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3-[4-(4-morpholin-4-ylmethyl-benzyloxy)-1-oxo-1,3-dihydro-isoindol-2-yl]-piperidine-2,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1323402-36-3

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1323402-36-3 Usage

General Description

3-[4-(4-morpholin-4-ylmethyl-benzyloxy)-1-oxo-1,3-dihydro-isoindol-2-yl]-piperidine-2,6-dione is a chemical compound with a complex structure that includes a piperidine-2,6-dione core with a benzylmorpholine substituent. 3-[4-(4-morpholin-4-ylmethyl-benzyloxy)-1-oxo-1,3-dihydro-isoindol-2-yl]-piperidine-2,6-dione has potential pharmacological activity due to its structural features, which may allow it to interact with biological targets in the body. The presence of a piperidine-2,6-dione moiety suggests that it may have an inhibitory effect on enzymes or receptors, while the presence of the benzylmorpholine group may contribute to its ability to bind to specific receptors or transporters. Further research and testing are needed to fully understand the potential uses and effects of 3-[4-(4-morpholin-4-ylmethyl-benzyloxy)-1-oxo-1,3-dihydro-isoindol-2-yl]-piperidine-2,6-dione.

Check Digit Verification of cas no

The CAS Registry Mumber 1323402-36-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,3,4,0 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1323402-36:
(9*1)+(8*3)+(7*2)+(6*3)+(5*4)+(4*0)+(3*2)+(2*3)+(1*6)=103
103 % 10 = 3
So 1323402-36-3 is a valid CAS Registry Number.

1323402-36-3Relevant academic research and scientific papers

METHODS FOR TREATING SOLID TUMORS AND THE USE OF BIOMARKERS AS A PREDICTOR OF CLINICAL SENSITIVITY TO IMMUNOMODULATORY THERAPIES

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, (2016/05/24)

A method of identifying a subject having a solid tumor who is likely to be responsive to a treatment compound, comprising: administering the treatment compound to a subject having the solid tumor; obtaining a sample from the subject; determining the level of a biomarker in the sample from the subject, and diagnosing the subject as being likely to be responsive to the treatment compound if the level of the biomarker in the sample of the subject changes as compared to a reference level of the biomarker.

3-(4-((4-(MORPHOLINOMETHYL-BENZYL)OXY)-1 -OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE FOR THE TREATMENT OF SYSTEMIC LUPUS ERYTHEMATOSUS

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, (2015/12/11)

Provided herein are methods of using compounds and compositions for treating, managing, and/or preventing systemic lupus erythematosus (SLE). Pharmaceutical compositions and dosing regimens for use in the methods are also provided herein.

METHODS OF TREATING CANCER USING 3-(4-((4-(MORPHOLINOMETHYL)BENZYL)OXY)-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE

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, (2014/03/21)

Provided herein are methods of treating, preventing and/or managing cancers, which comprise administering to a patient 3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione, or an enantiomer or a mixture of enantiomers thereof,

TREATMENT OF IMMUNE-RELATED AND INFLAMMATORY DISEASES

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, (2014/03/21)

Provided herein are methods of using compounds and compositions for modulating leukocytic activity, including activity of B cells and/or T cells monocytes, macrophages, and other lymphoid or myeloid-derived cell types, in immune-related diseases or inflam

METHODS FOR THE TREATMENT OF LOCALLY ADVANCED BREAST CANCER

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Page/Page column 63; 64, (2014/03/26)

Provided herein are methods of treating, preventing and/or managing locally advanced breast cancer, including inflammatory breast cancer, which comprise administering to a patient one or more immunomodulatory compounds or enantiomers or mixtures of enantiomers thereof, or pharmaceutically acceptable salts, solvates, hydrates, co-crystals, clathrates, or polymorphs thereof.

Arylmethoxy Isoindoline Derivatives and Compositions Comprising and Methods of Using the Same

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Page/Page column 50, (2011/08/22)

Provided are 4′-arylmethoxy isoindoline compounds, and pharmaceutically acceptable salts, solvates, clathrates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are disclosed.

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