TMPone (BioDeep_00000616769)
Main id: BioDeep_00000017521
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C9H17NO (155.1310072)
中文名称: 2,2,6,6-四甲基-4-哌啶酮
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 1.56%
分子结构信息
SMILES: CC1(C)CC(=O)CC(C)(C)N1
InChI: InChI=1S/C9H17NO/c1-8(2)5-7(11)6-9(3,4)10-8/h10H,5-6H2,1-4H3
描述信息
同义名列表
23 个代谢物同义名
2,2,6,6-tetramethylpiperidone-4-toluene-p- sulfonate; 4-Oxo-2,2,6,6-tetramethyl-4-piperidone; 4-Oxo-2,2,6,6-tetramethylpiperidine; 2,2,6, 6-Tetramethyl-4-piperidinone; 2,2,6,6-Tetramethyl-4-oxopiperidine; 2,2,6,6-Tetramethyl-4-piperidinone; 2,2,6,6-tetramethylpiperidin-4-one; 2,2,6,6-Tetramethyl-g-piperidone; 2,2,6,6-tetramethyl-4 piperidone; 2,2,6,6-Tetramethyl-4-piperidone; 2,2,6,6-Tetramethylpiperidinone; 2,2,6,6-Tetramethylpiperidone; Trojacetonoaminy; Triacetone amine; Triacetoneamine; Triacetonamine; Triacetonamin; Odoratin?; Vincubina; Odoratine; Vincubine; tempidon; TMPone
数据库引用编号
7 个数据库交叉引用编号
- ChEBI: CHEBI:177813
- PubChem: 13220
- Metlin: METLIN87472
- ChEMBL: CHEMBL117614
- CAS: 826-36-8
- LOTUS: LTS0239294
- wikidata: Q6120732
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)
2 个相关的物种来源信息
- 72715 - Agelas oroides: 10.1055/S-2006-957379
- 264975 - Caroxylon tetrandrum: 10.1016/S0031-9422(00)97401-6
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
- Eva Hideg, Zsuzsanna Deák, Marja Hakala-Yatkin, Maarit Karonen, A William Rutherford, Esa Tyystjärvi, Imre Vass, Anja Krieger-Liszkay. Pure forms of the singlet oxygen sensors TEMP and TEMPD do not inhibit Photosystem II.
Biochimica et biophysica acta.
2011 Dec; 1807(12):1658-61. doi:
10.1016/j.bbabio.2011.09.009
. [PMID: 21982982] - Ayaka Yoshida, Fumihiko Yoshino, Masahito Tsubata, Motoya Ikeguchi, Takeshi Nakamura, Masaichi-Chang-Il Lee. Direct assessment by electron spin resonance spectroscopy of the antioxidant effects of French maritime pine bark extract in the maxillofacial region of hairless mice.
Journal of clinical biochemistry and nutrition.
2011 Sep; 49(2):79-86. doi:
10.3164/jcbn.10-103
. [PMID: 21980222] - Marja Hakala-Yatkin, Esa Tyystjärvi. Inhibition of Photosystem II by the singlet oxygen sensor compounds TEMP and TEMPD.
Biochimica et biophysica acta.
2011 Mar; 1807(3):243-50. doi:
10.1016/j.bbabio.2010.11.014
. [PMID: 21130069] - Lingzhi Bao, An Xu, Liping Tong, Shaopeng Chen, Lingyan Zhu, Ye Zhao, Guoping Zhao, Erkang Jiang, Jun Wang, Lijun Wu. Activated toxicity of diesel particulate extract by ultraviolet a radiation in mammalian cells: role of singlet oxygen.
Environmental health perspectives.
2009 Mar; 117(3):436-41. doi:
10.1289/ehp.0800029
. [PMID: 19337519] - Joana Martins, Leonor Almeida, João Laranjinha. Simultaneous production of superoxide radical and singlet oxygen by sulphonated chloroaluminum phthalocyanine incorporated in human low-density lipoproteins: implications for photodynamic therapy.
Photochemistry and photobiology.
2004 Sep; 80(2):267-73. doi:
10.1562/2004-03-26-ra-124
. [PMID: 15362945] - F Takayama, T Egashira, Y Yamanaka. Singlet oxygen generation from phosphatidylcholine hydroperoxide in the presence of copper.
Life sciences.
2001 Mar; 68(15):1807-15. doi:
10.1016/s0024-3205(01)00956-0
. [PMID: 11270626] - M V Kumari, M Hiramatsu, M Ebadi. Free radical scavenging actions of hippocampal metallothionein isoforms and of antimetallothioneins: an electron spin resonance spectroscopic study.
Cellular and molecular biology (Noisy-le-Grand, France).
2000 May; 46(3):627-36. doi:
"
. [PMID: 10872749] - M V Kumari, T Yoneda, M Hiramatsu. Scavenging activity of 'beta catechin' on reactive oxygen species generated by photosensitization of riboflavin.
Biochemistry and molecular biology international.
1996 May; 38(6):1163-70. doi:
"
. [PMID: 8739038] - H Kikuchi, T Tetsuka. On the mechanism of lipoxygenase-like action of bleomycin-iron complexes.
The Journal of antibiotics.
1992 Apr; 45(4):548-55. doi:
10.7164/antibiotics.45.548
. [PMID: 1375591] - D Mikhaĭlova, V Ognianova, I Chobanova. [Pharmacokinetics of the original Bulgarian preparation, tempidon, in experimental animals].
Eksperimentalna meditsina i morfologiia.
1979; 18(1):5-12. doi:
NULL
. [PMID: 436713] - L Daleva, V Ognianova. [Determination of the plasma level and excretion to tempidon in man after oral use].
Eksperimentalna meditsina i morfologiia.
1978; 17(4):231-4. doi:
NULL
. [PMID: 743344] - L F Bjeldanes, G W Chang. Triacetonamine formation in fungal extracts.
Journal of agricultural and food chemistry.
1975 Sep; 23(5):1010-1. doi:
10.1021/jf60201a023
. [PMID: 1159172]