MONOSUBSTITUTED OR DISSUBSTITUTED INDOL DERIVATIVES USED AS DENGUE VIRUS REPLICATION INHIBITORS

MA42811AActive Publication Date: 2018-07-25JANSSEN PHARMACEUTICALS INC +1
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Patent Information

Application Number
MA42811
Authority / Receiving Office
MA · MA
Patent Type
Applications
Current Assignee / Owner
Priority Date
2016-09-15
Filing Date
2016-09-15
Publication Date
2018-07-25
Estimated Expiration
2036-09-15

AI Technical Summary

Technical Problem

Current treatments for dengue virus infection lack effective inhibitors that can target and inhibit the replication of the virus, posing a challenge in managing the disease effectively.

Method used

Development of monosubstituted or disubstituted indole derivatives in stereoisomeric, pharmaceutically acceptable forms, including solvates or polymorphs, which act as inhibitors of dengue virus replication.

Benefits of technology

The developed indole derivatives effectively inhibit dengue virus replication, providing a promising therapeutic option for managing dengue infection.

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Abstract

The present invention relates to mono- or di-substituted indole compounds, methods for preventing or treating dengue viral infections using said compounds, and also relates to said compounds for use as a drug, more preferably for use as a drug to treat or prevent dengue viral infections. The present invention further relates to pharmaceutical compositions or combination preparations of the compounds, compositions or preparations intended for use as a drug, more preferably for the prevention or treatment of dengue viral infections. The invention also relates to methods for preparing the compounds.
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Description

KINGDOM OF MOROCCO Moroccan Property Tax INDUSTRIAL AND COMMERCIAL WIPO Demands طةئمقئج ؛ تبمكجارية 1. Formula compound (I) stereoisomeric form, pharmaceutically acceptable, solvate or polymorphic thereof comprising an indole group mono- or disubstituted said component being chosen from the group in which: R] is H, R^ is F or R] is F, R^ is F and Cl and Rs is H or CH R is H; R] is CH, R^ is CCH and Rs is H; R] is CH, R^ is F and Rs is H; R] is CH, R^ is H and Rs is F; R] is Cl, R^ is H and Rs is CH; R] is OCFs, R^ is H or CCH and Rs is H and R] is OCFs, R^ is H and Rs is CHs. 2. Compound or its stereoisomeric form, salt pharmaceutically acceptable, solvate or polymorph of that- according to claim 1, said compound being chosen from the group:

Claims

comprising a compound of stereoisomers, a solvate or a polymorph of or 2 jointly with a diluent or vehicle 3, Pharmaceutical composition formula (I) or a pharmaceutically acceptable form, one or more pharmaceutically acceptable excipients according to claim 1. WIPO 4. Compound of formula (I) or stereoisomeric form, pharmaceutically acceptable salt, solvate or polymorph thereof according to claim 1 or pharmaceutical composition according to claim 3 for use as a medicinal product.

5. Compound of formula (I) or stereoisomeric form, pharmaceutically acceptable salt, solvate or polymorph thereof according to claim 1 or pharmaceutical composition according to claim 3 for use in the treatment of dengue. structural formula (I) stereoisomeric form. pharmaceutically acceptable salt. solvate or polymorph of it comprising an indole group mono- or disubstituted; said compound being chosen from the group in which: Ri is H, R2 is F or Ri is F, Ra is F and Cl and Fs is H or CH R is H; Ri is CH, R is OCH and R3 is H; Ri is CH, R is F and R3 is H; Ri is CH, R2 is H and R3 is F; Ri is Cl, R2 is H and Ra is CH; Ri is 0CF3, Rs is H or 0CH3 and R3 is H and صمحئقتثثثغرهه (مأ ئلئدتسة 0MPI.C Ri is 0CF3, Rs is H and R3 is CH, for use in 1. inhibition of dengue virus replication in a biological sample or patient.

7. Compound for use according to claim 6, further comprising the co-administration of an additional therapeutic agent.

8. Compound for use according to claim 7, said additional therapeutic agent being another antiviral agent.