Fluometuron (BioDeep_00000001979)
Industrial Pollutants
代谢物信息卡片
化学式: C10H11F3N2O (232.0823)
中文名称: 伏草隆
谱图信息:
最多检出来源 Viridiplantae(plant) 13.41%
Last reviewed on 2024-12-16.
Cite this Page
Fluometuron. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/fluometuron (retrieved
2025-02-24) (BioDeep RN: BioDeep_00000001979). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CN(C)C(=O)NC1=CC=CC(=C1)C(F)(F)F
InChI: InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)
描述信息
Fluometuron is a member of the class of 3-(3,4-substituted-phenyl)-1,1-dimethylureas that is urea in which one of the nitrogens is substituted by a 3-(trifluoromethyl)phenyl group while the other is substituted by two methyl groups. It is a herbicide used for the control of broadleaf weeds and annual grasses in cotton. It has a role as an agrochemical, an environmental contaminant, a herbicide, a xenobiotic and a photosystem-II inhibitor. It is a 3-(3,4-substituted-phenyl)-1,1-dimethylurea and a member of (trifluoromethyl)benzenes.
Fluometuron is a soil applied herbicide used to control annual grasses and broad-leaved weeds. In the United States it was approved for use on cotton and sugarcane crops in 1974, but since 1986 is only approved for use on cotton. Its mode of action is selective and inhibits photosynthesis.
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8414; ORIGINAL_PRECURSOR_SCAN_NO 8413
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8483; ORIGINAL_PRECURSOR_SCAN_NO 8479
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8454; ORIGINAL_PRECURSOR_SCAN_NO 8453
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8416; ORIGINAL_PRECURSOR_SCAN_NO 8415
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8468; ORIGINAL_PRECURSOR_SCAN_NO 8466
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4168; ORIGINAL_PRECURSOR_SCAN_NO 4167
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4190; ORIGINAL_PRECURSOR_SCAN_NO 4189
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4172; ORIGINAL_PRECURSOR_SCAN_NO 4171
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8464; ORIGINAL_PRECURSOR_SCAN_NO 8462
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4199; ORIGINAL_PRECURSOR_SCAN_NO 4198
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4184; ORIGINAL_PRECURSOR_SCAN_NO 4183
CONFIDENCE standard compound; INTERNAL_ID 921; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4155; ORIGINAL_PRECURSOR_SCAN_NO 4154
CONFIDENCE standard compound; EAWAG_UCHEM_ID 3709
Fluometuron. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=2164-17-2 (retrieved 2024-12-16) (CAS RN: 2164-17-2). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
同义名列表
数据库引用编号
43 个数据库交叉引用编号
- ChEBI: CHEBI:82012
- KEGG: C18853
- KEGGdrug: D90225
- PubChem: 16562
- Metlin: METLIN72615
- ChEMBL: CHEMBL1569926
- MoNA: CCMSLIB00001058223
- MoNA: CCMSLIB00001058389
- MoNA: CCMSLIB00001058242
- MoNA: CCMSLIB00001058933
- MoNA: EQ370904
- MoNA: EQ370906
- MoNA: LU092151
- MoNA: LU092106
- MoNA: LU092103
- MoNA: EQ370909
- MoNA: EQ370956
- MoNA: EQ370905
- MoNA: EQ370901
- MoNA: EQ370954
- MoNA: EQ370959
- MoNA: LU092105
- MoNA: LU092154
- MoNA: EQ370951
- MoNA: EQ370953
- MoNA: LU092102
- MoNA: EQ370952
- MoNA: LU092156
- MoNA: EQ370955
- MoNA: LU092104
- MoNA: LU092153
- MoNA: EQ370907
- MoNA: LU092101
- MoNA: LU092155
- MoNA: EQ370957
- MoNA: EQ370958
- MoNA: LU092152
- MoNA: EQ370903
- MoNA: EQ370908
- MoNA: EQ370902
- PMhub: MS000001589
- CAS: 2164-17-2
- KNApSAcK: 82012
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
- George P Balayiannis, Helen Karasali. Determination of azoxystrobin, topramezone, acetamiprid, fluometuron and folpet in their commercially available pesticide formulations by liquid chromatography.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes.
2021; 56(5):503-511. doi:
10.1080/03601234.2021.1903285
. [PMID: 33970794] - Amornrat Phongdara, Alisa Nakkaew, Sureeporn Nualkaew. Isolation of the detoxification enzyme EgP450 from an oil palm EST library.
Pharmaceutical biology.
2012 Jan; 50(1):120-7. doi:
10.3109/13880209.2011.631019
. [PMID: 22196587] - Randy Outward, Clyde E Sorenson, J R Bradley. Effects of vegetated field borders on arthropods in cotton fields in eastern North Carolina.
Journal of insect science (Online).
2008; 8(?):9. doi:
10.1673/031.008.0901
. [PMID: 20345293] - I Cydzik, J R Albert-García, J Martínez Calatayud. Photo-induced fluorescence of fluometuron in a continuous-flow multicommutation assembly.
Journal of fluorescence.
2007 Jan; 17(1):29-36. doi:
10.1007/s10895-006-0147-z
. [PMID: 17165123] - P Marquet, F Saint-Marcoux, T N Gamble, J C Y Leblanc. Comparison of a preliminary procedure for the general unknown screening of drugs and toxic compounds using a quadrupole-linear ion-trap mass spectrometer with a liquid chromatography-mass spectrometry reference technique.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2003 Jun; 789(1):9-18. doi:
10.1016/s1570-0232(03)00071-0
. [PMID: 12726839] - Fernando Peña, Soledad Cárdenas, Mercedes Gallego, Miguel Valcárcel. Analysis of phenylurea herbicides from plants by GC/MS.
Talanta.
2002 Mar; 56(4):727-34. doi:
10.1016/s0039-9140(01)00616-6
. [PMID: 18968549] - O S Mohamed, K E Ahmed, S E Adam, O F Idris. Toxicity of cotoran (fluometuron) in Desert sheep.
Veterinary and human toxicology.
1995 Jun; 37(3):214-6. doi:
. [PMID: 7571346]