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
名称をさらに表示
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
- 形式電荷
- 0
- 複雑度
- 151
実験および物理化学的性質
Physical Description
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
- 酸解離定数(Pka)
- 12.12 · 12.12±0.70(Predicted)
- 色
- ホワイトからオフホワイト
- 安定性
- 吸湿性
安全と法規制
GHS分類
GHS Classification
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
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
法規制情報
Regulatory Information
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
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
Pharmacodynamics
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
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.
Absorption, Distribution and Excretion
Tilactase is not absorbed in the GI tract and thus the pharmacokinetic parameters related to absorption are not relevant.
Tilactase is completely eliminated in the feces either unchanged or as metabolites.
Tilactase is not absorbed and thus the volume of distribution is not relevant.
Tilactase is not absorbed and thus the clearance rate is not relevant.
用途と製造
Uses
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
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.]
上流・下流製品情報
上流原料
下流製品
サプライヤー50 社
補足説明
定義ChEBI: A D-galactopyranose having beta-configuration at the anomeric centre.
関連反応
関連ノート
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