An integrated ligand-based modelling approach to explore the structure-property relationships of influenza endonuclease inhibitors
Abstract Influenza endonuclease plays important role in the viral transcription and translation processes. Inhibition of endonuclease enzyme may be an interesting choice to restrict influenza infection. This current study deals with validated multi-chemometric modelling approaches namely regression-based and classification-based quantitative structure-activity relationships (QSARs), hologram QSAR, comparative molecular similarity analysis (CoMSIA), Open3DQSAR study and pharmacophore mapping to identify the structural and physicochemical requirements along with the chemico-biological interactions of pyridinones and pyranones for anti-endonuclease activity. The results suggest that the pyridinone scaffold is more preferable than the pyranone ring. The keto function at 4th position and aryl tetrazole substitution at 1st position of the parent moiety may be important for endonuclease inhibition. Hydroxyl group at 5th position of the parent ring may act as hydrogen bond acceptor feature. The steric substituent is suitable at 2nd position whereas hydrophobic substitution is found to be unfavourable at this position. Bulky hydrophobic substituents are not preferred at the 3rd position of the parent moiety. The information revealed from these integrated ligand-based modelling methods may provide useful informations for designing newer potential anti-influenza agents in future..
Medienart: |
Artikel |
---|
Erscheinungsjahr: |
2017 |
---|---|
Erschienen: |
2017 |
Enthalten in: |
Zur Gesamtaufnahme - volume:28 |
---|---|
Enthalten in: |
Structural chemistry - 28(2017), 6 vom: 15. März, Seite 1663-1678 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Amin, Sk. Abdul [VerfasserIn] |
---|
Links: |
Volltext [lizenzpflichtig] |
---|
Themen: |
Bayesian classification modelling |
---|
Anmerkungen: |
© Springer Science+Business Media New York 2017 |
---|
doi: |
10.1007/s11224-017-0933-z |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
OLC2033890163 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | OLC2033890163 | ||
003 | DE-627 | ||
005 | 20230509082222.0 | ||
007 | tu | ||
008 | 200819s2017 xx ||||| 00| ||eng c | ||
024 | 7 | |a 10.1007/s11224-017-0933-z |2 doi | |
035 | |a (DE-627)OLC2033890163 | ||
035 | |a (DE-He213)s11224-017-0933-z-p | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
082 | 0 | 4 | |a 540 |q VZ |
100 | 1 | |a Amin, Sk. Abdul |e verfasserin |4 aut | |
245 | 1 | 0 | |a An integrated ligand-based modelling approach to explore the structure-property relationships of influenza endonuclease inhibitors |
264 | 1 | |c 2017 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
338 | |a Band |b nc |2 rdacarrier | ||
500 | |a © Springer Science+Business Media New York 2017 | ||
520 | |a Abstract Influenza endonuclease plays important role in the viral transcription and translation processes. Inhibition of endonuclease enzyme may be an interesting choice to restrict influenza infection. This current study deals with validated multi-chemometric modelling approaches namely regression-based and classification-based quantitative structure-activity relationships (QSARs), hologram QSAR, comparative molecular similarity analysis (CoMSIA), Open3DQSAR study and pharmacophore mapping to identify the structural and physicochemical requirements along with the chemico-biological interactions of pyridinones and pyranones for anti-endonuclease activity. The results suggest that the pyridinone scaffold is more preferable than the pyranone ring. The keto function at 4th position and aryl tetrazole substitution at 1st position of the parent moiety may be important for endonuclease inhibition. Hydroxyl group at 5th position of the parent ring may act as hydrogen bond acceptor feature. The steric substituent is suitable at 2nd position whereas hydrophobic substitution is found to be unfavourable at this position. Bulky hydrophobic substituents are not preferred at the 3rd position of the parent moiety. The information revealed from these integrated ligand-based modelling methods may provide useful informations for designing newer potential anti-influenza agents in future. | ||
650 | 4 | |a Influenza endonuclease inhibitors | |
650 | 4 | |a Bayesian classification modelling | |
650 | 4 | |a HQSAR | |
650 | 4 | |a CoMSIA | |
650 | 4 | |a Open3DQSAR | |
650 | 4 | |a Pharmacophore mapping | |
700 | 1 | |a Adhikari, Nilanjan |4 aut | |
700 | 1 | |a Gayen, Shovanlal |4 aut | |
700 | 1 | |a Jha, Tarun |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Structural chemistry |d Springer US, 1990 |g 28(2017), 6 vom: 15. März, Seite 1663-1678 |w (DE-627)130761478 |w (DE-600)1000614-X |w (DE-576)023035544 |x 1040-0400 |7 nnns |
773 | 1 | 8 | |g volume:28 |g year:2017 |g number:6 |g day:15 |g month:03 |g pages:1663-1678 |
856 | 4 | 1 | |u https://doi.org/10.1007/s11224-017-0933-z |z lizenzpflichtig |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a SYSFLAG_A | ||
912 | |a GBV_OLC | ||
912 | |a SSG-OLC-CHE | ||
912 | |a SSG-OLC-PHA | ||
912 | |a SSG-OLC-DE-84 | ||
912 | |a GBV_ILN_70 | ||
951 | |a AR | ||
952 | |d 28 |j 2017 |e 6 |b 15 |c 03 |h 1663-1678 |