beta-D-Galactopyranose

HCID 439353CAS 7296-64-2

基本情報

標準SMILES
OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O
InChIKey
WQZGKKKJIJFFOK-FPRJBGLDSA-N
分子式
C6H12O6
平均分子量
180.16 g/mol
単同位体質量
180.0633881

名称と識別子

優先名称
beta-D-Galactopyranose
IUPAC
(2R,3R,4S,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol
英語名
.beta.-D-Galactopyranose
分子式
C6H12O6
分子量
180.16

名称と別名

beta-D-galactosebeta-D-galactopyranose7296-64-2beta-Galactose(2R,3R,4S,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrolRQ6K52J67ACHEBI:27667DTXSID001015884RefChem:6900GlyTouCan:G65889KEDTXCID701474039G65889KE
名称をさらに表示
β-D-Galactoseβ-D-galactopyranose-β-D-Galactose.beta.-D-Galactopyranose(2R,3R,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol
b-D-Galactosebeta-D-Galbeta-D-GalactosideGalactitol,1,5-anhydro-1-C-phenyl-9031-11-2CHEMBL300520beta-Galactosidase(2R,3R,4S,5R,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol

データベース識別子

CAS
7296-64-2、9031-11-2
PubChem CID
439353
DTXSID
DTXSID001015884
ChEMBL
CHEMBL300520
ChEBI
CHEBI:27667
UNII
RQ6K52J67A
EC Number
232-864-1
Nikkaji
J292.886H

物性

構造計算による物性

XLogP
-2.6
極性表面積
110 Ų
水素結合供与体数
5
水素結合受容体数
6
回転可能結合数
1
重原子数
12

実験および物理化学的性質

SolubilitySlightly soluble
Isoelectric Point4.5
Physical Description · 2 件

Powder; [Sigma-Aldrich MSDS]

Solid

物理化学的性質

融点
179 · 179-179.5 °C
沸点
410.8 · 410.8±45.0 °C(Predicted)
比重(密度)
1.732 · 1.732±0.06 g/cm3(Predicted)
貯蔵温度
Hygroscopic, Refrigerator, under inert atmosphere
溶解性
水(少々)
外見
個体

安全と法規制

GHS分類

GHS Classification · 5 件

Danger

H334 (99.9%): May cause allergy or asthma symptoms or breathing difficulties if inhaled [Danger Sensitization, respiratory]

P233, P260, P271, P284, P304+P340, P342+P316, P403, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 1506 reports by companies from 4 notifications to the ECHA C&L Inventory.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

危険有害性情報

Regulatory Information · 3 件

Chemical: Galactosidase, .beta.-

Galactosidase, .beta.-: Does not have an individual approval but may be used under an appropriate group standard

.beta.-D-Galactopyranose: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Galactosidase, .beta.-: Environment tier I assessment
Hazards SummaryMay cause irritation; May cause allergic reactions in sensitive individuals; [Sigma-Aldrich MSDS] See ENZYMES.
Hazard Classes and CategoriesResp. Sens. 1 (99.9%)

法規制情報

Regulatory Information · 3 件

Chemical: Galactosidase, .beta.-

Galactosidase, .beta.-: Does not have an individual approval but may be used under an appropriate group standard

.beta.-D-Galactopyranose: Does not have an individual approval but may be used under an appropriate group standard

化学と産業

薬理情報

ATC Code · 2 件

A - Alimentary tract and metabolism;A09 - Digestives, incl. enzymes;A09A - Digestives, incl. enzymes;A09AA - Enzyme preparations;A09AA04 - Tilactase

QA - Alimentary tract and metabolism;QA09 - Digestives, incl. enzymes;QA09A - Digestives, incl. enzymes;QA09AA - Enzyme preparations;QA09AA04 - Tilactase

Protein BindingTilactase is not absorbed and thus the plasma protein binding is not possible.
Pharmacodynamics · 1 件

The use of a single oral administration of tilactase has been shown to be highly effective in decreasing the symptoms and hydrogen excretion of hypolactasia in tests of lactose H(2)-breath. The analysis has shown a decrease of approximately 80% in both malabsorbers and intolerants.The administration of tilacatase also decreases the presence of bloating and flatus.

Mechanism of Action · 1 件

Lactose is the primary disaccharide found in dairy products. Tilactase is a type of lactase which is the enzyme that is in charge of the breakdown of lactose to glucose and galactose which can be used by the body. Basically, tilactase acts by replacing the missing lactase in the body and allows avoidance of the reach of lactose to the small intestine and the normal bacteria and thus, preventing the symptoms of the lactose intolerance. Once tilactase has metabolized the lactose, the metabolism products are reabsorbed by the normal process of digestion.

Biological Half-LifeTilactase half-life at 35ºC is registered to be 123.77 min. This half-life can be affected by temperature in an inversely proportional manner.
Metabolism/MetabolitesTilactase is degraded by the stomach acid and by the normal flora bacterial metabolism.

用途と製造

Uses · 1 件

A group of enzymes that catalyzes the hydrolysis of terminal, non-reducing beta-D-galactose residues in beta-galactosides. Deficiency of beta-Galactosidase A1 may cause GANGLIOSIDOSIS, GM1. [ChemIDplus] Available commercially as a catalyst to hydrolyze milk lactose into glucose and galactose; [REPROTOX]

応用分野

使用β-D-Galactose s the beta anomer of D-Galactose (G155250), the C-4 epimer of Glucose (G595000). D-Galactose is found in milk and sugar beets as well as being synthesized by the body.

調製方法 · 1 件

純化方法D-Galactose (40g) is dissolved in hot H2O to establish the equilibrium of and anomers; then the solution is cooled to 0o and poured into absolute EtOH (500mL). Stir vigorously and crystallisation occurs within a few minutes, and more rapidly if seeded, filter the crystals immediately (7g, [] D 20 +65o (initial, c 4 in H2O). This mixture of and anomers is further separated by dissolving in an equal weight of cold H2O, filtering and adding to ice cold absolute EtOH (250mL) and stirring for 1minute when crystals separate, then filter them off. After two such crystallisations, the initial [] D 20 is +53o. This can be further purified by shaking with 80% EtOH for 2minutes, filtering, washing with EtOH and Et2O, and drying in a vacuum desiccator to give -Dgalactose (15g) with m 167o, [ ] D 20 +52o (initial, c 4 in H2O) mutarotating to +80.4o. Acetylation of Dgalactose with hot NaOAc/Ac2O gives -D-galactopyranoside pentaacetate m 1 4 2o, [ ] D 25 +25 (c 4 in CHCl3). [Wolfrom & Thompson Methods in Carbohydrate Chemistry I 120 1962, Academic Press, Beilstein 1 IV 4336.]

サプライヤー50 社

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
郑州阿尔法化工有限公司+86-18530059196 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
上海康朗生物科技有限公司021-61998208 18217752821 · [email protected]

補足説明

定義ChEBI: A D-galactopyranose having beta-configuration at the anomeric centre.

関連反応

6 件

関連ノート

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