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Some traditional herbal medicines, some mycotoxins, naphthalene and styrene

evaluation

[No authors listed]
GSID: fBOthiNFqWkJ
… Group on the Evaluation of Carcinogenic Risks to … - 2002 - books.google.com

Traditional herbal medicines encompass an extremely diverse group of preparations that originate from many different cultures. In recent years, such products have become widely available commercially in developed countries where mixtures prepared from medicinal plants …

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IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, & International Agency for Research on Cancer. (2002). Some traditional herbal medicines, some mycotoxins, naphthalene and styrene (Vol. 82). World Health Organization.
IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, and International Agency for Research on Cancer. Some traditional herbal medicines, some mycotoxins, naphthalene and styrene. Vol. 82. World Health Organization, 2002.
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Molecular Dynamics Simulation of Nitrobenzene Dioxygenase Using AMBER Force Field.

Journal of chemical theory and computation

Pabis A, Geronimo I, York DM, Paneth P.
PMID: 24955078
J Chem Theory Comput. 2014 Jun 10;10(6):2246-2254. doi: 10.1021/ct500205z. Epub 2014 Apr 24.

Molecular dynamics simulation of the oxygenase component of nitrobenzene dioxygenase (NBDO) system, a member of the naphthalene family of Rieske nonheme iron dioxygenases, has been carried out using the AMBER force field combined with a new set of parameters...

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Pabis A, Geronimo I, York DM, et al. Molecular Dynamics Simulation of Nitrobenzene Dioxygenase Using AMBER Force Field. J Chem Theory Comput. 2014;10(6):2246-2254doi: 10.1021/ct500205z.
Pabis, A., Geronimo, I., York, D. M., & Paneth, P. (2014). Molecular Dynamics Simulation of Nitrobenzene Dioxygenase Using AMBER Force Field. Journal of chemical theory and computation, 10(6), 2246-2254. https://doi.org/10.1021/ct500205z
Pabis, Anna, et al. "Molecular Dynamics Simulation of Nitrobenzene Dioxygenase Using AMBER Force Field." Journal of chemical theory and computation vol. 10,6 (2014): 2246-2254. doi: https://doi.org/10.1021/ct500205z
Pabis A, Geronimo I, York DM, Paneth P. Molecular Dynamics Simulation of Nitrobenzene Dioxygenase Using AMBER Force Field. J Chem Theory Comput. 2014 Jun 10;10(6):2246-2254. doi: 10.1021/ct500205z. Epub 2014 Apr 24. PMID: 24955078; PMCID: PMC4059247.
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Somatic embryogenesis and plant regeneration of cassava (Manihot esculenta Crantz) landraces from Cameroon.

SpringerPlus

Mongomake K, Doungous O, Khatabi B, Fondong VN.
PMID: 26361578
Springerplus. 2015 Sep 04;4:477. doi: 10.1186/s40064-015-1272-4. eCollection 2015.

A procedure to regenerate cassava (Manihot esculenta Crantz) cultivars from Cameroon via somatic embryogenesis (SE) was developed. Shoot apical meristems and immature leaf lobes were used as explants on Murashige and Skoog (MS) basal medium containing 33 or 50...

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Mongomake K, Doungous O, Khatabi B, et al. Somatic embryogenesis and plant regeneration of cassava (Manihot esculenta Crantz) landraces from Cameroon. Springerplus. 2015;4:477doi: 10.1186/s40064-015-1272-4.
Mongomake, K., Doungous, O., Khatabi, B., & Fondong, V. N. (2015). Somatic embryogenesis and plant regeneration of cassava (Manihot esculenta Crantz) landraces from Cameroon. SpringerPlus, 4477. https://doi.org/10.1186/s40064-015-1272-4
Mongomake, Kone, et al. "Somatic embryogenesis and plant regeneration of cassava (Manihot esculenta Crantz) landraces from Cameroon." SpringerPlus vol. 4 (2015): 477. doi: https://doi.org/10.1186/s40064-015-1272-4
Mongomake K, Doungous O, Khatabi B, Fondong VN. Somatic embryogenesis and plant regeneration of cassava (Manihot esculenta Crantz) landraces from Cameroon. Springerplus. 2015 Sep 04;4:477. doi: 10.1186/s40064-015-1272-4. eCollection 2015. PMID: 26361578; PMCID: PMC4559553.
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Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins.

The journal of physical chemistry. B

Favrelle A, Gouhier G, Guillen F, Martin C, Mofaddel N, Petit S, Mundy KM, Pitre SP, Wagner BD.
PMID: 26362021
J Phys Chem B. 2015 Oct 08;119(40):12921-30. doi: 10.1021/acs.jpcb.5b07157. Epub 2015 Sep 24.

Cyclodextrins (CDs) are the most widely used organic hosts for the inclusion of guest molecules. CDs can be readily modified through substitutions of the hydroxyl groups, and these modified CDs can have different host binding properties compared to those...

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Favrelle A, Gouhier G, Guillen F, et al. Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins. J Phys Chem B. 2015;119(40):12921-30doi: 10.1021/acs.jpcb.5b07157.
Favrelle, A., Gouhier, G., Guillen, F., Martin, C., Mofaddel, N., Petit, S., Mundy, K. M., Pitre, S. P., & Wagner, B. D. (2015). Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins. The journal of physical chemistry. B, 119(40), 12921-30. https://doi.org/10.1021/acs.jpcb.5b07157
Favrelle, Audrey, et al. "Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins." The journal of physical chemistry. B vol. 119,40 (2015): 12921-30. doi: https://doi.org/10.1021/acs.jpcb.5b07157
Favrelle A, Gouhier G, Guillen F, Martin C, Mofaddel N, Petit S, Mundy KM, Pitre SP, Wagner BD. Structure-Binding Effects: Comparative Binding of 2-Anilino-6-naphthalenesulfonate by a Series of Alkyl- and Hydroxyalkyl-Substituted β-Cyclodextrins. J Phys Chem B. 2015 Oct 08;119(40):12921-30. doi: 10.1021/acs.jpcb.5b07157. Epub 2015 Sep 24. PMID: 26362021.
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Is coronene better described by Clar's aromatic π-sextet model or by the AdNDP representation?.

Journal of computational chemistry

Kumar A, Duran M, Solà M.
PMID: 28394019
J Comput Chem. 2017 Jul 05;38(18):1606-1611. doi: 10.1002/jcc.24801. Epub 2017 Apr 10.

The bonding patterns in coronene are complicated and controversial as denoted by the lack of consensus of how its electronic structure should be described. Among the different proposed descriptions, the two most representative are those generated by Clar's aromatic...

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Kumar A, Duran M, Solà M. Is coronene better described by Clar's aromatic π-sextet model or by the AdNDP representation?. J Comput Chem. 2017;38(18):1606-1611doi: 10.1002/jcc.24801.
Kumar, A., Duran, M., & Solà, M. (2017). Is coronene better described by Clar's aromatic π-sextet model or by the AdNDP representation?. Journal of computational chemistry, 38(18), 1606-1611. https://doi.org/10.1002/jcc.24801
Kumar, Anand, et al. "Is coronene better described by Clar's aromatic π-sextet model or by the AdNDP representation?." Journal of computational chemistry vol. 38,18 (2017): 1606-1611. doi: https://doi.org/10.1002/jcc.24801
Kumar A, Duran M, Solà M. Is coronene better described by Clar's aromatic π-sextet model or by the AdNDP representation?. J Comput Chem. 2017 Jul 05;38(18):1606-1611. doi: 10.1002/jcc.24801. Epub 2017 Apr 10. PMID: 28394019.
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Tuning the Endocytosis Mechanism of Zr-Based Metal-Organic Frameworks through Linker Functionalization.

ACS applied materials & interfaces

Orellana-Tavra C, Haddad S, Marshall RJ, Abánades Lázaro I, Boix G, Imaz I, Maspoch D, Forgan RS, Fairen-Jimenez D.
PMID: 28925254
ACS Appl Mater Interfaces. 2017 Oct 18;9(41):35516-35525. doi: 10.1021/acsami.7b07342. Epub 2017 Oct 03.

A critical bottleneck for the use of metal-organic frameworks (MOFs) as drug delivery systems has been allowing them to reach their intracellular targets without being degraded in the acidic environment of the lysosomes. Cells take up particles by endocytosis...

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Orellana-Tavra C, Haddad S, Marshall RJ, et al. Tuning the Endocytosis Mechanism of Zr-Based Metal-Organic Frameworks through Linker Functionalization. ACS Appl Mater Interfaces. 2017;9(41):35516-35525doi: 10.1021/acsami.7b07342.
Orellana-Tavra, C., Haddad, S., Marshall, R. J., Abánades Lázaro, I., Boix, G., Imaz, I., Maspoch, D., Forgan, R. S., & Fairen-Jimenez, D. (2017). Tuning the Endocytosis Mechanism of Zr-Based Metal-Organic Frameworks through Linker Functionalization. ACS applied materials & interfaces, 9(41), 35516-35525. https://doi.org/10.1021/acsami.7b07342
Orellana-Tavra, Claudia, et al. "Tuning the Endocytosis Mechanism of Zr-Based Metal-Organic Frameworks through Linker Functionalization." ACS applied materials & interfaces vol. 9,41 (2017): 35516-35525. doi: https://doi.org/10.1021/acsami.7b07342
Orellana-Tavra C, Haddad S, Marshall RJ, Abánades Lázaro I, Boix G, Imaz I, Maspoch D, Forgan RS, Fairen-Jimenez D. Tuning the Endocytosis Mechanism of Zr-Based Metal-Organic Frameworks through Linker Functionalization. ACS Appl Mater Interfaces. 2017 Oct 18;9(41):35516-35525. doi: 10.1021/acsami.7b07342. Epub 2017 Oct 03. PMID: 28925254; PMCID: PMC5663390.
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Spectral and dynamical properties of a Zr-based MOF.

Physical chemistry chemical physics : PCCP

Gutiérrez M, Sánchez F, Douhal A.
PMID: 26400004
Phys Chem Chem Phys. 2016 Feb 21;18(7):5112-20. doi: 10.1039/c5cp04436g. Epub 2015 Sep 24.

We report on the spectra and dynamics of a Zr-naphthalene dicarboxylic acid (Zr-NDC) MOF in different diluted solvent suspensions and in a concentrated tetrahydrofuran (THF) one. In a diluted diethyl ether (DE) suspension, we observed intraparticle excimer formation between...

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Gutiérrez M, Sánchez F, Douhal A. Spectral and dynamical properties of a Zr-based MOF. Phys Chem Chem Phys. 2015;18(7):5112-20doi: 10.1039/c5cp04436g.
Gutiérrez, M., Sánchez, F., & Douhal, A. (2016). Spectral and dynamical properties of a Zr-based MOF. Physical chemistry chemical physics : PCCP, 18(7), 5112-20. https://doi.org/10.1039/c5cp04436g
Gutiérrez, Mario, et al. "Spectral and dynamical properties of a Zr-based MOF." Physical chemistry chemical physics : PCCP vol. 18,7 (2016): 5112-20. doi: https://doi.org/10.1039/c5cp04436g
Gutiérrez M, Sánchez F, Douhal A. Spectral and dynamical properties of a Zr-based MOF. Phys Chem Chem Phys. 2016 Feb 21;18(7):5112-20. doi: 10.1039/c5cp04436g. Epub 2015 Sep 24. PMID: 26400004.
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Thiophene-Fused π-Systems from Diarylacetylenes and Elemental Sulfur.

Journal of the American Chemical Society

Meng L, Fujikawa T, Kuwayama M, Segawa Y, Itami K.
PMID: 27501373
J Am Chem Soc. 2016 Aug 17;138(32):10351-5. doi: 10.1021/jacs.6b06486. Epub 2016 Aug 08.

A simple yet effective method for the formation of thiophene-fused π-systems is reported. When arylethynyl-substituted polycyclic arenes were heated in DMF in the presence of elemental sulfur, the corresponding thiophene-fused polycyclic arenes were obtained via cleavage of the ortho-C-H...

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Meng L, Fujikawa T, Kuwayama M, et al. Thiophene-Fused π-Systems from Diarylacetylenes and Elemental Sulfur. J Am Chem Soc. 2016;138(32):10351-5doi: 10.1021/jacs.6b06486.
Meng, L., Fujikawa, T., Kuwayama, M., Segawa, Y., & Itami, K. (2016). Thiophene-Fused π-Systems from Diarylacetylenes and Elemental Sulfur. Journal of the American Chemical Society, 138(32), 10351-5. https://doi.org/10.1021/jacs.6b06486
Meng, Lingkui, et al. "Thiophene-Fused π-Systems from Diarylacetylenes and Elemental Sulfur." Journal of the American Chemical Society vol. 138,32 (2016): 10351-5. doi: https://doi.org/10.1021/jacs.6b06486
Meng L, Fujikawa T, Kuwayama M, Segawa Y, Itami K. Thiophene-Fused π-Systems from Diarylacetylenes and Elemental Sulfur. J Am Chem Soc. 2016 Aug 17;138(32):10351-5. doi: 10.1021/jacs.6b06486. Epub 2016 Aug 08. PMID: 27501373.
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A theoretical study of low-lying singlet and triplet excited states of quinazoline, quinoxaline and phthalazine: insight into triplet formation.

Physical chemistry chemical physics : PCCP

Etinski M, Marian CM.
PMID: 28513683
Phys Chem Chem Phys. 2017 May 31;19(21):13828-13837. doi: 10.1039/c7cp02022h.

Quinazoline, quinoxaline and phthalazine are nitrogen containing heterocyclic aromatic molecules which belong to the class diazanaphthalenes. These isomers have low-lying nπ* and naphthalene-like ππ* states that interact via spin-orbit coupling. In this contribution, we study their structure and electronic...

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Etinski M, Marian CM. A theoretical study of low-lying singlet and triplet excited states of quinazoline, quinoxaline and phthalazine: insight into triplet formation. Phys Chem Chem Phys. 2017;19(21):13828-13837doi: 10.1039/c7cp02022h.
Etinski, M., & Marian, C. M. (2017). A theoretical study of low-lying singlet and triplet excited states of quinazoline, quinoxaline and phthalazine: insight into triplet formation. Physical chemistry chemical physics : PCCP, 19(21), 13828-13837. https://doi.org/10.1039/c7cp02022h
Etinski, Mihajlo, and Marian, Christel M. "A theoretical study of low-lying singlet and triplet excited states of quinazoline, quinoxaline and phthalazine: insight into triplet formation." Physical chemistry chemical physics : PCCP vol. 19,21 (2017): 13828-13837. doi: https://doi.org/10.1039/c7cp02022h
Etinski M, Marian CM. A theoretical study of low-lying singlet and triplet excited states of quinazoline, quinoxaline and phthalazine: insight into triplet formation. Phys Chem Chem Phys. 2017 May 31;19(21):13828-13837. doi: 10.1039/c7cp02022h. PMID: 28513683.
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Crystal structure of 1-isopropyl-4,7-dimethyl-3-nitro-naphthalene.

Acta crystallographica. Section E, Crystallographic communications

Benharref A, Elkarroumi J, El Ammari L, Saadi M, Berraho M.
PMID: 26396890
Acta Crystallogr E Crystallogr Commun. 2015 Aug 15;71:o659-60. doi: 10.1107/S2056989015014395. eCollection 2015 Sep 01.

The title compound, C15H17NO2, was synthesized from a mixture of α-himachalene (2-methyl-ene-6,6,9-tri-methylbi-cyclo-[5.4.0(1,7)]undec-8-ene) and β-himachalene (2,6,6,9-tetra-methylbi-cyclo-[5.4.0(1,7)]undeca-1,8-diene), which were isolated from an oil of the Atlas cedar (Cedrus Atlantica). The naphthalene ring system makes dihedral angles of 68.6 (2) and 44.3...

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Benharref A, Elkarroumi J, El Ammari L, et al. Crystal structure of 1-isopropyl-4,7-dimethyl-3-nitro-naphthalene. Acta Crystallogr E Crystallogr Commun. 2015;71:o659-60doi: 10.1107/S2056989015014395.
Benharref, A., Elkarroumi, J., El Ammari, L., Saadi, M., & Berraho, M. (2015). Crystal structure of 1-isopropyl-4,7-dimethyl-3-nitro-naphthalene. Acta crystallographica. Section E, Crystallographic communications, 71o659-60. https://doi.org/10.1107/S2056989015014395
Benharref, Ahmed, et al. "Crystal structure of 1-isopropyl-4,7-dimethyl-3-nitro-naphthalene." Acta crystallographica. Section E, Crystallographic communications vol. 71 (2015): o659-60. doi: https://doi.org/10.1107/S2056989015014395
Benharref A, Elkarroumi J, El Ammari L, Saadi M, Berraho M. Crystal structure of 1-isopropyl-4,7-dimethyl-3-nitro-naphthalene. Acta Crystallogr E Crystallogr Commun. 2015 Aug 15;71:o659-60. doi: 10.1107/S2056989015014395. eCollection 2015 Sep 01. PMID: 26396890; PMCID: PMC4555421.
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Polychlorinated naphthalene (PCN) emissions from scrap processing steel plants with electric-arc furnaces.

The Science of the total environment

Odabasi M, Dumanoglu Y, Kara M, Altiok H, Elbir T, Bayram A.
PMID: 27637279
Sci Total Environ. 2017 Jan 01;574:1305-1312. doi: 10.1016/j.scitotenv.2016.08.028. Epub 2016 Sep 13.

Polychlorinated naphthalene (PCN) emissions of scrap iron processing steel plants were explored by measuring concentrations in stack gases of five plants, in the atmosphere (n=11) at a site close to those plants, and in soil at several sites in...

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Odabasi M, Dumanoglu Y, Kara M, et al. Polychlorinated naphthalene (PCN) emissions from scrap processing steel plants with electric-arc furnaces. Sci Total Environ. 2016;574:1305-1312doi: 10.1016/j.scitotenv.2016.08.028.
Odabasi, M., Dumanoglu, Y., Kara, M., Altiok, H., Elbir, T., & Bayram, A. (2017). Polychlorinated naphthalene (PCN) emissions from scrap processing steel plants with electric-arc furnaces. The Science of the total environment, 5741305-1312. https://doi.org/10.1016/j.scitotenv.2016.08.028
Odabasi, Mustafa, et al. "Polychlorinated naphthalene (PCN) emissions from scrap processing steel plants with electric-arc furnaces." The Science of the total environment vol. 574 (2017): 1305-1312. doi: https://doi.org/10.1016/j.scitotenv.2016.08.028
Odabasi M, Dumanoglu Y, Kara M, Altiok H, Elbir T, Bayram A. Polychlorinated naphthalene (PCN) emissions from scrap processing steel plants with electric-arc furnaces. Sci Total Environ. 2017 Jan 01;574:1305-1312. doi: 10.1016/j.scitotenv.2016.08.028. Epub 2016 Sep 13. PMID: 27637279.
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Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II).

Journal of fluorescence

Ocak M, Ak T, Aktaş A, Özbek N, Çağılcı OC, Gümrükçüoğlu A, Kantekin H, Ocak Ü, Alp H.
PMID: 27633371
J Fluoresc. 2017 Jan;27(1):59-68. doi: 10.1007/s10895-016-1934-9. Epub 2016 Sep 16.

Four new Schiff base ligands carrying naphthalene groups were prepared from the reaction of 2,4-diamino-6-methyl-1,3,5-triazine and 2,4-diamino-6-undecyl-1,3,5-triazine with 2-hydroxy-1-naphthaldehyde. The influence of a series of metal ions including Cu

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Ocak M, Ak T, Aktaş A, et al. Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II). J Fluoresc. 2016;27(1):59-68doi: 10.1007/s10895-016-1934-9.
Ocak, M., Ak, T., Aktaş, A., Özbek, N., Çağılcı, O. C., Gümrükçüoğlu, A., Kantekin, H., Ocak, �. �., & Alp, H. (2017). Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II). Journal of fluorescence, 27(1), 59-68. https://doi.org/10.1007/s10895-016-1934-9
Ocak, Miraç, et al. "Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II)." Journal of fluorescence vol. 27,1 (2017): 59-68. doi: https://doi.org/10.1007/s10895-016-1934-9
Ocak M, Ak T, Aktaş A, Özbek N, Çağılcı OC, Gümrükçüoğlu A, Kantekin H, Ocak Ü, Alp H. Metal Complexation Properties of Schiff Bases Containing 1,3,5-Triazine Derived from 2-Hydroxy-1-Naphthaldehyde in Solution. A Simple Spectrofluorimetric Method to Determine Mercury (II). J Fluoresc. 2017 Jan;27(1):59-68. doi: 10.1007/s10895-016-1934-9. Epub 2016 Sep 16. PMID: 27633371.
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Showing 1 to 12 of 5263 entries