1-Phenylethylamine (BioDeep_00000003012)
Secondary id: BioDeep_00001868087
human metabolite Endogenous blood metabolite
代谢物信息卡片
化学式: C8H11N (121.0891)
中文名称: DL-α-苯乙胺, 1-苯乙胺
谱图信息:
最多检出来源 Homo sapiens(blood) 8.15%
分子结构信息
SMILES: CC(C1=CC=CC=C1)N
InChI: InChI=1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3
描述信息
1-Phenylethylamine, or alpha-phenethylamine, is an amine. Individual enantiomers of this basic compound are useful for performing chiral resolution of acidic compounds by forming diastereomeric salts. -- Wikipedia [HMDB]
1-Phenylethylamine, or alpha-phenethylamine, is an amine. Individual enantiomers of this basic compound are useful for performing chiral resolution of acidic compounds by forming diastereomeric salts. -- Wikipedia.
同义名列表
32 个代谢物同义名
1-Phenethylamine hydrochloride, (+-)-isomer; 1-Phenethylamine hydrochloride; alpha-Methylbenzenemethanamine; 1-Phenethylamine, (+-)-isomer; 1-Phenethylamine, (R)-isomer; 1-Phenethylamine, (S)-isomer; (S)-(-)-1-Phenylethylamine; a-Methylbenzenemethanamine; Α-methylbenzenemethanamine; (+/-)-α-methylbenzylamine; alpha-Aminoethylbenzene; alpha-Methylbenzylamine; 1-Amino-1-phenylethane; alpha-Phenylethylamine; (1-Aminoethyl)benzene; 1-Phenyl-1-ethanamine; 1-phenylethan-1-amine; alpha-Phenethylamine; Α-aminoethylbenzene; Α-methylbenzylamine; a-Methylbenzylamine; a-Aminoethylbenzene; 1-Phenylethanamine; a-Phenylethylamine; 1-Phenylethylamine; Α-phenylethylamine; a-Phenethylamine; 1-Phenethylamine; 1-Fenylethylamin; Sumine 2079; 1-Phenylethylamine; 1-Phenylethylamine
数据库引用编号
19 个数据库交叉引用编号
- ChEBI: CHEBI:670
- KEGG: C02455
- KEGGdrug: D77753
- PubChem: 7408
- HMDB: HMDB0002017
- Metlin: METLIN58
- ChEMBL: CHEMBL278059
- Wikipedia: 1-Phenylethylamine
- foodb: FDB022799
- chemspider: 7130
- CAS: 618-36-0
- CAS: 98-84-0
- PMhub: MS000007715
- PubChem: 5475
- NIKKAJI: J138.892D
- NIKKAJI: J66.056F
- LOTUS: LTS0263690
- wikidata: Q3560549
- KNApSAcK: 670
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)
10 个相关的物种来源信息
- 47037 - Alhagi maurorum: 10.1002/JPS.2600620942
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 3039 - Euglena gracilis: 10.3389/FBIOE.2021.662655
- 9606 - Homo sapiens: -
- 207710 - Prosopis alba: 10.1055/S-2006-960454
- 157169 - Ramalina fraxinea: 10.5586/ASBP.1979.002
- 138013 - Senegalia berlandieri:
- 867542 - Turbinicarpus lophophoroides: 10.1016/S0305-1978(99)00019-8
- 130183 - Turbinicarpus pseudomacrochele: 10.1016/S0305-1978(99)00019-8
- 867544 - Turbinicarpus pseudopectinatus: 10.1016/S0305-1978(99)00019-8
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
- Kazuyuki Yasukawa, Shogo Nakano, Yasuhisa Asano. Tailoring D-amino acid oxidase from the pig kidney to R-stereoselective amine oxidase and its use in the deracemization of α-methylbenzylamine.
Angewandte Chemie (International ed. in English).
2014 Apr; 53(17):4428-31. doi:
10.1002/anie.201308812. [PMID: 24644036] - Gholamreza Fazeli, Rajaraman Gnana Oli, Nicole Schupp, Helga Stopper. The role of the dopamine transporter in dopamine-induced DNA damage.
Brain pathology (Zurich, Switzerland).
2011 May; 21(3):237-48. doi:
10.1111/j.1750-3639.2010.00440.x. [PMID: 20875051] - Khozirah Shaari, Kee Cheng Ling, Zalilawati Mat Rashid, Tan Pei Jean, Faridah Abas, Salahudin Mohd Raof, Zurina Zainal, Nordin Hj Lajis, Habsah Mohamad, Abdul Manaf Ali. Cytotoxic aaptamines from Malaysian Aaptos aaptos.
Marine drugs.
2009; 7(1):1-8. doi:
10.3390/md7010001. [PMID: 19370166] - Hans-Jürgen Federsel, Martin Hedberg, Fredrik R Qvarnström, Magnus P T Sjögren, Wei Tian. Construction of a chiral central nervous system (CNS)-active aminotetralin drug compound based on a synthesis strategy using multitasking properties of (S)-1-phenylethylamine.
Accounts of chemical research.
2007 Dec; 40(12):1377-84. doi:
10.1021/ar700102c. [PMID: 17668920] - Paul E Harrington, Christopher Fotsch. Calcium sensing receptor activators: calcimimetics.
Current medicinal chemistry.
2007; 14(28):3027-34. doi:
10.2174/092986707782794096. [PMID: 18220738] - Mitsuhiro Wada, Shinichi Nakamura, Mamoru Tomita, Mihoko N Nakashima, Kenichiro Nakashima. Determination of MDMA and MDA in rat urine by semi-micro column HPLC-fluorescence detection with DBD-F and their monitoring after MDMA administration to rat.
Luminescence : the journal of biological and chemical luminescence.
2005 May; 20(3):210-5. doi:
10.1002/bio.821. [PMID: 15924321] - J F Van Bocxlaer, W E Lambert, L Thienpont, A P De Leenheer. Quantitative determination of amphetamine and alpha-phenylethylamine enantiomers in judicial samples using capillary gas chromatography.
Journal of analytical toxicology.
1997 Jan; 21(1):5-11. doi:
10.1093/jat/21.1.5. [PMID: 9013285] - E Meyer, J F Van Bocxlaer, W E Lambert, L Thienpont, A P De Leenheer. Identification of alpha-phenylethylamine in judicial samples.
Journal of analytical toxicology.
1996 Mar; 20(2):116-20. doi:
10.1093/jat/20.2.116. [PMID: 8868403] - M P Knadler, S D Hall. High-performance liquid chromatographic analysis of the enantiomers of flurbiprofen and its metabolites in plasma and urine.
Journal of chromatography.
1989 Sep; 494(?):173-82. doi:
10.1016/s0378-4347(00)82666-3. [PMID: 2584314] - A McCOUBREY. Depletion of adrenal ascorbic acid and cholesterol by p-cyclohexyloxy-alpha-phenylethylamine and related amines in rats.
British journal of pharmacology and chemotherapy.
1954 Sep; 9(3):295-8. doi:
10.1111/j.1476-5381.1954.tb01684.x. [PMID: 13199248]
