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110784-06-0

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110784-06-0 Usage

Derivation

Synthetic derivative of glutamic acid

Initial purpose

Sedative and antiemetic

Withdrawal from market

Due to teratogenic effects causing severe birth defects

Current uses

Treatment of conditions such as leprosy, multiple myeloma, and certain autoimmune diseases

Pharmacological properties

Immunomodulatory and anti-inflammatory

Chemical structure

Benzene ring with a methyl group and a carboxylic acid group, dioxo-isoindole ring

Check Digit Verification of cas no

The CAS Registry Mumber 110784-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,7,8 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110784-06:
(8*1)+(7*1)+(6*0)+(5*7)+(4*8)+(3*4)+(2*0)+(1*6)=100
100 % 10 = 0
So 110784-06-0 is a valid CAS Registry Number.

110784-06-0Downstream Products

110784-06-0Relevant articles and documents

Synthesis of cyclic imides (methylphtalimides, carboxylic acid phtalimides and itaconimides) and evaluation of their antifungal potential

Stiz, Dorimar,Corrêa, Rogério,D'Auria, Felicia D.,Simonetti, Giovanna,Cechinel-Filho, Valdir

, p. 647 - 654 (2016/10/18)

Background: This paper describes the synthesis of three different subfamilies of cyclic imides: methylphtalimides, carboxyl acid phtalimides and itaconimides. Methods: Fifteen compounds (five of each sub-family) were obtained by the reaction of appropriat

Design, synthesis, and structure-activity relationships of phthalimide- phenylpiperazines: A novel series of potent and selective {1a)-adrenergic receptor antagonists

Kuo, Gee-Hong,Prouty, Catherine,Murray, William V.,Pulito, Virginia,Jolliffe, Linda,Cheung, Peter,Varga, Sally,Evangelisto, Mary,Wang, Jian

, p. 2183 - 2195 (2007/10/03)

Beginning from the screening hit and literature α1-adrenergic compounds, a hybridized basic skeleton A was proposed as the pharmacophore for potent and selective α(1a)-AR antagonists. Introduction of a hydroxy group to increase the flexibility

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