5-Hydroxy-L-tryptophan (BioDeep_00000000117)

 

Secondary id: BioDeep_00000000221, BioDeep_00000398605, BioDeep_00000403185, BioDeep_00000896630, BioDeep_00001872968

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite


代谢物信息卡片


(S)-2-Amino-3-(5-hydroxy-1H-indol-3-yl)propanoic Acid (5-Hydroxytryptophan)

化学式: C11H12N2O3 (220.0847882)
中文名称: 5-羟基色氨酸, L-5-羟色氨酸, 5-羟基-色氨酸
谱图信息: 最多检出来源 Homo sapiens(blood) 0.02%

Reviewed

Last reviewed on 2024-07-02.

Cite this Page

5-Hydroxy-L-tryptophan. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/5-hydroxy-l-tryptophan (retrieved 2024-09-17) (BioDeep RN: BioDeep_00000000117). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C1=CC2=C(C=C1O)C(=CN2)CC(C(=O)O)N
InChI: InChI=1S/C11H12N2O3/c12-9(11(15)16)3-6-5-13-10-2-1-7(14)4-8(6)10/h1-2,4-5,9,13-14H,3,12H2,(H,15,16)

描述信息

5-Hydroxy-L-tryptophan is an aromatic amino acid naturally produced by the body from the essential amino acid L-tryptophan. 5-Hydroxy-L-tryptophan is the immediate precursor of the neurotransmitter serotonin. The conversion to serotonin is catalyzed by the enzyme aromatic L-amino acid decarboxylase (EC 4.1.1.28) (AADC1 also known as DOPA decarboxylase), an essential enzyme in the metabolism of the monoamine neurotransmitters. An accumulation of 5-hydroxy-L-tryptophan in cerebrospinal fluid occurs in aromatic L-amino acid decarboxylase deficiency (AADC deficiency) (OMIM: 608643) accompanied by an increased excretion in the urine of the patients, which are indicative of the disorder but not specific. 5-Hydroxy-L-tryptophan is also increased in other disorders such as in Parkinsons patients with severe postural instability and gait disorders. The amount of endogenous 5-hydroxy-L-tryptophan available for serotonin synthesis depends on the availability of tryptophan and on the activity of various enzymes, especially tryptophan hydroxylase (EC 1.14.16.4), indoleamine 2,3-dioxygenase (EC 1.13.11.52), and tryptophan 2,3-dioxygenase (TDO) (EC 1.13.11.11). 5-Hydroxy-L-tryptophan has been used clinically for over 30 years. In addition to its use in the treatment of depression, the therapeutic administration of 5-hydroxy-L-tryptophan has been shown to be effective in treating a wide variety of conditions, including fibromyalgia, insomnia, binge eating associated with obesity, cerebellar ataxia, and chronic headaches. 5-Hydroxy-L-tryptophan easily crosses the blood-brain barrier and effectively increases central nervous system (CNS) synthesis of serotonin. Supplementation with 5-hydroxy-L-tryptophan is hypothesized to normalize serotonin synthesis, which is putatively related to its antidepressant properties (PMID: 9295177, 17240182, 16023217). When present in sufficiently high levels, 5-hydroxytryptophan can be a neurotoxin and a metabotoxin. A neurotoxin is a compound that disrupts or attacks neural cells or tissue. A metabotoxin is an endogenously produced metabolite that causes adverse health effects at chronically high levels. Signs and symptoms of AADC deficiency generally appear in the first year of life. Affected infants may have severe developmental delay, weak muscle tone (hypotonia), muscle stiffness, difficulty moving, and involuntary writhing movements of the limbs (athetosis). They may be lacking in energy (lethargic), feed poorly, startle easily, and have sleep disturbances. Since 5-hydroxytryptophan is a precursor to serotonin, altered levels of serotonin can accumulate in the brain, which leads to abnormal neural signalling. Infants with AADC deficiency have very low levels of neural signalling molecules while individuals who consume high levels of 5-hydroxytryptophan will have very high levels of neural signalling molecules. Both conditions can lead to vomiting, nausea, extreme drowsiness, and lethargy. 5-Hydroxytryptophan (5-HTP), also known as oxitriptan (INN) is sold over-the-counter in the United Kingdom, the United States, and Canada as a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid. It is also marketed in many European countries for the indication of major depression under trade names such as Cincofarm, Levothym, Levotonine, Oxyfan, Telesol, Tript-OH, and Triptum. Several double-blind placebo-controlled clinical trials have demonstrated the effectiveness of 5-HTP in the treatment of depression, though a lack of high-quality studies has been noted. More and larger studies are needed to determine if 5-HTP is truly effective in treating depression.
5-hydroxy-L-tryptophan is the L-enantiomer of 5-hydroxytryptophan. It has a role as a human metabolite, a plant metabolite and a mouse metabolite. It is a 5-hydroxytryptophan, a hydroxy-L-tryptophan and a non-proteinogenic L-alpha-amino acid. It is an enantiomer of a 5-hydroxy-D-tryptophan. It is a tautomer of a 5-hydroxy-L-tryptophan zwitterion.
5-Hydroxytryptophan (5-HTP), also known as oxitriptan (INN), is a naturally occurring amino acid and metabolic intermediate in the synthesis of serotonin and melatonin. 5-HTP is sold over-the-counter in the United Kingdom, United States and Canada as a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid, and is also marketed in many European countries for the indication of major depression under trade names like Cincofarm, Levothym, Levotonine, Oxyfan, Telesol, Tript-OH, and Triptum. Several double-blind placebo-controlled clinical trials have demonstrated the effectiveness of 5-HTP in the treatment of depression, though a lack of high quality studies has been noted. More study is needed to determine efficacy in treating depression.
Oxitriptan is an aromatic amino acid with antidepressant activity. In vivo, oxitriptan (or 5-hydroxytryptophan) is converted into 5-hydroxytryptamine (5-HT or serotonin) as well as other neurotransmitters. Oxitriptan may exert its antidepressant activity via conversion to serotonin or directly by binding to serotonin (5-HT) receptors within the central nervous system (CNS). Endogenous oxitriptan is produced from the essential amino acid L-tryptophan. The exogenous therapeutic form is isolated from the seeds of the African plant Griffonia simplicifolia.
The immediate precursor in the biosynthesis of SEROTONIN from tryptophan. It is used as an antiepileptic and antidepressant.
See also: ... View More ...
5-Hydroxytryptophan (5-HTP), also known as oxitriptan (INN), is a naturally-occurring amino acid and chemical precursor as well as metabolic intermediate in the biosynthesis of the neurotransmitters serotonin and melatonin from tryptophan. 5-Hydroxy-L-tryptophan is found in french plantain.

5-Hydroxy-L-tryptophan. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=4350-09-8 (retrieved 2024-07-02) (CAS RN: 4350-09-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
L-5-Hydroxytryptophan (L-5-HTP), a naturally occurring amino acid and a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid, is the immediate precursor of the neurotransmitter serotonin and a reserpine antagonist[1]. L-5-Hydroxytryptophan (L-5-HTP) is used to treat fibromyalgia, myoclonus, migraine, and cerebellar ataxia[2][3][4][5].

同义名列表

89 个代谢物同义名

(S)-2-Amino-3-(5-hydroxy-1H-indol-3-yl)propanoic Acid (5-Hydroxytryptophan); 5-Hydroxy-L-tryptophan, United States Pharmacopeia (USP) Reference Standard; (2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid; (S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid; (2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoicacid; 2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoicacid; S(+)-1-alpha-Amino-5-hydroxyindole-3-propionic acid; (2S)-2-amino-3-(5-hydroxyindol-3-yl)propanoic acid; 2-Amino-3-(5-hydroxy-1H-indol-3-yl)propionic acid; 5-22-14-00278 (Beilstein Handbook Reference); N-ACETYLTRYPTOPHAN IMPURITY D [EP IMPURITY]; L-5-Hydroxytryptophan (L-5-HTP; Oxitriptan); TRYPTOPHAN IMPURITY D [EP IMPURITY]; 5-HYDROXYTRYPTOPHAN L-FORM [MI]; 5-HYDROXY-L-TRYPTOPHAN [USP-RS]; 5-Hydroxy-L-tryptophan, powder; 5-Hydroxytryptophan L form; Tryptophan, 5-hydroxy-, dl; Tryptophan, 5-hydroxy-, L-; 5-Hydroxytryptophan L-form; Oxitriptano (INN-Spanish); HYDROXYTRYPTOPHAN [VANDF]; Oxitriptano [INN-Spanish]; Oxitriptanum (INN-Latin); HYDROXYTRYPTOPHAN [INCI]; Oxitriptanum [INN-Latin]; 5-hydroxytryptophan, dl-; L-Tryptophan, 5-hydroxy-; Hydroxy-5 L-tryptophane; 5-Hydroxyl-L-tryptophan; (S)-5-Hydroxytryptophan; 5-hydroxy-L-tryptophane; Tryptophan, 5-hydroxy-; 5-hydroxy-L-tryptophan; 5-Hydroxy- Tryptophan; L-5-Hydroxytryptophan; Tryptophan, 5 Hydroxy; 5-Hydroxytryptophane; 5-HYDROXY-TRYPTOPHAN; 5-hydroxy tryptophan; OXITRIPTAN [WHO-DD]; 5-hydroxytryptophan; 5 Hydroxytryptophan; OXITRIPTAN [MART.]; OXITRIPTAN (MART.); hydroxytryptophan; Oxitriptan [INN]; Oxitriptan (INN); UNII-C1LJO185Q9; Tox21_111073_1; H-Trp(5-OH)-OH; 5-HTP Phenolic; Levothym (TN); Lopac0_000627; Dl-oxitriptan; Ro 3-5940 HCl; Oxytryptophan; Tox21_201032; Tox21_500627; Tox21_111073; Oxitriptan 1; Oxitriptanum; L-oxitriptan; Oxitriptano; Levotonine; C1LJO185Q9; Levotinine; Oxitriptan; Pretonine; Cincofarm; Serotonyl; Levothym; Serotain; Triptene; Tript-OH; Quietim; Telesol; Tripten; N06AX01; Triptum; L-5-Htp; Oxyfan; 5-HTP; 5HTP; 4PQ; 2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid; (+-)-5-Hydroxytryptophan; 5-Hydroxytryptophan; 5-Hydroxy-tryptophan



数据库引用编号

28 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

22 个相关的代谢反应过程信息。

Reactome(12)

BioCyc(0)

WikiPathways(4)

Plant Reactome(0)

INOH(1)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(5)

PharmGKB(0)

3 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

  • Xinying Fu, Siyang Yan, Zongren Hu, Wen Sheng, Wanyu Li, Shida Kuang, Xue Feng, Lumei Liu, Wei Zhang, Qinghu He. Guhan Yangsheng Jing mitigates hippocampal neuronal pyroptotic injury and manifies learning and memory capabilities in sleep deprived mice via the NLRP3/Caspase1/GSDMD signaling pathway. Journal of ethnopharmacology. 2024 May; 326(?):117972. doi: 10.1016/j.jep.2024.117972. [PMID: 38403005]
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  • Liguo Liu, Dongmei Xu, Fengxin Chen, Shengnan Cai, Jin Wei, Jiaheng Deng, Jianhua Zheng, Qi Jin, Wenhui Lun. Identification of potential biomarkers for diagnosis of syphilis from the cerebrospinal fluid based on untargeted metabolomic analysis. Molecular omics. 2023 Apr; ?(?):. doi: 10.1039/d3mo00026e. [PMID: 37185577]
  • Archana Sarangi, Mayukh Ghosh, Suman Sangwan, Rajesh Kumar, Sunesh Balhara, S K Phulia, R K Sharma, Subhasish Sahu, Sandeep Kumar, A K Mohanty, A K Balhara. Exploration of urinary metabolite dynamicity for early detection of pregnancy in water buffaloes. Scientific reports. 2022 09; 12(1):16295. doi: 10.1038/s41598-022-20298-1. [PMID: 36175438]
  • Ramkripa Raghavan, Neha S Anand, Guoying Wang, Xiumei Hong, Colleen Pearson, Barry Zuckerman, Hehuang Xie, Xiaobin Wang. Association between cord blood metabolites in tryptophan pathway and childhood risk of autism spectrum disorder and attention-deficit hyperactivity disorder. Translational psychiatry. 2022 07; 12(1):270. doi: 10.1038/s41398-022-01992-0. [PMID: 35810183]
  • Pan Luo, Jiawen Xu, Shiqiang Cheng, Ke Xu, Wensen Jing, Feng Zhang, Peng Xu. Large-scale genetic correlation scanning and causal association between deep vein thrombosis and human blood metabolites. Scientific reports. 2022 05; 12(1):7888. doi: 10.1038/s41598-022-12021-x. [PMID: 35551264]
  • Saurabh Bhatia, Ahmed Al-Harrasi, Arun Kumar, Tapan Behl, Aayush Sehgal, Sukhbir Singh, Neelam Sharma, Md Khalid Anwer, Deepak Kaushik, Vineet Mittal, Sridevi Chigurupati, Pritam Babu Sharma, Lotfi Aleya, Celia Vargas-de-la-Cruz, Md Tanvir Kabir. Anti-migraine activity of freeze-dried latex obtained from Calotropis gigantea Linn. Environmental science and pollution research international. 2022 Apr; 29(18):27460-27478. doi: 10.1007/s11356-021-17810-x. [PMID: 34981370]
  • Yingying Wang, Xueman Chen, Qiaoyu Chen, Ning Zhou, Xin Wang, Alei Zhang, Kequan Chen, Pingkai Ouyang. Construction of cell factory capable of efficiently converting L-tryptophan into 5-hydroxytryptamine. Microbial cell factories. 2022 Mar; 21(1):47. doi: 10.1186/s12934-022-01745-0. [PMID: 35331215]
  • ZhiFei Zhang, Wei Du, WenYi Liu, Braden T Wong, HuiLing Zheng. Increasing serotonin concentrations alter calcium metabolism in periparturient dairy goats. Journal of animal science. 2022 Mar; 100(3):. doi: 10.1093/jas/skac065. [PMID: 35235945]
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  • Jun Pan, Fengming Li, Caidie Wang, Xiaobin Li, Shiqi Zhang, Wenjie Zhang, Guodong Zhao, Chen Ma, Guoshi Liu, Kailun Yang. Effects of Duodenal 5-Hydroxytryptophan Perfusion on Melatonin Synthesis in GI Tract of Sheep. Molecules (Basel, Switzerland). 2021 Aug; 26(17):. doi: 10.3390/molecules26175275. [PMID: 34500708]
  • Ernesto Limón-Bernal, José E Roa-Coria, Ángel Zúñiga-Romero, Juan C Huerta-Cruz, Irma R C Ruíz-Velasco, Francisco J Flores-Murrieta, Eleazar Lara-Padilla, Juan G Reyes-García, Héctor I Rocha-González. Anorectic interaction and safety of 5-hydroxytryptophan/carbidopa plus phentermine or diethylpropion in rat. Behavioural pharmacology. 2021 08; 32(5):368-381. doi: 10.1097/fbp.0000000000000625. [PMID: 33660661]
  • E E L Valente, M L Damasceno, J L Klotz, D L Harmon. Residual effects of abomasal 5-hydroxytryptophan administration on serotonin metabolism in cattle. Domestic animal endocrinology. 2021 07; 76(?):106627. doi: 10.1016/j.domaniend.2021.106627. [PMID: 33882449]
  • Sena L Field, Marcela G Marrero, Lihe Liu, Francisco Peñagaricano, Jimena Laporta. Histological and transcriptomic analysis of adipose and muscle of dairy calves supplemented with 5-hydroxytryptophan. Scientific reports. 2021 05; 11(1):9665. doi: 10.1038/s41598-021-88443-w. [PMID: 33958639]
  • Yuying Liu, Nannan Zhou, Li Zhou, Jing Wang, Yabo Zhou, Tianzhen Zhang, Yi Fang, Jinwei Deng, Yunfeng Gao, Xiaoyu Liang, Jiadi Lv, Zhenfeng Wang, Jing Xie, Yuanbo Xue, Huafeng Zhang, Jingwei Ma, Ke Tang, Yiliang Fang, Feiran Cheng, Chengjuan Zhang, Bing Dong, Yuzhou Zhao, Peng Yuan, Quanli Gao, Haizeng Zhang, F Xiao-Feng Qin, Bo Huang. IL-2 regulates tumor-reactive CD8+ T cell exhaustion by activating the aryl hydrocarbon receptor. Nature immunology. 2021 03; 22(3):358-369. doi: 10.1038/s41590-020-00850-9. [PMID: 33432230]
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  • Shabbir Ahmad, Mujahid Mohammed, Lakshmi Prasuna Mekala, Sasikala Chintalapati, Venkata Ramana Chintalapati. Tryptophan, a non-canonical melanin precursor: New L-tryptophan based melanin production by Rubrivivax benzoatilyticus JA2. Scientific reports. 2020 06; 10(1):8925. doi: 10.1038/s41598-020-65803-6. [PMID: 32488041]
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  • Zheng Guan, Gabriel Jacobs, Hans van Pelt, Joop M A Van Gerven, Jacobus Burggraaf, Wei Zhao. PK/PD modeling of 5-hydroxytryptophan (5-HTP) challenge test with cortisol measurement in serum and saliva. Pharmacology research & perspectives. 2020 04; 8(2):e00574. doi: 10.1002/prp2.574. [PMID: 32168433]
  • Susanna D Mitro, Gloria T Larrabure-Torrealva, Sixto E Sanchez, Samantha A Molsberry, Michelle A Williams, Clary Clish, Bizu Gelaye. Metabolomic markers of antepartum depression and suicidal ideation. Journal of affective disorders. 2020 02; 262(?):422-428. doi: 10.1016/j.jad.2019.11.061. [PMID: 31744743]
  • Jacob P R Jacobsen, Adrianna Oh, Rachel Bangle, Wendy L Roberts, Elizabeth L Royer, Nathan Modesto, Sonora A Windermere, Zixuan Yi, Rebecca Vernon, Manuel Cajina, Nikhil M Urs, Joshua C Snyder, Peter J Nicholls, Benjamin D Sachs, Marc G Caron. Slow-release delivery enhances the pharmacological properties of oral 5-hydroxytryptophan: mouse proof-of-concept. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. 2019 11; 44(12):2082-2090. doi: 10.1038/s41386-019-0400-1. [PMID: 31035282]
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  • 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. [PMID: 31515284]
  • Yildirim Kayacan, Hayrullah Yazar, Günay Cerit, Babak Elmi Ghojebeigloo. A new oxidative stress indicator: Effect of 5-hydroxytryptophan on thiol-disulfide homeostasis in exercise. Nutrition (Burbank, Los Angeles County, Calif.). 2019 Jul; 63-64(?):114-119. doi: 10.1016/j.nut.2019.01.013. [PMID: 30939385]
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