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Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents |  SpringerLink
Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents | SpringerLink

Pyrimidine - an overview | ScienceDirect Topics
Pyrimidine - an overview | ScienceDirect Topics

The pyrimidine analog FNC inhibits cell proliferation and viral protein  synthesis in HTLV‑1‑infected cells
The pyrimidine analog FNC inhibits cell proliferation and viral protein synthesis in HTLV‑1‑infected cells

Figures and data in A chemical screen in zebrafish embryonic cells  establishes that Akt activation is required for neural crest development |  eLife
Figures and data in A chemical screen in zebrafish embryonic cells establishes that Akt activation is required for neural crest development | eLife

Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents |  SpringerLink
Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents | SpringerLink

Antibiotic capreomycin 115 and natural and synthetic derivatives of... |  Download Scientific Diagram
Antibiotic capreomycin 115 and natural and synthetic derivatives of... | Download Scientific Diagram

Pyrimidine Analogue - an overview | ScienceDirect Topics
Pyrimidine Analogue - an overview | ScienceDirect Topics

Marine Drugs | Free Full-Text | Recent Advances in Drug Discovery from  South African Marine Invertebrates
Marine Drugs | Free Full-Text | Recent Advances in Drug Discovery from South African Marine Invertebrates

Reduction of pyrimidine 23 and 53, oxidation of pyrimidine with... |  Download Scientific Diagram
Reduction of pyrimidine 23 and 53, oxidation of pyrimidine with... | Download Scientific Diagram

Betaine 107, synthesis of pyrimidinium betaines 21b, 108, and 109,... |  Download Scientific Diagram
Betaine 107, synthesis of pyrimidinium betaines 21b, 108, and 109,... | Download Scientific Diagram

Risperidone EP Impurity D|CAS. No. 1199589-74-6| 5-Fluoro Risperidone;  3-[2-[4-(5-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a] pyrimidin-4-one;|Impurity Standards, Research Chemicals|Simson Pharma  Limited
Risperidone EP Impurity D|CAS. No. 1199589-74-6| 5-Fluoro Risperidone; 3-[2-[4-(5-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a] pyrimidin-4-one;|Impurity Standards, Research Chemicals|Simson Pharma Limited

Structure–Activity Relationships of Pyrazolo[1,5-a]pyrimidin-7(4H)-ones as  Antitubercular Agents | ACS Infectious Diseases
Structure–Activity Relationships of Pyrazolo[1,5-a]pyrimidin-7(4H)-ones as Antitubercular Agents | ACS Infectious Diseases

The implication of Mycobacterium tuberculosis-mediated metabolism of  targeted xenobiotics | Nature Reviews Chemistry
The implication of Mycobacterium tuberculosis-mediated metabolism of targeted xenobiotics | Nature Reviews Chemistry

1-NM-PP1 (PP1 Analog II, CAS Number: 221244-14-0) | Cayman Chemical
1-NM-PP1 (PP1 Analog II, CAS Number: 221244-14-0) | Cayman Chemical

Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents |  SpringerLink
Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents | SpringerLink

Molecules | Free Full-Text | Probing the Highly Disparate Dual Inhibitory  Mechanisms of Novel Quinazoline Derivatives against Mycobacterium  tuberculosis Protein Kinases A and B
Molecules | Free Full-Text | Probing the Highly Disparate Dual Inhibitory Mechanisms of Novel Quinazoline Derivatives against Mycobacterium tuberculosis Protein Kinases A and B

EP2785184B1 - Compositions comprising jak inhibitors and haart drugs for  use in the prevention or treatment of hiv - Google Patents
EP2785184B1 - Compositions comprising jak inhibitors and haart drugs for use in the prevention or treatment of hiv - Google Patents

Pyrimidine-based antimalarials: design strategies and antiplasmodial  effects - MedChemComm (RSC Publishing) DOI:10.1039/C6MD00084C
Pyrimidine-based antimalarials: design strategies and antiplasmodial effects - MedChemComm (RSC Publishing) DOI:10.1039/C6MD00084C

Stereospecific α-(hetero)arylation of sulfoximines and sulfonimidamides |  Nature Synthesis
Stereospecific α-(hetero)arylation of sulfoximines and sulfonimidamides | Nature Synthesis

Current and future applications of GnRH, kisspeptin and neurokinin B  analogues | Nature Reviews Endocrinology
Current and future applications of GnRH, kisspeptin and neurokinin B analogues | Nature Reviews Endocrinology

Synthesis, Docking Study and Biological Evaluation of Amide‐Based Soluble  Epoxide Hydrolase Inhibitors with Novel Secondary Pharmacophore of Pyrimidin‐2‐ol  - Hejazi - 2022 - Chemistry & Biodiversity - Wiley Online Library
Synthesis, Docking Study and Biological Evaluation of Amide‐Based Soluble Epoxide Hydrolase Inhibitors with Novel Secondary Pharmacophore of Pyrimidin‐2‐ol - Hejazi - 2022 - Chemistry & Biodiversity - Wiley Online Library

Pharmaceuticals | July 2022 - Browse Articles
Pharmaceuticals | July 2022 - Browse Articles

Synthesis and Structure−Activity Relationships of Uracil Nucleotide  Derivatives and Analogues as Agonists at Human P2Y2, P2Y4, and P2Y6  Receptors | Journal of Medicinal Chemistry
Synthesis and Structure−Activity Relationships of Uracil Nucleotide Derivatives and Analogues as Agonists at Human P2Y2, P2Y4, and P2Y6 Receptors | Journal of Medicinal Chemistry

Pyrimidine - an overview | ScienceDirect Topics
Pyrimidine - an overview | ScienceDirect Topics

1-NA-PP1 (1-Naphthyl-PP1, PP1 Analog, CAS Number: 221243-82-9) | Cayman  Chemical
1-NA-PP1 (1-Naphthyl-PP1, PP1 Analog, CAS Number: 221243-82-9) | Cayman Chemical

General reaction of pyrimidine ring 23 and 29-32, singly activated... |  Download Scientific Diagram
General reaction of pyrimidine ring 23 and 29-32, singly activated... | Download Scientific Diagram

The pyrimidine analog FNC inhibits cell proliferation and viral protein  synthesis in HTLV‑1‑infected cells
The pyrimidine analog FNC inhibits cell proliferation and viral protein synthesis in HTLV‑1‑infected cells

Fluorescent nucleic acid base analogues | Quarterly Reviews of Biophysics |  Cambridge Core
Fluorescent nucleic acid base analogues | Quarterly Reviews of Biophysics | Cambridge Core