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A dozen years of retro-inverso peptidomimetics
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bip.360220806openalex-snapshot
Computer simulation of the conformational properties of retro–inverso peptides. I. Empirical force field calculations of rigid and flexible geometries of N‐acetylglycine‐N′‐ methylamide, bis(acetamido) methane, and N, N′‐ dimethylmalonamide and their corresponding Cα‐methylated analogs
inferredcites →https://doi.org/10.1002/bip.360220807openalex-snapshot
Computer simulation of the conformational properties of retro–inverso peptides. II. Ab initio study, spatial electron distribution, and population analysis of N‐formylglycine methylamide, N‐formyl N′‐acetyldiaminomethane, and N‐methylmalonamide
inferredcites →https://doi.org/10.1002/bip.360221207openalex-snapshot
Extended retro‐inverso analogs of somatostatin
inferredcites →https://doi.org/10.1002/bip.360260909openalex-snapshot
Conformational studies of diastereomeric cyclic enkephalins by 1H‐NMR and computer simulations
inferredcites →https://doi.org/10.1002/bip.360311307openalex-snapshot
Cyclic retro–inverso dipeptides with two aromatic side chains. I. Synthesis
inferredcites →https://doi.org/10.1002/bip.360311308openalex-snapshot
Cyclic retro–inverso dipeptides with two aromatic side chains. II. Conformational analysis
inferredcites →https://doi.org/10.1002/chir.530030410openalex-snapshot
Absolute configuration for peptidomimetic residues in bioactive peptides
inferredcites →https://doi.org/10.1016/0006-291x(85)91895-9openalex-snapshot
Octapeptide analogs of somatostatin exhibiting greatly enhanced in vivo and in vitro inhibition of growth hormone secretion in the rat
inferredcites →https://doi.org/10.1016/0006-291x(87)90627-9openalex-snapshot
Modified peptides which display potent and specific inhibition of human renin
inferredcites →https://doi.org/10.1016/0006-291x(89)92757-5openalex-snapshot
Inhibition of protein kinase C by retro-inverso pseudosubstrate analogues
inferredcites →https://doi.org/10.1016/0014-2999(86)90363-8openalex-snapshot
Metabolically stable analogues of substance P: Persistent action of partially modified retro-inverso analogues of substance P on rat parotid and hypothalamic slices
inferredcites →https://doi.org/10.1016/0196-9781(88)90130-1openalex-snapshot
Enzyme-resistant CCK analogs with high affinities for central receptors
inferredcites →https://doi.org/10.1016/0196-9781(89)90188-5openalex-snapshot
External pancreatic secretion in the rat: Supramaximal inhibition induced by the cholecystokinin octapeptide [CCK(26–33)] and analogs altered on the 28–29 bond
inferredcites →https://doi.org/10.1016/s0006-291x(87)80174-2openalex-snapshot
Relationship between the inhibitory potencies of thiorphan and retrothiorphan enantiomers on thermolysin and neutral endopeptidase 24.11 and their interactions with the thermolysin active site by computer modelling
inferredcites →https://doi.org/10.1016/s0040-4020(01)86144-5openalex-snapshot
Peptide and pseudopeptide analogues of cholecystokinin, chemical modifications of the met28-gly29 region
inferredcites →https://doi.org/10.1016/s0040-4039(00)99406-1openalex-snapshot
Reaction of trimethylsilyl derivatives with Meldrum's acid : A new and easy monofunctionalization of malonic acid
inferredcites →https://doi.org/10.1021/ar00061a001openalex-snapshot
Quantum-chemistry and catalysis in oxidation of hydrocarbons
inferredcites →https://doi.org/10.1021/ar50133a001openalex-snapshot
On the concept of linear modified retro-peptide structures
inferredcites →https://doi.org/10.1021/bi00329a020openalex-snapshot
Partial retro-inverso analogs of somatostatin: pairwise modifications at residues 7 and 8 and at residues 8 and 9
inferredcites →https://doi.org/10.1021/bi00371a050openalex-snapshot
Computer simulations of cyclic enkephalin analogs
inferredcites →https://doi.org/10.1021/bi00371a051openalex-snapshot
Conformational analysis of cyclic partially modified retro-inverso enkephalin analogs by proton NMR
inferredcites →https://doi.org/10.1021/bi00430a011openalex-snapshot
Thiorphan and retro-thiorphan display equivalent interactions when bound to crystalline thermolysin
inferredcites →https://doi.org/10.1021/ja00157a077openalex-snapshot
Temperature-dependent changes in the folding pattern of a simple triamide
inferredcites →https://doi.org/10.1021/ja00180a040openalex-snapshot
Crystal structure of two retro-inverso sweeteners
inferredcites →https://doi.org/10.1021/ja00249a040openalex-snapshot
Model for the sweet taste of stereoisomeric retro-inverso and dipeptide amides
inferredcites →https://doi.org/10.1021/ja00783a034openalex-snapshot
Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters
inferredcites →https://doi.org/10.1021/jm00086a017openalex-snapshot
Amide bond replacements incorporated into CCK-B selective "dipeptoids"
inferredcites →https://doi.org/10.1021/jm00116a005openalex-snapshot
Immunostimulation by a partially modified retro-inverso-tuftsin analog containing Thr1.sum..psi.[NHCO](R,S)Lys2 modification
inferredcites →https://doi.org/10.1021/jm00117a025openalex-snapshot
Retro-inverso concept applied to the complete inhibitors of enkephalin-degrading enzymes
inferredcites →https://doi.org/10.1021/jm00130a018openalex-snapshot
Synthesis and biological activity of some partially modified retro-inverso analogs of cholecystokinin
inferredcites →https://doi.org/10.1021/jm00155a027openalex-snapshot
Proton NMR configurational correlation for retro-inverso dipeptides: application to the determination of the absolute configuration of "enkephalinase" inhibitors. Relationships between stereochemistry and enzyme recognition
inferredcites →https://doi.org/10.1021/jm00354a008openalex-snapshot
Synthesis and pharmacological characterization in vitro of cyclic enkephalin analogs: effect of conformational constraints on opiate receptor selectivity
inferredcites →https://doi.org/10.1021/jm00356a003openalex-snapshot
Synthesis of partially modified retro-inverso substance P analogs and their biological activity
inferredcites →https://doi.org/10.1021/jm00383a013openalex-snapshot
Synthesis and pharmacological activity of partially modified retro-inverso dermorphin tetrapeptides
inferredcites →https://doi.org/10.1021/jo00294a042openalex-snapshot
Benzotriazole-assisted synthesis of monoacyl aminals and their peptide derivatives
inferredcites →https://doi.org/10.1021/jo00297a039openalex-snapshot
Synthesis, biological testing, and stereochemical assignment of an end group modified retro-inverso bombesin C-terminal nonapeptide
inferredcites →https://doi.org/10.1021/jo00364a055openalex-snapshot
N4-(Malonyl-D-cysteinyl)-L-2,4-diaminobutyrate: the end-group-modified retro-inverso isomer of glutathione
inferredcites →https://doi.org/10.1021/jo00369a035openalex-snapshot
Differentially protected .alpha.-aminoglycine
inferredcites →https://doi.org/10.1021/jo01324a048openalex-snapshot
New method for direct conversion of amides to amines
inferredcites →https://doi.org/10.1038/292055a0openalex-snapshot
A potent cyclic hexapeptide analogue of somatostatin
inferredcites →https://doi.org/10.1039/c39790000615openalex-snapshot
Cleavage of benzyl ethers with [bis(trifluoroacetoxy)iodo]benzene
inferredcites →https://doi.org/10.1039/c39820000280openalex-snapshot
Preparation of optically pure monoacyl 2-alkyl gem-diamines from peptide amides
inferredcites →https://doi.org/10.1039/c39830000195openalex-snapshot
Solid phase synthesis of retro-inverso peptide analogues. Synthesis of a partially modified retro-inverso analogue of substance P, [Glp 6 , gPhe 8 , mGly 9 ] SP 6–11 [gPhe =–NHCH(CH 2 Ph)NH–,mGly =–OCCH 2 CO–]
inferredcites →https://doi.org/10.1039/p19850000697openalex-snapshot
Synthesis, resolution, and assignment of configuration of potent hypotensive retro-inverso bradykinin potentiating peptide 5a(BPP5a) analogues
inferredcites →https://doi.org/10.1039/p19850002277openalex-snapshot
Some applications of the Curtius rearrangement
inferredcites →https://doi.org/10.1055/s-1985-31183openalex-snapshot
Synthesis of Optically Pure 5-Aminopyrrolidin-2-one Formic Acid Salt: A Key Intermediate for the Incorporation of the Pyroglutamyl Geminal Diamino Analogue intoRetro-InversoPeptides
inferredcites →https://doi.org/10.1073/pnas.77.12.7162openalex-snapshot
A cyclic enkephalin analog with high in vitro opiate activity.
inferredcites →https://doi.org/10.1073/pnas.80.11.3178openalex-snapshot
Complete differentiation between enkephalinase and angiotensin-converting enzyme inhibition by retro-thiorphan.
inferredcites →https://doi.org/10.1107/s0108768191011771openalex-snapshot
Synthesis and structure of new bronchospasmolytic agents. I
inferredcites →https://doi.org/10.1111/j.1399-3011.1979.tb01844.xopenalex-snapshot
THE SEPARATION OF PEPTIDE HORMONE DIASTEREOISOMERS BY REVERSE PHASE HIGH PRESSURE LIQUID CHROMATOGRAPHY
inferredcites →https://doi.org/10.1111/j.1399-3011.1981.tb01970.xopenalex-snapshot
TOPOCHEMICALLY RELATED HORMONE STRUCTURES: Synthesis of Partial Retro‐Inverso Analogs of LH‐RH
inferredcites →https://doi.org/10.1111/j.1399-3011.1983.tb03081.xopenalex-snapshot
Approaches to the synthesis of retro‐inverso peptides
inferredcites →https://doi.org/10.1111/j.1399-3011.1984.tb03133.xopenalex-snapshot
Synthesis of cyclic and acyclic partial retro‐inverso modified enkephalins
inferredcites →https://doi.org/10.1111/j.1399-3011.1984.tb03159.xopenalex-snapshot
Solid phase synthesis of retro‐inverso peptide analogues
inferredcites →https://doi.org/10.1111/j.1399-3011.1985.tb02206.xopenalex-snapshot
Synthesis and opioid activity of partial retro‐inverso analogs of dermorphin
inferredcites →https://doi.org/10.1111/j.1399-3011.1985.tb02222.xopenalex-snapshot
Synthesis and biological activity of linear and cyclic enkephalins modified at the Gly3‐Phe4amide bond
inferredcites →https://doi.org/10.1111/j.1399-3011.1988.tb00925.xopenalex-snapshot
Synthesis and activity of partial retro‐inverso modified atrial natriuretic factor analogs
inferredcites →https://doi.org/10.1111/j.1399-3011.1989.tb00200.xopenalex-snapshot
Enkephalin‐degrading enzyme inhibitors Crucial role of theC‐terminal residue on the inhibitory potencies of retro‐hydroxamate dipeptides
inferredcites →https://doi.org/10.1111/j.1399-3011.1989.tb01397.xopenalex-snapshot
Conformational perturbations in retro‐analogs of the tBuCO‐Ala‐Gly‐NHiPr dipeptide Crystal structure of the retro‐dipeptide with a reversed Ala‐Gly amide bond
inferredcites →https://doi.org/10.1111/j.1399-3011.1990.tb01300.xopenalex-snapshot
Cyclic hexapeptides related to somatostatin Synthesis and biological testing
inferredcites →https://doi.org/10.1111/j.1399-3011.1990.tb01301.xopenalex-snapshot
Cyclic hexapeptides related to somatostatin Conformational analysis employing 1H‐NMR and molecular dynamics
inferredcites →https://doi.org/10.1111/j.1399-3011.1992.tb00784.xopenalex-snapshot
14‐Membered cyclic opioids related to dermorphin and their partially retro‐inverso modified analogues
inferredcites →https://doi.org/10.1111/j.1399-3011.1992.tb00785.xopenalex-snapshot
14‐Membered cyclic opioids related to dermorphin and their partially retro‐inverso modified analogues II. Preferred conformations in solution as studied by1H‐NMR spectroscopy
inferredcites →https://doi.org/10.1126/science.451565openalex-snapshot
Partially Modified Retro-Inverso-Enkephalinamides: Topochemical Long-Acting Analogs in Vitro and in Vivo
inferredcites →https://doi.org/10.1135/cccc19882519openalex-snapshot
Partially modified retro-inverso enkephalin analogues containing Gly3Ψ(NH-CO)Phe4 modification, Configurational lability
inferredcites →https://doi.org/10.1248/cpb.38.3042openalex-snapshot
Synthesis of human renin inhibitory peptides, angiotensinogen transition-state analogs containing a Retro-inverso amide bond.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4601993openalex-extracted
Synthesis and Cytotoxicity Evaluation of Retro-Inverso Analog of Antitumor Bicyclic Hexapeptide Ra-Vii
inferred← citeshttps://doi.org/10.1002/(sici)1097-0282(1996)40:1<45::aid-bip3>3.0.co;2-3openalex-snapshot
Crystal structures of peptides and modified peptides
inferred← citeshttps://doi.org/10.1002/(sici)1097-0282(19970415)41:5<555::aid-bip7>3.0.co;2-lopenalex-snapshot
Peptides containing the sulfonamide junction: Synthesis, structure, and conformation of Z-Tau-Pro-Phe-NHiPr
inferred← citeshttps://doi.org/10.1002/(sici)1097-0282(19970415)41:5<569::aid-bip8>3.0.co;2-kopenalex-snapshot
Structural comparison between retro-inverso and parent peptides: Molecular basis for the biological activity of a retro-inverso analogue of the immunodominant fragment of VP1 coat protein from foot-and-mouth disease virus
inferred← citeshttps://doi.org/10.1002/(sici)1097-0282(199802)45:2<149::aid-bip5>3.0.co;2-sopenalex-snapshot
An experimental Ramachandran plot for retropeptide derivatives: Conformational features of derivatives of GEM-diamino and malonyl amino acids
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199805)1998:5<827::aid-ejoc827>3.0.co;2-bopenalex-snapshot
β-Homoalanyl-PNA: A Special Case of β-Peptides with β-Sheet-Like Backbone Conformation; Organization in Higher Ordered Structures
inferred← citeshttps://doi.org/10.1002/(sici)1521-4141(199908)29:08<2560::aid-immu2560>3.0.co;2-xopenalex-snapshot
Inhibition of experimental autoimmune encephalomyelitis in SJL mice by oral administration of retro-inverso derivative of encephalitogenic epitope P87 – 99
inferred← citeshttps://doi.org/10.1002/0471266949.bmc014openalex-snapshot
Peptidomimetics for Drug Design
inferred← citeshttps://doi.org/10.1002/1097-0282(2001)60:4<322::aid-bip9993>3.0.co;2-yopenalex-snapshot
Extended form of a retro-inverso peptide stabilized by ?-sheet unidirectional H-bonds: Crystallographic and NMR evidence
inferred← citeshttps://doi.org/10.1002/1873-3468.13558openalex-snapshot
Computational investigation of retro‐isomer equilibrium structures: Intrinsically disordered, foldable, and cyclic peptides
inferred← citeshttps://doi.org/10.1002/9783527613502.ch07openalex-snapshot
Combinatorial Synthetic Oligomers
inferred← citeshttps://doi.org/10.1002/9783527614912.ch02openalex-snapshot
Polymer Supported Organic Synthesis: A Review
inferred← citeshttps://doi.org/10.1002/9783527626038.ch7openalex-snapshot
Peptide and Protein Design, Pseudopeptides, and Peptidomimetics
inferred← citeshttps://doi.org/10.1002/ange.19941061705openalex-snapshot
Peptidmimetica – maßgeschneiderte Enzyminhibitoren
inferred← citeshttps://doi.org/10.1002/ange.19951070811openalex-snapshot
Festphasensynthese nicht natürlicher Biopolymere mit sich wiederholenden Harnstoffeinheiten
inferred← citeshttps://doi.org/10.1002/ange.19961080104openalex-snapshot
Organische Chemie an fester Phase
inferred← citeshttps://doi.org/10.1002/ange.200250711openalex-snapshot
Highly Stereoselective Tandem Aza‐Michael Addition–Enolate Protonation to Form Partially Modified Retropeptide Mimetics Incorporating a Trifluoroalanine Surrogate
inferred← citeshttps://doi.org/10.1002/ange.200460312openalex-snapshot
Verknoten und Durchfädeln von Molekülen: Chemie und Chiralität molekularer Knoten und ihrer Ensembles
inferred← citeshttps://doi.org/10.1002/ange.201405109openalex-snapshot
Rational Design and Identification of a Non‐Peptidic Aggregation Inhibitor of Amyloid‐β Based on a Pharmacophore Motif Obtained from cyclo[‐Lys‐Leu‐Val‐Phe‐Phe‐]
inferred← citeshttps://doi.org/10.1002/ange.201807298openalex-snapshot
Oral aktive Peptide: Gibt es ein Patentrezept?
inferred← citeshttps://doi.org/10.1002/anie.199416991openalex-snapshot
Peptidomimetics—Tailored Enzyme Inhibitors
inferred← citeshttps://doi.org/10.1002/anie.199509071openalex-snapshot
Solid‐Phase Syntheses of Unnatural Biopolymers Containing Repeating Urea Units
inferred← citeshttps://doi.org/10.1002/anie.199600171openalex-snapshot
Organic Chemistry on Solid Supports
inferred← citeshttps://doi.org/10.1002/anie.200250711openalex-snapshot
Highly Stereoselective Tandem Aza‐Michael Addition–Enolate Protonation to Form Partially Modified Retropeptide Mimetics Incorporating a Trifluoroalanine Surrogate
inferred← citeshttps://doi.org/10.1002/anie.200460312openalex-snapshot
Knotting and Threading of Molecules: Chemistry and Chirality of Molecular Knots and Their Assemblies
inferred← citeshttps://doi.org/10.1002/anie.201405109openalex-snapshot
Rational Design and Identification of a Non‐Peptidic Aggregation Inhibitor of Amyloid‐β Based on a Pharmacophore Motif Obtained from cyclo[‐Lys‐Leu‐Val‐Phe‐Phe‐]
inferred← citeshttps://doi.org/10.1002/anie.201807298openalex-snapshot
Orally Active Peptides: Is There a Magic Bullet?
inferred← citeshttps://doi.org/10.1002/bip.10202openalex-snapshot
Osteogenic growth peptide: From concept to drug design
inferred← citeshttps://doi.org/10.1002/bip.20219openalex-snapshot
The partial retro–inverso modification: A road traveled together
inferred← citeshttps://doi.org/10.1002/bip.20954openalex-snapshot
Bruce Merrifield's contribution to antimicrobial peptide research
inferred← citeshttps://doi.org/10.1002/chem.200304881openalex-snapshot
Synthesis, Structure and Conformation of Partially‐Modified Retro‐ and Retro‐Inverso ψ[NHCH(CF3)]Gly Peptides
inferred← citeshttps://doi.org/10.1002/chem.200600560openalex-snapshot
1,3,5‐Triazepan‐2,6‐diones as Structurally Diverse and Conformationally Constrained Dipeptide Mimetics: Identification of Malaria Liver Stage Inhibitors from a Small Pilot Library
inferred← citeshttps://doi.org/10.1002/chem.200800359openalex-snapshot
Supramolecular Bidentate Ligands by Metal‐Directed in situ Formation of Antiparallel β‐Sheet Structures and Application in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202002637openalex-snapshot
N,N‐Diacylaminals as Emerging Tools in Synthesis: From Peptidomimetics to Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/chin.199337336openalex-snapshot
ChemInform Abstract: A Dozen Years of Retro‐Inverso Peptidomimetics
inferred← citeshttps://doi.org/10.1002/chin.199748329openalex-snapshot
ChemInform Abstract: Design, Synthesis, and Study of Artificial β‐Sheets
inferred← citeshttps://doi.org/10.1002/cmdc.200800407openalex-snapshot
Synthesis and Conformational Analysis of Cyclotetrapeptide Mimetic β‐Turn Templates and Validation as 3D Scaffolds
inferred← citeshttps://doi.org/10.1002/eji.1830270614openalex-snapshot
A retro‐inverso analog mimicks the cognate peptide epitope of a CD4+ T cell clone
inferred← citeshttps://doi.org/10.1002/ejoc.200400242openalex-snapshot
Total Synthesis of Sequential Retro‐Peptide Oligomers
inferred← citeshttps://doi.org/10.1002/ejoc.200601010openalex-snapshot
Succinimidyl Carbamate Derivatives from N‐Protected α‐Amino Acids and Dipeptides―Synthesis of Ureidopeptides and Oligourea/Peptide Hybrids
inferred← citeshttps://doi.org/10.1002/ejoc.200700932openalex-snapshot
Cyclotetrapeptide Mimics Based on a 13‐Membered, Partially Modified Retro‐Inverso Structure
inferred← citeshttps://doi.org/10.1002/hlca.201100347openalex-snapshot
Preparation of Pseudo‐Peptide Building Blocks with retro‐Thioamide Bond Mediated via Thiocarbamoyl Meldrum's Acid
inferred← citeshttps://doi.org/10.1002/pep2.24048openalex-snapshot
Peptide therapeutics that directly target transcription factors
inferred← citeshttps://doi.org/10.1002/psc.1306openalex-snapshot
A retro‐inverso α‐melanocyte stimulating hormone analog with MC1R‐binding selectivity
inferred← citeshttps://doi.org/10.1002/psc.480openalex-snapshot
What to synthesize? from Emil Fischer to peptidomics
inferred← citeshttps://doi.org/10.1002/psc.833openalex-snapshot
Crystal‐state 3D‐structural characterization of novel, Aib‐based, turn and helical peptides
inferred← citeshttps://doi.org/10.1002/tcr.201600005openalex-snapshot
D‐Peptides as Recognition Molecules and Therapeutic Agents
inferred← citeshttps://doi.org/10.1006/jmre.2002.2573openalex-snapshot
Proton Dipolar Recoupling in Resin-Bound Peptides under High-Resolution Magic Angle Spinning
inferred← citeshttps://doi.org/10.1007/0-306-46864-6_269openalex-snapshot
Peptide analogues as vaccines and immunomodulators
inferred← citeshttps://doi.org/10.1007/0-306-46881-6_274openalex-snapshot
A CD28 CDR3 peptide analog inhibits CD4+ T-cell proliferation in vitro
inferred← citeshttps://doi.org/10.1007/0-306-46881-6_65openalex-snapshot
Partially-modified retro-inverso βturn tetrapeptidomimetic
inferred← citeshttps://doi.org/10.1007/128_052openalex-snapshot
Spatial Screening for the Identification of the Bioactive Conformation of Integrin Ligands
inferred← citeshttps://doi.org/10.1007/7081_2015_190openalex-snapshot
Synthesis of Constrained Peptidomimetics via the Pictet-Spengler Reaction
inferred← citeshttps://doi.org/10.1007/978-0-387-73657-0_160openalex-snapshot
A Peptide Vaccine Based on Retro-Inverso β-Amyloid Sequences Fails to Elicit a Cross-reactive Immune response
inferred← citeshttps://doi.org/10.1007/978-0-387-73657-0_54openalex-snapshot
Synthetic Peptide Vaccines: The Quest to Develop Peptide Vaccines for Influenza, HIV and Alzheimer's Disease
inferred← citeshttps://doi.org/10.1007/978-1-4614-2059-0_4openalex-snapshot
Anabolic Agents in Bone Repair
inferred← citeshttps://doi.org/10.1007/978-94-009-1679-1_7openalex-snapshot
Design, Synthesis, and Study of Artificial β-Sheets
inferred← citeshttps://doi.org/10.1007/978-94-010-9069-8_1openalex-snapshot
Retro and retroenantio analogs of cecropin-melittin hybrids
inferred← citeshttps://doi.org/10.1007/978-94-011-1468-4_296openalex-snapshot
Conformational differences of cyclic RGD-peptides and their retro-inverso isomers: The effect on antiadhesive activities
inferred← citeshttps://doi.org/10.1007/bf00119142openalex-snapshot
Design of superactive and selective integrin receptor antagonists containing the RGD sequence
inferred← citeshttps://doi.org/10.1007/bf00807938openalex-snapshot
Stereoconservative and stereoselective syntheses of rare and non-natural?-amino acids from (S)-aspartic acid and (S)-malic acid
inferred← citeshttps://doi.org/10.1007/bf02443538openalex-snapshot
Biochemical pharmacology of total retro-inverso analogues of bradykinin and angiotensin II: Molecular recognition by G-protein-coupled receptors and angiotensin converting enzyme
inferred← citeshttps://doi.org/10.1007/bf03348048openalex-snapshot
Synthetic peptides and their non-peptidyl mimetics in endocrinology: From synthesis to clinical perspectives
inferred← citeshttps://doi.org/10.1007/s00726-012-1428-2openalex-snapshot
Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement
inferred← citeshttps://doi.org/10.1007/s10822-005-9032-0openalex-snapshot
Force-field parametrization of retro-inverso modified residues: Development of torsional and electrostatic parameters
inferred← citeshttps://doi.org/10.1007/s10989-006-9046-zopenalex-snapshot
Microwave Assisted Alcoholysis of Isocyanates Derived from Nα-[(9-fluorenylmethyl)oxy]carbonyl Amino Acids: Synthesis of N-Fmoc-N1-Z-/Boc-/Alloc-/Bsmoc-gem-diamines
inferred← citeshttps://doi.org/10.1007/s12039-013-0519-2openalex-snapshot
Tandem synthesis of N,N′-alkylidenebisamides promoted by nano-SnCl4.SiO2
inferred← citeshttps://doi.org/10.1016/0006-2952(96)00047-0openalex-snapshot
Inhibition of angiotensin converting enzyme and potentiation of bradykinin by retro-inverso analogues of short peptides and sequences related to angiotensin I and bradykinin
inferred← citeshttps://doi.org/10.1016/0022-1139(94)00416-dopenalex-snapshot
New applications of fluorinated building blocks
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01374-qopenalex-snapshot
Synthesis of 'Retro-Inverso' Peptide Nucleic Acids: 1. Characterization of the Monomers
inferred← citeshttps://doi.org/10.1016/0167-0115(95)00049-hopenalex-snapshot
Pseudodipeptide analogs of the pyrokinin/PBAN (FXPRLa) insect neuropeptide family containing carbocyclic Pro-mimetic conformational components
inferred← citeshttps://doi.org/10.1016/0167-4838(95)00149-oopenalex-snapshot
Antigenicity of topochemically related peptides
inferred← citeshttps://doi.org/10.1016/0957-4166(94)80050-2openalex-snapshot
Optically active fluorinated β-lactam building blocks: A novel fluorinated retroamide isostere.
inferred← citeshttps://doi.org/10.1016/0960-894x(96)00414-3openalex-snapshot
Building blocks for peptide and carbamate libraries
inferred← citeshttps://doi.org/10.1016/0968-0896(96)00059-4openalex-snapshot
Solution-phase generation of tetraurea libraries
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00104-xopenalex-snapshot
1.6 Peptides and Chirality Effects on the Conformation and the Synthesis of Medicinally Relevant Peptides
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00123-3openalex-snapshot
1.17 Addition of Heteroatom Nucleophiles to CO and CN pi Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12413-8openalex-snapshot
Strategy and Tactics for Designing Analogs: Biochemical Characterization of the Large Molecules
inferred← citeshttps://doi.org/10.1016/j.apsb.2021.09.016openalex-snapshot
Whole-body PET tracking of a d-dodecapeptide and its radiotheranostic potential for PD-L1 overexpressing tumors
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.09.055openalex-snapshot
Synthesis and biological evaluation of phenolic Mannich bases of benzaldehyde and (thio)semicarbazone derivatives against the cysteine protease falcipain-2 and a chloroquine resistant strain of Plasmodium falciparum
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.02.019openalex-snapshot
Evaluation of retro-inverso modifications of HTLV-1 protease inhibitors containing a hydroxyethylamine isoster
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.08.013openalex-snapshot
Evaluation of dimerization–inhibitory activities of cyclic peptides containing a β-hairpin loop sequence of the EGF receptor
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.02.050openalex-snapshot
Effect of prime-site sequence of retro-inverso-modified HTLV-1 protease inhibitor
inferred← citeshttps://doi.org/10.1016/j.bmc.2015.10.004openalex-snapshot
New macrocyclic analogs of the natural histone deacetylase inhibitor FK228; design, synthesis and preliminary biological evaluation
inferred← citeshttps://doi.org/10.1016/j.bmc.2022.116785openalex-snapshot
Short peptide pharmacophores developed from protein phosphatase-1 disrupting peptides (PDPs)
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.06.105openalex-snapshot
New antifungal peptides. Synthesis, bioassays and initial structure prediction by CD spectroscopy
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.09.008openalex-snapshot
Formylated polyamines as peptidomimetics
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.11.026openalex-snapshot
Modification of amphipathic non-opioid dynorphin A analogues for rat brain bradykinin receptors
inferred← citeshttps://doi.org/10.1016/j.bpc.2006.05.028openalex-snapshot
The β-turn scaffold of tripeptide containing an azaphenylalanine residue
inferred← citeshttps://doi.org/10.1016/j.bpj.2008.12.3504openalex-snapshot
Phosphatidylserines Transduce Cell-Penetrating Peptides
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.04.015openalex-snapshot
Chemical protein synthesis-assisted high-throughput screening strategies for d-peptides in drug discovery
inferred← citeshttps://doi.org/10.1016/j.ejmech.2010.07.068openalex-snapshot
4-Aminoquinoline derived antimalarials: Synthesis, antiplasmodial activity and heme polymerization inhibition studies
inferred← citeshttps://doi.org/10.1016/j.exppara.2019.04.003openalex-snapshot
Semicarbazone derivatives as promising therapeutic alternatives in leishmaniasis
inferred← citeshttps://doi.org/10.1016/j.jconrel.2009.05.019openalex-snapshot
Enhanced intracellular delivery using arginine-rich peptides by the addition of penetration accelerating sequences (Pas)
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2026.113300openalex-snapshot
Metal-tuned antimicrobial peptides and zincophore pathways: from coordination chemistry to targeted therapeutics
inferred← citeshttps://doi.org/10.1016/j.jmb.2011.12.011openalex-snapshot
Inhibiting the Nucleation of Amyloid Structure in a Huntingtin Fragment by Targeting α-Helix-Rich Oligomeric Intermediates
inferred← citeshttps://doi.org/10.1016/j.tet.2005.07.018openalex-snapshot
A convenient and new approach to the synthesis of ω-heterocyclic amino acids from carboxy lactams through ring-chain-transformation. Part 2: Synthesis of (2R)-/(2S)-2-aminomethyl-3-(1-aryl-/1,5-diaryl-1H-pyrazol-3-yl)-propionic acid
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.06.069openalex-snapshot
Boron trifluoride-induced reactions of phenylglycidyl ethers: a convenient synthesis of enantiopure, stereodefined fluorohydrins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.10.066openalex-snapshot
Synthesis of retro-inverso peptides employing isocyanates of Nα-Fmoc-amino acids/peptide acids catalyzed by DMAP
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154839openalex-snapshot
Synthesis and cytotoxicity evaluation of retro-inverso analogue of antitumor bicyclic hexapeptide RA-VII
inferred← citeshttps://doi.org/10.1016/s0014-5793(03)00450-2openalex-snapshot
Inverse sequence similarity of proteins does not imply structural similarity
inferred← citeshttps://doi.org/10.1016/s0022-1139(01)00485-7openalex-snapshot
Solution and solid-phase synthesis of trifluoromethyl peptides and mimetics
inferred← citeshttps://doi.org/10.1016/s0022-3565(24)38886-xopenalex-snapshot
Retro-Inverso Prosaptide Peptides Retain Bioactivity, Are Stable In Vivo, and Are Blood-Brain Barrier Permeable
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00059-8openalex-snapshot
Synthetic studies on threonines. The preparation of protected derivatives of d-allo- and l-allo-threonine for peptide synthesis
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00333-5openalex-snapshot
Secondary Effects in Flexible Hydrogen Bonding Networks
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01044-3openalex-snapshot
Solid-phase synthesis of partially-modified retro and retro-inverso ψ[NHCH(CF3)]-peptides
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)61389-8openalex-snapshot
“Conformationally restricted β-amino acid isosteres prepared through regioselectively controlled aza-annulation.”
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)01787-8openalex-snapshot
Stereocontrolled solid-phase synthesis of fluorinated partially-modified retropeptides via tandem aza-Michael/enolate-protonation
inferred← citeshttps://doi.org/10.1016/s0040-4039(96)02297-6openalex-snapshot
Simple methods for the preparation of protected derivatives of and
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)00960-xopenalex-snapshot
Self-assembling urea-based peptidomimetics: A simple one-step synthesis and crystal structure of Core β-alanyl ureylene retro-bispeptides (MeOAaa[NHCONH]CH2CH2CONHAaaOMe; Aaa = amino acid A)
inferred← citeshttps://doi.org/10.1016/s0065-2490(97)80013-5openalex-snapshot
Peptidomimetics in Drug Design
inferred← citeshttps://doi.org/10.1016/s0149-6395(00)80050-1openalex-snapshot
Physicochemical factors in polypeptide and protein purification and analysis by high-performance liquid chromatographic techniques: current status and challenges for the future
inferred← citeshttps://doi.org/10.1016/s0161-5890(02)00095-0openalex-snapshot
A retro-inverso peptide analogue of influenza virus hemagglutinin B-cell epitope 91–108 induces a strong mucosal and systemic immune response and confers protection in mice after intranasal immunization
inferred← citeshttps://doi.org/10.1016/s0161-5890(97)00004-7openalex-snapshot
On the immunogenic properties of retro-inverso peptides. Total retro-inversion of T-Cell epitopes causes a loss of binding to MHC II molecules
inferred← citeshttps://doi.org/10.1016/s0167-7799(00)88999-4openalex-snapshot
Recent developments in retro peptides and proteins — an ongoing topochemical exploration
inferred← citeshttps://doi.org/10.1016/s0169-409x(97)00045-8openalex-snapshot
Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies
inferred← citeshttps://doi.org/10.1016/s0196-9781(01)00409-0openalex-snapshot
Retro-inverso peptide analogues of Trypanosoma cruzi B13 protein epitopes fail to be recognized by human sera and peripheral blood mononuclear cells
inferred← citeshttps://doi.org/10.1016/s0301-4622(99)00002-2openalex-snapshot
Observations on the origin of the non-linear van't Hoff behaviour of polypeptides in hydrophobic environments
inferred← citeshttps://doi.org/10.1016/s0960-894x(02)01004-1openalex-snapshot
Nociceptin/Orphanin FQ(1–13)NH2 analogues modified in the Phe1-Gly2 peptide bond
inferred← citeshttps://doi.org/10.1021/ac990369aopenalex-snapshot
Determination of Biophysical Parameters of Polypeptide Retro−Inverso Isomers and Their Analogues by Capillary Electrophoresis
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.5b00137openalex-snapshot
D-SP5 Peptide-Modified Highly Branched Polyethylenimine for Gene Therapy of Gastric Adenocarcinoma
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.7b00326openalex-snapshot
Novel Strategy Utilizing Extracellular Cysteine-Rich Domain of Membrane Receptor for Constructing d -Peptide Mediated Targeted Drug Delivery Systems: A Case Study on Fn14
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00041openalex-snapshot
Stronger Brønsted Acids: Recent Progress
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00673openalex-snapshot
Conversion of Hydroxyproline “Doubly Customizable Units” to Hexahydropyrimidines: Access to Conformationally Constrained Peptides
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00235openalex-snapshot
C(sp3)–H Azidation Reaction: A Protocol for Preparation of Aminals
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.6b01174openalex-snapshot
Highly Selective Targeting of Hepatic Stellate Cells for Liver Fibrosis Treatment Using a d -Enantiomeric Peptide Ligand of Fn14 Identified by Mirror-Image mRNA Display
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03946openalex-snapshot
Photoredox Approach to N-Acyl-N′-aryl-N,N′-aminals Using Enamides and Their Conversion to γ-Lactams
inferred← citeshttps://doi.org/10.1021/acschembio.7b00007openalex-snapshot
Structure–Activity Relationships of the Competence Stimulating Peptides (CSPs) in Streptococcus pneumoniae Reveal Motifs Critical for Intra-group and Cross-group ComD Receptor Activation
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.6c00358openalex-snapshot
Minimalist d -Tripeptide Prodrug Mimetics of the Myostatin Prodomain as Selective Inhibitors of Skeletal Muscle Atrophy Signaling
inferred← citeshttps://doi.org/10.1021/bc2002924openalex-snapshot
Enantiomer-Specific Bioactivities of Peptidomimetic Analogues of Mastoparan and Mitoparan: Characterization of Inverso Mastoparan as a Highly Efficient Cell Penetrating Peptide
inferred← citeshttps://doi.org/10.1021/bc500052ropenalex-snapshot
Phenylthiocarbamate or N -Carbothiophenyl Group Chemistry in Peptide Synthesis and Bioconjugation
inferred← citeshttps://doi.org/10.1021/bi100144mopenalex-snapshot
Development of a Proteolytically Stable Retro-Inverso Peptide Inhibitor of β-Amyloid Oligomerization as a Potential Novel Treatment for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1021/cr068373ropenalex-snapshot
Small-Molecule H-Bond Donors in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1021/cr970468topenalex-snapshot
Partially Modified Retro-Inverso Peptides: Development, Synthesis, and Conformational Behavior
inferred← citeshttps://doi.org/10.1021/ja026496xopenalex-snapshot
A Theoretical Study of Conformational Properties ofN-Methyl Azapeptide Derivatives
inferred← citeshttps://doi.org/10.1021/ja304095zopenalex-snapshot
Highly Enantioselective Electrophilic α-Bromination of Enecarbamates: Chiral Phosphoric Acid and Calcium Phosphate Salt Catalysts
inferred← citeshttps://doi.org/10.1021/ja961908lopenalex-snapshot
Stereoisomerism and Biological Activity of the Selective and Superactive αvβ3Integrin Inhibitor cyclo(-RGDfV-) and Its Retro-Inverso Peptide
inferred← citeshttps://doi.org/10.1021/jacs.6c02967openalex-snapshot
Photoredox-Catalyzed Lysine C(sp 3 )–H Functionalization for Peptide Editing
inferred← citeshttps://doi.org/10.1021/jm034012hopenalex-snapshot
Retroinverso Analogue of the Antiviral Octapeptide C8 Inhibits Feline Immunodeficiency Virus in Serum
inferred← citeshttps://doi.org/10.1021/jm061268popenalex-snapshot
Partial Retro−Inverso, Retro, and Inverso Modifications of Hydrazide Linked Bifunctional Peptides for Opioid and Cholecystokinin (CCK) Receptors
inferred← citeshttps://doi.org/10.1021/jm070304xopenalex-snapshot
Development of a Peptidomimetic Ligand for Efficient Isolation and Purification of Factor VIII via Affinity Chromatography
inferred← citeshttps://doi.org/10.1021/jm9013532openalex-snapshot
Antiangiogenic Effect of Dual/Selective α5β1/αvβ3 Integrin Antagonists Designed on Partially Modified Retro-Inverso Cyclotetrapeptide Mimetics
inferred← citeshttps://doi.org/10.1021/jm9509511openalex-snapshot
Partially Modified Retro-Inverso Pseudopeptides as Non-natural Ligands for the Human Class I Histocompatibility Molecule HLA-A2
inferred← citeshttps://doi.org/10.1021/jm990197+openalex-snapshot
Design, Synthesis, and Evaluation of Phe-Gly Mimetics: Heterocyclic Building Blocks for Pseudopeptides
inferred← citeshttps://doi.org/10.1021/jo011041wopenalex-snapshot
Ni-to-Ni+ 3-Ethylene-Bridged Partially Modified Retro-Inverso Tetrapeptide β-Turn Mimetic: Design, Synthesis, and Structural Characterization
inferred← citeshttps://doi.org/10.1021/jo801866zopenalex-snapshot
Macrolactamization versus Macrolactonization: Total Synthesis of FK228, the Depsipeptide Histone Deacetylase Inhibitor
inferred← citeshttps://doi.org/10.1021/jo9001867openalex-snapshot
New Fluorinated Peptidomimetics through Tandem Aza-Michael Addition to α-Trifluoromethyl Acrylamide Acceptors: Synthesis and Conformational Study in Solid State and Solution
inferred← citeshttps://doi.org/10.1021/jo9614102openalex-snapshot
Solid and Solution Phase Organic Syntheses of Oligomeric Thioureas
inferred← citeshttps://doi.org/10.1021/ol2019955openalex-snapshot
Cu(II)-Catalyzed Intermolecular Amidation of C -Acylimine: A Convenient Access to gem -Diamino Acid Derivatives
inferred← citeshttps://doi.org/10.1023/a:1008836814805openalex-snapshot
Biochemical pharmacology of total retro-inverso analogues of bradykinin and angiotensin II: Molecular recognition by G-protein-coupled receptors and angiotensin converting enzyme
inferred← citeshttps://doi.org/10.1038/s41467-018-05384-1openalex-snapshot
Enhanced immunocompatibility of ligand-targeted liposomes by attenuating natural IgM absorption
inferred← citeshttps://doi.org/10.1038/s41467-025-67162-0openalex-snapshot
Retro-inversion imparts antimycobacterial specificity to host defense peptides
inferred← citeshttps://doi.org/10.1038/s41598-018-24517-6openalex-snapshot
Immunosilencing peptides by stereochemical inversion and sequence reversal: retro-D-peptides
inferred← citeshttps://doi.org/10.1038/s42004-023-00890-wopenalex-snapshot
Stereochemical engineering yields a multifunctional peptide macrocycle inhibitor of Akt2 by fine-tuning macrocycle-cell membrane interactions
inferred← citeshttps://doi.org/10.1038/sj.bjp.0702857openalex-snapshot
Novel strategies for the design of receptor‐selective vasopressin analogues: Aib‐substitution and retro‐inverso transformation
inferred← citeshttps://doi.org/10.1039/b401485popenalex-snapshot
Topochemical exploration of potent compounds using retro-enantiomer libraries of cyclic pentapeptidesElectronic supplementary information (ESI) available: experimental procedures, procedures of biological assays, Table S1: characterization data of novel synthetic compounds and HPLC chromatograms…
inferred← citeshttps://doi.org/10.1039/b405955gopenalex-snapshot
Trifluoromethyl group: an effective xenobiotic function for peptide backbone modification
inferred← citeshttps://doi.org/10.1039/b607358aopenalex-snapshot
Zinc catalysed ester solvolysis. Application to the synthesis of tartronic acid derivatives
inferred← citeshttps://doi.org/10.1039/b709276hopenalex-snapshot
VAPOL phosphoric acid catalysis: the highly enantioselective addition of imides to imines
inferred← citeshttps://doi.org/10.1039/b904138aopenalex-snapshot
Mirror image phage display—a method to generate d -peptideligands for use in diagnostic or therapeutical applications
inferred← citeshttps://doi.org/10.1039/c2cc31530kopenalex-snapshot
Enantioselective direct aminalization with primary carboxamides catalyzed by chiral ammonium 1,1′-binaphthyl-2,2′-disulfonates
inferred← citeshttps://doi.org/10.1039/c2ob06692kopenalex-snapshot
Omegatides: constrained analogs of peptide primary sequence
inferred← citeshttps://doi.org/10.1039/c2ob06746copenalex-snapshot
Direct amination of α-substituted nitroacetates using di-tert-butyl azodicarboxylate catalyzed by Hatakeyama's catalyst β-ICD
inferred← citeshttps://doi.org/10.1039/c3ob41135dopenalex-snapshot
β3R3-Peptides: design and synthesis of novel peptidomimetics and their self-assembling properties at the air–water interface
inferred← citeshttps://doi.org/10.1039/c6ra00590jopenalex-snapshot
Advances in 1,3,5-triazepines chemistry
inferred← citeshttps://doi.org/10.1039/c7ob00882aopenalex-snapshot
Regioselective 1,2-addition of allenamides with N-haloimides: synthesis of 2-halo allylic aminal derivatives
inferred← citeshttps://doi.org/10.1039/c9ra08829fopenalex-snapshot
Synthesis and biological activity study of the retro-isomer of RhTx against TRPV1
inferred← citeshttps://doi.org/10.1039/cs9962500117openalex-snapshot
Asymmetric synthesis of ß-amino acids and α-substituted β-amino acids
inferred← citeshttps://doi.org/10.1039/d0nj04548aopenalex-snapshot
Iron-catalyzed C–O bond functionalization of butyrolactam derivatives with various N-/C-nucleophiles
inferred← citeshttps://doi.org/10.1039/d3ra00409kopenalex-snapshot
A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO 2 capture: synthesis, structural studies, and application
inferred← citeshttps://doi.org/10.1039/d3sc01944fopenalex-snapshot
Synthetic ramoplanin analogues are accessible by effective incorporation of arylglycines in solid-phase peptide synthesis
inferred← citeshttps://doi.org/10.1039/d4qo02332copenalex-snapshot
Interrupted intramolecular [3 + 2] to 5- endo-dig cyclization: [3 + 2] cycloaddition of nitrile ylides of diazo esters: photo-induced solvent-free gem -diamination to synthesize α-amino-α-substituted α-amino esters
inferred← citeshttps://doi.org/10.1039/d4sc07336copenalex-snapshot
Design of an abiotic unimolecular three-helix bundle
inferred← citeshttps://doi.org/10.1055/a-2854-0411openalex-snapshot
Amino Acid-Derived Isocyanates: A Comprehensive Review of Synthesis, Reactivity, and Stability
inferred← citeshttps://doi.org/10.1073/pnas.0915146107openalex-snapshot
From combinatorial peptide selection to drug prototype (II): Targeting the epidermal growth factor receptor pathway
inferred← citeshttps://doi.org/10.1073/pnas.92.8.3449openalex-snapshot
Retro and retroenantio analogs of cecropin-melittin hybrids.
inferred← citeshttps://doi.org/10.1073/pnas.94.23.12545openalex-snapshot
A retro-inverso peptide corresponding to the GH loop of foot-and-mouth disease virus elicits high levels of long-lasting protective neutralizing antibodies
inferred← citeshttps://doi.org/10.1074/jbc.270.20.11921openalex-snapshot
Cross-reactivity of Antibodies to Retro-Inverso Peptidomimetics with the Parent Protein Histone H3 and Chromatin Core Particle
inferred← citeshttps://doi.org/10.1074/jbc.270.35.20686openalex-snapshot
Retro-Inverso Peptidomimetics as New Immunological Probes
inferred← citeshttps://doi.org/10.1074/jbc.270.51.30422openalex-snapshot
Topological Mimicry of Cross-reacting Enantiomeric Peptide Antigens
inferred← citeshttps://doi.org/10.1074/jbc.274.6.3686openalex-snapshot
Solution Structure of a Retro-inverso Peptide Analogue Mimicking the Foot-and-Mouth Disease Virus Major Antigenic Site
inferred← citeshttps://doi.org/10.1074/jbc.m202063200openalex-snapshot
Exploring the Stereochemistry of CXCR4-Peptide Recognition and Inhibiting HIV-1 Entry with d-Peptides Derived from Chemokines
inferred← citeshttps://doi.org/10.1080/00397910802398256openalex-snapshot
Novel Route toN-Acyl-N′-formyl Aminal
inferred← citeshttps://doi.org/10.1088/1478-3975/7/1/016001openalex-snapshot
Molecular electroporation and the transduction of oligoarginines
inferred← citeshttps://doi.org/10.1107/s1600536805043096openalex-snapshot
10-Methyl-8,9,10,11,11a,12-hexahydro-5H,7H-isoquinolino[3,2-g][1,3,5]triazepine-7,11-dione
inferred← citeshttps://doi.org/10.1107/s1600536812039414openalex-snapshot
(2E)-2-[1-(2-Hydroxy-4-methoxyphenyl)ethylidene]-N-phenylhydrazinecarboxamide monohydrate
inferred← citeshttps://doi.org/10.1110/ps.8.6.1257openalex-snapshot
A functional protein pore with a “retro” transmembrane domain
inferred← citeshttps://doi.org/10.1111/cbdd.12143openalex-snapshot
Penetratin and Derivatives Acting as Antibacterial Agents
inferred← citeshttps://doi.org/10.1111/cbdd.13472openalex-snapshot
Peptide and protein mimetics by retro and retroinverso analogs
inferred← citeshttps://doi.org/10.1111/j.1399-3011.1995.tb01049.xopenalex-snapshot
End‐group modified retro‐inverso isomers of tripeptide oxytocin analogues: binding to neurophysin II and enhancement of its self‐association properties
inferred← citeshttps://doi.org/10.1111/j.1399-3011.1997.tb00883.xopenalex-snapshot
Synthesis and activity of partial retro‐inverso analogs of the antimetastatic laminin‐derived peptide, YIGSR‐NH2
inferred← citeshttps://doi.org/10.1111/j.1399-3011.1997.tb01187.xopenalex-snapshot
Antiproliferative and antitumor activities of D‐reverse peptides derived from the second type‐1 repeat of thrombospondin‐1
inferred← citeshttps://doi.org/10.1111/j.1399-3011.1997.tb01205.xopenalex-snapshot
Comparison of the solution conformations of a human immunodeficiency virus peptidomimetic and its retro‐inverso isomer using H NMR spectroscopy
inferred← citeshttps://doi.org/10.1111/j.1399-3011.1998.tb01221.xopenalex-snapshot
Conformational and topological requirements of cell‐permeable peptide function
inferred← citeshttps://doi.org/10.1111/j.1399-3011.2005.00224.xopenalex-snapshot
Exploring the stereochemical requirements for protease inhibition by ureidopeptides
inferred← citeshttps://doi.org/10.1128/iai.64.4.1413-1419.1996openalex-snapshot
Identification and characterization of epitopes on the 120-kilodalton surface protein antigen of Rickettsia prowazekii with synthetic peptides
inferred← citeshttps://doi.org/10.1135/cccc20021305openalex-snapshot
Parallel Solid-Phase Synthesis of Partially Modified Retro and Retro-Inverso ψ[NHCH(CF3)]-Gly Peptides
inferred← citeshttps://doi.org/10.1248/cpb.c15-00742openalex-snapshot
Medicinal Chemistry Focusing on Aggregation of Amyloid-β
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