Modulation of morphology and efficacy of new CB1 receptor antagonist using simple and benign polymeric additives (Record no. 16065)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220125142842.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220125b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 10280
Author Banerjee, Kaushik
245 ## - TITLE STATEMENT
Title Modulation of morphology and efficacy of new CB1 receptor antagonist using simple and benign polymeric additives
250 ## - EDITION STATEMENT
Volume, Issue number Vol.60(B), July
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. New Delhi
Name of publisher, distributor, etc. CSIR
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 1014-1021p.
520 ## - SUMMARY, ETC.
Summary, etc. The compound 1, [(1H-[1]benzoxepino[5,4-c]pyrazole-3-carboxamide, 8-chloro-1-(2,4-dichlorophenyl)-4,5-dihydro-N- 1-piperidinyl], a known CB1 modulator has been synthesized and characterized by IR, NMR and single Crystal X-ray study. The single crystal study of 1 displays a number of halogen bonds leading to 1-D network along with other weak noncovalent interactions. The CB1 modulator 1 inherently possesses extremely low solubility in water, which makes its application as drug difficult, and this may be attributed to multiple halogen bonds present in the crystal structure. A series of polymer additives, which are Generally Regarded As Safe (GRAS), have been explored to investigate whether they can modulate the halogen bond present in 1 through formation of various non-bonded interactions. Surprisingly, these polymers are found to change crystal morphology, crystal packing while retaining efficacy and bioavailability. The polymer molecular weight is found to play a significant role in crystal morphology modification especially in case of polyethylene glycol (PEG). The formation of new polymorphic forms of 1 and modification of halogen bond has been established using powder X-ray diffraction and IR study, respectively, in case of PEG 4000, PVPK-30, PVA polymers and compound 1 adducts.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 5009
Topical term or geographic name entry element GENERAL CHEMISTRY
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 15601
Co-Author Patel, Darshit R.
773 0# - HOST ITEM ENTRY
Title Indian journal of chemistry (Section B)
Place, publisher, and date of publication New Delhi NISCAIR-CSIR 2005
856 ## - ELECTRONIC LOCATION AND ACCESS
URL http://nopr.niscair.res.in/bitstream/123456789/58176/1/IJC%20%28Section%20B%29%2c%2060B%2c%201014-1021%20%28Jul%2c2021%29.pdf
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2022-01-25 2022-0210 2022-01-25 2022-01-25 Articles Abstract Database
Unique Visitors hit counter Total Page Views free counter
Implemented and Maintained by AIKTC-KRRC (Central Library).
For any Suggestions/Query Contact to library or Email: librarian@aiktc.ac.in | Ph:+91 22 27481247
Website/OPAC best viewed in Mozilla Browser in 1366X768 Resolution.

Powered by Koha