volume 14 issue 7 pages 2465-2478

Covalent assistance to supramolecular synthesis: modifying the drug functionality of the antituberculosis API isoniazidin situ during co-crystallization with GRAS and API compounds

Publication typeJournal Article
Publication date2012-01-01
scimago Q2
wos Q2
SJR0.520
CiteScore5.2
Impact factor2.6
ISSN14668033
General Chemistry
Condensed Matter Physics
General Materials Science
Abstract
The anti-tuberculosis molecule isonicotinic acid hydrazide (isoniazid) is a promising molecule in the supramolecular synthesis of multi-component molecular complexes and also allows for its biological activity to be improved and modified by a simple covalent reaction. The low temperature crystal structures of both isoniazid (1) and the related N′-(propan-2-ylidene)isonicotinohydrazide molecule (2), the latter known to be a more effective agent against Mycobacterium tuberculosis, are reported. In addition, these two molecules were then co-crystallized with the same three Generally Regarded As Safe (GRAS) molecules, succinic acid, 4-hydroxybenzoic acid and 2-hydroxybenzoic acid, to produce the following pharmaceutical co-crystals: (isonicotinic acid hydrazide)2·(succinic acid) 3, (N′-(propan-2-ylidene)isonicotinohydrazide)2·(succinic acid) 4, (isonicotinic acid hydrazide)·(4-hydroxybenzoic acid) 6, (N′-(propan-2-ylidene)isonicotinohydrazide)·(4-hydroxybenzoic acid) 7, (isonicotinic acid hydrazide)·(2-hydroxybenzoic acid) 8, and (N′-(propan-2-ylidene)isonicotinohydrazide)·(2-hydroxybenzoic acid) 9. In addition, a co-crystal using 2-butanone as a modifier is also reported, (N′-(butan-2-ylidene)isonicotinohydrazide)2·(succinic acid) 5. Drug–drug co-crystals were also made with the anti-HIV compound 2-chloro-4-nitrobenzoic acid: (isonicotinic acid hydrazide)·(2-chloro-4-nitrobenzoic acid) 10, and (N′-(propan-2-ylidene)isonicotinohydrazide)·(2-chloro-4-nitrobenzoic acid) 11. All the co-crystals use the carboxylic acid⋯pyridine hydrogen bond to connect the GRAS or drug molecule to the pyridine ring. In general, the co-crystals with the modified isoniazid feature the C(4) homosynthon, and those with the original isoniazid a variety of homo- and heterosynthons. By comparing the melting points of the co-crystals that use isoniazid and those that use the modified isoniazid, a reduction in melting point is observed.
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Lemmerer A. Covalent assistance to supramolecular synthesis: modifying the drug functionality of the antituberculosis API isoniazidin situ during co-crystallization with GRAS and API compounds // CrystEngComm. 2012. Vol. 14. No. 7. pp. 2465-2478.
GOST all authors (up to 50) Copy
Lemmerer A. Covalent assistance to supramolecular synthesis: modifying the drug functionality of the antituberculosis API isoniazidin situ during co-crystallization with GRAS and API compounds // CrystEngComm. 2012. Vol. 14. No. 7. pp. 2465-2478.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1039/C1CE06310C
UR - https://doi.org/10.1039/C1CE06310C
TI - Covalent assistance to supramolecular synthesis: modifying the drug functionality of the antituberculosis API isoniazidin situ during co-crystallization with GRAS and API compounds
T2 - CrystEngComm
AU - Lemmerer, Andreas
PY - 2012
DA - 2012/01/01
PB - Royal Society of Chemistry (RSC)
SP - 2465-2478
IS - 7
VL - 14
SN - 1466-8033
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2012_Lemmerer,
author = {Andreas Lemmerer},
title = {Covalent assistance to supramolecular synthesis: modifying the drug functionality of the antituberculosis API isoniazidin situ during co-crystallization with GRAS and API compounds},
journal = {CrystEngComm},
year = {2012},
volume = {14},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/C1CE06310C},
number = {7},
pages = {2465--2478},
doi = {10.1039/C1CE06310C}
}
MLA
Cite this
MLA Copy
Lemmerer, Andreas. “Covalent assistance to supramolecular synthesis: modifying the drug functionality of the antituberculosis API isoniazidin situ during co-crystallization with GRAS and API compounds.” CrystEngComm, vol. 14, no. 7, Jan. 2012, pp. 2465-2478. https://doi.org/10.1039/C1CE06310C.