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116 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Cmpds
Data
Article Title
Organization
38
SAR of amino pyrrolidines as potent and novel protein-protein interaction inhibitors of the PRC2 complex through EED binding.EBI
Abbvie
48
Integrated Platform for Expedited Synthesis-Purification-Testing of Small Molecule Libraries.EBI
Abbvie
2
Turning a Substrate Peptide into a Potent Inhibitor for the Histone Methyltransferase SETD8.EBI
Abbvie
3
Synthesis and Pharmacology of (Pyridin-2-yl)methanol Derivatives as Novel and Selective Transient Receptor Potential Vanilloid 3 Antagonists.EBI
Abbvie
11
Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2.EBI
Abbvie
5
Optimization of ADME Properties for Sulfonamides Leading to the Discovery of a T-Type Calcium Channel Blocker, ABT-639.EBI
Abbvie
18
Structure-guided design of a series of MCL-1 inhibitors with high affinity and selectivity.EBI
Abbvie
32
Discovery of (R)-1-(7-chloro-2,2-bis(fluoromethyl)chroman-4-yl)-3-(3-methylisoquinolin-5-yl)urea (A-1165442): a temperature-neutral transient receptor potential vanilloid-1 (TRPV1) antagonist with analgesic efficacy.EBI
Abbvie
22
Pyrimidine-based tricyclic molecules as potent and orally efficacious inhibitors of wee1 kinase.EBI
Abbvie
15
Discovery of a Potent and Selective BCL-XL Inhibitor with in Vivo Activity.EBI
Abbvie
16
Discovery and development of potent and selective inhibitors of histone methyltransferase g9a.EBI
Abbvie
2
Synthesis and SAR of 4-aminocyclopentapyrrolidines as orally active N-type calcium channel inhibitors for inflammatory and neuropathic pain.EBI
Abbvie
45
Validation, Key Pharmacophores, and X-ray Cocrystal Structures of Novel Biochemically and Cellularly Active WRN Inhibitors Derived from a DNA-Encoded Library Screen.EBI
Abbvie
76
Discovery and Development of CFTR Modulators for the Treatment of Cystic Fibrosis.EBI
Abbvie
34
Discovery of Potent Azetidine-Benzoxazole MerTK Inhibitors with In Vivo Target Engagement.EBI
Abbvie
6
Exploiting selective BCL-2 family inhibitors to dissect cell survival dependencies and define improved strategies for cancer therapy.EBI
Abbvie
1
The Histone Methyltransferase Inhibitor A-366 Uncovers a Role for G9a/GLP in the Epigenetics of Leukemia.EBI
Abbvie
9
Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours.EBI
AbbVie
18
Targeting the Tyrosine Kinase 2 (TYK2) Pseudokinase Domain: Discovery of the Selective TYK2 Inhibitor ABBV-712.EBI
Abbvie
1
Pipeline Impact of Radiolabeled Compounds in Drug Discovery and Development.EBI
Abbvie
49
Discovery of (R)-(3-fluoropyrrolidin-1-yl)(6-((5-(trifluoromethyl)pyridin-2-yl)oxy)quinolin-2-yl)methanone (ABBV-318) and analogs as small molecule NaEBI
Abbvie
16
Discovery and SAR of 4-aminopyrrolidine-2-carboxylic acid correctors of CFTR for the treatment of cystic fibrosis.EBI
Abbvie
24
Balancing Properties with Carboxylates: A Lead Optimization Campaign for Selective and Orally Active CDK9 Inhibitors.EBI
Abbvie
11
Development of Orally Efficacious Allosteric Inhibitors of TNFα via Fragment-Based Drug Design.EBI
Abbvie
1
Discovery of a Potent and Selective Covalent p300/CBP Inhibitor.EBI
Abbvie
13
Discovery of A-1331852, a First-in-Class, Potent, and Orally-Bioavailable BCL-XEBI
Abbvie
3
Structure-Based Design of A-1293102, a Potent and Selective BCL-XEBI
Abbvie
15
Discovery of 2-aminoisobutyric acid ethyl ester (AIBEE) phosphoramidate prodrugs for delivering nucleoside HCV NS5B polymerase inhibitors.EBI
Abbvie
24
Design and evaluation of pyrazolopyrimidines as KCNQ channel modulators.EBI
Abbvie
51
Discovery of EBI
Abbvie
17
Discovery of ABBV/GLPG-3221, a Potent Corrector of CFTR for the Treatment of Cystic Fibrosis.EBI
Abbvie
22
Hit-to-lead evaluation of a novel class of sphingosine 1-phosphate lyase inhibitors.EBI
Abbvie
27
Substituted Indazoles as Nav1.7 Blockers for the Treatment of Pain.EBI
Abbvie
4
Beyond the Rule of 5: Lessons Learned from AbbVie's Drugs and Compound Collection.EBI
Abbvie
1
Emerging Approaches for the Identification of Protein Targets of Small Molecules - A Practitioners' Perspective.EBI
Abbvie
5
Targeting lysine specific demethylase 4A (KDM4A) tandem TUDOR domain - A fragment based approach.EBI
Abbvie
28
Discovery and optimization of novel constrained pyrrolopyridone BET family inhibitors.EBI
Abbvie
25
Highlights of the Structure-Activity Relationships of Benzimidazole Linked Pyrrolidines Leading to the Discovery of the Hepatitis C Virus NS5A Inhibitor Pibrentasvir (ABT-530).EBI
Abbvie
32
De Novo Design, Synthesis, and Biological Evaluation of 3,4-Disubstituted Pyrrolidine Sulfonamides as Potent and Selective Glycine Transporter 1 Competitive Inhibitors.EBI
Abbvie
24
Discovery of Spiro Oxazolidinediones as Selective, Orally Bioavailable Inhibitors of p300/CBP Histone Acetyltransferases.EBI
Abbvie
41
Fragment-Based, Structure-Enabled Discovery of Novel Pyridones and Pyridone Macrocycles as Potent Bromodomain and Extra-Terminal Domain (BET) Family Bromodomain Inhibitors.EBI
Abbvie
40
Methylpyrrole inhibitors of BET bromodomains.EBI
Abbvie
48
SAR and characterization of non-substrate isoindoline urea inhibitors of nicotinamide phosphoribosyltransferase (NAMPT).EBI
Abbvie
32
Discovery of N-(4-(2,4-Difluorophenoxy)-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)ethanesulfonamide (ABBV-075/Mivebresib), a Potent and Orally Available Bromodomain and Extraterminal Domain (BET) Family Bromodomain Inhibitor.EBI
Abbvie
24
Are We There Yet? Applying Thermodynamic and Kinetic Profiling on Embryonic Ectoderm Development (EED) Hit-to-Lead Program.EBI
Abbvie
29
Tiparp Inhibitor CompoundsBDB
Abbvie
19
PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASEBDB
Abbvie
50
1,3,4,7-TETRAHYDRO-2H-PYRROLO[3',2':5,6]PYRIDO[2,3-B][1,4]OXAZEPINE BCL-2 INHIBITORSBDB
Abbvie
19
Pyrimidines for degrading Bruton's tyrosine kinaseBDB
Abbvie
85
Pyrrolidine Main Protease Inhibitors as Antiviral AgentsBDB
Abbvie
50
1,3,4,7-tetrahydro-2H-pyrrolo[3′,2′:5,6]pyrido[2,3-b][1,4]oxazepine bcl-2 inhibitorsBDB
Abbvie
19
PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASEBDB
Abbvie
372
APOPTOSIS INDUCING AGENTS FOR THE TREATMENT OF CANCER AND IMMUNE AND AUTOIMMUNE DISEASESBDB
Abbvie
39
THIAZOLO[5,4-B]PYRIDINE MALT-1 INHIBITORSBDB
Abbvie
18
Nicotinamide RIPK1 inhibitorsBDB
Abbvie
365
Melt-extruded solid dispersions containing an apoptosis-inducing agentBDB
Abbvie
42
Spiro-cyclic amine derivatives as S1P modulatorsBDB
Abbvie
53
Macrocyclic MCL-1 inhibitors and methods of useBDB
Abbvie
62
Glucocorticoid receptor agonist and immunoconjugates thereofBDB
Abbvie
130
Bromodomain inhibitorsBDB
Abbvie
100
Substituted isoxazolopyridazinones and isothiazolopyridazinones and methods of useBDB
Abbvie
184
Bromodomain inhibitorsBDB
Abbvie
69
Heterocyclic kinase inhibitorsBDB
Abbvie
370
Solid dispersions containing an apoptosis-inducing agentBDB
Abbvie
1352
Pyrrolo [2,3-B] pyridine CDK9 kinase inhibitorsBDB
Abbvie
25
Inhibitor compounds of phosphodiesterase type 10ABDB
Abbvie
356
Indazole ureas and method of useBDB
Abbvie
185
Furo-3-carboxamide derivatives and methods of useBDB
Abbvie
73
Isoindolone derivativesBDB
Abbvie
11
TRPA1 antagonistsBDB
Abbvie
42
Spiro-cyclic amine derivatives as S1P modulatorsBDB
Abbvie
790
Pyrrolidine derivatives, pharmaceutical compositions containing them, and their use in therapyBDB
Abbvie
335
Pyridine CDK9 kinase inhibitorsBDB
Abbvie
17
SMYD2 inhibitorsBDB
Abbvie
75
Substituted cyanoguanidines as oral anti-viralsBDB
Abbvie
354
Primary carboxamides as BTK inhibitorsBDB
Abbvie
21
Fused heterocyclic derivatives as S1P modulatorsBDB
Abbvie
44
Apoptosis-inducing agent for the treatment of cancer and immune and autoimmune diseasesBDB
Abbvie
619
6-heteroaryloxy- or 6-aryloxy-quinoline-2-carboxamides and method of useBDB
Abbvie
104
Bromodomain inhibitorsBDB
Abbvie
48
1,3,4,7-TETRAHYDRO-2H-PYRROLO[3',2':5,6]PYRIDO[2,3-B][1,4]OXAZEPINE BCL-2 INHIBITORSBDB
Abbvie
5
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseasesBDB
Abbvie
5
The EED protein-protein interaction inhibitor A-395 inactivates the PRC2 complex.BDB
Abbvie
4
The SUV4-20 inhibitor A-196 verifies a role for epigenetics in genomic integrity.BDB
Abbvie
193
Tetracyclic CDK9 kinase inhibitorsBDB
Abbvie
404
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseasesBDB
Abbvie
348
Bromodomain inhibitorsBDB
Abbvie
1518
NAMPT and rock inhibitorsBDB
Abbvie
725
Inhibitors of poly(ADP-ribose)polymeraseBDB
Abbvie
187
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseasesBDB
Abbvie
100
INHIBITORS OF TYROSINE KINASE 2 MEDIATED SIGNALINGBDB
Abbvie
15
Aminoindane derivatives, pharmaceutical compositions containing them, and their use in therapyBDB
Abbvie
59
Bicyclic carboxamide inhibitors of kinasesBDB
Abbvie
4
Mercaptoamidine derivatives and methods of useBDB
Abbvie
346
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseasesBDB
Abbvie
17
Anti-viral compoundsBDB
Abbvie
87
5-substituted indazoles as kinase inhibitorsBDB
Abbvie
44
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseasesBDB
Abbvie
8
Radiolabeled PDE10A ligandsBDB
Abbvie
431
Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseasesBDB
Abbvie
368
Pyrrolo[2,3-B]pyridine CDK9 kinase inhibitorsBDB
Abbvie
19
TRPA1 antagonistsBDB
Abbvie
291
TRPV3 modulatorsBDB
Abbvie
404
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseasesBDB
Abbvie
331
TRPV1 antagonistsBDB
Abbvie
180
Tetrahydroisoquinolines, pharmaceutical compositions containing them, and their use in therapyBDB
Abbvie
68
Chemokine receptor antagonistsBDB
Abbvie
38
Compounds as cannabinoid receptor ligandsBDB
Abbvie
15
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseasesBDB
Abbvie
64
Compounds as cannabinoid receptor ligandsBDB
Abbvie
65
Compounds as cannabinoid receptor ligandsBDB
Abbvie
8
N-substituted aminobenzocycloheptene, aminotetraline, aminoindane and phenalkylamine derivatives, pharmaceutical compositions containing them, and their use in therapyBDB
Abbvie
155
TRPV1 antagonistsBDB
Abbvie
23
4-substituted-2-amino-pyrimidine derivativesBDB
Abbvie
44
TRPV1 antagonistsBDB
Abbvie
5
Thieno[3,2-C]pyridine kinase inhibitors with improved CYP safety profileBDB
Abbvie