Log in

Relevant bibliographies by topics / Automatic Solid Phase Peptide Synthesis / Journal articles

To see the other types of publications on this topic, follow the link: Automatic Solid Phase Peptide Synthesis.

Journal articles on the topic 'Automatic Solid Phase Peptide Synthesis'

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 'Automatic Solid Phase Peptide Synthesis.'

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

Mäde, Veronika, Sylvia Els-Heindl, and Annette G. Beck-Sickinger. "Automated solid-phase peptide synthesis to obtain therapeutic peptides." Beilstein Journal of Organic Chemistry 10 (May 22, 2014): 1197–212. http://dx.doi.org/10.3762/bjoc.10.118.

Full text

Abstract:

The great versatility and the inherent high affinities of peptides for their respective targets have led to tremendous progress for therapeutic applications in the last years. In order to increase the drugability of these frequently unstable and rapidly cleared molecules, chemical modifications are of great interest. Automated solid-phase peptide synthesis (SPPS) offers a suitable technology to produce chemically engineered peptides. This review concentrates on the application of SPPS by Fmoc/t-Bu protecting-group strategy, which is most commonly used. Critical issues and suggestions for the s

APA, Harvard, Vancouver, ISO, and other styles

2

Maede, Veronika, Sylvia Els-Heindl, and Annette G. Beck-Sickinger. "ChemInform Abstract: Automated Solid-Phase Peptide Synthesis to Obtain Therapeutic Peptides." ChemInform 46, no. 6 (2015): no. http://dx.doi.org/10.1002/chin.201506294.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

NOKIHARA, Kiyoshi. "Highly Efficient Peptide Synthesis: Automated Simultaneous Multiple Solid-Phase Synthesis and Peptide Library." Journal of Synthetic Organic Chemistry, Japan 52, no. 5 (1994): 347–58. http://dx.doi.org/10.5059/yukigoseikyokaishi.52.347.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Zieleniewski, Francis, Derek N. Woolfson, and Jonathan Clayden. "Automated solid-phase concatenation of Aib residues to form long, water-soluble, helical peptides." Chemical Communications 56, no. 80 (2020): 12049–52. http://dx.doi.org/10.1039/d0cc04698a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Cammish, Linda E., and Steven A. Kates. "ChemInform Abstract: Instrumentation for Automated Solid Phase Peptide Synthesis." ChemInform 31, no. 45 (2000): no. http://dx.doi.org/10.1002/chin.200045267.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Stephenson, Karin A., Sangeeta Ray Banerjee, Nicole McFarlane, et al. "A convenient solid-phase synthesis methodology for preparing peptide-derived molecular imaging agents Synthesis, characterization, and in vitro screening of Tc(I) chemotactic peptide conjugates." Canadian Journal of Chemistry 83, no. 12 (2005): 2060–66. http://dx.doi.org/10.1139/v05-224.

Full text

Abstract:

A versatile solid-phase synthesis strategy for preparing peptidechelate conjugates was developed. The methodology was optimized using a series of ligands, designed to bind Tc(I)/Re(I), and a chemotactic peptide fMFL, which was exploited as a model targeting vector. The peptide derivatives were prepared in parallel using a conventional automated peptide synthesizer in multi-milligram quantities, which provided sufficient material to perform complete characterization, radiolabelling, and in vitro screening studies. Because of the robust nature of the metalchelate complexes, the Re complex of a

APA, Harvard, Vancouver, ISO, and other styles

7

Hurevich, Mattan, and Peter H. Seeberger. "Automated glycopeptide assembly by combined solid-phase peptide and oligosaccharide synthesis." Chem. Commun. 50, no. 15 (2014): 1851–53. http://dx.doi.org/10.1039/c3cc48761j.

Full text

Abstract:

Automated synthesis of glycopeptides was achieved using monosaccharide and amino acid building blocks. Using polystyrene beads equipped with photo-labile linker as solid support, all synthetic manipulations were performed using a single instrument.

APA, Harvard, Vancouver, ISO, and other styles

8

Buckman, Brad, Ameen Ghannam, Angela Li, Meina Liang, Raju Mohan, and Howard Ng. "Automated Parallel Solid-Phase Synthesis of Non-Peptide CCR1 Receptor Antagonists." Combinatorial Chemistry & High Throughput Screening 5, no. 3 (2002): 249–51. http://dx.doi.org/10.2174/1386207024607284.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Zhang, Jing, and Ya Dong Zhang. "Solid Phase Synthesis of Novel Fullerene Nucleotides Conjugates." Advanced Materials Research 266 (June 2011): 200–203. http://dx.doi.org/10.4028/www.scientific.net/amr.266.200.

Full text

Abstract:

N-substituted 3, 4-fullero pyrrolidine was synthesized according to 1, 3-dipolar cycloaddition of the azomethine ylide. Aspartic acid with protected α-amino and α-carboxyl groups was reacted with the activated hydroxyl group of N-substituted 3, 4-fullero pyrrolidine. The products were deprotected, affording the monofullerene aspartic acid (mFas). The conjugate FasT was synthesized by reaction of mFas containing protected amino group with the thymidylic acid derivatived controlled pore glass (CPG) using solid phase synthesis. All of the above fullerene derivatives were characterized by UV–vis,

APA, Harvard, Vancouver, ISO, and other styles

10

Ozerskay, A. V., K. V. Belugin, and O. N. Badmaev. "The use of prosthetic groups for synthesis of addressed RFLP molecules for positron emission tomography." Siberian Medical Review, no. 2 (2021): 84–86. http://dx.doi.org/10.20333/25000136-2021-2-84-86.

Full text

Abstract:

The aim of the research. An intensive research is underway to create new methods for the synthesis of fl uorine-18 labeled radiopharmaceuticals. Th e aim of this work is to select iodoaliphatic carboxylic acids and esters for radiopharmaceuticals labeling. Material and methods. A simple way to obtain z-yodalifi c carbonic acids and complex esters from commercially available cyclic ketones has been developed. Automatic synthesis of 18F-fl uoroproprostatic groups and 18F fl uoride peptide agents is successfully carried out using new original materials and various purifi cation methods with solid

APA, Harvard, Vancouver, ISO, and other styles

11

Sletten, Eric T., Manuel Nuño, Duncan Guthrie, and Peter H. Seeberger. "Real-time monitoring of solid-phase peptide synthesis using a variable bed flow reactor." Chemical Communications 55, no. 97 (2019): 14598–601. http://dx.doi.org/10.1039/c9cc08421e.

Full text

Abstract:

Integration of a pressure-based variable bed flow reactor into an automated solid-phase peptide synthesizer allowed for monitoring of on-resin aggregation and incomplete amide bond formation in real-time.

APA, Harvard, Vancouver, ISO, and other styles

12

Li, Wenyi, Neil M. O'Brien-Simpson, Mohammed Akhter Hossain, and John D. Wade. "The 9-Fluorenylmethoxycarbonyl (Fmoc) Group in Chemical Peptide Synthesis – Its Past, Present, and Future." Australian Journal of Chemistry 73, no. 4 (2020): 271. http://dx.doi.org/10.1071/ch19427.

Full text

Abstract:

The chemical formation of the peptide bond has long fascinated and challenged organic chemists. It requires not only the activation of the carboxyl group of an amino acid but also the protection of the Nα-amino group. The more than a century of continuous development of ever-improved protecting group chemistry has been married to dramatic advances in the chemical synthesis of peptides that, itself, was substantially enhanced by the development of solid-phase peptide synthesis by R. B. Merrifield in the 1960s. While the latter technology has continued to undergo further refinement and improveme

APA, Harvard, Vancouver, ISO, and other styles

13

Lebl, Michal. "Centrifugation Based Automated Synthesis Technologies." JALA: Journal of the Association for Laboratory Automation 8, no. 3 (2003): 30–35. http://dx.doi.org/10.1016/s1535-5535-04-00267-9.

Full text

Abstract:

Centrifugation is a powerful method for solid-liquid separation. It can be applied in numerous ways to simplify solid phase synthetic procedures. At the same time, centrifugation is the only totally parallel technique which can be scaled up for processing volume or number of simultaneously run reactions, without the limitation of overpressure or vacuum-driven filtration-based systems. We have developed synthesizers based on the power of centrifugation — peptide and small organic molecule synthesizers utilizing cotton as the synthetic substrate and inclusion volume chemistry, synthesizers for a

APA, Harvard, Vancouver, ISO, and other styles

14

Kim, Seongsoo, Sang-Myung Lee, Je Pil Yoon, et al. "Robust Magnetized Graphene Oxide Platform for In Situ Peptide Synthesis and FRET-Based Protease Detection." Sensors 20, no. 18 (2020): 5275. http://dx.doi.org/10.3390/s20185275.

Full text

Abstract:

Graphene oxide (GO)/peptide complexes as a promising disease biomarker analysis platform have been used to detect proteolytic activity by observing the turn-on signal of the quenched fluorescence upon the release of peptide fragments. However, the purification steps are often cumbersome during surface modification of nano-/micro-sized GO. In addition, it is still challenging to incorporate the specific peptides into GO with proper orientation using conventional immobilization methods based on pre-synthesized peptides. Here, we demonstrate a robust magnetic GO (MGO) fluorescence resonance energ

APA, Harvard, Vancouver, ISO, and other styles

15

Montanari, Vittorio, and Krishna Kumar. "A Fluorous Capping Strategy for Fmoc-Based Automated and Manual Solid-Phase Peptide Synthesis." European Journal of Organic Chemistry 2006, no. 4 (2006): 874–77. http://dx.doi.org/10.1002/ejoc.200500958.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Olsen, Christian, and Carlos Moreno-Yruela. "Synthesis of Trifluoromethyl Ketone Containing Amino Acid Building Blocks for the Preparation of Peptide-Based Histone Deacetylase (HDAC) Inhibitors." Synthesis 50, no. 20 (2018): 4037–46. http://dx.doi.org/10.1055/s-0037-1609945.

Full text

Abstract:

Trifluoromethyl ketones (TFMKs) are electrophilic moieties which hydrate readily in aqueous media to give geminal diols. This ability has been exploited for the development of histone deacetylase (HDAC) inhibitors, because HDAC enzymes contain a Zn2+ ion which may be chelated by this functionality. Interestingly, TFMKs are exceptional Zn2+-binding groups for targeting the intriguing class IIa HDAC isozymes, involved in transcription factor recruitment and gene regulation. Here, we have developed a scalable and inexpensive synthetic procedure for preparation of the enantiomerically pure TFMK-co

APA, Harvard, Vancouver, ISO, and other styles

17

Wu, Chi-Yue, Wen-Chao Chen, Hui-Ming Yu, Shui-Tein Chen, and Kung-Tsung Wang. "Side Reactions in Peptide Synthesis: Failure of Coupling in Solid-Phase Automatic Synthesis of a Fragment (Sequence 65-74) of the Acyl Carrier Protein." Journal of the Chinese Chemical Society 39, no. 2 (1992): 195–98. http://dx.doi.org/10.1002/jccs.199200032.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Gilpin, R. K., M. E. Gangoda, and S. S. Yang. "An Inlet Manifold for Carrying Out Automated Solid-Phase Peptide Synthesis Using a Standard Liquid Chromatograph." Journal of Chromatographic Science 26, no. 2 (1988): 74–76. http://dx.doi.org/10.1093/chromsci/26.2.74.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Winkler, Dirk F. H., and Kerry Tian. "Investigation of the automated solid-phase synthesis of a 38mer peptide with difficult sequence pattern under different synthesis strategies." Amino Acids 47, no. 4 (2015): 787–94. http://dx.doi.org/10.1007/s00726-014-1909-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Robillard, Marc S., Marina Bacac, Hans van den Elst, et al. "Automated Parallel Solid-Phase Synthesis and Anticancer Screening of a Library of Peptide-Tethered Platinum(II) Complexes." Journal of Combinatorial Chemistry 5, no. 6 (2003): 821–25. http://dx.doi.org/10.1021/cc030011z.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Mocanu, Cosmin Stefan, Monica Jureschi та Gabi Drochioiu. "Aluminium Binding to Modified Amyloid-β Peptides: Implications for Alzheimer’s Disease". Molecules 25, № 19 (2020): 4536. http://dx.doi.org/10.3390/molecules25194536.

Full text

Abstract:

Aluminium (Al) is clearly neurotoxic and considerable evidence exists that Al may play a role in the aetiology or pathogenesis of Alzheimer’s disease (AD). Nevertheless, the link between AD pathology and Al is still open to debate. Therefore, we investigated here the interaction of aluminium ions with two Aβ peptide fragments and their analogues. First, we synthesised by the Fmoc/tBu solid-phase peptide synthesis (SPPS) strategy using an automated peptide synthesiser two new peptides starting from the Aβ(1–16) native peptide fragment. For this purpose, the three histidine residues (H6, H13, an

APA, Harvard, Vancouver, ISO, and other styles

22

de Jong, Remco, Dirk T S. Rijkers, and Rob M J. Liskamp. "Automated Solid-Phase Synthesis and Structural Investigation of -Peptidosulfonamides and -Peptidosulfonamide/-Peptide Hybrids: -Peptidosulfonamide and -Peptide Foldamers are Two of a Different Kind." Helvetica Chimica Acta 85, no. 12 (2002): 4230–43. http://dx.doi.org/10.1002/hlca.200290008.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Coin, Irene, Rudolf Dölling, Eberhard Krause, et al. "Depsipeptide Methodology for Solid-Phase Peptide Synthesis: Circumventing Side Reactions and Development of an Automated Technique via Depsidipeptide Units†,‡." Journal of Organic Chemistry 71, no. 16 (2006): 6171–77. http://dx.doi.org/10.1021/jo060914p.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Serebryakova, L. I., I. M. Studneva, M. V. Ovchinnikov, et al. "Cardiometabolic efficacy and toxicological evaluation of a pharmacological galanin receptor agonist." Biomeditsinskaya Khimiya 65, no. 3 (2019): 231–38. http://dx.doi.org/10.18097/pbmc20196503231.

Full text

Abstract:

The goal of this study was to examine effects of a novel galanin receptor agonist GalR1-3 [bAla14, His15]-galanine 2-15 (G), obtained by automatic solid-phase synthesis, on the metabolic state of the area at risk and the size of acute myocardial infarction (MI) in rats in vivo and evaluate its toxicity in BALB /c mice. In anesthetized rats, regional ischemia was simulated by coronary artery occlusion and then coronary blood flow was restored. The peptide G was administered intravenously (i.v.) with a bolus after a period of regional ischemia in the dose range of 0.25-3.0 mg/kg. The sizes of MI

APA, Harvard, Vancouver, ISO, and other styles

25

Mende, Franziska, Michael Beisswenger, and Oliver Seitz. "Automated Fmoc-Based Solid-Phase Synthesis of Peptide Thioesters with Self-Purification Effect and Application in the Construction of Immobilized SH3 Domains." Journal of the American Chemical Society 132, no. 32 (2010): 11110–18. http://dx.doi.org/10.1021/ja101732a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Van Den Nest, Wim, Shov Yuval, and Fernando Albericio. "Cu(OBt)2 and Cu(OAt)2, copper(II)-based racemization suppressors ready for use in fully automated solid-phase peptide synthesis." Journal of Peptide Science 7, no. 3 (2001): 115–20. http://dx.doi.org/10.1002/psc.299.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Reid, Gavin E., and Richard J. Simpson. "Automated solid-phase peptide synthesis: Use of 2-(1H-benzotriazol-1-yl)-1,1,3,3,-tetramethyluronium tetrafluoroborate for coupling of ert- butyloxycarbonyl amino acids." Analytical Biochemistry 200, no. 2 (1992): 301–9. http://dx.doi.org/10.1016/0003-2697(92)90470-r.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Stephenson, Karin A., Sangeeta Ray Banerjee, Oyebola O. Sogbein, et al. "A New Strategy for the Preparation of Peptide-Targeted Technetium and Rhenium Radiopharmaceuticals. The Automated Solid-Phase Synthesis, Characterization, Labeling, and Screening of a Peptide-Ligand Library Targeted at the Formyl Peptide Receptor." Bioconjugate Chemistry 16, no. 5 (2005): 1189–95. http://dx.doi.org/10.1021/bc0500591.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Torchia, James A., Patrick P. Ng, Homer Chen, et al. "Targeting B-Cell Lymphoma with Idiotype-Specific Peptibodies: Toward a Personalized and Tumor-Specific Therapy." Blood 120, no. 21 (2012): 3713. http://dx.doi.org/10.1182/blood.v120.21.3713.3713.

Full text

Abstract:

Abstract Abstract 3713 Background: The complementarity determining region, or idiotype, of the surface immunoglobulin receptor is a tumor-specific marker on B-cell lymphomas that is unique to each patient. Antibodies against idiotype can induce complete regression of lymphoma in patients, but since this therapeutic approach requires the generation of a custom monoclonal antibody for each patient, it has not been practical. Objective: Here we describe a method for targeting the idiotype on the surface of a B-cell lymphoma by using synthetic idiotype-ligands covalently linked to a recombinant Ig

APA, Harvard, Vancouver, ISO, and other styles

30

Cameron, Linda R., Jill L. Holder, Morten Meldal, and Robert C. Sheppard. "Peptide synthesis. Part 13. Feedback control in solid phase synthesis. Use of fluorenylmethoxycarbonyl amino acid 3,4-dihydro-4-oxo-1,2,3-benzotriazin-3-yl esters in a fully automated system." Journal of the Chemical Society, Perkin Transactions 1, no. 10 (1988): 2895. http://dx.doi.org/10.1039/p19880002895.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Studneva, I. M., M. E. Palkeeva, O. M. Veselova, et al. "Protective action of a modified fragment of galanine in rats with doxorubicin-induced heart failure." Biomeditsinskaya Khimiya 65, no. 1 (2019): 51–56. http://dx.doi.org/10.18097/pbmc20196501051.

Full text

Abstract:

The use of the anticancer drug doxorubicin (Dox) is limited due to its cardiotoxic effect. Using the method of automatic solid-phase peptide synthesis, we obtained a synthetic agonist of galanin receptors GalR1-3 [RAla14, His15]-galanine (2-15) (G), exhibiting cardioprotective properties. It was purified by high performance liquid chromatography (HPLC). The homogeneity and structure of the peptide was confirmed by HPLC, 1H-NMR spectroscopy and mass spectroscopy. The purpose of this study was to study the effect of G on the metabolism and cardiac function of rats with chronic heart failure (CHF

APA, Harvard, Vancouver, ISO, and other styles

32

Gausepohl, Heinrich, and Christian Behn. "ChemInform Abstract: Automated Synthesis of Solid Phase Bound Peptides." ChemInform 33, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.200250243.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Lloyd-Williams, Paul, Fernando Albericio, and Ernest Giralt. "Convergent solid-phase peptide synthesis." Tetrahedron 49, no. 48 (1993): 11065–133. http://dx.doi.org/10.1016/s0040-4020(01)81800-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

LLOYD-WILLIAMS, PAUL, FERNANDO ALBERICIO, and ERNEST GIRALT. "Convergent solid-phase peptide synthesis." International Journal of Peptide and Protein Research 37, no. 1 (2009): 58–60. http://dx.doi.org/10.1111/j.1399-3011.1991.tb00733.x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

KISO, YOSHIAKI, YOICHI FUJIWARA, TOORU KIMURA, AKIKO NISHITANI, and KENICHI AKAJI. "Efficient solid phase peptide synthesis." International Journal of Peptide and Protein Research 40, no. 3-4 (2009): 308–14. http://dx.doi.org/10.1111/j.1399-3011.1992.tb00306.x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Grandas, A., E. Pedroso, E. Giralt, C. Granier, and J. Van Rietschoten. "Convergent solid phase peptide synthesis IV." Tetrahedron 42, no. 24 (1986): 6703–11. http://dx.doi.org/10.1016/s0040-4020(01)82111-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Le´ger, Roger, Rose Yen, Miles W. She, Ving J. Lee, and Scott J. Hecker. "N-Linked solid phase peptide synthesis." Tetrahedron Letters 39, no. 24 (1998): 4171–74. http://dx.doi.org/10.1016/s0040-4039(98)00777-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Felix, Arthur M. "SOLID-PHASE PEPTIDE SYNTHESIS. Bruce Merrifield." Kobunshi 51, no. 8 (2002): 630–32. http://dx.doi.org/10.1295/kobunshi.51.630.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Krchňák, Viktor, Josef Vágner, Martin Flegel, and Otakar Mach. "Continuous-flow solid-phase peptide synthesis." Tetrahedron Letters 28, no. 38 (1987): 4469–72. http://dx.doi.org/10.1016/s0040-4039(00)96541-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Giralt, Ernest, Ramon Eritja, Enrique Pedroso, Claude Granier, and Jurphaas Van Rietschoten. "Convergent solid phase peptide synthesis-III." Tetrahedron 42, no. 2 (1986): 691–98. http://dx.doi.org/10.1016/s0040-4020(01)87472-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Ramage, R., J. Green, and O. M. Ogunjobi. "Solid phase peptide synthesis of ubiquitin." Tetrahedron Letters 30, no. 16 (1989): 2149–52. http://dx.doi.org/10.1016/s0040-4039(01)93735-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

O'Donnell, Martin J., Changyou Zhou, and William L. Scott. "Solid-Phase Unnatural Peptide Synthesis (UPS)." Journal of the American Chemical Society 118, no. 25 (1996): 6070–71. http://dx.doi.org/10.1021/ja9601245.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

MERRIFIELD, B. "ChemInform Abstract: Solid-Phase Peptide Synthesis." ChemInform 27, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199629275.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

WALKER, B. "ChemInform Abstract: Solid-Phase Peptide Synthesis." ChemInform 27, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199629279.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

DAVIES, J. S. "ChemInform Abstract: Solid Phase Peptide Synthesis." ChemInform 26, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199532286.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Fields, Gregg B. "ChemInform Abstract: Solid-Phase Peptide Synthesis." ChemInform 30, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199913316.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Ferderigos, Nikolas, and Christos Zikos. "ChemInform Abstract: Solid-Phase Peptide Synthesis." ChemInform 43, no. 39 (2012): no. http://dx.doi.org/10.1002/chin.201239267.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

HANSEN, PAUL ROBERT, ARNE HOLM, and GUNNAR HOUEN. "Solid-phase peptide synthesis on proteins." International Journal of Peptide and Protein Research 41, no. 3 (2009): 237–45. http://dx.doi.org/10.1111/j.1399-3011.1993.tb00331.x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Ghassemian, Artin, Xavier Vila-Farrés, Paul F. Alewood, and Thomas Durek. "Solid phase synthesis of peptide-selenoesters." Bioorganic & Medicinal Chemistry 21, no. 12 (2013): 3473–78. http://dx.doi.org/10.1016/j.bmc.2013.03.076.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Stewart, John M. "Bradykinin in Solid-phase Peptide Synthesis." International Journal of Peptide Research and Therapeutics 13, no. 1-2 (2006): 3–5. http://dx.doi.org/10.1007/s10989-006-9043-2.

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!