Year |
Citation |
Score |
2018 |
Valenea A, Grindrod S, Jung M. Abstract A15: DNA damage response-targeted molecules for breast cancer therapy Molecular Cancer Research. 16. DOI: 10.1158/1557-3125.Advbc17-A15 |
0.391 |
|
2018 |
Grindrod S, Velena A, Jung M. Abstract A178: Targeting the ATM-mediated DNA damage response pathway for cancer treatment Molecular Cancer Therapeutics. 17. DOI: 10.1158/1535-7163.Targ-17-A178 |
0.43 |
|
2017 |
Paydar I, Velena A, Grindrod S, Jung M. Abstract 5855: Radiosensitization of cervical cancer cells by HDAC inhibitors Cancer Research. 77: 5855-5855. DOI: 10.1158/1538-7445.Am2017-5855 |
0.355 |
|
2017 |
Grindrod S, Velena A, Jung M. Abstract 4054: Development of dual function small molecules as therapeutic agents for cancer treatment Cancer Research. 77: 4054-4054. DOI: 10.1158/1538-7445.Am2017-4054 |
0.467 |
|
2017 |
Nicholas N, Velena A, Grindrod S, Jung M. Abstract 3215: Therapeutic potential of dual-function small molecules for breast cancers Cancer Research. 77: 3215-3215. DOI: 10.1158/1538-7445.Am2017-3215 |
0.372 |
|
2016 |
Cordova A, Woodrick J, Grindrod S, Zhang L, Saygideger-Kont Y, Wang K, DeVito S, Daniele S, Paige M, Brown ML. Aminopeptidase P mediated targeting for breast tissue specific conjugate delivery. Bioconjugate Chemistry. PMID 26965452 DOI: 10.1021/Acs.Bioconjchem.5B00481 |
0.489 |
|
2014 |
Ma Y, Tomita Y, Preet A, Clarke R, Englund E, Grindrod S, Nathan S, De Oliveira E, Brown ML, Rosen EM. Small-molecule "BRCA1-mimetics" are antagonists of estrogen receptor-α. Molecular Endocrinology (Baltimore, Md.). 28: 1971-86. PMID 25264941 DOI: 10.1210/Me.2014-1146 |
0.676 |
|
2014 |
Hou S, Yi YW, Kang HJ, Zhang L, Kim HJ, Kong Y, Liu Y, Wang K, Kong HS, Grindrod S, Bae I, Brown ML. Novel carbazole inhibits phospho-STAT3 through induction of protein-tyrosine phosphatase PTPN6. Journal of Medicinal Chemistry. 57: 6342-53. PMID 24978112 DOI: 10.1021/Jm4018042 |
0.554 |
|
2012 |
Walls TH, Grindrod SC, Beraud D, Zhang L, Baheti AR, Dakshanamurthy S, Patel MK, Brown ML, MacArthur LH. Synthesis and biological evaluation of a fluorescent analog of phenytoin as a potential inhibitor of neuropathic pain and imaging agent. Bioorganic & Medicinal Chemistry. 20: 5269-76. PMID 22863530 DOI: 10.1016/J.Bmc.2012.06.042 |
0.58 |
|
2011 |
Grindrod S, Suy S, Fallen S, Eto M, Toretsky J, Brown ML. Effects of a fluorescent Myosin light chain phosphatase inhibitor on prostate cancer cells. Frontiers in Oncology. 1: 27. PMID 22655237 DOI: 10.3389/Fonc.2011.00027 |
0.559 |
|
2011 |
Kong Y, Jung M, Wang K, Grindrod S, Velena A, Lee SA, Dakshanamurthy S, Yang Y, Miessau M, Zheng C, Dritschilo A, Brown ML. Histone deacetylase cytoplasmic trapping by a novel fluorescent HDAC inhibitor. Molecular Cancer Therapeutics. 10: 1591-9. PMID 21697394 DOI: 10.1158/1535-7163.Mct-10-0779 |
0.556 |
|
2011 |
Yenugonda VM, Deb TB, Grindrod SC, Dakshanamurthy S, Yang Y, Paige M, Brown ML. Fluorescent cyclin-dependent kinase inhibitors block the proliferation of human breast cancer cells. Bioorganic & Medicinal Chemistry. 19: 2714-25. PMID 21440449 DOI: 10.1016/J.Bmc.2011.02.052 |
0.603 |
|
2010 |
Ringer L, Sirajuddin P, Yenugonda VM, Ghosh A, Divito K, Trabosh V, Patel Y, Brophy A, Grindrod S, Lisanti MP, Rosenthal D, Brown ML, Avantaggiati ML, Rodriguez O, Albanese C. VMY-1-103, a dansylated analog of purvalanol B, induces caspase-3-dependent apoptosis in LNCaP prostate cancer cells. Cancer Biology & Therapy. 10: 320-5. PMID 20574155 DOI: 10.4161/Cbt.10.4.12208 |
0.547 |
|
2010 |
Sheikh KD, Banerjee PP, Jagadeesh S, Grindrod SC, Zhang L, Paige M, Brown ML. Fluorescent epigenetic small molecule induces expression of the tumor suppressor ras-association domain family 1A and inhibits human prostate xenograft. Journal of Medicinal Chemistry. 53: 2376-82. PMID 20184324 DOI: 10.1021/Jm9011615 |
0.683 |
|
2010 |
Hans SK, Camara F, Altiti A, Martín-Montalvo A, Brautigan DL, Heimark D, Larner J, Grindrod S, Brown ML, Mootoo DR. Synthesis of C-glycoside analogues of beta-galactosamine-(1-->4)-3-O-methyl-D-chiro-inositol and assay as activator of protein phosphatases PDHP and PP2Calpha. Bioorganic & Medicinal Chemistry. 18: 1103-10. PMID 20079654 DOI: 10.1016/J.Bmc.2009.12.056 |
0.458 |
|
2008 |
Chinigo GM, Paige M, Grindrod S, Hamel E, Dakshanamurthy S, Chruszcz M, Minor W, Brown ML. Asymmetric synthesis of 2,3-dihydro-2-arylquinazolin-4-ones: methodology and application to a potent fluorescent tubulin inhibitor with anticancer activity. Journal of Medicinal Chemistry. 51: 4620-31. PMID 18610995 DOI: 10.1021/Jm800271C |
0.734 |
|
2005 |
Brautigan DL, Brown M, Grindrod S, Chinigo G, Kruszewski A, Lukasik SM, Bushweller JH, Horal M, Keller S, Tamura S, Heimark DB, Price J, Larner AN, Larner J. Allosteric activation of protein phosphatase 2C by D-chiro-inositol-galactosamine, a putative mediator mimetic of insulin action. Biochemistry. 44: 11067-73. PMID 16101290 DOI: 10.1021/Bi0508845 |
0.683 |
|
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