Log in

Relevant bibliographies by topics / Perillyl alcohol / Journal articles

To see the other types of publications on this topic, follow the link: Perillyl alcohol.

Journal articles on the topic 'Perillyl alcohol'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Perillyl alcohol.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Wagner, Johanna E., Janice L. Huff, William L. Rust, Karl Kingsley, and George E. Plopper. "Perillyl Alcohol Inhibits Breast Cell Migration without Affecting Cell Adhesion." Journal of Biomedicine and Biotechnology 2, no. 3 (2002): 136–40. http://dx.doi.org/10.1155/s1110724302207020.

Full text

Abstract:

The monoterpene d-limonene exhibits chemotherapeutic and chemopreventive potential in breast cancer patients. D-limonene and its related compounds, perillyl alcohol and perillyl aldehyde, were chosen as candidate drugs for application in a screen for nontoxic inhibitors of cell migration. Using the nontumorigenic human breast cell line MCF-10A, we delineated the toxicity as greatest for the perillyl aldehyde, intermediate for perillyl alcohol, and least for limonene. A noncytotoxic concentration of 0.5 mmol/L perillyl alcohol inhibited the migration, while the same concentration of limonene failed to do so. Adhesion of the MCF-10A cell line and the human breast cancer cell line MDA-MB 435 to fibronectin was unaffected by 1.5 mmol/L perillyl alcohol. 0.4 mmol/L perillyl alcohol inhibited the growth of MDA-MB 435 cells. All migration-inhibiting concentrations of perillyl alcohol for MDA-MB 435 cells proved to be toxic. These results suggest that subtoxic doses of perillyl alcohol may have prophylactic potential in the treatment of breast cancer.

APA, Harvard, Vancouver, ISO, and other styles

2

Menéndez, Pilar, Carlos García, Paula Rodríguez, Patrick Moyna, and Horacio Heinzen. "Enzymatic systems involved in D-limonene biooxidation." Brazilian Archives of Biology and Technology 45, no. 2 (June 2002): 111–14. http://dx.doi.org/10.1590/s1516-89132002000200001.

Full text

Abstract:

The biooxidation of limonene by an Aspergillus strain resulted in the production of perillyl alcohol and short chain fatty acids. Addition of ketoconazole, a known inhibitor of cytochrome P450 oxydase, eliminated the production of free acids, but did not affect biotransformation to perillyl alcohol.

APA, Harvard, Vancouver, ISO, and other styles

3

van Beilen, Jan B., René Holtackers, Daniel Lüscher, Ulrich Bauer, Bernard Witholt, and Wouter A. Duetz. "Biocatalytic Production of Perillyl Alcohol from Limonene by Using a Novel Mycobacterium sp. Cytochrome P450 Alkane Hydroxylase Expressed in Pseudomonas putida." Applied and Environmental Microbiology 71, no. 4 (April 2005): 1737–44. http://dx.doi.org/10.1128/aem.71.4.1737-1744.2005.

Full text

Abstract:

ABSTRACT A number of oxygenated monoterpenes present at low concentrations in plant oils have anticarcinogenic properties. One of the most promising compounds in this respect is (−)-perillyl alcohol. Since this natural product is present only at low levels in a few plant oils, an alternative, synthetic source is desirable. Screening of 1,800 bacterial strains showed that many alkane degraders were able to specifically hydroxylate l-limonene in the 7 position to produce enantiopure (−)-perillyl alcohol. The oxygenase responsible for this was purified from the best-performing wild-type strain, Mycobacterium sp. strain HXN-1500. By using N-terminal sequence information, a 6.2-kb ApaI fragment was cloned, which encoded a cytochrome P450, a ferredoxin, and a ferredoxin reductase. The three genes were successfully coexpressed in Pseudomonas putida by using the broad-host-range vector pCom8, and the recombinant converted limonene to perillyl alcohol with a specific activity of 3 U/g (dry weight) of cells. The construct was subsequently used in a 2-liter bioreactor to produce perillyl alcohol on a scale of several grams.

APA, Harvard, Vancouver, ISO, and other styles

4

Geoghegan, Kimberly, and Paul Evans. "Synthesis of (+)-perillyl alcohol from (+)-limonene." Tetrahedron Letters 55, no. 8 (February 2014): 1431–33. http://dx.doi.org/10.1016/j.tetlet.2014.01.039.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Loutrari, Heleni, Maria Hatziapostolou, Vassoula Skouridou, Evangelia Papadimitriou, Charis Roussos, Fragiskos N. Kolisis, and Andreas Papapetropoulos. "Perillyl Alcohol Is an Angiogenesis Inhibitor." Journal of Pharmacology and Experimental Therapeutics 311, no. 2 (June 21, 2004): 568–75. http://dx.doi.org/10.1124/jpet.104.070516.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Xie, Fan, Nathan A. Seifert, Matthias Heger, Javix Thomas, Wolfgang Jäger, and Yunjie Xu. "The rich conformational landscape of perillyl alcohol revealed by broadband rotational spectroscopy and theoretical modelling." Physical Chemistry Chemical Physics 21, no. 28 (2019): 15408–16. http://dx.doi.org/10.1039/c9cp03028j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Benedito, Rubens Batista, Mateus Feitosa Alves, Wendel Batista Pereira, Paula de Arruda Torres, Jéssica Pereira Costa, Adriana da Rocha Tomé, Rita de Cássia da Silveira e Sá, et al. "Perillyl Alcohol: Antinociceptive Effects and Histopathological Analysis in Rodent Brains." Natural Product Communications 12, no. 9 (September 2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200902.

Full text

Abstract:

Perillyl alcohol (PA) is a natural compound found in essential oils. In this study, the antinociceptive activity of PA was evaluated using acetic acid and formalin tests. The involvement of the opioid system in its mechanism of action was investigated. Potential histological changes in the hippocampus and striatum were also assessed. In the acetic acid induced writhing tests, the mice pretreated with PA exhibited significant reductions in writhing. PA inhibited formalin injected paw licking response, and naloxone partially reversed the antinociceptive activity of perillyl alcohol during the writhing test. And as for the histopathological evaluation, PA did not cause significant tissue changes. This study suggests that PA possesses antinociceptive effects without significant hippocampus or striatum neurotoxicity, and that its activity involves opioid.

APA, Harvard, Vancouver, ISO, and other styles

8

García-Carnelli, Carlos, Paula Rodríguez, Horacio Heinzen, and Pilar Pilar Menéndez. "Influence of Culture Conditions on the Biotransformation of (+)-Limonene by Aspergillus niger." Zeitschrift für Naturforschung C 69, no. 1-2 (February 1, 2014): 61–67. http://dx.doi.org/10.5560/znc.2013-0048.

Full text

Abstract:

The influence of the cultivation system and of the culture medium on the biotransformation of (+)-limonene by a strain of Aspergillus niger was investigated. Biooxidation products were obtained in all conditions tested. Using a laboratory bioreactor, six terpenes were identified in every medium, predominantly terpineols and carveols, whereas terpinen-4-ol and perillyl alcohol were the only terpenes found when flasks were used for culture. Perillyl alcohol and carveols predominated when the medium was tryptic soy broth (TSB), whereas the formation of terpineols was clearly favoured in malt broth (MB). Thus, there was a marked influence of the culture conditions on the results of the biotransformation. Changes in the conditions led to variations both in the type and relative amount of products obtained.

APA, Harvard, Vancouver, ISO, and other styles

9

Said, Bastián, Iván Montenegro, Manuel Valenzuela, Yusser Olguín, Nelson Caro, Enrique Werner, Patricio Godoy, Joan Villena, and Alejandro Madrid. "Synthesis and Antiproliferative Activity of New Cyclodiprenyl Phenols against Select Cancer Cell Lines." Molecules 23, no. 9 (September 12, 2018): 2323. http://dx.doi.org/10.3390/molecules23092323.

Full text

Abstract:

Six new cyclodiprenyl phenols were synthesized by direct coupling of perillyl alcohol and the appropriate phenol. Their structures were established by IR, HRMS and mainly NMR. Three human cancer cell lines—breast (MCF-7), prostate (PC-3) and colon (HT-29)—were used in antiproliferative assays, with daunorubicin and dunnione as positive controls. Results described in the article suggest that dihydroxylated compounds 2–4 and monohydroxylated compound 5 display selectivity against cancer cell lines, cytotoxicity, apoptosis induction, and mitochondrial membrane impairment capacity. Compound 2 was identified as the most effective of the series by displaying against all cancer cell lines a cytotoxicity close to dunnione antineoplastic agent, suggesting that the cyclodiprenyl phenols from perillyl alcohol deserve more extensive investigation of their potential medicinal applications.

APA, Harvard, Vancouver, ISO, and other styles

10

Kiran, Ismail. "Microbial Hydroxylation of S-(-)-Perillyl Alcohol by Fusarium heterosporium." Natural Product Communications 6, no. 12 (December 2011): 1934578X1100601. http://dx.doi.org/10.1177/1934578x1100601203.

Full text

Abstract:

S-(-)-Perillyl alcohol ( p-mentha-1, 8-diene-7-ol) (1) (500 mg) was converted by Fusarium heterosporium ATCC 15625 over 10 days at 25°C to a new metabolite, 1,2-dihydroxyperillyl alcohol ( p-mentha-8-en-1,2,7-triol) (3) in a yield of 13% (70 mg). The structure of 3 was established by IR and NMR spectroscopic, specific rotation, and mass spectral studies.

APA, Harvard, Vancouver, ISO, and other styles

11

Fatima, Zeeshan. "Antimycobacterial Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol." SOJ Microbiology & Infectious Diseases 4, no. 4 (December 5, 2016): 1–6. http://dx.doi.org/10.15226/sojmid/4/4/00160.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Geoghegan, Kimberly, and Paul Evans. "ChemInform Abstract: Synthesis of (+)-Perillyl Alcohol from (+)-Limonene." ChemInform 45, no. 30 (July 10, 2014): no. http://dx.doi.org/10.1002/chin.201430198.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Gupta, Abhishek, and Paul B. Myrdal. "Development of a perillyl alcohol topical cream formulation." International Journal of Pharmaceutics 269, no. 2 (January 2004): 373–83. http://dx.doi.org/10.1016/j.ijpharm.2003.09.026.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Miastkowska, Małgorzata, and Paweł Śliwa. "Influence of Terpene Type on the Release from an O/W Nanoemulsion: Experimental and Theoretical Studies." Molecules 25, no. 12 (June 13, 2020): 2747. http://dx.doi.org/10.3390/molecules25122747.

Full text

Abstract:

The interaction between a drug molecule and its carrier’s components is an important factor which influences the drug release profile. For this purpose, molecular dynamics (MD) may be the in silico tool which can help to understand the mechanism of drug loading/release. The aim of this work is to explain the effect of interactions between different types of terpenes, namely perillyl alcohol, forskolin, ursolic acid, and the nanoemulsion droplet core, on the release by means of experimental and theoretical studies. The basic nanoemulsion was composed of caprylic/capric triglyceride as the oil phase, polysorbate 80 as the emulsifier, and water. The in vitro release tests from a terpene-loaded nanoemulsion were carried out to determine the release profiles. The behavior of terpenoids in the nanoemulsion was also theoretically investigated using the molecular dynamics method. The forskolin-loaded nanoemulsion showed the highest percentage of drug release (almost 80% w/w) in contrast to ursolic acid and perillyl alcohol-loaded nanoemulsions (about 53% w/w and 19% w/w, respectively). The results confirmed that the kinetic model of release was terpene-type dependent. The zero-order model was the best to describe the ursolic acid release profile, while the forskolin and the perillyl alcohol followed a first-order and Higuchi model, respectively. Molecular dynamics simulations, especially energetical analysis, confirmed that the driving force of terpenes diffusion from nanoemulsion interior was their interaction energy with a surfactant.

APA, Harvard, Vancouver, ISO, and other styles

15

Matos, Jesus M., C. Max Schmidt, Howard J. Thomas, Oscar W. Cummings, Eric A. Wiebke, James A. Madura, Loehrer J. Patrick, and P. L. Crowell. "A Pilot Study of Perillyl Alcohol in Pancreatic Cancer." Journal of Surgical Research 147, no. 2 (June 2008): 194–99. http://dx.doi.org/10.1016/j.jss.2008.02.005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Cho, Hee-Yeon, Weijun Wang, Niyati Jhaveri, Shering Torres, Joshua Tseng, Michelle N. Leong, David Jungpa Lee, et al. "Perillyl Alcohol for the Treatment of Temozolomide-Resistant Gliomas." Molecular Cancer Therapeutics 11, no. 11 (August 28, 2012): 2462–72. http://dx.doi.org/10.1158/1535-7163.mct-12-0321.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Rajesh, Deepika, Rachelle A. Stenzel, and Steven P. Howard. "Perillyl Alcohol as a Radio-/Chemosensitizer in Malignant Glioma." Journal of Biological Chemistry 278, no. 38 (June 12, 2003): 35968–78. http://dx.doi.org/10.1074/jbc.m303280200.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Stark, M. Jennifer, Yvette D. Burke, Jamie H. McKinzie, A. Siar Ayoubi, and Pamela L. Crowell. "Chemotherapy of pancreatic cancer with the monoterpene perillyl alcohol." Cancer Letters 96, no. 1 (September 1995): 15–21. http://dx.doi.org/10.1016/0304-3835(95)03912-g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Erland, Lauren AE, Christopher R. Bitcon, Ashley D. Lemke, and Soheil S. Mahmoud. "Antifungal Screening of Lavender Essential oils and Essential Oil Constituents on three Post-harvest Fungal Pathogens." Natural Product Communications 11, no. 4 (April 2016): 1934578X1601100. http://dx.doi.org/10.1177/1934578x1601100427.

Full text

Abstract:

A growing body of literature indicates that many synthetic pesticides have adverse effects on human, animal, and environmental health. As a result, plant-derived natural products are quickly gaining momentum as safer and less ecologically damaging alternatives due to their low toxicity, high biodegradability, and good specificity. Essential oils of Lavandula angustifolia, Lavandula x intermedia cv Grosso, and Lavandula x intermedia cv Provence as well as various mono- and sesquiterpene essential oil constituents were tested in order to assess their antifungal potential on three important agricultural pathogens: Botrytis cinerea, Mucor piriformis, and Penicillium expansum. Fungal susceptibility testing was performed using disk diffusion assays. The majority of essential oil constituents tested did not have a significant effect; however, 3-carene, carvacrol, geraniol, nerol and perillyl alcohol demonstrated significant inhibition at concentrations as low as 1 μL/mL. In vivo testing using strawberry fruit as a model system supported in vitro results and revealed that perillyl alcohol, carvacrol and 3-carene were effective in limiting infection by postharvest pathogens.

APA, Harvard, Vancouver, ISO, and other styles

20

Hui, Zi, Meihui Zhang, Lin Cong, Mingyu Xia, and Jinhua Dong. "Synthesis and Antiproliferative Effects of Amino-Modified Perillyl Alcohol Derivatives." Molecules 19, no. 5 (May 22, 2014): 6671–82. http://dx.doi.org/10.3390/molecules19056671.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Matos, Jesus M., Christian M. Schmidt, Thomas J. Howard, Oscar W. Cummings, Eric A. Wiebke, James A. Madura, Patrick J. Loehrer, and Pamela L. Crowell. "QS104. A Pilot Study of Perillyl Alcohol in Pancreatic Cancer." Journal of Surgical Research 144, no. 2 (February 2008): 309. http://dx.doi.org/10.1016/j.jss.2007.12.344.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Yeruva, Laxmi, Casey Hall, John Abiodun Elegbede, and Stephen W. Carper. "Perillyl alcohol and methyl jasmonate sensitize cancer cells to cisplatin." Anti-Cancer Drugs 21, no. 1 (January 2010): 1–9. http://dx.doi.org/10.1097/cad.0b013e32832a68ad.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Nandurkar, Nitin S., Jianjun Zhang, Qing Ye, Larissa V. Ponomareva, Qing-Bai She, and Jon S. Thorson. "The Identification of Perillyl Alcohol Glycosides with Improved Antiproliferative Activity." Journal of Medicinal Chemistry 57, no. 17 (August 25, 2014): 7478–84. http://dx.doi.org/10.1021/jm500870u.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Lee, Chong Ho, Kyung Ho Row, Youn-Woo Lee, Jae-Duck Kim, and Youn Yong Lee. "SUPERCRITICAL FLUID EXTRACTION OF PERILLYL ALCOHOL IN KOREAN ORANGE PEEL." Journal of Liquid Chromatography & Related Technologies 24, no. 13 (August 31, 2001): 1987–96. http://dx.doi.org/10.1081/jlc-100104440.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Silva, Eduardo, Filipe Oliveira, Joana M. Silva, Ana Matias, Rui L. Reis, and Ana Rita C. Duarte. "Optimal Design of THEDES Based on Perillyl Alcohol and Ibuprofen." Pharmaceutics 12, no. 11 (November 20, 2020): 1121. http://dx.doi.org/10.3390/pharmaceutics12111121.

Full text

Abstract:

Therapeutic deep eutectic systems (THEDES) have dramatically expanded their popularity in the pharmaceutical field due to their ability to increase active pharmaceutical ingredients (APIs) bioavailability. However, their biological performance has not yet been carefully scrutinized. Herein, THEDES based on the binary mixture of perillyl alcohol (POH) and ibuprofen (IBU) were prepared using different molar ratios. Our comprehensive strategy includes the characterization of their thermal and structural behavior to identify the molar ratios that successfully form deep eutectic systems. The in vitro solubility of the different systems prepared has demonstrated that, unlike other reported examples, the presence of the terpene did not affect the solubility of the anti-inflammatory agent in a physiological simulated media. The biological performance of the systems was studied in terms of their antimicrobial activity against a wide panel of microorganisms. The examined THEDES showed relevant antimicrobial activity against all tested microbial strains, with the exception of P. aeruginosa. A synergistic effect from the combination of POH and IBU as a eutectic system was verified. Furthermore, the cytotoxic profile of these eutectic systems towards colorectal cancer (CRC) in vitro cell models was also evaluated. The results provide the indication that the cell viability varies in a dose-dependent manner, with a selective THEDES action towards CRC cells. With tunable bioactivities in a ratio-dependent manner, THEDES enhanced the antimicrobial and anticancer properties, representing a possible alternative to conventional therapies. Therefore, this study provides foreseeable indications about the utility of THEDES based on POH and IBU as strong candidates for novel active pharmaceutical systems.

APA, Harvard, Vancouver, ISO, and other styles

26

Imamura, Mitsuru, Oh Sasaki, Katsuhide Okunishi, Kazuyuki Nakagome, Hiroaki Harada, Kimito Kawahata, Ryoichi Tanaka, Kazuhiko Yamamoto, and Makoto Dohi. "Perillyl alcohol suppresses antigen-induced immune responses in the lung." Biochemical and Biophysical Research Communications 443, no. 1 (January 2014): 266–71. http://dx.doi.org/10.1016/j.bbrc.2013.11.106.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Fulton, Gregory J., Lizzie Barber, Einar Svendsen, Per-Otto Hagen, and Mark G. Davies. "Oral Monoterpene Therapy (Perillyl Alcohol) Reduces Vein Graft Intimal Hyperplasia." Journal of Surgical Research 69, no. 1 (April 1997): 128–34. http://dx.doi.org/10.1006/jsre.1997.5047.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Durço, Aimée Obolari, Lino Sérgio Rocha Conceição, Diego Santos de Souza, Carlos Anselmo Lima, Jullyana de Souza Siqueira Quintans, and Márcio Roberto Viana dos Santos. "Perillyl alcohol as a treatment for cancer: A systematic review." Phytomedicine Plus 1, no. 3 (August 2021): 100090. http://dx.doi.org/10.1016/j.phyplu.2021.100090.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Pires Mello, Camilly, Thereza Quirico-Santos, Lídia Fonte Amorim, Viveca Giongo Silva, Lucianne Madeira Fragel, David C. Bloom, and Izabel Palmer Paixão. "Perillyl alcohol and perillic acid exert efficient action upon HSV-1 maturation and release of infective virus." Antiviral Therapy 25, no. 1 (2019): 1–11. http://dx.doi.org/10.3851/imp3315.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Miastkowska, Malgorzata, Monika Konieczna, Elwira Lason, Malgorzata Tabaszewska, Elzbieta Sikora, and Jan Ogonowski. "The Release of Perillyl Alcohol from the Different Kind of Vehicles." Current Pharmaceutical Biotechnology 19, no. 7 (October 1, 2018): 573–80. http://dx.doi.org/10.2174/1389201019666180730165330.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Chen, Thomas, Clovis da Fonseca, and Axel Schönthal. "Intranasal Perillyl Alcohol for Glioma Therapy: Molecular Mechanisms and Clinical Development." International Journal of Molecular Sciences 19, no. 12 (December 6, 2018): 3905. http://dx.doi.org/10.3390/ijms19123905.

Full text

Abstract:

Intracranial malignancies, such as primary brain cancers and brain-localized metastases derived from peripheral cancers, are particularly difficult to treat with therapeutic agents, because the blood-brain barrier (BBB) effectively minimizes brain entry of the vast majority of agents arriving from the systemic circulation. Intranasal administration of cancer drugs has the potential to reach the brain via direct nose-to-brain transport, thereby circumventing the obstacle posed by the BBB. However, in the field of cancer therapy, there is a paucity of studies reporting positive results with this type of approach. A remarkable exception is the natural compound perillyl alcohol (POH). Its potent anticancer activity was convincingly established in preclinical studies, but it nonetheless failed in subsequent clinical trials, where it was given orally and displayed hard-to-tolerate gastrointestinal side effects. Intriguingly, when switched to intranasal delivery, POH yielded highly promising activity in recurrent glioma patients and was well tolerated. As of 2018, POH is the only intranasally delivered compound in the field of cancer therapy (outside of cancer pain) that has advanced to active clinical trials. In the following, we will introduce this compound, summarize its molecular mechanisms of action, and present the latest data on its clinical evaluation as an intranasally administered agent for glioma.

APA, Harvard, Vancouver, ISO, and other styles

32

KOYAMA, MAKOTO, YOSHIHIRO SOWA, TOSHIAKI HITOMI, YOSUKE IIZUMI, MOTOKI WATANABE, TOMOYUKI TANIGUCHI, MASAMI ICHIKAWA, and TOSHIYUKI SAKAI. "Perillyl alcohol causes G1 arrest through p15INK4b and p21WAF1/Cip1 induction." Oncology Reports 29, no. 2 (December 6, 2012): 779–84. http://dx.doi.org/10.3892/or.2012.2167.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Murren, John R., Giuseppe Pizzorno, Susan A. DiStasio, Anne McKeon, Kathleen Peccerillo, Ashwin Gollerkari, Walter McMurray, et al. "Phase I Study of Perillyl Alcohol in Patients with Refractory Malignancies." Cancer Biology & Therapy 1, no. 2 (March 7, 2002): 130–35. http://dx.doi.org/10.4161/cbt.57.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Alonso-Gutierrez, Jorge, Rossana Chan, Tanveer S. Batth, Paul D. Adams, Jay D. Keasling, Christopher J. Petzold, and Taek Soon Lee. "Metabolic engineering of Escherichia coli for limonene and perillyl alcohol production." Metabolic Engineering 19 (September 2013): 33–41. http://dx.doi.org/10.1016/j.ymben.2013.05.004.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Ahn, Ki-Jung, Chung K. Lee, Eun Kyung Choi, Robert Griffin, Chang W. Song, and Heon Joo Park. "Cytotoxicity of perillyl alcohol against cancer cells is potentiated by hyperthermia." International Journal of Radiation Oncology*Biology*Physics 57, no. 3 (November 2003): 813–19. http://dx.doi.org/10.1016/s0360-3016(03)00737-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Fischer, Juliana de Saldanha da Gama, Lujian Liao, Paulo C. Carvalho, Valmir C. Barbosa, Gilberto B. Domont, Maria da Gloria da Costa Carvalho, and John R. Yates. "Dynamic proteomic overview of glioblastoma cells (A172) exposed to perillyl alcohol." Journal of Proteomics 73, no. 5 (March 2010): 1018–27. http://dx.doi.org/10.1016/j.jprot.2010.01.003.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Ansari, Moiz A., Zeeshan Fatima, and Saif Hameed. "Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans." PLOS ONE 11, no. 9 (September 14, 2016): e0162465. http://dx.doi.org/10.1371/journal.pone.0162465.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

LEE, YOUN WOO, CHONG HO LEE, JAE DUCK KIM, YOUN YONG LEE, and KYUNG HO ROW. "Extraction of Perillyl Alcohol in Korean Orange Peel by Supercritical CO2." Separation Science and Technology 35, no. 7 (January 7, 2000): 1069–76. http://dx.doi.org/10.1081/ss-100100211.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Berchtold, Craig M., Kai-Shun Chen, Shigeki Miyamoto, and Michael N. Gould. "Perillyl Alcohol Inhibits a Calcium-Dependent Constitutive Nuclear Factor-κB Pathway." Cancer Research 65, no. 18 (September 15, 2005): 8558–66. http://dx.doi.org/10.1158/0008-5472.can-04-4072.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Ren, Zhibin, and Michael N. Gould. "Inhibition of ubiquinone and cholesterol synthesis by the monoterpene perillyl alcohol." Cancer Letters 76, no. 2-3 (January 30, 1994): 185–90. http://dx.doi.org/10.1016/0304-3835(94)90396-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

d'Alessio, Patrizia A., Jean-François Bisson, and Marie C. Béné. "Anti-Stress Effects of d-Limonene and Its Metabolite Perillyl Alcohol." Rejuvenation Research 17, no. 2 (April 2014): 145–49. http://dx.doi.org/10.1089/rej.2013.1515.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Sundin, Tabetha, Dennis M. Peffley, David Gauthier, and Patricia Hentosh. "The isoprenoid perillyl alcohol inhibits telomerase activity in prostate cancer cells." Biochimie 94, no. 12 (December 2012): 2639–48. http://dx.doi.org/10.1016/j.biochi.2012.07.028.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Row, Kyung Ho, Chong Ho Lee, and Ji Hoon Kang. "Parameter estimation of perillyl alcohol in RP-HPLC by moment analysis." Biotechnology and Bioprocess Engineering 7, no. 1 (February 2002): 16–20. http://dx.doi.org/10.1007/bf02935874.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Garcia, Diogo G., Lidia M. F. Amorim, Mauro V. de Castro Faria, Aline S. Freire, Ricardo E. Santelli, Clóvis O. Da Fonseca, Thereza Quirico-Santos, and Patricia Burth. "The anticancer drug perillyl alcohol is a Na/K-ATPase inhibitor." Molecular and Cellular Biochemistry 345, no. 1-2 (August 6, 2010): 29–34. http://dx.doi.org/10.1007/s11010-010-0556-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Morgan-Meadows, Sherry, Sarita Dubey, Michael Gould, Kendra Tutsch, Rebecca Marnocha, Rhoda Arzoomanin, Dona Alberti, et al. "Phase I trial of perillyl alcohol administered four times daily continuously." Cancer Chemotherapy and Pharmacology 52, no. 5 (November 1, 2003): 361–66. http://dx.doi.org/10.1007/s00280-003-0684-y.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Yeruva, Laxmi, Keon J. Pierre, Abiodun Elegbede, Robert C. Wang, and Stephen W. Carper. "Perillyl alcohol and perillic acid induced cell cycle arrest and apoptosis in non small cell lung cancer cells." Cancer Letters 257, no. 2 (November 2007): 216–26. http://dx.doi.org/10.1016/j.canlet.2007.07.020.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Yapa, Asanka S., Tej B. Shrestha, Sebastian O. Wendel, Madumali Kalubowilage, Jing Yu, Hongwang Wang, Marla Pyle, et al. "Peptide Nanosponges Designed for the Delivery of Perillyl Alcohol to Glioma Cells." ACS Applied Bio Materials 2, no. 1 (December 11, 2018): 49–60. http://dx.doi.org/10.1021/acsabm.8b00305.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

d'Alessio, Patrizia, Massoud Mirshahi, Jean-Francois Bisson, and Marie Bene. "Skin Repair Properties of d-Limonene and Perillyl Alcohol in Murine Models." Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry 13, no. 1 (January 31, 2014): 29–35. http://dx.doi.org/10.2174/18715230113126660021.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Zhang, Zhihong, Haitao Chen, Kenneth K. Chan, Thomas Budd, and Ram Ganapathi. "Gas chromatographic–mass spectrometric analysis of perillyl alcohol and metabolites in plasma." Journal of Chromatography B: Biomedical Sciences and Applications 728, no. 1 (May 1999): 85–95. http://dx.doi.org/10.1016/s0378-4347(99)00065-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

CHANG, HAE C., and PATRICK ORIEL. "Bioproduction of Perillyl Alcohol and Related Monoterpenes by Isolates of Bacillus stearothermophilus." Journal of Food Science 59, no. 3 (May 1994): 660–62. http://dx.doi.org/10.1111/j.1365-2621.1994.tb05588.x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!