Council of Scientific and Industrial Research

[24]7.Ai, Inc.

Prashant Joshi

Ram Asrey Vishwakarma

Sandip Bibishan Bharate

Ajay Kumar

Sonali Sandip Bharate

Shashi Bhushan

Santosh Kumar Guru

Abir Chakraborty

Dilip Manikrao Mondhe

Suresh Kumar

Sudhakar Manda

Abubakar Wani

Naresh Kumar Satti

Ajit Kumar Saxena

Inshad Ali Khan

Girish Badrinath Mahajan

Ashok Kumar

Shreyans Kumar Jain

Asif Khurshid Qazi

Rohit Sharma

Mubashir Javed Mintoo

Samdarshi Meena

Aashiq Hussain

Parduman Sharma

Ramesh Mudududdla

Abhishek Ghose

Samsher Singh

Jaideep Bharate

Rammohan Rao Yadav

Anup S Pathania

Akanksha Behl

Baljinder Singh

Abid Hamid

Sadhana Sharma

Zahoor Wani

Anup Singh Pathania

Naresh Satti

A computer-implemented method and an apparatus dynamically select content for online visitors. The method includes receiving information related to activity of an online visitor on an enterprise interaction channel and identifying channel data related to the activity. A plurality of content pieces capable of being provided to the online visitor during the ongoing journey is identified. A correlation score is computed for each content piece using the channel data to generate a plurality of correlation scores. The plurality of content pieces are rank-ordered by sorting the plurality of correlation scores. A display of at least one content piece is effected during the ongoing journey of the online visitor on the enterprise interaction channel based on the rank-ordering of the plurality of content pieces.

Method and apparatus for dynamically selecting content for online visitors

A computer-implemented method and an apparatus for improving experiences of an online visitor visiting a website detects a website access event. A visitor profile is generated by defining a plurality of attributes related to visitor activities on the website. A data field is allocated to each attribute to configure the visitor profile including a plurality of data fields. Each data field is capable of accommodating a respective fixed number of entries determined based on a temporal threshold value computed to determine a number of entries required for storing of information related to past activities that are relevant to current activity of the online visitor on the website. The visitor profile is dynamically updated based on the current activity. At least one intention of the online visitor is predicted based on a state of the visitor profile selected at a chosen time instant during the current activity of the online visitor.

Method and apparatus for improving experiences of online visitors to a website

The present invention relates to the alkylidene phosphonate esters of formula I wherein, Ris selected from a group consisting of hydrogen or alkyl group; Ris selected from a group consisting of hydrogen, hydroxy, alkyl, alkoxy, nitro, halogen, amino, N-substituted alkylamino; alkyl group is selected from a group consisting of methyl, ethyl and isopropyl; Ar is selected from a group consisting of aryl, substituted aryl, fused aryl, heteroaryl, and substituted heteroaryl. The present invention particularly relates to synthesis and p-glycoprotein induction activity of the alkylidene phosphonate esters. In addition, the invention relates to methods of using compounds for treating or preventing Alzheimer's disease. 

Alkylidene phosphonate esters as p-glycoprotein inducers

The present invention relates to 6-aryl-4-phenylamino quinazolines of formula I wherein, R and R' are as herein described. The present invention particularly relates to synthesis and anticancer and phoshpoinositide-3-kinase-&#x3b1; (PI3K-&#x3b1;) inhibitory activity. In addition, the invention relates to methods of using compounds for treating or preventing various cancers such as pancreatic, prostate, breast and melanoma. 

6-aryl-4-phenylamino-quinazoline analogs as phosphoinositide-3-kinase inhibitors

The present invention relates to the polyprenylated phloroglucinol compounds of formulae I and II. The present invention also provides synthesis and p-glycoprotein induction activity of the alkyl- and acyl-polyprenylated phloroglucinol compounds. Further, use of the compounds as p-glycoprotein inducers and methods of treatment of Alzheimer's disease using compounds of the invention are also provided.

Polyprenylated phloroglucinol compounds as potent P-glycoprotein inducers

The present invention relates to the N-substituted beta-carbolinium compounds of general formula A and formulae I and II wherein, Rand Rgroups are selected from halogens or trifluoromethyl; Rgroup is selected from hydrogen or methyl; Ar is selected from aryl and heteroaryl, X is selected from halogens; and Rand Rgroups may be attached to any position on ring E. The present invention particularly relates to synthesis and p-glycoprotein induction activity of the N-substituted beta-carbolinium compounds. In addition, the invention relates to methods of using compounds for treating or preventing Alzheimer's disease. 

N-substituted beta-carbolinium compounds as potent P-glycoprotein inducers

A pharmaceutical composition for the treatment of multi-drug resistant infections includes an antimicrobial agent in combination the benzopyrano[3,4-b][1]benzopyran-12(6H)-one class of compound boeravinone B of Formula 1: The bio-efficacy of anti-infective drugs can be potentiated, when used in combination with boeravinone B. Boeravinone B can overcome the resistance or multi-drug resistance developed by bacteria against quinolone, mupirocin and macrolide class of anti-bacterial agents via inhibition of bacterial efflux pumps. Thus, the compositions can be used to treat or prevent drug-resistant bacterial diseases.

Pharmaceutical composition for the treatment of multi-drug resistant infections

The present invention relates to the rohitukine (5,7-dihydroxy-8-(3-hydroxy-1-methyl-piperidin-4-yl)-4H-chromen-4-ones) analogs of formula A and pharmaceutically acceptable salts thereof. In addition, the invention relates to pharmaceutically acceptable compositions comprising at least one such compound, and methods of using the compounds for treating or preventing various proliferative disorders such as melanoma, leukemia, breast cancer and prostate cancer etc. [insert Formula A here] wherein, n=0 or 1, when n=1, the dotted line indicates the double bond. 

Rohitukine analogs as cyclin-dependent kinase inhibitors and a process for the preparation thereof

The present invention relates to the compounds of formula I wherein R is as herein described. The present invention particularly relates to synthesis and antiproliferative activity of 10-substituted colchicinoids. Compounds of the invention can be used for prevention or in the treatment of cancer disease. 

10-substituted colchicinoids as potent anticancer agents

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Jammu, India

Prashant Joshi