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ラクツロース

Lactulose

HCID 11333
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基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
4618-18-2
標準SMILES
OC[C@H]1O[C@@H](O[C@@H]2[C@@H](CO)O[C@](O)(CO)[C@H]2O)[C@H](O)[C@@H](O)[C@H]1O
InChIKey
JCQLYHFGKNRPGE-FCVZTGTOSA-N
分子式
C12H22O11
平均分子量
342.3 g/mol
単同位体質量
342.11621151

概要

Lactulose is a synthetic galactosylfructose disaccharide used in the treatment of constipation and hepatic encephalopathy. It has a role as a laxative and a gastrointestinal drug.

名称と識別子

優先名称
Lactulose
IUPAC
(2S,3R,4S,5R,6R)-2-[(2R,3S,4S,5R)-4,5-dihydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
現地名
ラクツロース
英語名
Lactulose
分子式
C12H22O11
分子量
342.3

名称と別名

lactuloseD-LactuloseBifiteralCephulacChronulacConstilacLactulosaAcilacCholac4618-18-2ConstuloseLactulosum
名称をさらに表示
ラクツロースレボラックD-ラクツロース4-O-β-D-ガラクトピラノシル-D-フルクトースラクツロースPモニラックラグノスピアーレ4-O-β-D-ガラクトピラノシル-D-フルクトフラノースカロリール4-O-β-D-ガラクトピラノシル-β-D-フルクトフラノースリフォロースピアーレDSラクツロース (JP17)Lactulose Concentrateruguotang[UL-13C12]lactulose4-O-hexopyranosylhex-2-ulofuranoseLactulose for peak identification CRS(3S,4R,5R)-1,3,5,6-tetrahydroxy-4-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxyMethyl)tetrahydro-2H-pyran-2-yl)oxy)hexan-2-one
EnuloseGenerlacHeptalacLaxilosePortalacKristaloseLattulosioDTXSID5045833

物性

構造計算による物性

XLogP
-4.3
極性表面積
190 Ų
水素結合供与体数
8
水素結合受容体数
11
回転可能結合数
5
重原子数
23
形式電荷
0
複雑度
395

実験および物理化学的性質

DrugsPharmaceuticals -> Listed in ZINC15
Cosmetics · 2 件

Cosmetic ingredients (Lactulose) -> CIR (Cosmetic Ingredient Review)

Humectant; Skin conditioning

LogP-4.3
Solubility · 2 件

Soluble in cold water, hot water. Solubility in water: 76.4% @ 30 deg. C

764.0 mg/mL

Human Drugs · 4 件

Breast Feeding; Lactation; Milk, Human; Gastrointestinal Agents; Laxatives

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Medicines for other common symptoms in palliative care

Melting Point169 °C
Physical DescriptionSolid
Collision Cross Section · 4 件

171.3 Ų [M+K]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

180.1 Ų [M+Na]+ [CCS Type: DT; Method: stepped-field]

169.2 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

179 Ų [M+Na]+

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 3 件

This chemical does not meet GHS hazard criteria for 100% (9 of 9) of all reports.

Not Classified

Aggregated GHS information provided per 9 reports by companies from 2 notifications to the ECHA C&L Inventory.

危険有害性情報

Regulatory InformationLactulose: Does not have an individual approval but may be used under an appropriate group standard
Hazard Classes and CategoriesNot Classified

毒性情報

Adverse Effects · 1 件

Because lactulose has insignificant absorption by the gut and undergoes rapid excretion by the kidneys, its effects remain localized to the gut microenvironment. Side effects would include increased bowel sounds (borborygmi), increased flatus, and a sensation of bloating. Since lactulose's intended use is to soften the stool quantity and increase the stool amount, its most significant side effect remains diarrhea. The diarrhea is dose-dependent and decreases in severity with a reduction in the dose of lactulose.

Toxicity Summary · 2 件

Safe in the present practices of use and concentration. Ingredient, concentration, and use information are available in documents discoverable at https://cir-reports.cir-safety.org

Clinically, documentation on lactulose toxicity is lacking. Specific studies using rats inoculated with various concentrations of lactulose syrup ranging from 0.5% to 5% revealed no evidence of toxicity. However, there have been study results indicating the ability of lactulose to induce lithium toxicity in psychiatric patients. This effect is more broadly attributable to lactulose's ability to induce dehydration through its osmotic action, depletion of total body volume, and the resultant poor renal excretion of lithium. Although rare, documented allergic reactions to lactulose have been recorded in patients with milk allergies.

化学と産業

薬理情報

ATC Code · 4 件

A06AD11

A - Alimentary tract and metabolism

QA - Alimentary tract and metabolism

A06AD11

Protein BindingNegligible amounts of lactulose - metabolized or non-metabolized - are absorbed into the body.. Regardless, data regarding the protein binding of lactulose is not readily available or accessible.
Pharmacodynamics · 1 件

Lactulose formulations are most commonly administered via the oral route or the rectal route. Consequently, because the substance experiences minimal absorption by the gut it typically remains localized in the gastrointestinal tract environment and ultimately demonstrates almost all of its pharmacologic effects within the gut. In particular, as lactulose elicits its laxative effects in enhancing stool amounts and softening stool, such biochemical and physiologic activities can cause increased bowel sounds (borborygmi), a feeling of bloatedness, belching, frequent flatus, and diarrhea.

Mechanism of Action · 1 件

Lactulose is a synthetic disaccharide derivative of lactose that consists of one molecule of galactose and one molecule of fructose. Saccharolytic bacteria present in the large intestine subsequently break the substance down into organic acids like lactic acid and small amounts of formic and acetic acids. Such resultant volatile fatty acid metabolites, in combination with hydrogen and methane that is also generated consequently enhance intraluminal gas formation, peristaltic gut motility, and elicit an osmotic effect that facilitates an increase in the water content of stool as well as associated stool softening. All of these actions ultimately assist in facilitating and increasing the frequency of bowel movements in patients experiencing constipation, although it may take 24 to 48 hours after using the medication for this laxative effect to become evident. At the same time, the formation of such acids via the metabolism of lactulose by colonic bacteria also acidifies the contents of the colon, thereby contributing to the treatment of portal-systemic encephalopathy (PSE). As one of the principal features of PSE involves the accumulation of nitrogenous waste products like ammonia in the systemic circulation, a state in which the colonic contents become more acidic than blood allows ammonia in the circulation to diffuse into the colon.. Furthermore, ammonia that diffuses into the acidic colon is ionized to ammonium ions that are incapable of being absorbed back into the blood. These effects, combined with the laxative action of lactulose facilitates the excretion of excess ammonia. And finally, it is also believed that an acidic colonic environment results in the elimination of urease-producing bacteria that contribute to the formation of ammonia while surviving colonic bacteria use up any trapped ammonia in the colon as a source of nitrogen for protein synthesis.

関連反応

9 件
反応記録を作成
HRID 1726 の反応式
HRID 1726生成物としてuspto-grants-1998_03
HRID 1727 の反応式
HRID 1727反応物としてuspto-grants-1998_03
HRID 215682 の反応式
HRID 215682反応物としてuspto-grants-2012_06
HRID 324923 の反応式
HRID 324923生成物としてuspto-grants-2001_04
HRID 485636 の反応式
HRID 485636反応物としてuspto-grants-1985_08
HRID 1076820 の反応式
HRID 1076820反応物としてuspto-grants-1976_05
HRID 1086962 の反応式
HRID 1086962生成物としてuspto-grants-1991_07
HRID 1174429 の反応式
HRID 1174429反応物としてuspto-grants-2010_11
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化合物ノート

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データベース識別子

CAS
4618-18-2、58166-24-8、58166-25-9
PubChem CID
11333
DTXSID
DTXSID5045833
ChEMBL
CHEMBL296306
ChEBI
CHEBI:6359
UNII
9XH2P2N8EP
EC Number
225-027-7
Nikkaji
J3.412F

物理化学的性質

融点
169 °C · ~169 °C (dec.)
比旋光度
-47 · -47 º (C=5, H2O, 12HR)
沸点
397.76 °C · 397.76°C (rough estimate)
比重(密度)
1 · 1,32g/cm
屈折率
1 · 1,45-1,47
貯蔵温度
Refrigerator
溶解性
水に溶けやすく、メタノールにやや溶けにくく、トルエンにほとんど溶けない。
外見
粉
酸解離定数(Pka)
11.67 · 11.67±0.20(Predicted)
色
白~ほぼ白
水溶解度
76.4 G/100 · 76.4 G/100 ML (30 °C)
Merck
5346 · 5346
BRN
93773 · 93773
BCS Class
2 · 2
化粧品成分の機能
保湿剤スキンコンディショニング
InChI
1S/C12H22O11/c13-1-4-6(16)7(17)8(18)11(21-4)22-9-5(2-14)23-12(20,3-15)10(9)19/h4-11,13-20H,1-3H2/t4-,5-,6+,7+,8-,9-,10+,11+,12+/m1/s1
InChIKey
PFCRQPBOOFTZGQ-VZXVHDRGSA-N
SMILES
OC[C@H]1O[C@@H](O[C@@H]2[C@@H](CO)O[C@@](O)(CO)[C@H]2O)[C@H](O)[C@@H](O)[C@H]1O
LogP
-2.885 · -2.885 (est)
CAS データベース
4618 · 4618-18-2(CAS DataBase Reference)
EPAの化学物質情報
4 · D-Fructose, 4-O-.beta.-D-galactopyranosyl- (4618-18-2)
CAS Number Unlabeled
4618 · 4618-18-2

化学的性質

化学的特性White Powder

Drug Induced Liver Injury · 6 件

Drug Induced Liver Injury Rank (DILIrank 2.0)

Lactulose

vNo-DILI-concern

0

No match

DOI:10.1016/j.drudis.2016.02.015

Effects During Pregnancy and Lactation◉ Summary of Use during Lactation

安全データ

wgk
2
tsca
TSCA listed
rtecs
LS6965000
hs_code
29400090
safety_code
24/25
ストレージクラス
11 - Combustible Solids
Biological Half-LifeThe data regarding the half-life of lactulose is not readily available or accessible.
Metabolism/Metabolites · 1 件

Lactulose is essentially only metabolized in the colon by saccharolytic bacteria that are present there. In particular, the substance is broken down into lactic acid and small amounts of acetic and formic acid. Specific examples of bacteria that normally inhabit the large intestine that are capable of lactulose metabolism include Lactobacilli, Bacteroides, Escherichia coli, and Clostridia.

FDA Pharmacological Classification · 6 件

9U7D5QH5AE

LACTULOSE

Established Pharmacologic Class [EPC] - Osmotic Laxative

Mechanisms of Action [MoA] - Osmotic Activity

Mechanisms of Action [MoA] - Acidifying Activity

Physiologic Effects [PE] - Stimulation Large Intestine Fluid/Electrolyte Secretion

MeSH Pharmacological ClassificationDrugs used for their effects on the gastrointestinal system, as to control gastric acidity, regulate gastrointestinal motility and water flow, and improve digestion.
Absorption, Distribution and Excretion · 4 件

After administration by the oral route, less than 3% of the given dose of lactulose solution is absorbed by the small intestine. The remaining unabsorbed lactulose reaches the large intestine where it is metabolized - but even then, negligible quantities of unchanged lactulose or its metabolites are absorbed across the colon.

The renal excretion of any lactulose that manages to be absorbed into the circulation has been determined to be 3% or less and is generally complete within 24 hours. Any unabsorbed lactulose is largely excreted with stool.

Negligible amounts of lactulose - metabolized or non-metabolized - are absorbed into the body.. Most lactulose that is administered subsequently remains predominantly around the gastrointestinal tract area.

Negligible amounts of lactulose - metabolized or non-metabolized - are absorbed into the body.. Regardless, data regarding the clearance of lactulose is not readily available or accessible.

Tissue LocationsIntestine
Cellular LocationsCytoplasm

用途と製造

UsesCIR ingredient: Lactulose
Use ClassificationCosmetics -> Humectant; Skin conditioning

応用分野

解説ラクツロース,ガラクトースとフルクトースからなる2糖類.ラクツロース,白色の結晶.粉末で涼甘味を有する.融点169 ℃.[α]20D-51.4°(水).乳糖が異性化したもので,加熱処理した乳製品中に見いだされる.ミルクオリゴ糖ともよばれる.ラクツロースは難消化性で胃や小腸で吸収されず,大腸にとどく.そこでビフィズス菌のえさになり,ビフィズス菌を増殖させる結果,腸内の悪玉菌や病原菌の増殖を抑え,整腸作用を発揮する.森北出版「化学辞典(第2版)

使用Lactulose is is a synthetic, non-digestible sugar used in the treatment of chronic constipation; laxative.

調製方法 · 2 件

Industrial production of lactulose relies on isomerization of lactose in alkaline media (pH 11) at 70–80 °C, with yields reaching 70–80% when complexing catalysts such as aluminates or borates are used; lactose for this process can be sourced from secondary dairy raw materials including cheese whey, curd whey, and ultrafiltration permeates of skim milk and whey[3]. Lactulose can be purified from commercial syrups by selective enzymatic hydrolysis of residual lactose and epilactose using four commercial β-galactosidase preparations combined with biological and physicochemical methods, yielding a product containing over 94% lactulose[3]. Lactulose can also be produced by isomerization of lactose in ultrafiltrated whey permeate, where optimization and electroactivation achieve a 37% conversion[3].

純化方法Crystallise lactulose from MeOH or 50% MeOH. It mutarotates from [] D 20 -11.9o to –50.7o (c 1, H2O). [Montgomery & Hudson J Am Chem Soc 32 2101, 2104 1930, Beilstein 17 III/IV 3094, 17/7 V 214.] NMR in Me2SO at 24o shows 0% -pyranose, 27% -pyranose, 20% -furanose and 52% -furanose fforms [Angyal Adv Carbohydr Chem 42 15 1984].

上流・下流製品情報

上流原料

β-D-フルクトピラノースラクトース一水和物1-[2-(2-アジドエトキシ)エトキシ]エチル 2,3,4,6-テトラ-O-アセチル-D-ガラクトピラノシドアルミン酸ナトリウムD-(-)-フルクトース

補足説明

定義ChEBI: A synthetic galactosylfructose disaccharide used in the treatment of constipation and hepatic encephalopathy.