基本情報
- 標準SMILES
O=C(O)CCNC(=O)c1ccc(N=Nc2ccc(O)c(C(=O)O)c2)cc1- InChIKey
IPOKCKJONYRRHP-UHFFFAOYSA-N- 分子式
- C17H15N3O6
- 平均分子量
- 357.32 g/mol
- 単同位体質量
- 357.0960852
概要
Balsalazide is a monohydroxybenzoic acid consisting of 5-aminosalicylic acid (mesalazine) linked to 4-aminobenzoyl-beta-alanine via an azo bond. It has a role as a non-steroidal anti-inflammatory drug, an anti-ulcer drug, a prodrug and a gastrointestinal drug. It is a conjugate acid of a balsalazide(2-).
名称と識別子
- 優先名称
- 5-((4-((2-Carboxyethyl)carbamoyl)phenyl)diazenyl)-2-hydroxybenzoic acid
- IUPAC
- 5-[[4-(2-carboxyethylcarbamoyl)phenyl]diazenyl]-2-hydroxybenzoic acid
- 現地名
- バルサラジド
- 英語名
- Balsalazide
- 分子式
- C17H15N3O6
- 分子量
- 357.32
名称と別名
名称をさらに表示
データベース識別子
- CAS
80573-04-2- PubChem CID
- 54585
- DTXSID
DTXSID50861027- ChEMBL
CHEMBL1208641- ChEBI
CHEBI:267413- UNII
- P80AL8J7ZP
物性
構造計算による物性
- XLogP
- 2.2
- 極性表面積
- 149 Ų
- 水素結合供与体数
- 4
- 水素結合受容体数
- 8
- 回転可能結合数
- 7
- 重原子数
- 26
- 形式電荷
- 0
- 複雑度
- 545
実験および物理化学的性質
物理化学的性質
- 融点
- 254 · 254-255C
- 沸点
- 729.6 · 729.6±60.0 °C(Predicted)
- 比重(密度)
- 1.44 · 1.44±0.1 g/cm3(Predicted)
- 蒸気圧
- 0 Pa · 0Pa at 20℃
- 貯蔵温度
- -20 °C · -20°C Freezer
- 溶解性
- DMSO(微量)、メタノール(微量)
- 外見
- 個体
- 酸解離定数(Pka)
- 2.97 · 2.97±0.10(Predicted)
- 色
- 黄色からベージュ
- InChI
- InChI=1S/C17H15N3O6/c21-14-6-5-12(9-13(14)17(25)26)20-19-11-3-1-10(2-4-11)16(24)18-8-7-15(22)23/h1-6,9,21H,7-8H2,(H,18,24)(H,22,23)(H,25,26)/b20-19+
- InChIKey
- IPOKCKJONYRRHP-FMQUCBEESA-N
- SMILES
- C(O)(=O)C1=CC(/N=N/C2=CC=C(C(NCCC(O)=O)=O)C=C2)=CC=C1O
- LogP
- 1 at · 1 at 25℃ and pH7.5
- EPAの化学物質情報
- 5 · Benzoic acid, 5-[(1E)-2-[4-[[(2-carboxyethyl)amino]carbonyl]phenyl]diazenyl]-2-hydroxy- (80573-04-2)
化学的性質
化学的特性Yellow Solid
化学と産業
薬理情報
Pharmacodynamics
Balsalazide is a prodrug that has little or no pharmacologic activity until it is enzymatically cleaved in the colon to produce mesalamine (5-aminosalicylic acid), an anti inflammatory drug indicated for the treatment of mildly to moderately active ulcerative colitis. Balsalazide disodium is delivered intact to the colon where it is cleaved by bacterial azoreduction to release equimolar quantities of mesalamine, which is the therapeutically active portion of the molecule, and the intert 4-aminobenzoyl-(beta)-alanine. As a result, the spectrum of pharmacologic activity of balsalazide is similar to that of mesalamine.
Mechanism of Action
The mechanism of action of 5-aminosalicylic acid is unknown, but appears to exert its anti-inflammatory effects locally (in the GI tract) rather than systemically. Mucosal production of arachidonic acid metabolites, both through the cyclooxygenase pathways (catalyzes the formation of prostaglandin precursors from arachidonic acid), and through the lipoxygenase pathways (catalyzes the formation of leukotrienes and hydroxyeicosatetraenoic acids from arachidonic acid and its metabolites), is increased in patients with chronic inflammatory bowel disease. Therefore, it is possible that 5-aminosalicylic acid diminishes inflammation by blocking production of arachidonic acid metabolites in the colon through both the inhibition of cyclooxygenase and lipoxygenase.
Absorption, Distribution and Excretion
Low and variable, intact balsalazide is poorly absorbed systemically.
The products of the azoreduction of this compound, 5-ASA and 4-aminobenzoyl-ß-alanine, and their N-acetylated metabolites have been identified in plasma, urine and feces. Following single-dose administration of 2.25 g COLAZAL (three 750 mg capsules) under fasting conditions in healthy subjects, mean urinary recovery of balsalazide, 5-ASA, and N-Ac-5-ASA was 0.20%, 0.22% and 10.2%, respectively.
応用分野
説明Balsalazide is a prodrug form of 5-aminosalicylic acid (5-ASA; ). It is cleaved by bacterial azoreductases in the intestinal lumen to release 5-ASA. Balsalazide (600 mg/kg per day) decreases IL-2 levels and increases IL-6 levels in the serum and colonic mucosa membrane, as well as decreases micro- and macroscopic colonic damage, in a rat model of colitis induced by 2,4-dinitrochlorobenzene (DNCB). Formulations containing balsalazide have been used in the treatment of ulcerative colitis.
使用An analogue of Sulfasalazine, A prodrug of 5-Aminosalicylic Acid
上流・下流製品情報
上流原料
サプライヤー50 社
補足説明
定義ChEBI: A monohydroxybenzoic acid consisting of 5-aminosalicylic acid (mesalazine) linked to 4-aminobenzoyl-beta-alanine via an azo bond.
関連反応
関連ノート
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