![IJMS | Free Full-Text | AI-Driven De Novo Design and Molecular Modeling for Discovery of Small-Molecule Compounds as Potential Drug Candidates Targeting SARS-CoV-2 Main Protease IJMS | Free Full-Text | AI-Driven De Novo Design and Molecular Modeling for Discovery of Small-Molecule Compounds as Potential Drug Candidates Targeting SARS-CoV-2 Main Protease](https://www.mdpi.com/ijms/ijms-24-08083/article_deploy/html/images/ijms-24-08083-g001.png)
IJMS | Free Full-Text | AI-Driven De Novo Design and Molecular Modeling for Discovery of Small-Molecule Compounds as Potential Drug Candidates Targeting SARS-CoV-2 Main Protease
![2206825-87-6 | 5-[[4-[3-(Aminocarbonyl)-1,4,5,7-tetrahydro-1-(4-methoxyphenyl)-7-oxo-6H-pyrazolo[3,4-c] pyridin-6-yl]phenyl]amino]pentanoic Acid | Apixaban Open Chain Acid; 5-[[4-[3-(Aminocarbonyl)-1,4,5,7-tetrahydro-1-(4-methoxyphenyl)-7-oxo-6H ... 2206825-87-6 | 5-[[4-[3-(Aminocarbonyl)-1,4,5,7-tetrahydro-1-(4-methoxyphenyl)-7-oxo-6H-pyrazolo[3,4-c] pyridin-6-yl]phenyl]amino]pentanoic Acid | Apixaban Open Chain Acid; 5-[[4-[3-(Aminocarbonyl)-1,4,5,7-tetrahydro-1-(4-methoxyphenyl)-7-oxo-6H ...](https://www.trc-canada.com/prod-img/A875620.png)
2206825-87-6 | 5-[[4-[3-(Aminocarbonyl)-1,4,5,7-tetrahydro-1-(4-methoxyphenyl)-7-oxo-6H-pyrazolo[3,4-c] pyridin-6-yl]phenyl]amino]pentanoic Acid | Apixaban Open Chain Acid; 5-[[4-[3-(Aminocarbonyl)-1,4,5,7-tetrahydro-1-(4-methoxyphenyl)-7-oxo-6H ...
![tert-butyl N-[5-(hydroxymethyl)pyridin-2-yl]carbamate_Pyridines_Hetero 6-membered Rings +_By Structure_Diversity Oriented Building Blocks_affinitychem tert-butyl N-[5-(hydroxymethyl)pyridin-2-yl]carbamate_Pyridines_Hetero 6-membered Rings +_By Structure_Diversity Oriented Building Blocks_affinitychem](http://affinitychem.com/images/201806/source_img/10634_G_1528158572284.jpg)
tert-butyl N-[5-(hydroxymethyl)pyridin-2-yl]carbamate_Pyridines_Hetero 6-membered Rings +_By Structure_Diversity Oriented Building Blocks_affinitychem
![Synthesis of N-Alkylpyridin-4-ones and Thiazolo[3,2-A]pyridin-5-ones Through Pummerer-Type Reactions | Organic Chemistry | ChemRxiv | Cambridge Open Engage Synthesis of N-Alkylpyridin-4-ones and Thiazolo[3,2-A]pyridin-5-ones Through Pummerer-Type Reactions | Organic Chemistry | ChemRxiv | Cambridge Open Engage](https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/60c742b0bdbb8971b9a3854c/largeThumb/synthesis-of-n-alkylpyridin-4-ones-and-thiazolo-3-2-a-pyridin-5-ones-through-pummerer-type-reactions.jpg)
Synthesis of N-Alkylpyridin-4-ones and Thiazolo[3,2-A]pyridin-5-ones Through Pummerer-Type Reactions | Organic Chemistry | ChemRxiv | Cambridge Open Engage
![Metallation of pyridin-2-yldiazines. Use of pyridine ring as ortho-directing group. Diazines. Part 45 - ScienceDirect Metallation of pyridin-2-yldiazines. Use of pyridine ring as ortho-directing group. Diazines. Part 45 - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402005012044-sc1.gif)
Metallation of pyridin-2-yldiazines. Use of pyridine ring as ortho-directing group. Diazines. Part 45 - ScienceDirect
Novel Pyridyl Ring C5 Substituted Analogues of Epibatidine and 3-(1-Methyl-2(S)- pyrrolidinylmethoxy)pyridine (A-84543) as Highly Selective Agents for Neuronal Nicotinic Acetylcholine Receptors Containing β2 Subunits | Journal of Medicinal Chemistry
![AMINO-BENZAZOLES AS P2Y1 RECEPTOR INHIBITORS WITH PYRIDINE RING AND HETEROCYCLIC COMPONENTS - diagram, schematic, and image 29 AMINO-BENZAZOLES AS P2Y1 RECEPTOR INHIBITORS WITH PYRIDINE RING AND HETEROCYCLIC COMPONENTS - diagram, schematic, and image 29](https://www.patentsencyclopedia.com/img/20080275090_29.png)
AMINO-BENZAZOLES AS P2Y1 RECEPTOR INHIBITORS WITH PYRIDINE RING AND HETEROCYCLIC COMPONENTS - diagram, schematic, and image 29
Synthesis of naphthyridin-2(1H)-one derivatives via ring expansion of 3-substituted-1H-pyrrolo[2,3-b]pyridin-2(3H)-one derivatives - Chemical Communications (RSC Publishing)
![PYRIDINE-2-CARBOXALDEHYDE,99%,100G | Heterocyclus (ungesättigt, 1 N, Pyridin mit H, Alkyl-, Arylgruppe, [O] , Labor) | Heterocycl. Kohlenw. (1 Ring, 1 Het., Labor) | Chemikalie (organisch, Labor) | Labormaterial, Labortechnik | Fisher Scientific ... PYRIDINE-2-CARBOXALDEHYDE,99%,100G | Heterocyclus (ungesättigt, 1 N, Pyridin mit H, Alkyl-, Arylgruppe, [O] , Labor) | Heterocycl. Kohlenw. (1 Ring, 1 Het., Labor) | Chemikalie (organisch, Labor) | Labormaterial, Labortechnik | Fisher Scientific ...](https://b11b9n4iy7xjijdm4i8nmcj.blob.core.windows.net/images/FIS/FIS0323_chemical-structure-cas-1121-60-4.jpg-650.jpg)
PYRIDINE-2-CARBOXALDEHYDE,99%,100G | Heterocyclus (ungesättigt, 1 N, Pyridin mit H, Alkyl-, Arylgruppe, [O] , Labor) | Heterocycl. Kohlenw. (1 Ring, 1 Het., Labor) | Chemikalie (organisch, Labor) | Labormaterial, Labortechnik | Fisher Scientific ...
![Optimization of novel benzofuro[3,2-b]pyridin-2(1H)-one derivatives as dual inhibitors of BTK and PI3Kδ - ScienceDirect Optimization of novel benzofuro[3,2-b]pyridin-2(1H)-one derivatives as dual inhibitors of BTK and PI3Kδ - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0223523418311012-fx1.jpg)