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ALRESTATIN

CAS No.
51411-04-2
Chemical Name:
ALRESTATIN
Synonyms
AY-22284;ALRESTATIN;AURORA 5841;AKOS BBS-00007376;IFLAB-BB F0863-0248;Alrestatin free acid;1,3-dioxo-1h-benz(de)isoquinoline-2(3h)-aceticaci;2-(1,3-dioxobenzo[de]isoquinolin-2-yl)acetic acid;1,3-Dioxo-1H-benzo[de]isoquinoline-2(3H)-acetic acid;1,3-DIOXO-1H-BENZ[D,E]ISOQUINOLINE-2(3H)-ACETIC ACID
CBNumber:
CB4392682
Molecular Formula:
C14H9NO4
Molecular Weight:
255.23
MDL Number:
MFCD00181399
MOL File:
51411-04-2.mol
MSDS File:
SDS
Last updated:2023-06-08 09:03:01

ALRESTATIN Properties

Melting point 266-267 °C
Boiling point 512.7±33.0 °C(Predicted)
Density 1.511±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility DMSO : 50 mg/mL (195.90 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
form White crystalline solid.
pka 3.61±0.10(Predicted)
FDA UNII 515DHK15LG

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
NFPA 704
0
2 0

ALRESTATIN price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 29888 Alrestatin 51411-04-2 5mg $86 2024-03-01 Buy
Cayman Chemical 29888 Alrestatin 51411-04-2 50mg $951 2024-03-01 Buy
Cayman Chemical 29888 Alrestatin 51411-04-2 10mg $135 2024-03-01 Buy
Cayman Chemical 29888 Alrestatin 51411-04-2 25mg $315 2024-03-01 Buy
Tocris 0485 Alrestatin 51411-04-2 50 $411 2021-12-16 Buy
Product number Packaging Price Buy
29888 5mg $86 Buy
29888 50mg $951 Buy
29888 10mg $135 Buy
29888 25mg $315 Buy
0485 50 $411 Buy

ALRESTATIN Chemical Properties,Uses,Production

Originator

Alrestatin,BIOMOL

Uses

Enzyme inhibitor (aldose reductase).

Uses

Alrestatin is an inhibitor of aldose reductase and has been shown to display inhibitory activity on aldose reductase prepared and purified from the human brain.

Manufacturing Process

1,3-Dioxo-1H-benz[de]isoquinoline-2(3H)-acetic acid:
1,8-Naphthalic acid anhydride (110 g, 0.556 mole), glycine (48 g, 0.64 mole) and dimethylformamide (750 ml) are heated and stirred at reflux for 2 hr. The homogeneous dark solution is cooled to about 100°C and 750 ml of hot water is added slowly to the stirred solution. The reaction mixture is cooled and allowed to stand in a refrigerator for 16 hr. The precipitate is collected and recrystallized from ethanol, using decolorizing charcoal, to give the title compound, MP: 271°-272°C.
In practice it is usually used as sodium salt.

Therapeutic Function

Aldose reductase inhibitor

Biological Activity

Specific inhibitor of aldose reductase (IC 50 = 148 μ M). Attenuates glucose-induced angiotensin II production in rat vascular smooth muscle in vitro .

Enzyme inhibitor

This aldose reductase inhibitor and drug (FWfree-acid = 255.23 g/mol; CAS 51411-04-2), also known as 1,3-dioxo-1H-benz[de]isoquinoline-2(3H)- acetic acid) suppresses diabetes-associated, osmotic cell and tissue damage by inhibiting aldose reduction and thereby reducing the accumulation intracellular sorbitol. Primary Mode of Action of Aldose Reductase Inhibitors: A major cause of diabetic neuropathy is the intraneural osmotic pressure that builds up as a consequence of the over-accumulation of sorbitol, a polyol formed by aldose reductase (Reaction: Glucose + NADPH ? Sorbitol + NADP+ + H+). Similar considerations apply to cataract formation in the lens, another tissue rich in aldose reductase. In diabetes, aldose reductase activity increases as the concentration of glucose rises in the lens, peripheral nerves and glomerulus (tissues that are insulininsensitive); because sorbitol lacks a membrane carrier, its contributes to intracellular osmotic pressure, disrupting cell-cell interactions (especially synapses), eventually leading to retinopathy and neuropathy. The additive effects of aldose reductase (AR) and polyol dehydrogenase in producing sorbitol from glucose and fructose, acting in combination with agedependent decreased hexokinase is believed to account for diabetic cataract formation in human lenses under high glucose stress. AR’s Km for glucose of AR is roughly 200 mM, whereas its Km for NADPH is 0.06 mM. NADP inhibits human lens AR noncompetitively and has a K1 that is roughly equal to the Km for NADPH. Notably. The Km for fructose is 40 mM and that for NADH is 0.02 mM in the polyol dehydrogenase (PD) reaction. Therefore, although sorbitol formation is modest during normoglycemia, such is not the case for diabetic hyperglycemia. Moreover, the recent increased reliance on high-fructose corn syrup as a sweetener is problematic, in that glucose-sensing mechanisms in humans are largely unresponsive to fructose. Because sorbitol is not transported out of the lens, any increase in intracellular sortbitol must be compensated osmotically by the considerable uptake of water, a well-characterized cataractogenic event. By inhibiting sorbitol dehydrogenase, alrestatin lowers tha undesirable net accumulatrion of sorbitol during hyperglycemic episodes. At high enough concentrations, alrestatin also inhibits PD. Target(s): aldose reductase, or aldehyde reductase; 4-aminobutyrate aminotransferase; carbonyl reductase; succinate-semialdehyde dehydrogenase; polyol dehydrogenase, weakly inhibited, except at elevated concentrations; hexonate dehydrogenase, or glucuronate reductase.

ALRESTATIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 108)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Finetech Industry Limited
+86-27-87465837 +8618971612321 info@finetechnology-ind.com China 9635 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24738 58
Nantong HI-FUTURE Biology Co., Ltd.
+undefined18051384581 sales@chemhifuture.com China 3136 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
ZHEJIANG JIUZHOU CHEM CO., LTD
+86-0576225566889 +86-13454675544 admin@jiuzhou-chem.com;jamie@jiuzhou-chem.com;alice@jiuzhou-chem.com China 20000 58

View Lastest Price from ALRESTATIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-(1,3-dioxobenzo[de]isoquinolin-2-yl)acetic acid pictures 2019-07-10 2-(1,3-dioxobenzo[de]isoquinolin-2-yl)acetic acid
51411-04-2
US $8.80 / KG 1KG 97%-99% 100kg Career Henan Chemical Co

ALRESTATIN Spectrum

1,3-DIOXO-1H-BENZ[D,E]ISOQUINOLINE-2(3H)-ACETIC ACID (1,3-DIOXO-1H-BENZO[DE]ISOQUINOLIN-2(3H)-YL)ACETIC ACID AKOS BBS-00007376 ALRESTATIN IFLAB-BB F0863-0248 AURORA 5841 1,3-dioxo-1h-benz(de)isoquinoline-2(3h)-aceticaci 1,3-Dioxo-1H-benzo[de]isoquinoline-2(3H)-acetic acid 1,3-Dioxo-2,3-dihydro-1H-benzo[de]isoquinoline-2-acetic acid 2,3-Dihydro-1,3-dioxo-1H-benzo[de]isoquinoline-2-acetic acid AY-22284 (1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-acetic acid 2-(1,3-dioxobenzo[de]isoquinolin-2-yl)acetic acid 2-(1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)acetic acid 1H-Benz[de]isoquinoline-2(3H)-acetic acid, 1,3-dioxo- Alrestatin free acid 51411-04-2