| Record Information |
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| Version | 1.0 |
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| Creation date | 2010-04-08 22:06:07 UTC |
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| Update date | 2025-11-18 22:55:26 UTC |
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| Primary ID | FDB004181 |
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| Secondary Accession Numbers | Not Available |
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| Chemical Information |
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| FooDB Name | Lithium |
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| Description | Lithium (Li) is an alkali metal. First described as a mood stabilizer in 1949, it remains an efficacious treatment for bipolar disorders. Recent emerging evidence of its neuroprotective and neurogenic effects alludes to lithium's potential therapeutic use in stroke and neurodegenerative diseases. One intriguing clinical application is in the treatment of Alzheimer's disease. Ongoing clinical trials are evaluating lithium's abilities to lower tau and beta-amyloid levels in cerebrospinal fluid in Alzheimer's patients. Lithium reduces brain inositol levels by inhibiting the enzyme inositol monophosphatase. This suggests that inositol monophosphatase inhibition is a key mechanism of Li's therapeutic action and that design of new inositol monophosphatase inhibitors may be a practical strategy to create new compounds with Li-like therapeutic effects. Lithium reduces the severity of some behavioral complications of Alzheimer's disease (AD). And there are growing indications that Li may be of benefit to the underlying pathology of AD, as well as an array of other common CNS disorders, including stroke, Parkinson's disease, and Huntington's disease. Physiologically, it exists as an ion in the body. Despite these demonstrated and prospective therapeutic benefits, Li's mechanism of action remains elusive, and opinions differ regarding the most relevant molecular targets. Lithium inhibits several enzymes; significant among these are inositol monophosphatase (IMPase), glycogen synthase kinase-3 (GSK-3), and the proteasome. Lithium has a narrow therapeutic range, and several well characterised adverse effects limit the potential usefulness of higher doses. Acute ingestion in Li-naive patients is generally associated with only short-lived exposure to high concentrations, due to extensive distribution of Li throughout the total body water compartment. Conversely, chronic toxicity and acute-on-therapeutic ingestion are associated with prolonged exposure to higher tissue concentrations and, therefore, greater toxicity. Lithium toxicity may be life threatening, or result in persistent cognitive and neurological impairment. Therefore, enhanced Li clearance has been explored as a means of minimizing exposure to high tissue concentrations. Although haemodialysis is highly effective in removing circulating Li, serum concentrations often rebound so repeated or prolonged treatment may be required. Continuous arteriovenous haemodiafiltration and continuous venovenous haemodiafiltration increase Li clearance, albeit to a lesser extent than haemodialysis, and are more widely accessible. Lithium reduces brain inositol levels by inhibiting IMPase, suggesting that IMPase's inhibition is a key mechanism of Li's therapeutic action and that design of new IMPase inhibitors may be a practical strategy to create new compounds with Li-like therapeutic effects. (PMID: 17688381, 17316163, 8110911, 17288494). Lithium is found in many foods, some of which are endive, yellow zucchini, romaine lettuce, and common bean. |
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| CAS Number | 7439-93-2 |
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| Structure | |
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| Synonyms | | Synonym | Source |
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| 3Li | ChEBI | | Li | ChEBI | | Litio | ChEBI | | Normothymin-e | Kegg | | Lithium-7 | MeSH | | Lithium 7 | MeSH | | Apo-lithium carbonate | biospider | | Apo-lithium carbonate SR | biospider | | Carbolith Cap 150mg | biospider | | Carbolith Cap 300mg | biospider | | Carbolith Capsules 600mg | biospider | | Eskalith | biospider | | Eskalith CR | biospider | | LI | biospider | | Li(+) | biospider | | Li(+) cation | biospider | | Li(+) ion | biospider | | Li+ | biospider | | Lithane | biospider | | Lithium atom | biospider | | Lithium benziocum | biospider | | Lithium carbonate | biospider | | Lithium carbonicum | biospider | | Lithium cation | biospider | | Lithium citrate | biospider | | Lithium element | biospider | | Lithium ion | biospider | | Lithium, ion | biospider | | Lithium, ion (Li1+) | biospider | | lithium(+1) cation | biospider | | lithium(1+) | biospider | | lithium(1+) ion | biospider | | Lithium(I) cation | biospider | | Lithobid | biospider | | Pal-lithium carbonate | biospider | | PHL-lithium carbonate | biospider | | Pms-Lithium Carbonate - Cap 150mg | biospider | | Pms-Lithium Carbonate - Cap 300mg | biospider | | Pms-Lithium Carbonate - Cap 600mg | biospider | | Pms-Lithium Citrate Syr 8mmo/5ml | biospider |
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| Predicted Properties | |
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| Chemical Formula | Li |
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| IUPAC name | lithium |
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| InChI Identifier | InChI=1S/Li |
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| InChI Key | WHXSMMKQMYFTQS-UHFFFAOYSA-N |
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| Isomeric SMILES | [Li] |
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| Average Molecular Weight | 6.941 |
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| Monoisotopic Molecular Weight | 7.016004049 |
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| Classification |
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| Description | Belongs to the class of inorganic compounds known as homogeneous alkali metal compounds. These are inorganic compounds containing only metal atoms,with the largest atom being a alkali metal atom. |
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| Kingdom | Inorganic compounds |
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| Super Class | Homogeneous metal compounds |
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| Class | Homogeneous alkali metal compounds |
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| Sub Class | Not Available |
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| Direct Parent | Homogeneous alkali metal compounds |
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| Alternative Parents | Not Available |
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| Substituents | |
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| Molecular Framework | Not Available |
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| External Descriptors | |
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| Ontology |
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| Ontology | No ontology term |
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| Physico-Chemical Properties |
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| Physico-Chemical Properties - Experimental | | Property | Value | Reference |
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| Physical state | Solid | |
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| Physical Description | Not Available | |
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| Mass Composition | Not Available | |
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| Melting Point | 190 oC | |
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| Boiling Point | Not Available | |
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| Experimental Water Solubility | Not Available | |
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| Experimental logP | Not Available | |
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| Experimental pKa | Not Available | |
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| Isoelectric point | Not Available | |
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| Charge | Not Available | |
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| Optical Rotation | Not Available | |
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| Spectroscopic UV Data | Not Available | |
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| Density | Not Available | |
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| Refractive Index | Not Available | |
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| Spectra |
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| Spectra | |
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| EI-MS/GC-MS | Not Available |
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| MS/MS | | Type | Description | Splash Key | View |
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| Predicted MS/MS | Predicted LC-MS/MS Spectrum - 10V, Positive | splash10-0a4i-9000000000-cbe4de9c65cbd09ee945 | 2016-08-03 | View Spectrum | | Predicted MS/MS | Predicted LC-MS/MS Spectrum - 20V, Positive | splash10-0a4i-9000000000-cbe4de9c65cbd09ee945 | 2016-08-03 | View Spectrum | | Predicted MS/MS | Predicted LC-MS/MS Spectrum - 40V, Positive | splash10-0a4i-9000000000-cbe4de9c65cbd09ee945 | 2016-08-03 | View Spectrum | | Predicted MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-0a4i-9000000000-ae882b48ac0e9bfbedb2 | 2016-08-03 | View Spectrum | | Predicted MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-0a4i-9000000000-ae882b48ac0e9bfbedb2 | 2016-08-03 | View Spectrum | | Predicted MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-0a4i-9000000000-ae882b48ac0e9bfbedb2 | 2016-08-03 | View Spectrum |
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| NMR | Not Available |
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| External Links |
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| ChemSpider ID | 26502 |
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| ChEMBL ID | Not Available |
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| KEGG Compound ID | C15473 |
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| Pubchem Compound ID | 28486 |
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| Pubchem Substance ID | Not Available |
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| ChEBI ID | 30145 |
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| Phenol-Explorer ID | Not Available |
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| DrugBank ID | DB01356 |
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| HMDB ID | HMDB05949 |
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| CRC / DFC (Dictionary of Food Compounds) ID | Not Available |
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| EAFUS ID | Not Available |
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| Dr. Duke ID | LITHIUM |
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| BIGG ID | Not Available |
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| KNApSAcK ID | Not Available |
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| HET ID | LI |
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| Food Biomarker Ontology | Not Available |
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| VMH ID | Not Available |
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| Flavornet ID | Not Available |
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| GoodScent ID | Not Available |
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| SuperScent ID | Not Available |
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| Wikipedia ID | Lithium |
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| Phenol-Explorer Metabolite ID | Not Available |
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| Duplicate IDS | Not Available |
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| Old DFC IDS | Not Available |
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| Associated Foods |
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| Food | Content Range | Average | Reference |
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| Food | | | Reference |
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| Biological Effects and Interactions |
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| Health Effects / Bioactivities | | Descriptor | ID | Definition | Reference |
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| Anti depressant | 52217 | An agent that regulates mood, reducing symptoms of depression and anxiety by altering neurotransmitter levels in the brain, commonly used in managing depression, anxiety disorders, and other mood disorders. | DUKE | | Anti hyperthyroid | 52217 | An agent that reduces thyroid hormone production, used to manage hyperthyroidism by decreasing thyroid-stimulating hormone (TSH) and thyroid hormone levels, commonly used to treat conditions such as Graves' disease and thyroid storm. | DUKE | | Anti-manic | | An agent that stabilizes mood by controlling symptoms of mania, used to manage bipolar disorder, reducing excessive excitement and impulsivity, and preventing manic episodes. | DUKE | | Anti premenstrual syndrome | 52217 | An agent that alleviates symptoms of premenstrual syndrome (PMS), reducing physical and emotional discomfort. Its biological role involves regulating hormonal fluctuations, and its therapeutic applications include managing mood swings, bloating, and breast tenderness. Key medical uses include treating PMS, premenstrual dysphoric disorder (PMDD), and other menstrual-related disorders. | DUKE | | Anti psychotic | 35476 | An agent that reduces psychotic symptoms, commonly used in managing schizophrenia, bipolar disorder, and other mental health conditions by blocking dopamine receptors in the brain, thereby alleviating hallucinations, delusions, and disordered thinking. | DUKE | | Anti-schizophrenic | 52217 | An agent that reduces psychotic symptoms, commonly used in managing schizophrenia and other psychotic disorders, by modulating dopamine and serotonin levels in the brain, thereby alleviating hallucinations, delusions, and disorganized thinking. | DUKE | | Anti-viral | 22587 | An agent that inhibits the replication of viruses, playing a crucial role in preventing and treating viral infections. Therapeutically, anti-virals are used to manage diseases such as HIV, herpes, and influenza, reducing symptoms and slowing disease progression. Key medical uses include treating viral hepatitis, respiratory syncytial virus, and COVID-19. | DUKE | | Cholinergic | 38323 | An agent that stimulates the parasympathetic nervous system by mimicking acetylcholine, enhancing muscle contraction, and regulating various bodily functions. Therapeutically, it treats conditions like glaucoma, myasthenia gravis, and Alzheimer's disease, improving muscle tone, cognition, and eye pressure. | DUKE | | Deliriant | | A class of hallucinogen that induces solid hallucinations, seamlessly integrating into waking consciousness. It has no established therapeutic applications, but is sometimes used in research to study psychosis and altered states of consciousness. Medical uses are limited due to its potent hallucinogenic effects. | DUKE | | Natriuretic | | An agent that promotes the excretion of sodium in the urine, aiding in blood pressure regulation and fluid balance. It plays a biological role in managing hypertension and heart failure, with therapeutic applications in treating edema and cardiovascular diseases. Key medical uses include diuretic therapy and management of congestive heart failure. | DUKE | | Nephrotoxic | 50909 | An agent that damages or harms the kidneys, disrupting their ability to filter waste. It has no therapeutic applications, but is often a side effect of certain medications, such as antibiotics and chemotherapy. Key medical uses involve monitoring and managing kidney damage in patients receiving nephrotoxic treatments. | DUKE |
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| Enzymes | | Name | Gene Name | UniProt ID |
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| Glycogen synthase kinase-3 beta | GSK3B | P49841 | | Catenin beta-1 | CTNNB1 | P35222 |
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| Pathways | Not Available |
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| Metabolism | Not Available |
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| Biosynthesis | Not Available |
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| Organoleptic Properties |
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| Flavours | Not Available |
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| Files |
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| MSDS | show |
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| References |
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| Synthesis Reference | Not Available |
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| General Reference | Not Available |
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| Content Reference | — Duke, James. 'Dr. Duke's Phytochemical and Ethnobotanical Databases. United States Department of Agriculture.' Agricultural Research Service, Accessed April 27 (2004).
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