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The 50 checked references that resolve
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resolves10.1016/S0968-0896(01)00116-XIn vitro antifungal evaluation and structure–activity relationships of a new series of chalcone derivatives and synthetic analogues, with inhibitory properties against polymers of the fungal cell wall
resolves10.1016/j.bbrc.2004.07.094Licochalcone-A, a novel flavonoid isolated from licorice root (Glycyrrhiza glabra), causes G2 and late-G1 arrests in androgen-independent PC-3 prostate cancer cells
resolves10.1016/j.bmc.2008.01.058Interactive effects of polymethoxy flavones from Citrus on cell growth inhibition in human neuroblastoma SH-SY5Y cells
resolves10.1016/j.bmc.2007.11.048Synthesis and biological evaluation of imidazol-2-one derivatives as potential antitumor agents
resolves10.1016/j.bmc.2006.12.001Synthesis of furopyrazole analogs of 1-benzyl-3-(5-hydroxymethyl-2-furyl)indazole (YC-1) as novel anti-leukemia agents
resolves10.1021/jm701240cStructure-Based Optimization of Pyrazolo[3,4-<i>d</i>]pyrimidines as Abl Inhibitors and Antiproliferative Agents toward Human Leukemia Cell Lines
resolves10.1016/j.bmc.2007.08.021Synthesis and structure–activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5-carbohydrazide derivatives as potential agents against A549 lung cancer cells
resolves10.1016/j.ejmech.2008.01.021Synthesis and structure–activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5-carbohydrazide hydrazone derivatives as potential agents against A549 lung cancer cells
resolves10.1016/j.bmcl.2004.03.013New pyrazolo[3,4-d]pyrimidines endowed with A431 antiproliferative activity and inhibitory properties of Src phosphorylation
resolves10.1016/j.ejmech.2003.11.012Synthesis and antiproliferative activity of triazenoindazoles and triazenopyrazoles: a comparative study
resolves10.1016/j.bmcl.2006.08.017Design and synthesis of a series of novel pyrazolopyridines as HIF 1-α prolyl hydroxylase inhibitors
resolves10.1016/j.bmcl.2005.03.121Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents
resolves10.1007/BF02977319Synthesis of thiazolo[4,5-d]pyrimidine derivatives as potential antimicrobial agents
resolves10.1016/j.bmcl.2008.09.057One-pot synthesis and antibacterial activities of pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine-dione derivatives
resolves10.1007/BF02978199Synthesis of new 2-thiouracil-5-sulphonamide derivatives with antibacterial and antifungal activity
resolves10.1021/jm701159tDerivatives of 4-Amino-6-hydroxy-2-mercaptopyrimidine as Novel, Potent, and Selective A<sub>3</sub>Adenosine Receptor Antagonists
resolves10.1016/j.ejmech.2011.02.057Discovery, synthesis, and investigation of the antitumor activity of novel piperazinylpyrimidine derivatives
resolves10.1016/S0014-827X(01)01167-3Synthesis and structure elucidation of some new thioether derivatives of 1,2,4-triazoline-3-thiones and their antimicrobial activities
resolves10.1002/ardp.200390011Substituted Quinazolines, Part 2. Synthesis and In‐Vitro Anticancer Evaluation of New 2‐Substituted Mercapto‐3<i>H</i>‐quinazoline Analogs
resolves10.1021/jm050744tParallel Solution-Phase and Microwave-Assisted Synthesis of New <i>S</i>-DABO Derivatives Endowed with Subnanomolar Anti-HIV-1 Activity
resolves10.1002/ardp.200300734Synthesis andin vitro evaluation of the anticancer activity of novel fluorinated thiazolo[4, 5-d]pyrimidines
resolves10.3797/scipharm.aut-03-08Synthesis and in vitro Anti-HIV Screening of Certain 2-(Benzoxazol-2-ylamino)-3H-4-oxopyrimidines
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resolves10.1016/j.bmc.2006.06.020Synthesis and in vitro antitumor evaluation of some indeno[1,2-c]pyrazol(in)es substituted with sulfonamide, sulfonylurea(-thiourea) pharmacophores, and some derived thiazole ring systems
resolves10.1007/s00044-007-9033-8Synthesis of some sulfonamides, disubstituted sulfonylureas or thioureas and some structurally related variants. A class of promising antitumor agents
resolves10.1002/ardp.2007001783‐Methyl‐2‐(4‐substituted phenyl)‐4,5‐dihydronaphtho[1,2‐<i>c</i>]‐pyrazoles: Synthesis and <i>in‐vitro</i> Biological Evaluation as Antitumour Agents
resolves10.1002/ardp.200800026Synthesis and Biological Evaluation of Some 2,4,5‐Trisubstituted Thiazole Derivatives as Potential Antimicrobial and Anticancer Agents
resolves10.1002/ardp.200800223Synthesis and Biological Evaluation of Some Novel Polysubstituted Pyrimidine Derivatives as Potential Antimicrobial and Anticancer Agents
resolves10.1002/ardp.200900062Synthesis and Biological Evaluation of Some Polymethoxylated Fused Pyridine Ring Systems as Antitumor Agents
resolves10.1016/j.bmc.2010.02.006Polysubstituted pyrazoles, part 6. Synthesis of some 1-(4-chlorophenyl)-4-hydroxy-1H-pyrazol-3-carbonyl derivatives linked to nitrogenous heterocyclic ring systems as potential antitumor agents
resolves10.1016/j.bmcl.2006.07.06714β-Hydroxy-10-deacetylbaccatin III as a convenient, alternative substrate for the improved synthesis of methoxylated second-generation taxanes
resolves10.1002/ddr.430340203Some practical considerations and applications of the national cancer institute in vitro anticancer drug discovery screen
resolves10.1093/jnci/83.11.757Feasibility of a High-Flux Anticancer Drug Screen Using a Diverse Panel of Cultured Human Tumor Cell Lines
resolves10.1093/jnci/81.8.577New Soluble-Formazan Assay for HIV-1 Cytopathic Effects: Application to High-Flux Screening of Synthetic and Natural Products for AIDS-Antiviral Activity
resolves10.1021/jm00040a010Anticancer Specificity of Some Ellipticinium Salts against Human Brain Tumors in vitro
resolves10.1093/jac/dkl393Bactericidal agents in the treatment of MRSA infections--the potential role of daptomycin
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