Keywords: گروه اتصال دهنده روی; FK228 (PubChem CID: 5352062); PXD101 (PubChem CID: 6918638); SAHA (PubChem CID: 5311); LBH-589 (PubChem CID: 6918837); tubacin (PubChem CID: 6675804); tubastatin A (PubChem CID: 49850262); ACY-1215 (PubChem CID: 53340666); ACY-241 (PubChem CID: 53340426);
مقالات ISI گروه اتصال دهنده روی (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: گروه اتصال دهنده روی; HDAC; histone deacetylase; HDACi; histone deacetylase inhibitors; COX; cyclooxygenases; NSAIDs; non-steroidal anti-inflammatory drugs; AR; androgen receptor; ZBG; zinc binding group; PGE2; prostaglandin E2;
Design, synthesis and evaluation of antiproliferative activity of melanoma-targeted histone deacetylase inhibitors
Keywords: گروه اتصال دهنده روی; HDAC; histone deacetylase; HDACi; histone deacetylase inhibitors; ZBG; zinc binding group;
Keywords: گروه اتصال دهنده روی; Histone deacetylase inhibitors; Coumarin; 2-AminoBenzamide; Docking; Molecular dynamics; HDAC; Histone Deacetylases; HATs; Histone Acetyl Transferases; HSP 90; Heat Shock Protein 90; SAHA; suberoylanilide hydroxamic acid; TSA; Trichostatin A; ZBG; Zinc Bi
Keywords: گروه اتصال دهنده روی; Carbonic anhydrase inhibitors; Isoform selectivity; Zinc binding group; Primary sulfonamide; Aromatic sulfochlorination; Alternative binding mode;
Design, synthesis and structure-activity relationship evaluation of novel LpxC inhibitors as Gram-negative antibacterial agents
Keywords: گروه اتصال دهنده روی; Gram-negative bacteria infection; LpxC inhibitor; Structure-activity relationship; Zinc binding group; Liver microsomal stability;
Structure-activity relationships of HDAC8 inhibitors: Non-hydroxamates as anticancer agents
Keywords: گروه اتصال دهنده روی; Vorinostat (PubChem CID: 5311); Romidepsin (PubChem CID: 5352062); PCI-34051 (PubChem CID: 24753719); Cancer; Histone deacetylase; HDAC8 inhibitor; Non-hydroxamates; Zinc binding group; Structure-activity relationship (SAR);
Design, synthesis and biological screening of 2-aminobenzamides as selective HDAC3 inhibitors with promising anticancer effects
Keywords: گروه اتصال دهنده روی; B16F10; murine melanoma cells; CDCl3; deuterated chloroform; CTCL; cutaneous T-cell lymphoma; DCM; dichloromethane; DFT; density functional theory; DMAP; 4-Dimethylaminopyridine; DMEM; Dulbecco's modified Eagle's media; DMF; dimethylformamide; DMSO; dimet
Structural insights of SmKDAC8 inhibitors: Targeting Schistosoma epigenetics through a combined structure-based 3D QSAR, in vitro and synthesis strategy
Keywords: گروه اتصال دهنده روی; 3D QSAR; Three-Dimensional Quantitative Structure-Activity Relationships; BZDs; Benzodiazepine Derivatives; hKDAC; Human Lysine Deacetylase; KDACI; Lysine Deacetylase Inhibitor; NCI; National Cancer Institute; NEt3; Triethylamine; SLAs; Simplified Largazo
Arylsulfonamides and selectivity of matrix metalloproteinase-2: An overview
Keywords: گروه اتصال دهنده روی; Metalloenzyme; Matrix metalloproteinase-2; Zinc binding group; Selectivity; Arylsulfonamide; Structure-activity relationship (SAR);
Potent dual inhibitors of Plasmodium falciparum M1 and M17 aminopeptidases through optimization of S1 pocket interactions
Keywords: گروه اتصال دهنده روی; Plasmodium falciparum; Malaria; Aminopeptidase inhibitors; Hydroxamic acid; Zinc-binding group; MAP; metalloaminopeptidase; ZBG; zinc binding group; Pf; Plasmodium falciparum; Dd2 SpiroR; NITD609-RDd2 clone#2; CDI; carbonyldiimidazole; FCC; flash column c
An efficient synthesis of SK-658 and its analogs as potent histone deacetylase inhibitors
Keywords: گروه اتصال دهنده روی; Histone deacetylase inhibitor; Zinc binding group; SK-658 analogs; SS-hybrid
A dual inhibitor of matrix metalloproteinases and a disintegrin and metalloproteinases, [18F]FB-ML5, as a molecular probe for non-invasive MMP/ADAM-targeted imaging
Keywords: گروه اتصال دهنده روی; ACN; acetonitrile; AcOH; acetic acid; ADAM; a disintegrin and metalloproteinase; CD; catalytic domain; DCC; N,Nâ²-dicyclohexylcarbodiimide; DCM; dichloromethane; DMF; N,N-dimethylformamide; ECM; extracellular matrix; EOB; end of bombardment; EOS; end of
Saccharin: A lead compound for structure-based drug design of carbonic anhydrase IX inhibitors
Keywords: گروه اتصال دهنده روی; CA; carbonic anhydrase; Ki; inhibition constant; ZBG; zinc binding group; Saccharin; Metalloenzyme; Carbonic anhydrase IX; CA IX-mimic; Structure-based drug design;
Novel β-dicarbonyl derivatives as inhibitors of aminopeptidase N (APN)
Keywords: گروه اتصال دهنده روی; Aminopeptidase N; Zinc binding group; β-Dicarbonyl; Inhibitor; Anti-tumor;
Arylamino methylene bisphosphonate derivatives as bone seeking matrix metalloproteinase inhibitors
Keywords: گروه اتصال دهنده روی; Matrix metalloproteinase inhibitors; Zinc binding group; Bone targeting; Bisphosphonates;
Salicylaldoxime derivatives as new leads for the development of carbonic anhydrase inhibitors
Keywords: گروه اتصال دهنده روی; Carbonic anhydrase; Salicylaldoxime; Docking; QM/MM calculation; Zinc binding group
Metal–ligand interactions: An analysis of zinc binding groups using the Protein Data Bank
Keywords: گروه اتصال دهنده روی; Metal–ligand interaction; Zinc metalloproteins; Protein Data Bank; Zinc binding group
Histone deacetylase inhibitors with a primary amide zinc binding group display antitumor activity in xenograft model
Keywords: گروه اتصال دهنده روی; HDAC inhibitors; Primary carboxamide; Zinc binding group
Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isoforms I and II and transmembrane, tumor-associated isoforms IX and XII with boronic acids
Keywords: گروه اتصال دهنده روی; Carbonic anhydrase; Isoform CA I, II, IX, XII; Boronic acid; Enzyme inhibitor; Zinc binding group
Optimization of a series of potent and selective ketone histone deacetylase inhibitors
Keywords: گروه اتصال دهنده روی; HDAC inhibitors; Alkyl ketone; Zinc binding group
Carbonic anhydrase inhibitors: The X-ray crystal structure of the adduct of N-hydroxysulfamide with isozyme II explains why this new zinc binding function is effective in the design of potent inhibitors
Keywords: گروه اتصال دهنده روی; Carbonic anhydrase; N-Hydroxysulfamide; Zinc binding group; Enzyme inhibitor; X-ray crystallography