Induction of apoptosis in human leukemia cell (Jurkat) by neolignans isolated from seeds of Licaria puchury-major.
Biological & pharmaceutical bulletin.
2009 Oct; 32(10):1749-53. doi:
10.1248/bpb.32.1749
. [PMID: 19801838] - Christin Fellenberg, Christoph Böttcher, Thomas Vogt. Phenylpropanoid polyamine conjugate biosynthesis in Arabidopsis thaliana flower buds.
Phytochemistry.
2009 Jul; 70(11-12):1392-400. doi:
10.1016/j.phytochem.2009.08.010
. [PMID: 19762055] - Ali Mahjoub, Michel Hernould, Jérôme Joubès, Alain Decendit, Mohamed Mars, François Barrieu, Saïd Hamdi, Serge Delrot. Overexpression of a grapevine R2R3-MYB factor in tomato affects vegetative development, flower morphology and flavonoid and terpenoid metabolism.
Plant physiology and biochemistry : PPB.
2009 Jul; 47(7):551-61. doi:
10.1016/j.plaphy.2009.02.015
. [PMID: 19375343] - Ling Fan, Wei-Jun Shi, Wen-Ran Hu, Xiao-Yan Hao, Dong-Mei Wang, Hui Yuan, Hong-Ying Yan. Molecular and biochemical evidence for phenylpropanoid synthesis and presence of wall-linked phenolics in cotton fibers.
Journal of integrative plant biology.
2009 Jul; 51(7):626-37. doi:
10.1111/j.1744-7909.2009.00840.x
. [PMID: 19566641] - Damla D Bilgin, Mihai Aldea, Bridget F O'Neill, Marisol Benitez, Min Li, Steven J Clough, Evan H DeLucia. Elevated ozone alters soybean-virus interaction.
Molecular plant-microbe interactions : MPMI.
2008 Oct; 21(10):1297-308. doi:
10.1094/mpmi-21-10-1297
. [PMID: 18785825] - Dirk Meissner, Andreas Albert, Christoph Böttcher, Dieter Strack, Carsten Milkowski. The role of UDP-glucose:hydroxycinnamate glucosyltransferases in phenylpropanoid metabolism and the response to UV-B radiation in Arabidopsis thaliana.
Planta.
2008 Sep; 228(4):663-74. doi:
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. [PMID: 18563436] - Alexandra Lanot, Denise Hodge, Eng-Kiat Lim, Fabián E Vaistij, Dianna J Bowles. Redirection of flux through the phenylpropanoid pathway by increased glucosylation of soluble intermediates.
Planta.
2008 Sep; 228(4):609-16. doi:
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Phytochemistry.
2008 Jul; 69(10):2016-21. doi:
10.1016/j.phytochem.2008.04.014
. [PMID: 18534638] - Tomonori Shinya, Ivan Gális, Tomoko Narisawa, Mami Sasaki, Hiroo Fukuda, Hideaki Matsuoka, Mikako Saito, Ken Matsuoka. Comprehensive analysis of glucan elicitor-regulated gene expression in tobacco BY-2 cells reveals a novel MYB transcription factor involved in the regulation of phenylpropanoid metabolism.
Plant & cell physiology.
2007 Oct; 48(10):1404-13. doi:
10.1093/pcp/pcm115
. [PMID: 17761750] - Filippos Ververidis, Emmanouil Trantas, Carl Douglas, Guenter Vollmer, Georg Kretzschmar, Nickolas Panopoulos. Biotechnology of flavonoids and other phenylpropanoid-derived natural products. Part II: Reconstruction of multienzyme pathways in plants and microbes.
Biotechnology journal.
2007 Oct; 2(10):1235-49. doi:
10.1002/biot.200700184
. [PMID: 17935118] - Zara Merali, Melinda J Mayer, Mary L Parker, Anthony J Michael, Andrew C Smith, Keith W Waldron. Metabolic diversion of the phenylpropanoid pathway causes cell wall and morphological changes in transgenic tobacco stems.
Planta.
2007 Apr; 225(5):1165-78. doi:
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Planta.
2007 Feb; 225(3):665-79. doi:
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Phytochemistry.
2006 Apr; 67(8):800-4. doi:
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. [PMID: 16540132] - Inna Guterman, Tania Masci, Xinlu Chen, Florence Negre, Eran Pichersky, Natalia Dudareva, David Weiss, Alexander Vainstein. Generation of phenylpropanoid pathway-derived volatiles in transgenic plants: rose alcohol acetyltransferase produces phenylethyl acetate and benzyl acetate in petunia flowers.
Plant molecular biology.
2006 Mar; 60(4):555-63. doi:
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. [PMID: 16525891] - Shinichi Tanimoto, Hitoshi Tominaga, Yoshiharu Okada, Masato Nomura. Synthesis and cosmetic whitening effect of glycosides derived from several phenylpropanoids.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.
2006 Mar; 126(3):173-7. doi:
10.1248/yakushi.126.173
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Chemistry & biodiversity.
2006 Jan; 3(1):41-8. doi:
10.1002/cbdv.200690005
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Journal of chromatography. A.
2005 Oct; 1092(1):55-64. doi:
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Natural product research.
2005 Sep; 19(6):547-50. doi:
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Plant & cell physiology.
2005 Mar; 46(3):454-66. doi:
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The Journal of pharmacy and pharmacology.
2004 Dec; 56(12):1607-11. doi:
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Cellular & molecular biology letters.
2004; 9(4B):829-42. doi:
"
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Archives of pharmacal research.
2003 Dec; 26(12):1014-7. doi:
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Journal of mass spectrometry : JMS.
2003 Aug; 38(8):845-53. doi:
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Plant physiology.
2003 May; 132(1):146-53. doi:
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Plant & cell physiology.
2003 May; 44(5):510-7. doi:
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Plant & cell physiology.
2003 Apr; 44(4):437-46. doi:
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Planta.
2003 Mar; 216(5):881-9. doi:
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TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik.
2003 Feb; 106(3):375-83. doi:
10.1007/s00122-002-0999-9
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The Plant journal : for cell and molecular biology.
2002 Jun; 30(6):663-77. doi:
10.1046/j.1365-313x.2002.01323.x
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Planta.
2002 May; 215(1):79-89. doi:
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Journal of ethnopharmacology.
2002 Mar; 79(3):389-92. doi:
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Journal of ethnopharmacology.
2002 Feb; 79(2):193-7. doi:
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Bioscience, biotechnology, and biochemistry.
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