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1 ral energies are spatially controlled within peptidic 1-D nanostructures to create localized energy g
2 derivative of acetazolamide, a spacer, and a peptidic (99m)Tc chelator, was labeled using sodium pert
3 ancer cells can process and present a shared peptidic Ag to TCR alphabeta+ T cells via a nonclassical
4 the delta receptor by centrally administered peptidic agonists and intravenously administered JOM-13
5 ects without producing convulsions, and some peptidic agonists can increase BDNF mRNA expression, how
6 n of VEK-30 with mK2Pg demonstrated that the peptidic alpha-helical structure increased substantially
7                                              Peptidic alpha-toxins AahI to AahIV are responsible for
8                              When homologous peptidic amide and ester substrates were compared, a ser
9 work investigates the influence of the first peptidic amino acid (P1) on peptide binding to B*2705 an
10 ould be exploited for the development of non-peptidic amyloid-specific inhibitors.
11 own approach to study a series of alpha/beta-peptidic analogs of anginex, a beta-sheet-forming antian
12               NMR spectroscopy of all of the peptidic analogs of BK or HOE-140 revealed a beta-turn a
13 d species with that of the corresponding non-peptidic analogs, reveals that the peptide component enh
14                                        Other peptidic analogues, chosen because of specific substitut
15  quantitation of translation termination and peptidic analysis identified lncRNAs that produce peptid
16 ernalized DRM proteins show varied lipid and peptidic anchors indicating that, contrary to the prevai
17 nce for overlapping ligand-binding sites for peptidic and nonpeptidic agonists.
18                 It also competes weakly with peptidic and nonpeptidic antagonists.
19                          We used an array of peptidic and nonpeptidic arginine-glycine-aspartic acid
20    Thus, the CSP approach distinguishes both peptidic and nonpeptidic delta opioid agonists and antag
21 ned models for a structurally diverse set of peptidic and nonpeptidic delta opioid ligands offer good
22      In addition, results indicate that both peptidic and nonpeptidic ligands have the same binding m
23 Because of its critical role in cancer, many peptidic and nonpeptidic ligands with different modes of
24 access to folded objects beyond the reach of peptidic and nucleotidic backbones.
25  have relevance for the development of other peptidic and peptidomimetic drugs such as inhibitors of
26                                              Peptidic and peptidomimetic hydroxamates are increasingl
27 jor progress has recently been achieved with peptidic and proteinaceous compounds.
28 o binding of Tat protein and of a variety of peptidic and small molecule ligands, indicating that its
29 es a platform for the further development of peptidic and/or small molecule agents directed toward th
30 notoxin GVIA, a well-characterized ICK-motif peptidic antagonist of voltage-gated calcium channels.
31 caconitine, further opens to accommodate the peptidic antagonist, alpha-conotoxin ImI, but wraps arou
32 e recent development of orally available non-peptidic antagonists and genetically modified mice defic
33 I and class II molecules bind to and display peptidic antigens acquired from pathogens that are recog
34 riant T (MAIT) cells recognize microbial non-peptidic antigens presented by non-classical MHC MR1.
35 ructural relationships with other classes of peptidic antimicrotubule agents, or for modeling studies
36 mode of HTI-286, a synthetic analogue of the peptidic antimitotic agent hemiasterlin, to tubulin is p
37 translocation signal is comprised of unique, peptidic (approximately equal to 40-aa) sequences.
38                                        These peptidic arrays are used to purge self-reactive T cells,
39 ts for human Cdc25A with respect to a set of peptidic, artificial, and natural substrates.
40                   To date, a large number of peptidic as well as nonpeptidic SH2 domain inhibitors ha
41              Second, B cells specific to the peptidic B cell epitope in pCol(28-40) were absent among
42  that the anti-GBM Ab was not related to the peptidic B cell epitope nested in pCol(28-40); that is,
43 ACE1 for activity and inhibition by selected peptidic BACE inhibitors.
44 n-2-ylamine], the first orally available non-peptidic BACE1 inhibitor that produces profound Abeta-lo
45 sure to UV light induces an oxidation of its peptidic backbone and a concomitant reduction of the coo
46 multaneously improved by replacing the polar peptidic backbone of the inhibitor with nonpeptidic moie
47 lator natural product, which contains in its peptidic backbone two S-methylated l-cysteine residues.
48       Here we report a new type of unnatural peptidic backbone, containing alpha-, beta-, and gamma-a
49 y-D-glucitol-gamma-glutamate subunits into a peptidic backbone, was synthesized.
50 are seen also in helices formed by unnatural peptidic backbones, e.g., those containing beta- or gamm
51 e 1 were conceived as "minimalist" mimics of peptidic beta-turn structures.
52 t reported crystal structure of a two-tailed peptidic bilayer reveals similarities in thickness to a
53 , a strategy for the iterative conversion of peptidic blockers of protein-protein interactions into p
54 the A' pocket of the groove, whereas its two peptidic branches protrude along the F' pocket to the ou
55 ers of 4-hydroxyphenylglycine as non-natural peptidic building blocks synthesized via a copper-comple
56            We investigated the effect of the peptidic C3 inhibitor, compstatin Cp40, and its long-act
57 c binding of the substrate; hydration of the peptidic carbonyl by an active site water; proton transl
58 n amine-containing PS forms amide bonds with peptidic cargo, a thiol derivative is designed for conju
59  conjugation of a small receptor ligand to a peptidic carrier to potentially facilitate transport acr
60 ates has predominantly focused on the use of peptidic carriers to deliver the phosphotyrosine moiety
61             Incubation of the cells with the peptidic caspase inhibitor z-valine-alanine-asparagine-C
62 ort peptides, the design and optimization of peptidic catalysts by rational structural modifications
63          In recent years, numerous versatile peptidic catalysts have been developed that bear Xaa-Pro
64  stereoselectivity of H-Pro-Pro-Xaa-NH2-type peptidic catalysts in conjugate addition reactions.
65 diastereoselectivity of structurally related peptidic catalysts.
66 ool to optimize the catalytic performance of peptidic catalysts.
67 radiography and compared with an established peptidic CCK agonist radioligand.
68 rom these studies revealed not only that the peptidic CCK2R ligands were unstable in vivo but also th
69 s of the Lck SH2 domain which are reduced in peptidic character and in which the three carboxyl group
70 o acid residues of 1 with moieties with less peptidic character was done with retention of BACE enzym
71 ncy of this lead, as well as attenuating its peptidic character, an analogue program was undertaken.
72 h higher conformational definition and lower peptidic character.
73  and KGHK-Rev, which also contain N-terminal peptidic chelators (ATCUN motifs), were studied for comp
74  activity can be conveniently monitored with peptidic chromogenic or fluorogenic substrates, with cer
75 e site specificity (PICS), we identified 286 peptidic cleavage sites spanning from P6 to P6' from whi
76 stent with the kinetic data, the affinity of peptidic competitive inhibitors is diminished at acidic
77 hese studies yield new insight into critical peptidic components composing one side of the prion repl
78  and robustly with PrP(Sc), likely represent peptidic components of one flank of the prion replicativ
79                                Defensins are peptidic components of the innate immune system of plant
80 d was specific for structure of the acyl and peptidic components of these antigens.
81 of 70.37%, was characterised in terms of its peptidic composition using mass spectrometry and 1882 pe
82                                         This peptidic compound, termed LirAzo, possesses an azobenzen
83                                        These peptidic compounds and their advantageous biological pro
84  have constructed and tested a library of 45 peptidic compounds based on this loop sequence.
85 LACE as an effective strategy for converting peptidic compounds to more pharmaceutically relevant com
86 (including apamin, scyllatoxin and newer non-peptidic compounds) showed these homomeric SK3 channels
87 ity, nonreceptor-mediated interaction of the peptidic conantokins with synaptic membranes in conjunct
88 t a study on MMP-12 inhibitors with a common peptidic core but different ZBGs.
89 ss-section EM to reveal a nanostructure with peptidic core.
90 pharmacokinetic properties relative to their peptidic counterparts.
91 cleoside amino acid fragment was followed by peptidic coupling of the two components, leading to the
92 onalized pyrolytic graphite electrodes using peptidic coupling.
93 r antagonist, and alpha-helical CRH(9-41), a peptidic CRHR1/CRHR2 antagonist to attempt to determine
94                        Previously documented peptidic cross-linking strategies remain operative in th
95 and the synthesis of our first series of non-peptidic cyclophilin ligands, along with the preliminary
96  present study examined whether a variety of peptidic delta agonists, DPDPE, JOM-13, a systemically a
97 TEEI (4), VYGGG (5), and YGFGG (6) to afford peptidic derivatives for exploring pentapeptide-based hy
98  process and convert exogenous antigens into peptidic determinants capable of interaction with MHC cl
99 own to be very efficacious at insertion into peptidic disulfide bonds.
100 cerning the rate by which TCEP reduces other peptidic disulfide bonds.
101 s an engineered nanocontainer for delivering peptidic drugs across the BBB encapsulating the analgesi
102 ffector molecule, resembles the mechanism of peptidic entry inhibitors based on portions of the gp41
103 tion of gluten and gliadin 33-mer equivalent peptidic epitopes (33EPs) in human feces.
104 oach can become a tool for rapid creation of peptidic expression domains in a eukaryotic environment.
105 ot substrates for farnesylation, do not have peptidic features, and have no hydrolyzable bonds.
106 ioid receptors, for which relatively few non-peptidic fluorescent probes currently exist.
107                             In this respect, peptidic foldamers are perhaps the best-characterized sy
108               We describe efforts to develop peptidic foldamers that bind to the irregular receptor-r
109                                              Peptidic foldamers, consisting of various amino acid bas
110 mes to stabilize the folding in a variety of peptidic foldamers.
111 bundles composed of either alpha-peptides or peptidic foldamers.
112                                          The peptidic fraction of carotenoproteins (PFCP) contained 8
113 s and in vitro antioxidative activity of the peptidic fraction of carotenoproteins from shrimp (Parap
114     Results from this study suggest that the peptidic fraction of carotenoproteins is a good source o
115 rties of Pacific hake hydrolysates and their peptidic fractions varying in molecular size were assess
116 (procyanidin B3) and different wheat-derived peptidic fractions.
117  is stabilized by hydrogen bonds between the peptidic fragment and the sugar.
118 restrictive properties of media differing in peptidic fragment content and reveal unusual signalling
119  markedly enhanced production of informative peptidic fragment ions during CID that dramatically incr
120             CLIP is substituted by exogenous peptidic fragments in an exchange reaction catalyzed by
121  were obtained for isolated protein domains, peptidic fragments, or mutants.
122  with MALDI-TOF MS analysis of the resulting peptidic fragments.
123 can be widely used to improve the potency of peptidic fusion inhibitors against other enveloped virus
124 cretagogue receptor 1a (ghrelin receptor), a peptidic G-protein-coupled receptor.
125                                              Peptidic glucagon antagonists have been shown to lower b
126                                          All peptidic guests in all solvent systems have association
127   Macrocyclization could also provide a less peptidic HCV inhibitor.
128 ins DS40M6 and DS40M8, each contain a unique peptidic head group that coordinates iron(III) and an ap
129 tin has the same Tris-hydroxamate-containing peptidic headgroup composed of three ornithine residues
130 rection for the discovery of more potent non-peptidic HIV protease inhibitors as potential therapeuti
131  Our broad screening program to discover non-peptidic HIV protease inhibitors previously identified c
132 re made of selected steroidal components and peptidic hormones in blood serum, and cognitive and phys
133 uretic peptides (PNPs), are a novel class of peptidic hormones that signal via guanosine 3',5'-cyclic
134                                  No specific peptidic hydrolysed bond was detected.
135 acterize the engagement of hTS with one such peptidic inhibitor in cell lysates.
136 ng and subsequent removal of a high affinity peptidic inhibitor increased the apparent molecular mass
137                      Fasciculin, a selective peptidic inhibitor of acetylcholinesterase, is a member
138                                            A peptidic inhibitor of caspase-3, Z-Asp-Glu-Val-Asp-fluor
139   Aclacinomycin A is the first described non-peptidic inhibitor showing discrete selectivity for the
140 nerated viruses with resistance to VIR165, a peptidic inhibitor that binds the fusion peptide of the
141                                      The non-peptidic inhibitor tipranavir is distinctive in its cons
142 ee cases the enzyme forms a complex with the peptidic inhibitor U-89360E.
143                                  A synthetic peptidic inhibitor, diphenyl N alpha-benzoxycarbonyl-l-A
144        Recently, we successfully developed a peptidic inhibitor, RRYGTSKYQ ("SKY" peptide), that show
145 association of acetylcholinesterase with its peptidic inhibitor, the neurotoxin fasciculin.
146                                   The potent peptidic inhibitor, Y1, of the basic residue-specific ye
147                                 The designed peptidic inhibitors are 12-amino-acids-long and target t
148  the importance of evaluating the potency of peptidic inhibitors at physiologically relevant pH value
149 in-coupled receptors, for which chemical and peptidic inhibitors have been extensively explored, few
150 vel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases.
151 esis and in vitro characterization of potent peptidic inhibitors of dengue virus protease that incorp
152                  This is the first report on peptidic inhibitors of heme oxygenase.
153   We recently discovered new, unconventional peptidic inhibitors of hTS that are active against cance
154                     Potent and selective non-peptidic inhibitors of human endothelin-converting enzym
155       A series of P2-modified, orally active peptidic inhibitors of human neutrophil elastase (HNE) a
156 gn and structural characterization of potent peptidic inhibitors of influenza hemagglutinin.
157 trated that the rational design of small non-peptidic inhibitors of large protein-protein interfaces
158 e of action of Elec410 as one of the largest peptidic inhibitors targeting the acetylcholinesterase p
159 benzamide, belongs to a family of potent non-peptidic inhibitors that have large P1' groups.
160 y demonstrates the feasibility of developing peptidic inhibitors to functionally relevant sites on PC
161       With the caspases fully inactivated by peptidic inhibitors, GrB induced in Jurkat cells growth
162          Using this assay, we found that the peptidic inhibitors, leupeptin and aprotinin, exhibited
163         Structure-based design of potent non-peptidic inhibitors, utilizing crystal structures of HIV
164  to give irreversible cruzain inhibition for peptidic inhibitors.
165 as a starting structure to rationally design peptidic inhibitors.
166 y classified as either peptidomimetic or non-peptidic inhibitors.
167 ied structurally diverse small molecule (non-peptidic) inhibitors (SMNPIs) of the botulinum neurotoxi
168 re were employed to mine small molecule (non-peptidic) inhibitors from the National Cancer Institute'
169 nd a domain motion enabling enclosure of the peptidic ligand and formation of specific hydrogen bonds
170 in was recently identified as the endogenous peptidic ligand for human APJ.
171 that targets the ATP-binding cleft and (2) a peptidic ligand that enhances selectivity between kinase
172 settled in the apo-cluster and the PR-957 (a peptidic ligand) complex in the pep-cluster.
173 he potency of a recently described linear SE peptidic ligand.
174  subunits of the unliganded species with the peptidic liganded forms demonstrates a greatly enhanced
175                          The manner by which peptidic ligands bind and activate their corresponding G
176                                              Peptidic ligands can be used for specific cell targeting
177                                 In contrast, peptidic ligands failed to promote expression or rescue
178 ve biopanning for isolation of high affinity peptidic ligands for a single cancer type and expands th
179              One of the better characterized peptidic ligands is the chemotactic cytokine complement
180 r phylogeny has accelerated the discovery of peptidic ligands targeted to ion channels and receptors.
181 pioid efficacy pharmacophore, is extended to peptidic ligands using replica exchange molecular dynami
182 rcine pancreatic elastase (PPE) complexed to peptidic ligands, we have developed a new series of nonp
183 residues is compared with that of biotin and peptidic ligands.
184 iopanning for the isolation of TM transiting peptidic ligands.
185 and the pep-cluster comprises complexes with peptidic ligands.
186 H1-hinge domains of mAb2 are fused through a peptidic linker to the N terminus of mAb1 H chain, and p
187  the latter, the two peptides are joined via peptidic linkers of variable lengths to produce a range
188 glycosidic attachment of thymine at C-1, and peptidic linking of the C-6 amine with the 1,2-aminocycl
189 peptides proved efficient in the ligation to peptidic, lipidic and fluorescently labeled amines and i
190 cule modulators of CXCR7 have been reported, peptidic macrocycles may provide advantages in terms of
191                      We produced a series of peptidic macrocycles that incorporate an N-linked peptoi
192 ning the activity and physical properties of peptidic macrocycles.
193 ate and selectively redissolve CS versus the peptidic material and (3) the selective purification and
194                            Administration of peptidic MC4R antagonists (usually by intracerebro ventr
195 alternatives, we replaced one or both of the peptidic membrane anchors of exocytic vesicle (v)- and t
196 ndocaensis results in the discovery of three peptidic metabolites (cahuitamycins A-C), with cahuitamy
197 effectively mine microbial strains for novel peptidic metabolites.
198               These results suggest that all peptidic mimics of Tat induce the same dynamics in TAR w
199 talling isosteric chemical substituents in a peptidic model system and using NMR spectroscopy, X-ray
200  of the myristoyl chain and repulsion of the peptidic moiety from the phospholipid headgroup region.
201 a1-selective peptidomimetic, or an RGD/PHSRN peptidic molecule.
202                                           As peptidic molecules find increasing value in therapeutic
203 e energy associated with the transfer of the peptidic molecules from water to membrane.
204 ade to develop technologies for selection of peptidic molecules that act as substrates or binders to
205 o link the acids to DNA major groove-binding peptidic motifs known to adopt alpha-helical conformatio
206 xylation of conserved prolyl residues within peptidic motifs present in the HIFalpha family members.
207 second and fourth amino acid residues in the peptidic mu opioid lead agonist Dmt-d-Arg-Phe-Lys-NH(2)
208 s, we show that intraarticular delivery of a peptidic nanoparticle complexed to NF-kappaB siRNA signi
209                                         This peptidic natural product exhibited an amino acid sequenc
210 A number of seemingly structurally disparate peptidic natural products inhibit tubulin polymerization
211 y towards high-throughput discovery of novel peptidic natural products.
212  endothelin-A (ET(A)) receptor; however, its peptidic nature leads to poor oral absorption characteri
213 nvironmental responsiveness, morphology, and peptidic nature make this hydrogel a possible material c
214                                          The peptidic nature of pantocin B facilitated a series of st
215 lic dipeptide moiety would also decrease the peptidic nature of the inhibitors.
216 ochemistry was employed to detect changes in peptidic neurotransmitter expression in identified dural
217 amics simulations were performed with 13 non-peptidic neurotransmitters (NTs) in three different memb
218  methylmalonyl CoA is hydrogen bonded to the peptidic NH group of Gly 110 and the imidazole ring of H
219                 The oxyanion hole, formed by peptidic NH groups from Gly121, Gly122, and Ala204, is a
220 d between the carbonyl oxygen of ACh and the peptidic NH groups of Gly121 and Gly122.
221 the inhibitors are mediated through backbone peptidic NH groups, carbonyl oxygens, and/or solvents.
222 gen bonds with backbone carbonyl oxygens and peptidic NH groups.
223  that the stimulatory compounds were neither peptidic nor lipidic but instead were composed of sulfur
224  structure prediction and design of five non-peptidic oligomer scaffolds (noncanonical backbones), ol
225                                              Peptidic oligomers that contain both alpha- and beta-ami
226                                          The peptidic opioid delta(1) agonist [D-Pen(2),D-Pen(5)]enke
227 ibitors relies on a core zinc chelator and a peptidic or nonpeptidic scaffold that provides supplemen
228 letely novel set of antibacterial compounds, peptidic or peptidomimetic, if the interacting bacterial
229  is first halogenated and then elaborated by peptidic or polyketide extensions.
230 een used to screen approximately 150,000 non-peptidic organic compounds in a molecular data base and
231 ecule that occupies the same position as the peptidic oxygen in the tetrahedral intermediate.
232       On the contrary, we identified the non-peptidic part as the determining factor of differences b
233 n classes of rhodesain inhibitors, including peptidic, peptidomimetic, and nonpeptidic structures, em
234 zed by conjugating fluorescent dyes to a non-peptidic, pharmacophore-based ligand, based on a molecul
235  alpha,beta-unsaturated ketones catalyzed by peptidic phosphine ligands and (CuOTf)(2).C(6)H(6).
236                                    While the peptidic portion of these compounds serves an enzyme tar
237 ligand can bind simultaneously to a flexible peptidic PPI recognition motif and to a well-structured
238  downregulation in cancer cells by designing peptidic precursors as the substrates of both carboxyles
239 ) in complex with a substrate analogue and a peptidic product to 2.5 and 2.7 A, respectively, and com
240  A similar configuration was evident for the peptidic product, although decreasing electron density t
241 ompared efficacy and safety of the novel non-peptidic protease inhibitor tipranavir co-administered w
242  a well-known family of aldehyde-containing, peptidic protease inhibitors, including antipain, chymos
243 fluence of (EH)3 on the biodistribution of 2 peptidic radiopharmaceuticals, Glu-urea-Lys(Ahx)-HBED-CC
244 to improve the pharmacokinetic properties of peptidic radiopharmaceuticals, leading to reduced uptake
245      Here we investigate the ability of such peptidic receptor ligands to target the liver.
246 and their bioderivatization with a selective peptidic receptor modified with a SERS transducer.
247 potential to interact with broad surfaces of peptidic receptors rather than within their narrow folds
248                           Boronic acid based peptidic receptors, derived from a combinatorial library
249  we biochemically generated the potential Tg peptidic repertoire available to HLA-DR3 by separately t
250 ot affect the binding of the four C-terminal peptidic residues to PDZ, as revealed by the crystal str
251 he catalytic domain of human MMP9 bound to a peptidic reverse hydroxamate inhibitor as well as the co
252                      The introduction of non-peptidic scaffolds into macrocycles is highly desirable
253 unit of the ligand and the AA2 moiety of the peptidic segment of the chiral ligand associates and del
254  yields highly conjugated backbones when the peptidic segment of the PAs has a linear, as opposed to
255 , we further identified within this region a peptidic segment that exhibits membrane interaction prop
256 olism through their binding, via a conserved peptidic sequence, into a universally conserved pocket.
257                                   A discrete peptidic sequence, termed the amyloid-converting motif (
258 rupting the DNA stretch encoding a conserved peptidic sequence.
259 pine nucleus is introduced internally to the peptidic sequence.
260 s of beta-sheet folding and design for alpha-peptidic sequences are well established, while those for
261 ere, we used phage display to identify novel peptidic sequences that bind Cx43CT and modify Cx43 regu
262 s further exemplified in combining optimized peptidic sequences with effective N-terminal capping gro
263 dels or, as in previous studies, zinc finger peptidic sequences.
264  novo-designed bioactive beta- or alpha,beta-peptidic sequences.
265 ile substantially different from that of the peptidic series, particularly with regard to the require
266 the membrane permeability of matched sets of peptidic small molecules bearing natural or bioisosteric
267        Our approach relies on the use of non-peptidic small molecules, which selectively bind fungal
268 inus of VEK30 (VEK32) maintained a monomeric peptidic structure, but exhibited similar K2hPg binding
269 eation of rationally designed and functional peptidic structures, the roles of these forces on purely
270 ma-imino)triphosphate), but not ADP, or of a peptidic substrate induces depolymerization of FLAG-BiP.
271 proteolysis rate of the folded protein and a peptidic substrate mimicking the sequence at the cleavag
272 iabetic compound such a the organic vanadate peptidic substrate was possible the toxicity problems cu
273      Ligand interactions, as reported in one peptidic substrate, are favorable so that complementarit
274 ic phosphate derivatives, the more realistic peptidic substrates allow evaluating substrate specifici
275 e results also suggest the design of optimal peptidic substrates and inhibitors.
276 re efficient substrates than the most potent peptidic substrates ever reported for VHR.
277  employing 3-nitrophosphotyrosine containing peptidic substrates is described.
278 ytic efficiency than glycan-free KLK2 toward peptidic substrates with P2-Phe, the situation was rever
279 nown to process a large variety of different peptidic substrates, although the mechanism behind this
280 ng enzyme (IDE) cleaves insulin, among other peptidic substrates, but its function in insulin signali
281                               In contrast to peptidic substrates, Cdc25A and dN25A are highly active
282 ction from 3-nitrophosphotyrosine containing peptidic substrates, which are accepted by many PTPs.
283 atases-tailoring the number of phosphates on peptidic substrates-is able to regulate the rate of mole
284 onfirms a mode of binding similar to that of peptidic substrates.
285 aturation and are capable of acting on large peptidic substrates.
286 e show that gp33 variants substituted at the peptidic termini at the putative CDR1 contact regions sh
287 e and robust synthesis of highly substituted peptidic thiazole derivatives using Ugi-multicomponent r
288 ctivating regions characterized thus far are peptidic, this function can be served by other kinds of
289  MII, isolated from Conus magus, is a potent peptidic toxin which specifically targets the mammalian
290 , it is likely that the discovery of similar peptidic toxins will rapidly expand to existing and emer
291              Endothelin-1 is the most potent peptidic vasoconstrictor discovered to date.
292 h 7 daily subcutaneous injections of VIPhyb (peptidic VIP-antagonist) or phosphate-buffered saline (P

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