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owl:Thing dbo:ChemicalCompound wikidata:Q11173 umbel-rc:ChemicalSubstanceType n69:ChemicalObject dbo:ChemicalSubstance
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락트산 Kwas mlekowy Milchsäure Mjölksyra Aigéad lachtach Acido lattico Молочна кислота Asam laktat حمض اللبنيك Γαλακτικό οξύ 乳酸 Laktata acido 乳酸 Ácido láctico Молочная кислота Azido laktiko Àcid làctic Kyselina mléčná Melkzuur Lactic acid Acide lactique Ácido láctico
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حمض اللاكتيك أو حمض اللبنيك أو حمض اللبن هو مركب حيوي مهم يدخل في العديد من العمليات الكيميائية الحيوية، أثناء الأيض مثلا . وهو يصنف كيميائياً على أنه حمض كربوكسيلي له الصيغة C2H4OHCOOH. ينتج في العضلات عند الحركة، حيث تحرق الخلايا العضلية الجلوكوز . 乳酸(にゅうさん、lactic acid)は、有機化合物で、カルボン酸の1種である。キラル中心を1つ持つため鏡像異性体が存在するので、R体かS体かの区別が必要な場合がある。乳酸の塩やエステルは ラクタート あるいは ラクテート(lactate)と呼ぶ。解糖系の生成物として現れる。 락트산(lactic酸, Lactic acid), 유산(乳酸) 또는 젖산(―酸)은 체내에서 에너지를 만드는 글리코겐이 근육의 사용으로 분해되면서 생성되는 물질이다.흔히 락트산을 강도가 높은 운동 후에 발생하는 근육의 피로의 주범으로 많이 생각하는데, 한편으로는 락트산은 (slow muscle fiber 또는 slow twitch fiber)에서의 간단한 젖산 탈수소화 효소 반응으로 쉽게 산화시켜 에너지원으로서 TCA 회로로 들어갈 수 있다. Asam lakta (CH3-CHOH-COOH), dikenal juga sebagai asam susu) adalah senyawa kimia penting dalam beberapa proses biokimia. Seorang ahli kimia Swedia, Carl Wilhelm Scheele, kali meng pada tahun 1780. Secara struktur, ia adalah asam karboksilat dengan satu gugus hidroksil yang menempel pada gugus karboksil. Dalam air, ia terlarut epas proton (H+), membentuk ion laktat. Asam ini juga larut dalam alkohol dan bersifat menyerap air (higroskopik). Melkzuur is een organische verbinding met als brutoformule C3H6O3. In de scheikunde is de zuivere stof melkzuur vast, maar het racemisch mengsel van melkzuur is een olieachtige kleurloze hygroscopische vloeistof, die goed oplosbaar is in water. In de biologie is melkzuur een stof (metaboliet) die bij verschillende biologische processen vrijkomt, met name bij de onvolledige, zuurstofloze afbraak van glucose, zogeheten anaerobe dissimilatie. Melkzuur wordt niet tot de koolhydraten gerekend. Het E-nummer van melkzuur is E270. Kwas mlekowy, kwas 2-hydroksypropanowy (łac. acidum lacticum), E270 – organiczny związek chemiczny z grupy hydroksykwasów, obecny w skwaśniałym mleku (skąd pochodzi jego nazwa) oraz powstający w mięśniach w trakcie intensywnego wysiłku fizycznego, kiedy dochodzi do procesu beztlenowego oddychania zwanego fermentacją mleczanową. Sole tego kwasu to mleczany. Ze względu na to, że atom węgla, do którego przyłącza się grupa hydroksylowa, jest asymetryczny, kwas mlekowy wykazuje chiralność i ma dwa enancjomery: W organizmie ludzkim występuje wyłącznie forma L(+). Моло́чна кислота́ — α-оксіпропіонова одноосновна оксикарбонова кислота, хімічна формула СН3-СН(ОН)-СООН. Важливий проміжний продукт обміну живих організмів. Була відкрита шведським хіміком Карлом Шеєле у 1780 році. Milchsäure (lat. acidum lacticum) ist eine Hydroxycarbonsäure, enthält somit sowohl eine Carboxygruppe als auch eine Hydroxygruppe. Sie wird deswegen auch als 2-Hydroxypropionsäure bezeichnet, nach den Nomenklaturempfehlungen der IUPAC ist jedoch die Bezeichnung 2-Hydroxypropansäure zu verwenden. Die Salze und Ester der Milchsäure heißen Lactate. Kyselina mléčná má kyselou chuť, je lehce rozpustná a tvoří bezbarvé krystaly s chemickým vzorcem CH3CH(OH)COOH. Po kyselině glykolové jde o druhou nejjednodušší hydroxykyselinu. Tato kyselina vzniká mléčným kvašením cukrů, např. v mléce, sýrech, kyselém zelí. Používá se proto v pekařství, pivovarnictví (E270), koželužství, k přípravě limonád a při barvení a zušlechťování textilií (pohmat, lesk). Většinou se vyskytuje jako opticky neaktivní (kyselina DL-mléčná). Pro její antiseptické vlastnosti se požívá také v mastech, ústních vodách a jako prostředek k ošetřování vlasů. Její L-enantiomer[zdroj?] je koncovým produktem mléčného kvašení cukrů, a proto je přítomen v kyselém mléku a zelí. Konjugovaná báze kyseliny mléčné (její anion) se nazývá - CH3CH(OH)COO−. 乳酸(IUPAC學名:2-羥基丙酸)是一种化合物,它在多种生物化学过程中起作用。它是一种羧酸,分子式是C3H6O3。它是一个含有羟基的羧酸,因此是一个α-羟酸(AHA)。在水溶液中它的羧基释放出一个质子,而产生乳酸根离子 - 乳酸質(Lactate) - CH3CHOHCOO−。 乳酸有手性,有两个旋光异构体。一个被称为L-(+)-乳酸或(S)-乳酸,另一个被称为D-(-)-乳酸或(R)-乳酸。L-(+)-是在生物学上重要的异构体。 Azido laktikoa (laktatoa, ionizatzen denean) H3C-CH(OH)-COOH formula duen azido karboxilikoa da (C3H6O3), hainbat prozesu biokimiko eta fisiologikotan agertzen dena (esaterako, hartzidura laktikoan). Bi isomero optiko ditu: destrogiroa (D-laktikoa) eta lebogiroa (L-laktikoa), azken hau garrantzi biologikoa duena izanik. L'àcid làctic, o en la seva forma ionitzada, el lactat, en nomenclatura IUPAC oficial: àcid 2-hidroxi-propanoic o àcid α-hidroxi-propanoic, és un compost químic amb un important paper en diversos processos bioquímics, com el de la fermentació làctica. Es tracta d'un àcid carboxílic, amb un grup hidroxil en el carboni adjacent al grup carboxil, cosa que el converteix en un (AHA) de fórmula H₃C-CH(OH)-COOH (C₃H₆O₃). En solució pot perdre l'oxoni i convertir-se en l'anió lactat. L'àcid làctic és un , per la qual cosa posseeix dos isòmers òptics. El ácido láctico, o su forma ionizada, el lactato (del lat. lac, lactis, leche), también conocido por su nomenclatura oficial ácido 2-hidroxi-propanoico o ácido α-hidroxi-propanoico, es un compuesto químico que desempeña importantes roles en varios procesos bioquímicos, como la fermentación láctica. Es un ácido carboxílico, con un grupo hidroxilo en el carbono adyacente al grupo carboxilo, lo que lo convierte en un (AHA) de fórmula H3C-CH(OH)-COOH (C3H6O3). En solución puede perder el hidrógeno unido al grupo carboxilo y convertirse en el anión lactato. Lactic acid is an organic acid. It has a molecular formula CH3CH(OH)COOH. It is white in the solid state and it is miscible with water. When in the dissolved state, it forms a colorless solution. Production includes both artificial synthesis as well as natural sources. Lactic acid is an alpha-hydroxy acid (AHA) due to the presence of a hydroxyl group adjacent to the carboxyl group. It is used as a synthetic intermediate in many organic synthesis industries and in various biochemical industries. The conjugate base of lactic acid is called lactate (or the lactate anion). The name of the derived acyl group is lactoyl. Laktata acido (aŭ laktacido; kemia formulo: C3H6O3) estas acida kemia kombinaĵo kiu rolas en multaj biokemiaj procezoj. Ĝi estas uzata en pluraj manĝaĵoj por konservi kaj reguli aliajn acidojn. En solvaĵo, ĝi povas perdi protonon el la acida grupo. Tiel estiĝas la laktata jono CH3CH(OH)COO−, kiu miksiĝas kun akvo aŭ etanolo kaj estas higroskopa. Aigéad orgánach gan dath is ea Aigéad lachtach (CH3-CH(OH)-COOH). I láthair i mbainne géar. Cruthaítear é i matáin tar éis a gcraptha, agus mar staid inmheánach i meitibileacht carbaihiodráití. Déantar ar bhonn trádalach é trí choipeadh glúcóis le baictéir. In úsáid i súdaireacht, ruaimneoireacht agus míochaine. Tá dhá fhoirm eanaintiméireacha de sa nádúr. Les acides lactiques (acides hydroxypropanoïques) sont des acides organiques dont la chaîne est composée de trois atomes de carbone. Les ions lactate sont les bases conjuguées de ces acides (autrement dit, la forme ionisée des acides lactiques). Les acides lactiques sont des acides α-hydroxylés, de formule brute C3H6O3. Leur structure se reflète dans leur nom systématique : acide 2-hydroxypropanoïque. L'acido lattico (nome IUPAC: acido 2-idrossipropanoico) è un composto chimico di formula CH3-CHOH-COOH, che svolge un ruolo rilevante in diversi processi biochimici. L'acido lattico è un acido carbossilico, la sua struttura si distingue da quella dell'acido propionico per la presenza di un gruppo -OH all'atomo centrale (stereocentro) di carbonio. La sua deprotonazione dà origine allo ione lattato. La costante di ionizzazione (pKa = 3.1 a 25 °C) è tale che a pH fisiologico la sostanza sia presente quasi interamente sotto forma di lattato. Sia l'acido che i suoi sali alcalini sono solubili in acqua. Mjölksyra eller ɑ-hydroxipropionsyra (kemisk formel: CH3CH(OH)COOH) är en karboxylsyra (α-hydroxisyra) som spelar en stor roll inom biokemi. Laktat är mjölksyrans konjugata bas. O ácido láctico ou lático (do latim lac, lactis, leite), é um composto orgânico de função mista ácido carboxílico - álcool que apresenta fórmula molecular C3H6O3 e estrutural CH3 - CH ( OH ) - COOH. Participa de vários processos bioquímicos, e o lactato é a forma ionizada deste ácido. Foi descoberto pelo químico sueco Carl Wilhelm Scheele, no leite coalhado. Pela nomenclatura IUPAC é conhecido como ácido 2-hidroxipropanóico ou ácido α-hidroxipropanóico. Το γαλακτικό οξύ (αγγλικά: lactic acid) είναι οργανική χημική ένωση, με μοριακό τύπο C3H6O3, αν και συνηθέστερα παριστάνεται ως CH3CH(OH)CO2H. Το χημικά καθαρό γαλακτικό οξύ, στις κανονικές συνθήκες περιβάλλοντος, είναι λευκό στερεό, αναμείξιμο με το νερό. Όταν διαλύεται στο τελευταίο (νερό) σχηματίζει ένα άχρωμο διάλυμα. Η παραγωγή του συμπεριλαμβάνει τόσο φυσικές όσο και τεχνητές μεθόδους. Το γαλακτικό οξύ είναι ένα α- (AHA, A-HydroxyAcid), λόγω της παρουσίας υδροξυομάδας δίπλα ακριβώς από την καρβοξυλομάδα του. Χρησιμοποιήθηκε βιομηχανικά ως ενδιάμεσο συνθετικό σύνθεσης διαφόρων οργανικών και βιοχημικών προϊόντων. Η συζυγής βάση του γαλακτικού οξέος είναι το γαλακτικό ανιόν [CH3C(OH)CO2–]. Моло́чная кислота́ (химическая формула — C3H6O3) — cлабая химическая органическая кислота, относящаяся к классу предельных карбоновых кислот. При стандартных условиях молочная кислота — это одноосновная карбоновая оксикислота белого цвета с характерным запахом. Соли и эфиры молочной кислоты называются лактатами. Малотоннажная химия производит молочную кислоту 4 сортов: химически чистую, «фармакопейную», «техническую» и «пищевую».
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Lactic acid
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Lactic acid
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dbo:abstract
Melkzuur is een organische verbinding met als brutoformule C3H6O3. In de scheikunde is de zuivere stof melkzuur vast, maar het racemisch mengsel van melkzuur is een olieachtige kleurloze hygroscopische vloeistof, die goed oplosbaar is in water. In de biologie is melkzuur een stof (metaboliet) die bij verschillende biologische processen vrijkomt, met name bij de onvolledige, zuurstofloze afbraak van glucose, zogeheten anaerobe dissimilatie. Melkzuur wordt niet tot de koolhydraten gerekend. Het E-nummer van melkzuur is E270. 락트산(lactic酸, Lactic acid), 유산(乳酸) 또는 젖산(―酸)은 체내에서 에너지를 만드는 글리코겐이 근육의 사용으로 분해되면서 생성되는 물질이다.흔히 락트산을 강도가 높은 운동 후에 발생하는 근육의 피로의 주범으로 많이 생각하는데, 한편으로는 락트산은 (slow muscle fiber 또는 slow twitch fiber)에서의 간단한 젖산 탈수소화 효소 반응으로 쉽게 산화시켜 에너지원으로서 TCA 회로로 들어갈 수 있다. Mjölksyra eller ɑ-hydroxipropionsyra (kemisk formel: CH3CH(OH)COOH) är en karboxylsyra (α-hydroxisyra) som spelar en stor roll inom biokemi. Laktat är mjölksyrans konjugata bas. Kwas mlekowy, kwas 2-hydroksypropanowy (łac. acidum lacticum), E270 – organiczny związek chemiczny z grupy hydroksykwasów, obecny w skwaśniałym mleku (skąd pochodzi jego nazwa) oraz powstający w mięśniach w trakcie intensywnego wysiłku fizycznego, kiedy dochodzi do procesu beztlenowego oddychania zwanego fermentacją mleczanową. Sole tego kwasu to mleczany. Ze względu na to, że atom węgla, do którego przyłącza się grupa hydroksylowa, jest asymetryczny, kwas mlekowy wykazuje chiralność i ma dwa enancjomery: * L(+) (o konfiguracji absolutnej S): kwas (S)-2-hydroksypropanowy * D(–) (o konfiguracji absolutnej R): kwas (R)-2-hydroksypropanowy W organizmie ludzkim występuje wyłącznie forma L(+). Laktata acido (aŭ laktacido; kemia formulo: C3H6O3) estas acida kemia kombinaĵo kiu rolas en multaj biokemiaj procezoj. Ĝi estas uzata en pluraj manĝaĵoj por konservi kaj reguli aliajn acidojn. En solvaĵo, ĝi povas perdi protonon el la acida grupo. Tiel estiĝas la laktata jono CH3CH(OH)COO−, kiu miksiĝas kun akvo aŭ etanolo kaj estas higroskopa. Aigéad orgánach gan dath is ea Aigéad lachtach (CH3-CH(OH)-COOH). I láthair i mbainne géar. Cruthaítear é i matáin tar éis a gcraptha, agus mar staid inmheánach i meitibileacht carbaihiodráití. Déantar ar bhonn trádalach é trí choipeadh glúcóis le baictéir. In úsáid i súdaireacht, ruaimneoireacht agus míochaine. Tá dhá fhoirm eanaintiméireacha de sa nádúr. El ácido láctico, o su forma ionizada, el lactato (del lat. lac, lactis, leche), también conocido por su nomenclatura oficial ácido 2-hidroxi-propanoico o ácido α-hidroxi-propanoico, es un compuesto químico que desempeña importantes roles en varios procesos bioquímicos, como la fermentación láctica. Es un ácido carboxílico, con un grupo hidroxilo en el carbono adyacente al grupo carboxilo, lo que lo convierte en un (AHA) de fórmula H3C-CH(OH)-COOH (C3H6O3). En solución puede perder el hidrógeno unido al grupo carboxilo y convertirse en el anión lactato. El ácido láctico es quiral, por lo que se pueden encontrar dos enantiómeros (isómeros ópticos). Uno es el dextrógiro ácido D-(+)-láctico o d-ácido láctico (en este caso, el ácido (R)-láctico); el otro es el levógiro ácido L-(-)-láctico o ℓ-ácido láctico (en este caso, ácido (S)-láctico), que es el que tiene importancia biológica. La mezcla racémica (cantidades idénticas de estos isómeros) se llama d,ℓ-ácido láctico. Lactic acid is an organic acid. It has a molecular formula CH3CH(OH)COOH. It is white in the solid state and it is miscible with water. When in the dissolved state, it forms a colorless solution. Production includes both artificial synthesis as well as natural sources. Lactic acid is an alpha-hydroxy acid (AHA) due to the presence of a hydroxyl group adjacent to the carboxyl group. It is used as a synthetic intermediate in many organic synthesis industries and in various biochemical industries. The conjugate base of lactic acid is called lactate (or the lactate anion). The name of the derived acyl group is lactoyl. In solution, it can ionize by loss of a proton to produce the lactate ion CH3CH(OH)CO−2. Compared to acetic acid, its pKa is 1 unit less, meaning lactic acid is ten times more acidic than acetic acid. This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group. Lactic acid is chiral, consisting of two enantiomers. One is known as L-lactic acid, (S)-lactic acid, or (+)-lactic acid, and the other, its mirror image, is D-lactic acid, (R)-lactic acid, or (−)-lactic acid. A mixture of the two in equal amounts is called DL-lactic acid, or racemic lactic acid. Lactic acid is hygroscopic. DL-Lactic acid is miscible with water and with ethanol above its melting point, which is about 16 to 18 °C (61 to 64 °F). D-Lactic acid and L-lactic acid have a higher melting point. Lactic acid produced by fermentation of milk is often racemic, although certain species of bacteria produce solely D-lactic acid. On the other hand, lactic acid produced by anaerobic respiration in animal muscles has the (L) enantiomer and is sometimes called "sarcolactic" acid, from the Greek sarx, meaning "flesh". In animals, L-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation during normal metabolism and exercise. It does not increase in concentration until the rate of lactate production exceeds the rate of lactate removal, which is governed by a number of factors, including monocarboxylate transporters, concentration and isoform of LDH, and oxidative capacity of tissues. The concentration of blood lactate is usually 1–2 mM at rest, but can rise to over 20 mM during intense exertion and as high as 25 mM afterward. In addition to other biological roles, L-lactic acid is the primary endogenous agonist of hydroxycarboxylic acid receptor 1 (HCA1), which is a Gi/o-coupled G protein-coupled receptor (GPCR). In industry, lactic acid fermentation is performed by lactic acid bacteria, which convert simple carbohydrates such as glucose, sucrose, or galactose to lactic acid. These bacteria can also grow in the mouth; the acid they produce is responsible for the tooth decay known as caries. In medicine, lactate is one of the main components of lactated Ringer's solution and Hartmann's solution. These intravenous fluids consist of sodium and potassium cations along with lactate and chloride anions in solution with distilled water, generally in concentrations isotonic with human blood. It is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or burns. Моло́чная кислота́ (химическая формула — C3H6O3) — cлабая химическая органическая кислота, относящаяся к классу предельных карбоновых кислот. При стандартных условиях молочная кислота — это одноосновная карбоновая оксикислота белого цвета с характерным запахом. Соли и эфиры молочной кислоты называются лактатами. Малотоннажная химия производит молочную кислоту 4 сортов: химически чистую, «фармакопейную», «техническую» и «пищевую». Kyselina mléčná má kyselou chuť, je lehce rozpustná a tvoří bezbarvé krystaly s chemickým vzorcem CH3CH(OH)COOH. Po kyselině glykolové jde o druhou nejjednodušší hydroxykyselinu. Tato kyselina vzniká mléčným kvašením cukrů, např. v mléce, sýrech, kyselém zelí. Používá se proto v pekařství, pivovarnictví (E270), koželužství, k přípravě limonád a při barvení a zušlechťování textilií (pohmat, lesk). Většinou se vyskytuje jako opticky neaktivní (kyselina DL-mléčná). Pro její antiseptické vlastnosti se požívá také v mastech, ústních vodách a jako prostředek k ošetřování vlasů. Její L-enantiomer[zdroj?] je koncovým produktem mléčného kvašení cukrů, a proto je přítomen v kyselém mléku a zelí. Konjugovaná báze kyseliny mléčné (její anion) se nazývá - CH3CH(OH)COO−. Azido laktikoa (laktatoa, ionizatzen denean) H3C-CH(OH)-COOH formula duen azido karboxilikoa da (C3H6O3), hainbat prozesu biokimiko eta fisiologikotan agertzen dena (esaterako, hartzidura laktikoan). Bi isomero optiko ditu: destrogiroa (D-laktikoa) eta lebogiroa (L-laktikoa), azken hau garrantzi biologikoa duena izanik. 乳酸(IUPAC學名:2-羥基丙酸)是一种化合物,它在多种生物化学过程中起作用。它是一种羧酸,分子式是C3H6O3。它是一个含有羟基的羧酸,因此是一个α-羟酸(AHA)。在水溶液中它的羧基释放出一个质子,而产生乳酸根离子 - 乳酸質(Lactate) - CH3CHOHCOO−。 乳酸有手性,有两个旋光异构体。一个被称为L-(+)-乳酸或(S)-乳酸,另一个被称为D-(-)-乳酸或(R)-乳酸。L-(+)-是在生物学上重要的异构体。 Το γαλακτικό οξύ (αγγλικά: lactic acid) είναι οργανική χημική ένωση, με μοριακό τύπο C3H6O3, αν και συνηθέστερα παριστάνεται ως CH3CH(OH)CO2H. Το χημικά καθαρό γαλακτικό οξύ, στις κανονικές συνθήκες περιβάλλοντος, είναι λευκό στερεό, αναμείξιμο με το νερό. Όταν διαλύεται στο τελευταίο (νερό) σχηματίζει ένα άχρωμο διάλυμα. Η παραγωγή του συμπεριλαμβάνει τόσο φυσικές όσο και τεχνητές μεθόδους. Το γαλακτικό οξύ είναι ένα α- (AHA, A-HydroxyAcid), λόγω της παρουσίας υδροξυομάδας δίπλα ακριβώς από την καρβοξυλομάδα του. Χρησιμοποιήθηκε βιομηχανικά ως ενδιάμεσο συνθετικό σύνθεσης διαφόρων οργανικών και βιοχημικών προϊόντων. Η συζυγής βάση του γαλακτικού οξέος είναι το γαλακτικό ανιόν [CH3C(OH)CO2–]. Το γαλακτικό οξύ σε υδατικό διάλυμα διίσταται, σχηματίζοντας γαλακτικό ανιόν και υδροξώνιο (Η3Ο+). Σε σύγκριση με το οξικό οξύ, το γαλακτικό οξύ έχει pKa = 3,86 έναντι 4,756 του πρώτου (δηλαδή του οξικού οξέος), γεγονός που σημαίνει ότι το γαλακτικό οξύ είναι περίπου κατά 10 φορές ισχυρότερο οξύ από αυτό (δηλαδή το οξικό οξύ). Η υψηλότερη οξύτητά του είναι συνέπεια του ενδομοριακού δεσμού υδρογόνου μεταξύ του ατόμου υδρογόνου του υδροξυλίου και του ενός ατόμου οξυγόνου του καρβοξυλίου. Το γαλακτικό οξύ είναι χειρόμορφο, αποτελούμενο από δυο εναντιομερή. Το ένα είναι γνωστό ως L-(+)- ή S- γαλακτικό οξύ, ενώ το άλλο, που όμοιο με κατοπτρική εικόνα του πρώτου, είναι γνωστό ως D-(-)- ή R- γαλακτικό οξύ. Ένα ισομοριακό μείγμα των δυο εναντιομερών ονομάζεται DL- ή ρακεμεικό γαλακτικό οξύ. Το DL-γαλακτικό οξύ είναι υγροσκοπικό και αναμείξιμο με το νερό, αλλά και με την αιθανόλη, πάνω από την κανονική θερμοκρασία τήξης του, που είναι 16,8 °C. Τα διαχωρισμένα εναντιομερή έχουν αρκετά υψηλότερη θερμοκρασία τήξης (53°C). Το γαλακτικό οξύ που παράγεται με ζύμωση γάλακτος είναι συχνά ρακεμεικό, παρόλο που υπάρχουν κάποια συγκεκριμένα είδη βακτηριδίων που παράγουν μόνο D-γαλακτικό οξύ. Από την άλλη, το γαλακτικό οξύ που παράγεται με αναερόβεια αναπνοή των ζωικών μυών είναι το L-γαλακτικό οξύ και γι' αυτόν το λόγο ενίοτε το εναντιομερές αυτό ονομάζεται «σαρκογαλακτικό οξύ», δηλαδή με πρόθεμα που προέρχεται από την ελληνική λέξη «σάρξ» (δηλαδή σάρκα). Στα ζώα, το L-γαλακτικό οξύ παράγεται σταθερά από το πυροσταφυλικό οξύ, μέσω ενός ενζύμου που ονομάζεται (LDH, Lactate DeHydrogenase), σε μια διεργασία ζύμωσης που συμβαίνει κατά τον κανονικό μεταβολισμό και την άσκηση. Η συγκέντρωση του L-γαλακτικού οξέος δεν αυξάνεται, παρά μόνο αν ο ρυθμός παραγωγής του ξεπεράσει το ρυθμό αποσύνθεσής του, που ρυθμίζεται από έναν αριθμό παραμέτρων, που συμπεριλαμβάνουν μεταφορείς μονοκαρβοξυλικών, τη συγκέντρωση και τον ισοφορμισμό της LDH, καθώς και την οξειδωτική χωρητικότητα των ιστών. Η συγκέντρωση του L-γαλακτικού οξέος στο αίμα είναι συνήθως 1-2 mM σε ηρεμία, αλλά μπορεί να ξεπεράσει τα 20 mM, κατά τη διάρκεια έντονης άσκησης, καθώς και τα 25 mM μετά την άσκηση. Απομονώθηκε για πρώτη φορά το 1780, από το Σουηδό χημικό (Carl Wilhelm Scheele). Στη βιομηχανία, η πραγματοποιείται από βακτήρια του γαλακτικού οξέος, που μετατρέπουν γλυκόζη και σουκρόζη σε γαλακτικό οξύ. Αυτά τα βακτήρια μπορούν επίσης να αναπτυχθούν στο στόμα: Το γαλακτικό οξύ που παράγουν είναι υπεύθυνο για τη φθορά των δοντιών. Στην ιατρική, το γαλακτικό οξύ είναι ένα από τα κύρια συστατικά του (lactated Ringer's solution) και του (lactated Hartmann's solution). Αυτά τα ενδοφλέβια διαλύματα περιέχουν γαλακτικό οξύ, χλωριούχο νάτριο (NaCl) και χλωριούχο κάλιο (KCl) σε αποσταγμένο νερό, σε ισοτονικές με το ανθρώπινο αίμα συγκεντρώσεις, Η πιο συνηθισμένη χρήση αυτών των διαλυμάτων είναι η αντικατάσταση απωλειών σε υγρά του αίματος, μετά από αιμορραγία από τραύμα, εγχείρηση ή έγκαυμα. Les acides lactiques (acides hydroxypropanoïques) sont des acides organiques dont la chaîne est composée de trois atomes de carbone. Les ions lactate sont les bases conjuguées de ces acides (autrement dit, la forme ionisée des acides lactiques). Les acides lactiques doivent leur nom par référence au lait, d'où un des énantiomères (l'acide L-lactique, ou S) a été extrait pour la première fois par le chimiste suédois Carl Wilhelm Scheele, mais il est largement présent (souvent dissocié sous forme de lactate) dans les organismes vivants où il joue un rôle dans divers processus biochimiques (notamment la production d'énergie lors d'effort musculaire anaérobie), et dans des produits d'origine vivante, par exemple dans le vin, certains fruits et légumes, la choucroute et d'autres produits fermentés, etc. Les acides lactiques sont des acides α-hydroxylés, de formule brute C3H6O3. Leur structure se reflète dans leur nom systématique : acide 2-hydroxypropanoïque. 乳酸(にゅうさん、lactic acid)は、有機化合物で、カルボン酸の1種である。キラル中心を1つ持つため鏡像異性体が存在するので、R体かS体かの区別が必要な場合がある。乳酸の塩やエステルは ラクタート あるいは ラクテート(lactate)と呼ぶ。解糖系の生成物として現れる。 L'acido lattico (nome IUPAC: acido 2-idrossipropanoico) è un composto chimico di formula CH3-CHOH-COOH, che svolge un ruolo rilevante in diversi processi biochimici. L'acido lattico è un acido carbossilico, la sua struttura si distingue da quella dell'acido propionico per la presenza di un gruppo -OH all'atomo centrale (stereocentro) di carbonio. La sua deprotonazione dà origine allo ione lattato. La costante di ionizzazione (pKa = 3.1 a 25 °C) è tale che a pH fisiologico la sostanza sia presente quasi interamente sotto forma di lattato. Sia l'acido che i suoi sali alcalini sono solubili in acqua. La molecola dell'acido lattico è chirale, ne esistono pertanto due enantiomeri. L'enantiomero che compare nei cicli metabolici dei sistemi viventi è l'acido S-(+)-lattico o acido L-(+)-lattico (in figura). حمض اللاكتيك أو حمض اللبنيك أو حمض اللبن هو مركب حيوي مهم يدخل في العديد من العمليات الكيميائية الحيوية، أثناء الأيض مثلا . وهو يصنف كيميائياً على أنه حمض كربوكسيلي له الصيغة C2H4OHCOOH. ينتج في العضلات عند الحركة، حيث تحرق الخلايا العضلية الجلوكوز . L'àcid làctic, o en la seva forma ionitzada, el lactat, en nomenclatura IUPAC oficial: àcid 2-hidroxi-propanoic o àcid α-hidroxi-propanoic, és un compost químic amb un important paper en diversos processos bioquímics, com el de la fermentació làctica. Es tracta d'un àcid carboxílic, amb un grup hidroxil en el carboni adjacent al grup carboxil, cosa que el converteix en un (AHA) de fórmula H₃C-CH(OH)-COOH (C₃H₆O₃). En solució pot perdre l'oxoni i convertir-se en l'anió lactat. L'àcid làctic és un , per la qual cosa posseeix dos isòmers òptics. Asam lakta (CH3-CHOH-COOH), dikenal juga sebagai asam susu) adalah senyawa kimia penting dalam beberapa proses biokimia. Seorang ahli kimia Swedia, Carl Wilhelm Scheele, kali meng pada tahun 1780. Secara struktur, ia adalah asam karboksilat dengan satu gugus hidroksil yang menempel pada gugus karboksil. Dalam air, ia terlarut epas proton (H+), membentuk ion laktat. Asam ini juga larut dalam alkohol dan bersifat menyerap air (higroskopik). Asam ini memiliki simetri cermin (kiralitas), dengan dua isomer: asam L-(+)-laktat atau asam (S)-laktat dan, cerminannya, iasam D-(-)-laktat atau asam (R)-laktat. Hanya isomer yang pertama (S) aktif secara biologi Milchsäure (lat. acidum lacticum) ist eine Hydroxycarbonsäure, enthält somit sowohl eine Carboxygruppe als auch eine Hydroxygruppe. Sie wird deswegen auch als 2-Hydroxypropionsäure bezeichnet, nach den Nomenklaturempfehlungen der IUPAC ist jedoch die Bezeichnung 2-Hydroxypropansäure zu verwenden. Die Salze und Ester der Milchsäure heißen Lactate. Моло́чна кислота́ — α-оксіпропіонова одноосновна оксикарбонова кислота, хімічна формула СН3-СН(ОН)-СООН. Важливий проміжний продукт обміну живих організмів. Була відкрита шведським хіміком Карлом Шеєле у 1780 році. O ácido láctico ou lático (do latim lac, lactis, leite), é um composto orgânico de função mista ácido carboxílico - álcool que apresenta fórmula molecular C3H6O3 e estrutural CH3 - CH ( OH ) - COOH. Participa de vários processos bioquímicos, e o lactato é a forma ionizada deste ácido. Foi descoberto pelo químico sueco Carl Wilhelm Scheele, no leite coalhado. Pela nomenclatura IUPAC é conhecido como ácido 2-hidroxipropanóico ou ácido α-hidroxipropanóico. O lactato proporciona uma valiosa fonte de energia química que se acumula como resultado de exercícios físicos intensos, quando a respiração aeróbia não da conta da demanda para geração de energia. Normalmente, o organismo degrada a glicose presente no nosso corpo juntamente com o oxigênio proveniente da respiração, produzindo energia. Entretanto, se o esforço desempenhado pela pessoa está acima da sua condição física,o organismo começa a quebrar glicose sozinha e produzir ácido lático. Quando essa molécula se encontra em excesso nos músculos (na qual ela é muito mais formada do que eliminada) causa cansaço e dores musculares.
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