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(3R,4R)-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(1H-indol-3-yl)pyrrolidine-2,5-dione is a complex organic molecule characterized by a pyrrolidine-dione core structure with various substituted functional groups. It features a pyrroloquinoline moiety and an indole group, both of which are significant structural motifs in many biologically active compounds. The molecule's stereochemistry, designated as (3R,4R), specifies the configuration of its chiral centers. This unique structure and the presence of biologically relevant functional groups suggest potential pharmaceutical applications, although further research and investigation are required to fully understand its properties and potential uses.

1000873-98-2

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1000873-98-2 Usage

Uses

Used in Pharmaceutical Industry:
(3R,4R)-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(1H-indol-3-yl)pyrrolidine-2,5-dione is used as a potential pharmaceutical candidate for [specific application reason] due to its unique structure and the presence of biologically relevant functional groups, such as the pyrroloquinoline moiety and the indole group. These structural motifs are commonly found in many biologically active compounds, which may contribute to the molecule's potential therapeutic effects.
[Note: The specific application reason is not provided in the materials. It should be filled in based on the actual research findings and potential therapeutic effects of the molecule.]
Please provide more information or specific application reasons if you would like a more detailed description of the uses of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 1000873-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,8,7 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1000873-98:
(9*1)+(8*0)+(7*0)+(6*0)+(5*8)+(4*7)+(3*3)+(2*9)+(1*8)=112
112 % 10 = 2
So 1000873-98-2 is a valid CAS Registry Number.

1000873-98-2Relevant academic research and scientific papers

COMBINATIONAL COMPOSITIONS AND METHODS FOR TREATMENT OF CANCER

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Paragraph 0314, (2015/12/23)

The present invention provides methods of treating a cell proliferative disorder, such as a cancer, by administering to a subject in need thereof a therapeutically effective amount of a pyrroloquinolinyl-pyrrole-2,5-dione compound or a pyrroloquinolinyl-pyrrolidine-2,5-dione compound in combination with a therapeutically effective amount of a second anti-proliferative agent.

Highly Pure Pyrroloquinolinyl-Pyrrole-2,5-Dione and Pyrroloquinolinyl-Pyrrolidine-2,5-Dione and Methods of Preparing Same

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Paragraph 0128; 0129, (2013/11/05)

The present invention relates to highly-pure pyrroloquinolinyl-pyrrole-2,5-dione and pyrroloquinolinyl-pyrrolidine-2,5-dione, for example, 3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione, 3-(5,6-dihydro-4H-pyrrolo[

Purified Pyrroloquinolinyl-Pyrrolidine-2,5-Dione Compositions And Methods For Preparing And Using Same

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Page/Page column 25, (2011/07/08)

The present invention relates to a form 1 and form 2 polymorph of (?)-trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(1H-indol-3-yl)pyrrolidine-2,5-dione. The present invention also relates to (?)-trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinol

MELEIMIDE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS AND METHODS FOR TREATMENT OF CANCER

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Page/Page column 56, (2008/06/13)

The present invention relates to pyrroloquinolinyl-pyrrole-2,5-dione compounds and pyrroloquinolinyl-pyrrolidine-2,5-dione compounds, and methods of preparation of these compounds. The present invention also relates to pharmaceutical compositions comprising pyrroloquinolinyl-pyrrole-2,5-dione compounds and pyrroloquinolinyl-pyrrolidine-2,5-dione compounds. The present invention provides methods of treating a cell proliferative disorder, such as a cancer, by administering to a subject in need thereof a therapeutically effective amount of a pyrroloquinolinyl-pyrrole-2,5-dione compound or pyrroloquinolinyl-pyrrolidine-2,5-dione compound of the present invention.

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