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rdf:type
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http://linked.open...gbank/description
| - A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851) (en)
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http://linked.open...gy/drugbank/group
| - approved (en)
- nutraceutical (en)
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http://linked.open...ugbank/indication
| - For nutritional supplementation, also for treating dietary shortage or imbalance (en)
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sameAs
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Title
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adms:identifier
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http://linked.open...mechanismOfAction
| - Succinate is an essential component of the Krebs or citric acid cycle and serves an electron donor in the production of fumaric acid and FADH2. It also has been shown to be a good "natural" antibiotic because of its relative acidic or caustic nature (high concentrations can even cause burns). Succinate supplements have been shown to help reduce the effects of hangovers by activating the degradation of acetaldehyde - a toxic byproduct of alcohol metabolism - into CO2 and H2O through aerobic metabolism. Succinic acid has been shown to stimulate neural system recovery and bolster the immune system. Claims have also been made that it boosts awareness, concentration and reflexes. (en)
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http://linked.open...drugbank/packager
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http://linked.open.../drugbank/synonym
| - Succinic acid (en)
- 1,2-Ethanedicarboxylic acid (en)
- Amber acid (en)
- Asuccin (en)
- Bernsteinsaure (en)
- Butanedioic acid (en)
- Butanedionic acid (en)
- Spirit of amber (en)
- Succinate (en)
- Acide butanedioique (en)
- Acide succinique (en)
- Acidum succinicum (en)
- Bernsteinsaeure (en)
- Butandisaeure (en)
- Dihydrofumaric acid (en)
- Ethylenesuccinic acid (en)
- HOOC-CH2-CH2-COOH (en)
- e363 (en)
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http://linked.open...drugbank/toxicity
| - Oral rat LD<sub>50</sub>: 2260 mg/kg (en)
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http://linked.open.../drug/hasAHFSCode
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http://linked.open.../drugbank/mixture
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http://linked.open...ynthesisReference
| - Michael Diamantoglou, Gerhard Meyer, "Process for the production of water-insoluble fibers of cellulose monoesters of maleic acid, succinic acid and phthalic acid, having an extremely high absorbability for water and physiological liquids." U.S. Patent US4734239, issued April, 1941. (en)
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http://linked.open...y/mesh/hasConcept
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http://linked.open...ugbank/IUPAC-Name
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http://linked.open...gy/drugbank/InChI
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http://linked.open...Molecular-Formula
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http://linked.open.../Molecular-Weight
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http://linked.open...noisotopic-Weight
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http://linked.open...y/drugbank/SMILES
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http://linked.open.../Water-Solubility
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http://linked.open...ogy/drugbank/logP
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http://linked.open...ogy/drugbank/logS
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http://linked.open...logy/drugbank/pKa
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http://linked.open...nd-Acceptor-Count
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http://linked.open...-Bond-Donor-Count
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http://linked.open...drugbank/InChIKey
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http://linked.open...urface-Area--PSA-
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http://linked.open...nk/Polarizability
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http://linked.open...bank/Refractivity
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http://linked.open...atable-Bond-Count
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http://linked.open.../affectedOrganism
| - Humans and other mammals (en)
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http://linked.open...casRegistryNumber
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http://linked.open...drugbank/category
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http://linked.open...gbank/containedIn
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http://linked.open...k/Bioavailability
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http://linked.open...ank/Boiling-Point
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http://linked.open...bank/Ghose-Filter
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http://linked.open...nk/MDDR-Like-Rule
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http://linked.open...ank/Melting-Point
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http://linked.open...k/Number-of-Rings
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http://linked.open...siological-Charge
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http://linked.open...bank/Rule-of-Five
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http://linked.open...tional-IUPAC-Name
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http://linked.open...strongest-acidic-
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