ゼナレスタット

Zenarestat

HCID 5724

基本情報

CAS
112733-06-9
標準SMILES
O=C(O)Cn1c(=O)n(Cc2ccc(Br)cc2F)c(=O)c2ccc(Cl)cc21
InChIKey
SXONDGSPUVNZLO-UHFFFAOYSA-N
分子式
C17H11BrClFN2O4
平均分子量
441.6 g/mol
単同位体質量
439.95747483

名称と識別子

優先名称
Zenarestat
IUPAC
2-[3-[(4-bromo-2-fluorophenyl)methyl]-7-chloro-2,4-dioxoquinazolin-1-yl]acetic acid
現地名
ゼナレスタット
英語名
Zenarestat
分子式
C17H11BrClFN2O4
分子量
441.639

名称と別名

Zenarestat112733-06-9FR-74366FK-366ZenarestatumFR 74366Fk366CI-1014DTXSID0047296FR74366180C9PJ8JT2-[3-[(4-bromo-2-fluorophenyl)methyl]-7-chloro-2,4-dioxoquinazolin-1-yl]acetic acid
名称をさらに表示
ゼナレスタット[[3-(4-ブロモ-2-フルオロベンジル)-7-クロロ-2,4-ジオキソ-1,2,3,4-テトラヒドロキナゾリン]-1-イル]酢酸ゼナレスタト3-[(4-ブロモ-2-フルオロフェニル)メチル]-7-クロロ-3,4-ジヒドロ-2,4-ジオキソ-1(2H)-キナゾリン酢酸3-(2-フルオロ-4-ブロモベンジル)-7-クロロ-2,4(1H,3H)-ジオキソキナゾリン-1-酢酸3-(4-ブロモ-2-フルオロベンジル)-7-クロロ-2,4-ジオキソ-1,2,3,4-テトラヒドロキナゾリン-1-酢酸2-{3-[(4-ブロモ-2-フルオロフェニル)メチル]-7-クロロ-2,4-ジオキソ-1,2,3,4-テトラヒドロキナゾリン-1-イル}酢酸CI10143-(2-Fluoro-4-bromobenzyl)-7-chloro-2,4(1H,3H)-dioxoquinazoline-1-acetic acid[3-(4-Bromo-2-fluorobenzyl)-7-chloro-2,4-dioxo-3,4-dihydro-1(2H)- quinazolinyl]acetic acid3-[(4-Bromo-2-fluorophenyl)methyl]-7-chloro-3,4-dihydro-2,4-dioxo-1(2H)-quinazolineacetic acid1(2H)-Quinazolineacetic acid, 3-[(4-bromo-2-fluorophenyl)methyl]-7-chloro-3,4-dihydro-2,4-dioxo-
DTXCID80272962-(3-((4-bromo-2-fluorophenyl)methyl)-7-chloro-2,4-dioxoquinazolin-1-yl)acetic acidRefChem:904824[3-(4-bromo-2-fluorobenzyl)-7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2h)-yl]acetic acidCHEMBL104132-(3-(4-bromo-2-fluorobenzyl)-7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl)acetic acid1(2H)-Quinazolineaceticacid, 3-[(4-bromo-2-fluorophenyl)methyl]-7-chloro-3,4-dihydro-2,4-dioxo-3-(4-Bromo-2-fluorobenzyl)-7-chloro-3,4-dihydro-2,4-dioxo-1(2H)-quinazolineacetic acid

データベース識別子

CAS
112733-06-9
PubChem CID
5724
DTXSID
DTXSID0047296
ChEMBL
CHEMBL10413
UNII
180C9PJ8JT
Nikkaji
J248.078F

物性

構造計算による物性

XLogP
3.3
極性表面積
77.9 Ų
水素結合供与体数
1
水素結合受容体数
5
回転可能結合数
4
重原子数
26

実験および物理化学的性質

DrugsPharmaceuticals -> Listed in ZINC15
Collision Cross Section188.9 Ų [M-H]- [CCS Type: DT; Buffer gas: N2; Ionization: ESI-; Dataset: TOXCAST; Source Identifier: DTXSID0047296]

物理化学的性質

融点
223 · 223-224°
沸点
624.4 · 624.4±65.0 °C(Predicted)
比重(密度)
1.737 · 1.737
溶解性
100 mg/mL · DMSO : 100 mg/mL (226.43 mM; Need ultrasonic)
酸解離定数(Pka)
3.76 · 3.76±0.10(Predicted)
外見
Solid

化学と産業

薬理情報

Mechanism of Action · 1 件

Polyneuropathy, damage of peripheral neurons, is common in diabetes mellitus patients and causes pain, sensory and motor deficits in the limbs. Zenarestat is an aldose reductase inhibitor which inhibits the metabolism of glucose by the polyol pathway, which possibly slows or reduces progression of polyneuropathy. Chronic hyperglycemia affects peripheral nerves by an extracellular mechanism with many types of glycation reactions and chemical rearrangements, and an intracellular route involving increased amounts of glucose passing through the polyol pathway. The polyol pathway allows cells to produce fructose from glucose, and has two steps, which require energy and enzymes. Aldose reductase catalyzes the conversion of glucose to sorbitol in the first step, while the second involves the oxidation of nicotinamide adenine dicnucleotide phosphate (conversion of NADPH to NADP). Chronic hyperglycemia causes damage by overactivity of the polyol pathway, causing a decrease in cellular NADPH levels, reducing the amount of glutathione (a free radical scavenger), and nitric oxide (a vasodilator), as well as increasing cellular sorbital levels, causing decreased levels of myo-inositol (necessary for Na-K ATPase function) and increased fructose, thus increasing AGE (advanced glycosylation end products), the byproduct of the polyol pathway. The suppression of the first step in the polyol pathway by zenarestat prevents these deleterious processes from occuring.

MeSH Pharmacological ClassificationCompounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction.

応用分野

使用Treatment of diabetic neuropathy (aldose reductase inhibitor).

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関連反応

3 件

化合物ノート

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