Search Results - "Pinori, M" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

The interaction of myristylated peptides with the catalytic domain of protein kinase C revealed by their sequence palindromy and the identification of a myristyl binding site

The interaction of myristylated peptides with the catalytic domain of protein kinase C revealed by their sequence palindromy and the identification of a myristyl binding site

by Zaliani, A, Pinori, M, Ball, H L, DiGregorio, G, Cremonesi, P, Mascagni, P
Published in Protein engineering (01.09.1998)

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Journal Article

Detection of human antibodies against Plasmodium falciparum sporozoites using synthetic peptides

Detection of human antibodies against Plasmodium falciparum sporozoites using synthetic peptides

by DEL GIUDICE, G, VERDINI, A. S, PINORI, M, PESSI, A, VERHAVE, J.-P, TOUGNE, C, IVANOFF, B, LAMBERT, P.-H, ENGERS, H. D
Published in Journal of Clinical Microbiology (01.01.1987)

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Journal Article

Cyclic pentapeptides of chiral sequence DLDDL as scaffold for antagonism of G-protein coupled receptors: Synthesis, activity and conformational analysis by NMR and molecular dynamics of ITF 1565 a substance P inhibitor

Cyclic pentapeptides of chiral sequence DLDDL as scaffold for antagonism of G-protein coupled receptors: Synthesis, activity and conformational analysis by NMR and molecular dynamics of ITF 1565 a substance P inhibitor

by Porcelli, Massimiliano, Casu, Mariano, Lai, Adolfo, Saba, Giuseppe, Pinori, Massimo, Cappelletti, Silvana, Mascagni, Paolo
Published in Biopolymers (01.08.1999)

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Journal Article

THE USE OF CROWN-ETHERS IN PEPTIDE CHEMISTRY .4. SOLID-PHASE SYNTHESIS OF PEPTIDES USING PEPTIDE-FRAGMENTS N-ALPHA PROTECTED WITH 18-CROWN-6

THE USE OF CROWN-ETHERS IN PEPTIDE CHEMISTRY .4. SOLID-PHASE SYNTHESIS OF PEPTIDES USING PEPTIDE-FRAGMENTS N-ALPHA PROTECTED WITH 18-CROWN-6

by BOTTI, P, BALL, HL, RIZZI, E, LUCIETTO, P, PINORI, M, MASCAGNI, P
Published in Tetrahedron (01.05.1995)

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Journal Article

IMMUNOSTIMULATION BY A PARTIALLY MODIFIED RETRO-INVERSO-TUFTSIN ANALOG CONTAINING THR1-PSI[NHCO](R,S)LYS2 MODIFICATION

IMMUNOSTIMULATION BY A PARTIALLY MODIFIED RETRO-INVERSO-TUFTSIN ANALOG CONTAINING THR1-PSI[NHCO](R,S)LYS2 MODIFICATION

by VERDINI, AS, SILVESTRI, S, BECHERUCCI, C, LONGOBARDI, MG, PARENTE, L, PEPPOLINI, S, PERRETTI, M, PILERI, P, PINORI, M, VISCOMI, GC, NENCIONI, L
Published in Journal of medicinal chemistry (01.12.1991)

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Journal Article

The use of crown ethers in peptide chemistry-V. Solid-phase synthesis of peptides by the fragment condensation approach using crown ethers as non-covalent protecting groups

The use of crown ethers in peptide chemistry-V. Solid-phase synthesis of peptides by the fragment condensation approach using crown ethers as non-covalent protecting groups

by Botti, P, Ball, H L, Lucietto, P, Pinori, M, Rizzi, E, Mascagni, P
Published in Journal of peptide science (01.11.1996)

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Journal Article

Rational design of a new C-myristylamido peptide exerting potent and selective PKC inhibitory activity

Rational design of a new C-myristylamido peptide exerting potent and selective PKC inhibitory activity

by Zaliani, A, Gromo, G, Pinori, M, Mascagni, P
Published in Drug design and discovery (01.04.1996)

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Journal Article

Partially modified and retro-inverted tetrapeptides analogues of c-reactive protein fragments and medicinal composition

Partially modified and retro-inverted tetrapeptides analogues of c-reactive protein fragments and medicinal composition

by S. CAPPELLETTI, A. S. VERDINI, M. PINORI
Year of Publication 15.07.1998

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Patent

Peptide synthesis. VI: Protection of the sulphydryl group of cysteine in solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino acids. Linear oxytocin derivatives

Peptide synthesis. VI: Protection of the sulphydryl group of cysteine in solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino acids. Linear oxytocin derivatives

by ATHERTON, E, PINORI, M, SHEPPARD, R. C
Published in Perkin transactions. 1 (1985)

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Journal Article

Analysis of a bioactive synthetic analogue of tuftsin by tandem mass spectrometry: anomalous fast atom bombardment activated processes

Analysis of a bioactive synthetic analogue of tuftsin by tandem mass spectrometry: anomalous fast atom bombardment activated processes

by De Angelis, F, Nicoletti, R, Kuster, T, Heizmann, C W, Pinori, M, Verdini, A S
Published in Biological mass spectrometry (01.05.1994)

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Journal Article

Solid phase synthesis of retro-inverso peptide analogues. Synthesis of a partially modified retro-inverso analogue of substance P, (Glp super(6), gPhe super(8), mGly super(9))SP sub(6-11) (gPhe = -NHCH (CH sub(2)Ph)NH-, mGly = -OCCH sub(2)CO-)

Solid phase synthesis of retro-inverso peptide analogues. Synthesis of a partially modified retro-inverso analogue of substance P, (Glp super(6), gPhe super(8), mGly super(9))SP sub(6-11) (gPhe = -NHCH (CH sub(2)Ph)NH-, mGly = -OCCH sub(2)CO-)

by Pessi, A, Pinori, M, Verdini, A, Viscomi, G C
Published in Journal of the Chemical Society. Chemical communications (01.01.1983)

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Journal Article

Fast atom bombardment mass spectrometry and selective acid hydrolysis for the analysis of partially modified retro-inverso peptide analogues

Fast atom bombardment mass spectrometry and selective acid hydrolysis for the analysis of partially modified retro-inverso peptide analogues

by De Angelis, F, Ceccarelli, S, Viscomi, G C, Pinori, M, Verdini, A S
Published in Biomedical & environmental mass spectrometry (01.10.1989)

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Journal Article