Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 13 to 24 of 943 entries
Sorted by: Best Match Show Resources per page
Visible-light-mediated C2-amination of thiophenes by using DDQ as an organophotocatalyst.

Chemical communications (Cambridge, England)

Song C, Yi H, Dou B, Li Y, Singh AK, Lei A.
PMID: 28294249
Chem Commun (Camb). 2017 Mar 28;53(26):3689-3692. doi: 10.1039/c7cc01339f.

In this work, a direct C-H activation of thiophenes was presented via an oxidation pathway under visible-light irradiation, in which the thiophene radical cation serves as the key intermediate. Various thiophenes and azoles could be transformed into the corresponding...

Cite
Song C, Yi H, Dou B, et al. Visible-light-mediated C2-amination of thiophenes by using DDQ as an organophotocatalyst. Chem Commun (Camb). 2017;53(26):3689-3692doi: 10.1039/c7cc01339f.
Song, C., Yi, H., Dou, B., Li, Y., Singh, A. K., & Lei, A. (2017). Visible-light-mediated C2-amination of thiophenes by using DDQ as an organophotocatalyst. Chemical communications (Cambridge, England), 53(26), 3689-3692. https://doi.org/10.1039/c7cc01339f
Song, Chunlan, et al. "Visible-light-mediated C2-amination of thiophenes by using DDQ as an organophotocatalyst." Chemical communications (Cambridge, England) vol. 53,26 (2017): 3689-3692. doi: https://doi.org/10.1039/c7cc01339f
Song C, Yi H, Dou B, Li Y, Singh AK, Lei A. Visible-light-mediated C2-amination of thiophenes by using DDQ as an organophotocatalyst. Chem Commun (Camb). 2017 Mar 28;53(26):3689-3692. doi: 10.1039/c7cc01339f. PMID: 28294249.
Copy Download .nbib Format: NLM
Lonafarnib synergizes with azoles against Aspergillus spp. and Exophiala spp.

Medical mycology

Qiao J, Sun Y, Gao L, He C, Zheng W.
PMID: 29514275
Med Mycol. 2019 Feb 01;57(2):e1. doi: 10.1093/mmy/myx072.

No abstract available.

Cite
Qiao J, Sun Y, Gao L, et al. Lonafarnib synergizes with azoles against Aspergillus spp. and Exophiala spp. Med Mycol. 2019;57(2):e1doi: 10.1093/mmy/myx072.
Qiao, J., Sun, Y., Gao, L., He, C., & Zheng, W. (2019). Lonafarnib synergizes with azoles against Aspergillus spp. and Exophiala spp. Medical mycology, 57(2), e1. https://doi.org/10.1093/mmy/myx072
Qiao, Jianjun, et al. "Lonafarnib synergizes with azoles against Aspergillus spp. and Exophiala spp." Medical mycology vol. 57,2 (2019): e1. doi: https://doi.org/10.1093/mmy/myx072
Qiao J, Sun Y, Gao L, He C, Zheng W. Lonafarnib synergizes with azoles against Aspergillus spp. and Exophiala spp. Med Mycol. 2019 Feb 01;57(2):e1. doi: 10.1093/mmy/myx072. PMID: 29514275.
Copy Download .nbib Format: NLM
[No title available]

Frontiers in microbiology

Lv QZ, Qin YL, Yan L, Wang L, Zhang C, Jiang YY.
PMID: 29515531
Front Microbiol. 2018 Feb 20;9:218. doi: 10.3389/fmicb.2018.00218. eCollection 2018.

Antifungal azole drugs inhibit the synthesis of ergosterol and cause the accumulation of sterols containing a 14α-methyl group, which is related to the properties of cell membrane. Due to the frequent recurrence of fungal infections and clinical long-term prophylaxis,...

Cite
Lv QZ, Qin YL, Yan L, et al. . Front Microbiol. 2018;9:218doi: 10.3389/fmicb.2018.00218.
Lv, Q. Z., Qin, Y. L., Yan, L., Wang, L., Zhang, C., & Jiang, Y. Y. (2018). . Frontiers in microbiology, 9218. https://doi.org/10.3389/fmicb.2018.00218
Lv, Quan-Zhen, et al. "." Frontiers in microbiology vol. 9 (2018): 218. doi: https://doi.org/10.3389/fmicb.2018.00218
Lv QZ, Qin YL, Yan L, Wang L, Zhang C, Jiang YY. . Front Microbiol. 2018 Feb 20;9:218. doi: 10.3389/fmicb.2018.00218. eCollection 2018. PMID: 29515531; PMCID: PMC5826172.
Copy Download .nbib Format: NLM
Photo-induced oxidant-free oxidative C-H/N-H cross-coupling between arenes and azoles.

Nature communications

Niu L, Yi H, Wang S, Liu T, Liu J, Lei A.
PMID: 28145410
Nat Commun. 2017 Feb 01;8:14226. doi: 10.1038/ncomms14226.

Direct cross-coupling between simple arenes and heterocyclic amines under mild conditions is undoubtedly important for C-N bonds construction. Selective C(sp

Cite
Niu L, Yi H, Wang S, et al. Photo-induced oxidant-free oxidative C-H/N-H cross-coupling between arenes and azoles. Nat Commun. 2017;8:14226doi: 10.1038/ncomms14226.
Niu, L., Yi, H., Wang, S., Liu, T., Liu, J., & Lei, A. (2017). Photo-induced oxidant-free oxidative C-H/N-H cross-coupling between arenes and azoles. Nature communications, 814226. https://doi.org/10.1038/ncomms14226
Niu, Linbin, et al. "Photo-induced oxidant-free oxidative C-H/N-H cross-coupling between arenes and azoles." Nature communications vol. 8 (2017): 14226. doi: https://doi.org/10.1038/ncomms14226
Niu L, Yi H, Wang S, Liu T, Liu J, Lei A. Photo-induced oxidant-free oxidative C-H/N-H cross-coupling between arenes and azoles. Nat Commun. 2017 Feb 01;8:14226. doi: 10.1038/ncomms14226. PMID: 28145410; PMCID: PMC5296647.
Copy Download .nbib Format: NLM
Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp.

Chemical communications (Cambridge, England)

Xing Q, Lv H, Xia C, Li F.
PMID: 28612071
Chem Commun (Camb). 2017 Jun 22;53(51):6914-6917. doi: 10.1039/c7cc03274a.

An efficient palladium-catalyzed oxidative aminocarbonylation of azoles has been developed. This system allows for intermolecular carbonylative cross-coupling of aromatic C(sp

Cite
Xing Q, Lv H, Xia C, et al. Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp. Chem Commun (Camb). 2017;53(51):6914-6917doi: 10.1039/c7cc03274a.
Xing, Q., Lv, H., Xia, C., & Li, F. (2017). Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp. Chemical communications (Cambridge, England), 53(51), 6914-6917. https://doi.org/10.1039/c7cc03274a
Xing, Qi, et al. "Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp." Chemical communications (Cambridge, England) vol. 53,51 (2017): 6914-6917. doi: https://doi.org/10.1039/c7cc03274a
Xing Q, Lv H, Xia C, Li F. Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp. Chem Commun (Camb). 2017 Jun 22;53(51):6914-6917. doi: 10.1039/c7cc03274a. PMID: 28612071.
Copy Download .nbib Format: NLM
Microwave-assisted one pot three-component synthesis of some novel pyrazole scaffolds as potent anticancer agents.

Chemistry Central journal

Gomha SM, Edrees MM, Faty RAM, Muhammad ZA, Mabkhot YN.
PMID: 29086808
Chem Cent J. 2017 May 08;11(1):37. doi: 10.1186/s13065-017-0266-4.

BACKGROUND: Pyrazoles, thiazoles and 1,3,4-thiadiazoles have been reported to possess various pharmacological activities.RESULTS: An efficient and a novel approach for the synthesis of some novel pyrazole based-azoles are described via multi-component reaction under controlled microwave heating conditions. The structures...

Cite
Gomha SM, Edrees MM, Faty RAM, et al. Microwave-assisted one pot three-component synthesis of some novel pyrazole scaffolds as potent anticancer agents. Chem Cent J. 2017;11(1):37doi: 10.1186/s13065-017-0266-4.
Gomha, S. M., Edrees, M. M., Faty, R. A. M., Muhammad, Z. A., & Mabkhot, Y. N. (2017). Microwave-assisted one pot three-component synthesis of some novel pyrazole scaffolds as potent anticancer agents. Chemistry Central journal, 11(1), 37. https://doi.org/10.1186/s13065-017-0266-4
Gomha, Sobhi M, et al. "Microwave-assisted one pot three-component synthesis of some novel pyrazole scaffolds as potent anticancer agents." Chemistry Central journal vol. 11,1 (2017): 37. doi: https://doi.org/10.1186/s13065-017-0266-4
Gomha SM, Edrees MM, Faty RAM, Muhammad ZA, Mabkhot YN. Microwave-assisted one pot three-component synthesis of some novel pyrazole scaffolds as potent anticancer agents. Chem Cent J. 2017 May 08;11(1):37. doi: 10.1186/s13065-017-0266-4. PMID: 29086808; PMCID: PMC5422217.
Copy Download .nbib Format: NLM
A DFT study of adsorption of imidazole, triazole, and tetrazole on oxidized copper surfaces: Cu₂O(111) and Cu₂O(111)-w/o-CuCUS.

Physical chemistry chemical physics : PCCP

Gustinčič D, Kokalj A.
PMID: 26443103
Phys Chem Chem Phys. 2015 Nov 21;17(43):28602-15. doi: 10.1039/c5cp03647j.

Azoles and their derivatives are known for their corrosion inhibition ability for copper. For this reason the bonding of imidazole, triazole, and tetrazole-used as archetypal models of azole corrosion inhibitors-to Cu2O(111) and Cu2O(111)-w/o-Cu(CUS) was characterized using density functional theory...

Cite
Gustinčič D, Kokalj A. A DFT study of adsorption of imidazole, triazole, and tetrazole on oxidized copper surfaces: Cu₂O(111) and Cu₂O(111)-w/o-CuCUS. Phys Chem Chem Phys. 2015;17(43):28602-15doi: 10.1039/c5cp03647j.
Gustinčič, D., & Kokalj, A. (2015). A DFT study of adsorption of imidazole, triazole, and tetrazole on oxidized copper surfaces: Cu₂O(111) and Cu₂O(111)-w/o-CuCUS. Physical chemistry chemical physics : PCCP, 17(43), 28602-15. https://doi.org/10.1039/c5cp03647j
Gustinčič, Dunja, and Kokalj, Anton. "A DFT study of adsorption of imidazole, triazole, and tetrazole on oxidized copper surfaces: Cu₂O(111) and Cu₂O(111)-w/o-CuCUS." Physical chemistry chemical physics : PCCP vol. 17,43 (2015): 28602-15. doi: https://doi.org/10.1039/c5cp03647j
Gustinčič D, Kokalj A. A DFT study of adsorption of imidazole, triazole, and tetrazole on oxidized copper surfaces: Cu₂O(111) and Cu₂O(111)-w/o-CuCUS. Phys Chem Chem Phys. 2015 Nov 21;17(43):28602-15. doi: 10.1039/c5cp03647j. PMID: 26443103.
Copy Download .nbib Format: NLM
Antifungal prophylaxis in stem cell transplantation centers in Turkey.

Turkish journal of haematology : official journal of Turkish Society of Haematology

Akan H.
PMID: 27264583
Turk J Haematol. 2011 Dec 05;28(4):271-5. doi: 10.5152/tjh.2011.81.

OBJECTIVE: This study aimed to determine the current state of antifungal prophylaxis in Turkish stem cell transplantation (SCT) centers.METHODS: he were 38 active stem cell transplantation centers in Turkey, 28 of which were registered with the European Group for...

Cite
Akan H. Türkiye'deki kök hücre nakli merkezlerinde antifungal profilaksi. Antifungal prophylaxis in stem cell transplantation centers in Turkey. Turk J Haematol. 2011;28(4):271-5doi: 10.5152/tjh.2011.81.
Akan, H. (2011). Türkiye'deki kök hücre nakli merkezlerinde antifungal profilaksi. Antifungal prophylaxis in stem cell transplantation centers in Turkey. Turkish journal of haematology : official journal of Turkish Society of Haematology, 28(4), 271-5. https://doi.org/10.5152/tjh.2011.81
Akan, Hamdi. "Türkiye'deki kök hücre nakli merkezlerinde antifungal profilaksi." Antifungal prophylaxis in stem cell transplantation centers in Turkey. Turkish journal of haematology : official journal of Turkish Society of Haematology vol. 28,4 (2011): 271-5. doi: https://doi.org/10.5152/tjh.2011.81
Akan H. Türkiye'deki kök hücre nakli merkezlerinde antifungal profilaksi. Antifungal prophylaxis in stem cell transplantation centers in Turkey. Turk J Haematol. 2011 Dec 05;28(4):271-5. doi: 10.5152/tjh.2011.81. PMID: 27264583.
Copy Download .nbib Format: NLM
Cyclosporine/ketoconazole reduces treatment costs for nephrotic syndrome.

Indian journal of nephrology

Iyengar A, Kamath N, Phadke KD, Bitzan M.
PMID: 24339519
Indian J Nephrol. 2013 Nov;23(6):419-23. doi: 10.4103/0971-4065.120338.

Cyclosporine A (CyA) is an effective agent for the treatment of glucocorticoid-dependent idiopathic nephrotic syndrome (GCDNS), but costs are prohibitive in resource-poor societies. The objectives of this study were to evaluate the efficacy and safety of reducing the dose...

Cite
Iyengar A, Kamath N, Phadke KD, et al. Cyclosporine/ketoconazole reduces treatment costs for nephrotic syndrome. Indian J Nephrol. 2013;23(6):419-23doi: 10.4103/0971-4065.120338.
Iyengar, A., Kamath, N., Phadke, K. D., & Bitzan, M. (2013). Cyclosporine/ketoconazole reduces treatment costs for nephrotic syndrome. Indian journal of nephrology, 23(6), 419-23. https://doi.org/10.4103/0971-4065.120338
Iyengar, A, et al. "Cyclosporine/ketoconazole reduces treatment costs for nephrotic syndrome." Indian journal of nephrology vol. 23,6 (2013): 419-23. doi: https://doi.org/10.4103/0971-4065.120338
Iyengar A, Kamath N, Phadke KD, Bitzan M. Cyclosporine/ketoconazole reduces treatment costs for nephrotic syndrome. Indian J Nephrol. 2013 Nov;23(6):419-23. doi: 10.4103/0971-4065.120338. PMID: 24339519; PMCID: PMC3841509.
Copy Download .nbib Format: NLM
Fluconazole Resistance Candida albicans in Females With Recurrent Vaginitis and Pir1 Overexpression.

Jundishapur journal of microbiology

Nasrollahi Z, Yadegari MH, Roudbar Mohammadi S, Roudbary M, Hosseini Poor M, Nikoomanesh F, Rajabi Bazl M.
PMID: 26495107
Jundishapur J Microbiol. 2015 Sep 23;8(9):e21468. doi: 10.5812/jjm.21468. eCollection 2015 Sep.

BACKGROUND: Some genes may be associated with Candida albicans resistance to azoles. Pir1 gene is described as responsible to induce resistance in C. albicans.OBJECTIVES: The current study aimed to find the relationship between fluconazole resistance and Pir1 protein (Pir1p)...

Cite
Nasrollahi Z, Yadegari MH, Roudbar Mohammadi S, et al. Fluconazole Resistance Candida albicans in Females With Recurrent Vaginitis and Pir1 Overexpression. Jundishapur J Microbiol. 2015;8(9):e21468doi: 10.5812/jjm.21468.
Nasrollahi, Z., Yadegari, M. H., Roudbar Mohammadi, S., Roudbary, M., Hosseini Poor, M., Nikoomanesh, F., & Rajabi Bazl, M. (2015). Fluconazole Resistance Candida albicans in Females With Recurrent Vaginitis and Pir1 Overexpression. Jundishapur journal of microbiology, 8(9), e21468. https://doi.org/10.5812/jjm.21468
Nasrollahi, Zahra, et al. "Fluconazole Resistance Candida albicans in Females With Recurrent Vaginitis and Pir1 Overexpression." Jundishapur journal of microbiology vol. 8,9 (2015): e21468. doi: https://doi.org/10.5812/jjm.21468
Nasrollahi Z, Yadegari MH, Roudbar Mohammadi S, Roudbary M, Hosseini Poor M, Nikoomanesh F, Rajabi Bazl M. Fluconazole Resistance Candida albicans in Females With Recurrent Vaginitis and Pir1 Overexpression. Jundishapur J Microbiol. 2015 Sep 23;8(9):e21468. doi: 10.5812/jjm.21468. eCollection 2015 Sep. PMID: 26495107; PMCID: PMC4609386.
Copy Download .nbib Format: NLM
Reversible solid-to-liquid phase transition of coordination polymer crystals.

Journal of the American Chemical Society

Umeyama D, Horike S, Inukai M, Itakura T, Kitagawa S.
PMID: 25530162
J Am Chem Soc. 2015 Jan 21;137(2):864-70. doi: 10.1021/ja511019u. Epub 2015 Jan 09.

The solid-to-liquid phase transition, a fundamental process commonly observed for various types of substances with significant potential for application, has been given little attention in the field of coordination polymers (CPs) despite the rich functionality of these compounds. In...

Cite
Umeyama D, Horike S, Inukai M, et al. Reversible solid-to-liquid phase transition of coordination polymer crystals. J Am Chem Soc. 2015;137(2):864-70doi: 10.1021/ja511019u.
Umeyama, D., Horike, S., Inukai, M., Itakura, T., & Kitagawa, S. (2015). Reversible solid-to-liquid phase transition of coordination polymer crystals. Journal of the American Chemical Society, 137(2), 864-70. https://doi.org/10.1021/ja511019u
Umeyama, Daiki, et al. "Reversible solid-to-liquid phase transition of coordination polymer crystals." Journal of the American Chemical Society vol. 137,2 (2015): 864-70. doi: https://doi.org/10.1021/ja511019u
Umeyama D, Horike S, Inukai M, Itakura T, Kitagawa S. Reversible solid-to-liquid phase transition of coordination polymer crystals. J Am Chem Soc. 2015 Jan 21;137(2):864-70. doi: 10.1021/ja511019u. Epub 2015 Jan 09. PMID: 25530162.
Copy Download .nbib Format: NLM
NOV-002, A Glutathione Disulfide Mimetic, Suppresses Tumor Cell Invasion and Metastasis.

Journal of carcinogenesis & mutagenesis

Gumireddy K, Li A, Cao L, Yan J, Liu L, Xu X, Pazoles C, Huang Q.
PMID: 24377058
J Carcinog Mutagen. 2013 Apr 30;2013. doi: 10.4172/2157-2518.S7-002.

Metastasis is the major cause of death in cancer. Most therapies currently in the clinic aim to eradicate primary tumor, but do not have ideal effects on metastasis. The lack of effective therapy in metastasis prevention and treatment results...

Cite
Gumireddy K, Li A, Cao L, et al. NOV-002, A Glutathione Disulfide Mimetic, Suppresses Tumor Cell Invasion and Metastasis. J Carcinog Mutagen. 2013;2013doi: 10.4172/2157-2518.S7-002.
Gumireddy, K., Li, A., Cao, L., Yan, J., Liu, L., Xu, X., Pazoles, C., & Huang, Q. (2013). NOV-002, A Glutathione Disulfide Mimetic, Suppresses Tumor Cell Invasion and Metastasis. Journal of carcinogenesis & mutagenesis, 2013. https://doi.org/10.4172/2157-2518.S7-002
Gumireddy, Kiranmai, et al. "NOV-002, A Glutathione Disulfide Mimetic, Suppresses Tumor Cell Invasion and Metastasis." Journal of carcinogenesis & mutagenesis vol. 2013 (2013). doi: https://doi.org/10.4172/2157-2518.S7-002
Gumireddy K, Li A, Cao L, Yan J, Liu L, Xu X, Pazoles C, Huang Q. NOV-002, A Glutathione Disulfide Mimetic, Suppresses Tumor Cell Invasion and Metastasis. J Carcinog Mutagen. 2013 Apr 30;2013. doi: 10.4172/2157-2518.S7-002. PMID: 24377058; PMCID: PMC3872994.
Copy Download .nbib Format: NLM
Showing 13 to 24 of 943 entries