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2-(2,5-dioxopyrrolidin-1-yl)-2-phenylacetic acid is a complex organic compound with the molecular formula C11H10O4N. It is a derivative of phenylacetic acid, featuring a pyrrolidine-2,5-dione moiety attached to the 2-position of the phenyl ring. 2-(2,5-dioxopyrrolidin-1-yl)-2-phenylacetic acid is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates. Its structure is characterized by a phenyl ring attached to a 2-oxopyrrolidine-1-yl group, which in turn is connected to an acetic acid moiety. The compound's properties, such as its reactivity and solubility, can be influenced by the presence of the carbonyl groups within the pyrrolidine ring, making it a versatile building block in organic synthesis.

1500-58-9

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1500-58-9 Usage

Molecular Weight

227.23 g/mol

Structure

Cyclic structure with a pyrrolidin-2,5-dione ring and a phenylacetic acid moiety

Classification

Non-proteinogenic amino acid

Usage

Commonly used in the synthesis of pharmaceuticals and as an intermediate in organic chemistry

Biological Activities

Studied for its potential antimicrobial and antitumor properties, and investigated for its role as a chiral building block in asymmetric synthesis

Importance

Valuable molecule in the field of medicinal and pharmaceutical chemistry due to its diverse applications and potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 1500-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1500-58:
(6*1)+(5*5)+(4*0)+(3*0)+(2*5)+(1*8)=49
49 % 10 = 9
So 1500-58-9 is a valid CAS Registry Number.

1500-58-9Relevant academic research and scientific papers

The search for new anticonvulsants in a group of (2,5-dioxopyrrolidin-1-yl)(phenyl)acetamides with hybrid structure—synthesis and in vivo/in vitro studies

Abram, Micha?,Jakubiec, Marcin,Rapacz, Anna,Mogilski, Szczepan,Latacz, Gniewomir,Kamiński, Rafa? M.,Kamiński, Krzysztof

, p. 1 - 27 (2020)

Epilepsy belongs to the most common and debilitating neurological disorders with multifactorial pathophysiology and a high level of drug resistance. Therefore, with the aim of searching for new, more effective, and/or safer therapeutics, we discovered a focused series of original hybrid pyrrolidine-2,5-dione derivatives with potent anticonvulsant properties. We applied an optimized coupling reaction yielding several hybrid compounds that showed broad-spectrum activity in widely accepted animal seizure models, namely, the maximal electroshock (MES) test and the psychomotor 6 Hz (32 mA) seizure model in mice. The most potent anticonvulsant activity and favorable safety profile was demonstrated for compound 30 (median effective dose (ED50) MES = 45.6 mg/kg, ED50 6 Hz (32 mA) = 39.5 mg/kg, median toxic dose (TD50) (rotarod test) = 162.4 mg/kg). Anticonvulsant drugs often show activity in pain models, and compound 30 was also proven effective in the formalin test of tonic pain, the capsaicin-induced pain model, and the oxaliplatin (OXPT)-induced neuropathic pain model in mice. Our studies showed that the most plausible mechanism of action of 30 involves inhibition of calcium currents mediated by Cav1.2 (L-type) channels. Importantly, 30 revealed high metabolic stability on human liver microsomes, negligible hepatotoxicity, and relatively weak inhibition of CYP3A4, CYP2D6, and CYP2C9 isoforms of cytochrome P450, compared to reference compounds. The promising in vivo activity profile and drug-like properties of compound 30 make it an interesting candidate for further preclinical development.

Multitargeted Compounds Derived from (2,5-Dioxopyrrolidin-1-yl)(phenyl)-Acetamides as Candidates for Effective Anticonvulsant and Antinociceptive Agents

Abram, Micha?,Kamiński, Krzysztof,Kamiński, Rafa? M.,Latacz, Gniewomir,Lubelska, Annamaria,Mogilski, Szczepan,Rapacz, Anna

, p. 1996 - 2008 (2020/07/14)

We developed a focused set of original hybrid pyrrolidine-2,5-dione derivatives with potent anticonvulsant and antinociceptive properties. These hybrid compounds demonstrated broad-spectrum protective activity in a range of mouse models, such as the maximal electroshock (MES) test, the pentylenetetrazole-induced seizures (scPTZ), and the 6 Hz (32 mA) seizures. Compound 22 showed the most potent anticonvulsant activity (ED50 MES = 23.7 mg/kg, ED50 6 Hz (32 mA) = 22.4 mg/kg, ED50 scPTZ = 59.4 mg/kg). In addition, 22 revealed potent efficacy in the formalin-induced tonic pain. These in vivo activities of 22 are likely mediated by several targets and may result from the inhibition of central sodium/calcium currents and transient receptor potential vanilloid 1 (TRPV1) receptor antagonism. Finally, the lead compound 22 revealed drug-like absorption, distribution, metabolism, excretion, toxicity (ADME-Tox) properties in the in vitro assays, making it a potential candidate for further development in epilepsy and neuropathic pain indications.

(2,5-DIOXOPYRROLIDIN-L-YL)(PHENYL)-ACETAMIDE DERIVATIVES AND THEIR USE IN THE TREATMENT OF NEUROLOGICAL DISEASES

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Page/Page column 15, (2020/07/25)

The first object of the invention is the compound of general formula (I) or pharmaceutically acceptable salts thereof. A second object of the invention is the use of compounds described by general formula (I) as active ingredient in pharmaceutical compositions for the treatment of epileptic seizures or neuropathic pain or migraine.

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