Relevant bibliographies by topics / Indole compound

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Indole compound'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Indole compound"

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CHAUBAN, Vishal, Sbivkanya FULORIA, Neeraj K. FULORIA, Syed R. HASHIM, and Sokindra KUMAR. "SYNTHESIS, CHARACTERIZATION AND COMPARATIVE SCREENING OF SOME NEWER 2-PHENYL INDOLE AND 5-CHLORO-2-PHENYL INDOLE DERIVATIVES." SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 20, no. 20 (2012): 69–76. http://dx.doi.org/10.48141/sbjchem.v20.n20.2012.71_revista_2012a.pdf.

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Biologically active phenyl indole and chloro phenyl indole derivatives were efficiently synthesized. The reaction of 2-phenyl-1H-indole A and 5-chloro-2-phenyl-1H-indole B, with chloroacetylchloride yielded 2-chloro-1-(2-phenyl-1H-indol-1-yl)ethanone 1 and 2-chloro-1-(5-chloro-2-phenyl-1H-indol-1-yl)ethanone 4 respectively. Compound 1 and 4 on Friedal Crafts cyclization in presence of aluminium chloride and nitrobenzene yielded indolo[2,1 -alfa]isoquinolin-6(5H)-one 2 and 10-chloroindolo [2,1-alfa]isoquinolin-6(5H)-one 5 respectively, which upon hydrolysis afforded 2-(2-(1H-indol-2-yl)phenyl)a
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Boraei, Ahmed T. A., Ahmed A. M. Sarhan, Sammer Yousuf, and Assem Barakat. "Synthesis of a New Series of Nitrogen/Sulfur Heterocycles by Linking Four Rings: Indole; 1,2,4-Triazole; Pyridazine; and Quinoxaline." Molecules 25, no. 3 (2020): 450. http://dx.doi.org/10.3390/molecules25030450.

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A new series of nitrogen and sulfur heterocyclic systems were efficiently synthesized by linking the following four rings: indole; 1,2,4-triazole; pyridazine; and quinoxaline hybrids. The strength of the acid that catalyzes the condensation of 4-amino-5-(1H-indol-2-yl)-2,4-dihydro-3H-1,2,4-triazole-3-thione 1 with aromatic aldehydes controlled the final product. Reflux in glacial acetic acid yielded Schiff bases 2–6, whereas concentrated HCl in ethanol resulted in a cyclization product at C-3 of the indole ring to create indolo-triazolo-pyridazinethiones 7–16. This fascinating cyclization appr
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Zendah, Imene, Khaled A. Shaaban, Elisabeth Helmke, Armin Maier, Heinz H. Fiebig, and Hartmut Laatsch. "Barakacin: A Thiazolyl-indole Alkaloid Isolated from a Ruminal Pseudomonas sp." Zeitschrift für Naturforschung B 67, no. 5 (2012): 417–20. http://dx.doi.org/10.5560/znb.2011-0277.

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A new thiazolyl-indole alkaloid, barakacin (1), has been isolated from the ruminal bacterium Pseudomonas aeruginosa strain ZIO. On the basis of detailed spectroscopic analyses and comparison with the data of related compounds, its structure has been determined as 2-{4-[bis-(1H-indol-3- yl)-methyl]-thiazol-2-yl}-phenol. In addition, the known compounds phenazine-1-carboxylic acid, 3-(hydroxyacetyl)-indole, indole-3-carbaldehyde, and glycolipid A were isolated. The discovery of compounds with a new skeleton emphasizes the importance for exploring new ecological niches like the rumen of bovines f
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Verma, Vaijinath A., Anand R. Saundane, and Rajkumar S. Meti. "Synthesis of Schiff Base Indolyl-1,3,4-Oxadiazole, Thiazolidinone and Azetidinone as Efficient Antimicrobial, Antioxidant, Antituberculosis and Anticancer Agents." Asian Journal of Organic & Medicinal Chemistry 4, no. 2 (2019): 77–88. http://dx.doi.org/10.14233/ajomc.2019.ajomc-p175.

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The present investigation was under-taken to synthesize the Schiff base indole derivatives bearing of 1,3,4-oxadiazole thiazolidinone and azetidinone moieties. New series of 5-(5-substituted-3-phenyl-1H-indol-2-yl)-N-[(5-substituted-2-phenyl-1H-indol-3-yl)methylene]-1,3,4-oxadiazol-2-amines and screened their biological activities. Compound 4a showed excellent antibacterial and radical scavenging activities. Compound 5a revealed efficient to antifungal activity. In addition, compound 4a was found to be most active against H37Rv strain Mycobacterium tuberculosis. In case of anticancer activity
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Ramkissoon, Antonio, Mohindra Seepersaud, Anderson Maxwell, Jayaraj Jayaraman, and Adesh Ramsubhag. "Isolation and Antibacterial Activity of Indole Alkaloids from Pseudomonas aeruginosa UWI-1." Molecules 25, no. 16 (2020): 3744. http://dx.doi.org/10.3390/molecules25163744.

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In this study, we report the first isolation of three antibiotic indole alkaloid compounds from a Pseudomonad bacterium, Pseudomonas aeruginosa UWI-1. The bacterium was batch fermented in a modified Luria Broth medium and compounds were solvent extracted and isolated by bioassay-guided fractionation. The three compounds were identified as (1) tris(1H-indol-3-yl) methylium, (2) bis(indol-3-yl) phenylmethane, and (3) indolo (2, 1b) quinazoline-6, 12 dione. A combination of 1D and 2D NMR, high-resolution mass spectrometry data and comparison from related data from the literature was used to deter
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Mandadi, Manoj Kumar, Ramana Reddy Bobbala, Balakrishna Kolli, and Rambabu Gundla. "Synthesis and Anticancer Activity of Novel Amide Tagged Trifluoromethyl Indole and Pyrimido Indole Derivatives." Asian Journal of Chemistry 33, no. 10 (2021): 2327–32. http://dx.doi.org/10.14233/ajchem.2021.23313.

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A series of novel amide tagged trifluoromethyl indole and pyrimido indole derivatives 4a-e & 5a-e and 6a-d & 7a-d were synthesized from 4-methyl-2-(methylamino)-6-(trifluoromethyl)isophthalonitrile (1) on reaction with bromoethyl acetate to obtain 2a and 2b isomers. Compound 2a treated with hydrazine hydrate followed by Schiff base reaction to get compounds 4a-e. In another way, compound 2a on reaction with aliphatic primary amine to get compounds 6a-d. For cyclization, compounds 4a-e & 6a-d treated with trifluoroacetic acid to obtain compounds 5a-e and 7a-d, respectively. All the
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Sweidan, Kamal, Dima A. Sabbah, Sanaa Bardaweel, et al. "Facile synthesis, characterization, and cytotoxicity study of new 3-(indol-2-yl)bicyclotetrazatridecahexaens." Canadian Journal of Chemistry 95, no. 8 (2017): 858–62. http://dx.doi.org/10.1139/cjc-2017-0120.

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A new series of thiosemicarbazone-based indole derivatives 12–15 has been prepared by condensation reaction of indole-2-carboxamide derivatives 8–11 with thiosemicarbazide. The former compounds underwent intracyclization in the presence of chloroacetic acid and sodium acetate to afford a set of new 3-(indol-2-yl)bicyclotetrazatridecahexaens 16–19. These newly synthesized compounds have been characterized by means of FTIR, 1H NMR, 13C NMR, and HRMS and by elemental analyses. Cytotoxic activities of the prepared compounds along with LY294002 were evaluated in vitro against normal human skin fibr
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Golubeva, I. S., N. P. Yavorskaya, L. V. Ektova, et al. "ANTITUMOR ACTIVITY OF SOME DERIVATIVES OF INDOLO[2,3-A]CARBAZOLES N-GLYCOSIDES WITH XYLOSE CARBOHYDRATE RESIDUE." Russian Journal of Biotherapy 19, no. 4 (2020): 86–93. http://dx.doi.org/10.17650/1726-9784-2020-19-4-86-93.

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Introduction. The search for new antineoplastic agents in a series of indolo[2,3-a]-carbazole derivatives is an urgent and promising direction, since compounds with antitumor activity have been found in this class. In the chemical fusion laboratory, N.N. Blokhin National Medical Research Center оf the Ministry of Health of Russia has developed an original and effective method for the synthesis of glycosides of indolo[2,3-a]-pyrrolo[3,4-c]carbazoles, which makes it possible to synthesize derivatives of N-glycosides of indolo[2,3-a]carbazoles with different substituents in the heterocyclic parts
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MahamadAlli Shaikh, Tanveer, and Habtamu Debebe. "Synthesis and Evaluation of Antimicrobial Activities of Novel N-Substituted Indole Derivatives." Journal of Chemistry 2020 (April 14, 2020): 1–9. http://dx.doi.org/10.1155/2020/4358453.

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Indole motifs are one of the most significant scaffolds in the discovery of new drugs. We have described a synthesis of new N-substituted indole derivatives (1-3), and their in vitro antimicrobial activities were investigated. The synthesis of titled compounds has been demonstrated by utilizing commercially available starting materials. The antibacterial and antifungal activities were performed using new strains of bacteria Staphylococcus aureus, Escherichia coli, and Candida albicans using the disc diffusion method. Notably, the compound 4-(1-(2-(1H-indol-1-yl) ethoxy) pentyl)-N,N-dimethyl an
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Almutairi, Maha S., Adnan A. Kadi, Reem I. Al-Wabli, Mohamed W. Attwa, and Mohamed I. Attia. "Fragmentation pattern of certain isatin–indole antiproliferative conjugates with application to identify their in vitro metabolic profiles in rat liver microsomes by liquid chromatography tandem mass spectrometry." Open Chemistry 18, no. 1 (2020): 503–15. http://dx.doi.org/10.1515/chem-2020-0095.

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AbstractThe fragmentation pattern of certain isatin-based compounds was carried out using collision-induced dissociation inside the triple quadrupole mass analyzer. These data were used as a clue for the identification of metabolites of the recently reported isatin-based antiproliferative agent, namely, N′-[5-bromo-1-methyl-2-oxo-1,2-dihydro-3H-indol-3-ylidene]-5-methoxy-1H-indole-2-carbohydrazide (1) in rat liver microsomes (RLMs) using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Prediction of the vulnerable sites for metabolic pathways in compound 1 was performed by WhichP450
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Dissertations / Theses on the topic "Indole compound"

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Seira, Naofumi, Naoki Yanagisawa, Akiko Suganami, et al. "Anti-cancer Effects of MW-03, a Novel Indole Compound, by Inducing 15-Hydroxyprostaglandin Dehydrogenase and Cellular Growth Inhibition in the LS174T Human Colon Cancer Cell Line." PHARMACEUTICAL SOC JAPAN, 2017. http://hdl.handle.net/10150/626040.

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Increases in the expression of prostaglandin E2 (PGE2) are widely known to be involved in aberrant growth in the early stage of colon cancer development. We herein demonstrated that the novel indole compound MW-03 reduced PGE2-induced cAMP formation by catalization to an inactive metabolite by inducing 15-hydroxyprostaglandin dehydrogenase through the activation of peroxisome proliferator-activated receptor-γ. MW-03 also inhibited colon cancer cell growth by arresting the cell cycle at the S phase. Although the target of MW-03 for cell cycle inhibition has not yet been identified, these dual a
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Koulibaly, Issa. "Automatisation et optimisation de la synthèse du ((pyridyl-4)-2 ethyl)-3 indole, précurseur d'un antidépresseur." Paris 6, 1986. http://www.theses.fr/1986PA066413.

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Dans le cadre des recherches concernant l'application des techniques d'automatisation et des méthodes d'optimisation, sur les procédés de fabrications industrielles de produits pharmaceutiques, nous avons choisi l'automatisation et l'optimisation de la synthèse d'un précurseur de l'indalpine, qui est un produit pharmaceutique important par ses propriétés d'antidépresseur. Nous montrons, dans la première partie de ce travail, qu'il est possible d'automatiser, à l'échelle du laboratoire, et pour un cout réduit, une synthèse organique complexe à l'aide d'un automate de bas de gamme et de capteurs
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Roffey, Jonathan R. A. "The synthesis of indole containing anticancer compounds." Thesis, Loughborough University, 1996. https://dspace.lboro.ac.uk/2134/10935.

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The concept of bioreductive prodrug chemotherapy is introduced in chapter 1. Tumour cell hypoxia is a significant factor in limiting tumour growth control with conventional radiotherapy and some chemotherapeutic agents. Following therapy these cells can repopulate and cause a relapse of the cancer. On the other hand, hypoxia is unique to tumours, and is therefore potentially exploitable. Bioreductive prodrugs are compounds in which a oxygen inhibited redox-based bioactivation step triggers a reaction leading to a lethal intermediate. The concept of bioreductive DNA alkylators and DNA topoisome
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Souchet, Michel. "Synthese de la (+) anticapsine et d'analogues structuraux : evaluation de leurs proprietes biologiques." Paris 6, 1988. http://www.theses.fr/1988PA066545.

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Synthese du compose du titre et de ses derives perhydro indoliques via la synthese stereoselective d'alcools allyliques. Etude de l'activite inhibatrice des composes synthetises sur la glucosamine synthetase et sur l'enzyme de conversion de l'angiotensine
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Razmutė-Razmė, Inga. "Vibrational spectroscopic studies on the structure and interaction with solution components of bifunctional organic compounds adsorbed at metal electrodes." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2009. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2009~D_20091215_091605-81688.

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The indole and phenole rings comprise the main part of tryptophan and tyrosine side chains in proteins and play an important role in the stabilization of tertiary structure, interaction with active centers in biomolecules, and electron transfer phenomena. To get better insight into the interactions of these functional groups, the artificial monomolecular structures have been constructed from the synthesized bifuncional compounds with thiol and indole or phenole ring functional groups able to form self-assembled monolayers on gold, silver and copper electrodes. Properties of these monolayers we
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Wang, Mingzhong, and 汪明中. "Selective alkylation of indoles catalyzed by gold (I) phosphine complexes and ruthenium (II) porphyrin complexes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B45699501.

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Lam, Shuk-mei, and 林淑媚. "Studies on diazoketone rearrangements and application toward the synthesis of welwistatin." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hdl.handle.net/10722/196009.

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Engqvist, Robert. "Syntheses of some tri- and tetracyclic heterocycles containing an indole moiety /." Stockholm, 2004. http://diss.kib.ki.se/2004/91-7140-161-X/.

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Iwata, Akira. "Development of Novel Methods for Synthesis of Fused Indole-Type Compounds." Kyoto University, 2018. http://hdl.handle.net/2433/232328.

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Somphol, Kittiya Chemistry Faculty of Science UNSW. "Synthesis of new heterocyclic structures based on indoles." Awarded by:University of New South Wales. Chemistry, 2007. http://handle.unsw.edu.au/1959.4/40829.

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Novel indolo-macrocycles have been generated from the attempts to synthesise bis-indolo-cyclotriveratrylenes by the condensation of I, I'-diindolyl-3,3'-dimethanols catalysed by p-toluenesulfonic acid. The addition of substituents on indoles led to enhanced solubilities of the macrocycles. Nine- and six-membered ring compounds have been synthesized from the acid-catalysed reaction of I,I'-diindolyl compounds and aryl aldehydes. Some reactions of these compounds and the attempted synthesis of 2,2' diindolylmethanes from the cyclic compounds have also been described. The electrophilic substitu
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Books on the topic "Indole compound"

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Tirkkonen, Birgit. Stereoselective syntheses in the corynantheine series and of related model compounds. Suomalainen Tiedeakatemia, 1994.

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service), SpringerLink (Online, ed. Heterocyclic Scaffolds II: Reactions and Applications of Indoles. Springer-Verlag Berlin Heidelberg, 2011.

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Costa, Gabriele. I composti indoeuropei con *dus- e *su-. Giardini, 1990.

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Eklund, B. Recommended practices manual for making decisions about vapor intrusion. URS Corp., 2006.

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Charles, Humfrey, Shuker Linda, and Harrison Paul 1953-, eds. IEH assessment on indoor air quality in the home: Nitrogen dioxide, formaldehyde, volatile organic compounds, house dust mites, fung, and bacteria. Institue for Environment and Health, 1996.

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Żarski, Waldemar. Wyrazy złożone w sanskrycie i języku polskim: Z dziejów pojmowania i opisu kategorii morfologicznych. Wydawn. Uniwersytetu Wrocławskiego, 1991.

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1969-, Formichelli Linda, ed. The complete idiot's guide to green cleaning. 2nd ed. Alpha Books, 2009.

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Saarela, Kristina. Rakennusmateriaalien orgaaniset päästöt ja niiden vähentäminen. VAPK-kustannus, 1992.

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Järnström, Helena. Muovimattopinnoitteisen lattiarakenteen VOC-emissiot sisäilmaongelmatapauksissa. VTT, 2005.

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1957-, Kumar M., and Gupta V. 1966-, eds. Heterocyclic chemistry. Springer, 1998.

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Book chapters on the topic "Indole compound"

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Rush, Kent. "Oxidized Nitrogen Derivatives of Indole and Indoline." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186930.ch5.

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Wu, Yong-Jin. "New Indole-Containing Medicinal Compounds." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/7081_2010_37.

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Hess-Kosa, Kathleen. "Volatile Organic Compounds." In Indoor Air Quality. CRC Press, 2018. http://dx.doi.org/10.1201/9781315098180-8.

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Remers, William A. "Indole Aldehydes and Ketones." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186947.ch2.

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Parry, Ronald J. "Biosynthesis of Compounds Containing an Indole Nucleus." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186930.ch1.

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Lebuhn, M., and A. Hartmann. "Indolic and Phenolic Compounds." In Methods in Soil Biology. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-60966-4_17.

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Brown, Robert K. "Synthesis of the Indole Nucleus." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186923.ch2.

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Spande, Thomas F. "Hydroxyindoles, Indole Alcohols, and Indolethiols." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186947.ch1.

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Hess-Kosa, Kathleen. "Microbial Volatile Organic Compounds and Mold Detection." In Indoor Air Quality. CRC Press, 2018. http://dx.doi.org/10.1201/9781315098180-9.

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Tabor, M. Wilson, Eugene Coats, Malcolm Sainsbury, and Howard G. Shertzer. "Antioxidation Potential of Indole Compounds — Structure Activity Studies." In Advances in Experimental Medicine and Biology. Springer New York, 1991. http://dx.doi.org/10.1007/978-1-4684-5877-0_116.

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Conference papers on the topic "Indole compound"

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Jiang, Duohua, Ting Xiao, Weijun Liu, Gang Liu, and Shiqiang Cui. "Sythesis of a novel unsymmetrical photochromic diarylethene compound bearing indole unit." In 2011 4th International Congress on Image and Signal Processing (CISP 2011). IEEE, 2011. http://dx.doi.org/10.1109/cisp.2011.6100548.

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Kanehara, Keigo, Shinobu Ohnuma, Takeshi Naitoh, Michiaki Uuno, and Takaaki Abe. "Abstract 6123: An indole compound MA-35 attenuates tumorigenesis in an inflammation-induced colon cancer model." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-6123.

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Lu, Jianyu, Lihong Hu, Ping Wang, et al. "Abstract 1804: Novel indole compound LX-039 as an oral selective estrogen receptor degrader (SERD) for treating estrogen receptor positive (ER+) breast cancer." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-1804.

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Sevo, Igor, and Tijana Mijatovic. "Segmentation-based compound figure detection and separation methods." In 2016 International Symposium on Industrial Electronics (INDEL). IEEE, 2016. http://dx.doi.org/10.1109/indel.2016.7797794.

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Garcia, Jorge, and Camilo Valencia-Estrada. "Freeform compound concentrators for indoor optical wireless communications." In Nonimaging Optics: Efficient Design for Illumination and Solar Concentration XVII, edited by Roland Winston and Eli Yablonovitch. SPIE, 2020. http://dx.doi.org/10.1117/12.2570779.

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Zhou, Caifa, and Andreas Wieser. "CDM: Compound Dissimilarity Measure and an Application to Fingerprinting-Based Positioning." In 2018 International Conference on Indoor Positioning and Indoor Navigation (IPIN). IEEE, 2018. http://dx.doi.org/10.1109/ipin.2018.8533681.

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PETRAUSKAITĖ, Erika, and Rasa VAIŠKŪNAITĖ. "EXPERIMENTAL STUDY OF DROPLET BIOFILTER PACKED WITH GREEN SPHAGNUM TO CLEAN AIR FROM VOLATILE ORGANIC COMPOUNDS." In Conference for Junior Researchers „Science – Future of Lithuania“. VGTU Technika, 2017. http://dx.doi.org/10.3846/aainz.2017.015.

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Volatile organic compound pollution is one of the problems of outdoor and indoor environment air quality. In order to maintain good air quality, air cleaning technologies are being engaged. One of the recent biological air treatment technology is biofiltration. It is a promising treatment of air from volatile organic compounds (VOCs). Experimental research of droplet biofilter for cleaning VOCs was carried out. Biofilter load of green sphagnum was used with the aim to clean three different concentrations of pollutant toluene. Measurements of biofiltration processes were recorded after 20 and 4
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Liang, Yingbin, Gerhard Kramer, H. Vincent Poor, and Shlomo Shamai. "Recent results on compound wire-tap channels." In 2008 IEEE 19th International Symposium on Personal, Indoor and Mobile Radio Communications (PIMRC). IEEE, 2008. http://dx.doi.org/10.1109/pimrc.2008.4699909.

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Vilcekova, Silvia. "INDOOR AIR POLLUTION CAUSED BY VOLATILE ORGANIC COMPOUNDS." In 15th International Multidisciplinary Scientific GeoConference SGEM2015. Stef92 Technology, 2011. http://dx.doi.org/10.5593/sgem2015/b41/s19.122.

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Neculai, Ana-Maria. "STUDIES ON NATURAL COMPOUNDS WITH GLYCOZIDES WITH RING INDOLIC." In 15th International Multidisciplinary Scientific GeoConference SGEM2015. Stef92 Technology, 2015. http://dx.doi.org/10.5593/sgem2015/b61/s25.076.

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Reports on the topic "Indole compound"

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Loy, Michael David Van. Dynamic behavior of semivolatile organic compounds in indoor air. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/7364.

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McCann, J., L. Horn, J. Girman, and A. V. Nero. Potential risks from exposure to organic compounds in indoor air. Office of Scientific and Technical Information (OSTI), 1988. http://dx.doi.org/10.2172/6111476.

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Essigmann, John M., and Robert G. Croy. Development of Novel Bifunctional Compounds That Induce Apoptosis in Prostate Cancer Cells. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada502889.

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Essigmann, John M. Development of Novel Bifunctional Compounds that Induce Apoptosis in Prostate Cancer Cells. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada437129.

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Essigmann, John M. Development of Novel Bifunctional Compounds that Induce Apoptosis in Prostate Cancer Cells. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada454067.

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Essigmann, John M. Development of Novel Bifunctional Compounds that Induce Apoptosis in Prostate Cancer Cells. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada468546.

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Essigmann, John M. Development of Novel Bifunctional Compounds That Induce Apoptosis in Prostate Cancer Cells. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada425127.

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Essigmann, John M., and Robert G. Croy. Development of Novel Bifunctional Compounds that Induce Apoptosis in Prostate Cancer Cells. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada481546.

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Kuder, Tomasz, Monika Klisch, R. P. Philp, and Thomas McHugh. Use of Compound Specific Stable Isotope Analysis to Distinguish Between Vapor Intrusion and Indoor Sources of VOCs. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada579119.

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McHugh, Thomas, Tomasz Kuder, Monika Klisch, and R. P. Philp. Use of Compound-Specific Stable Isotope Analysis to Distinguish Between Vapor Intrusion and Indoor Sources of VOCs. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada579218.

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