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1                               Abiraterone, a steroidal 17alpha-hydroxylase/17,20-lyase (CYP17A1) inhi
2 Two additional subclasses were prepared: bis(steroidal)-4,7-ACQ derivatives and bis(4,7-ACQ)cholate d
3 ty and is structurally similar to endogenous steroidal 5alpha-reductase substrates, such as testoster
4 oline (HHII) scaffold as a surrogate for the steroidal A-B ring system is described.
5 ucocorticoid receptor antagonism by studying steroidal active antagonists such as RU-38486 (1).
6 an 100 Food and Drug Administration-approved steroidal agents are prescribed daily for indications in
7  products, are glycosides of triterpenoid or steroidal aglycones (sapogenins).
8 onally defined a novel pharmacophore for the steroidal agonist site.
9  even the best clinically approved synthetic steroidal agonists are prone to cross-reactivity and off
10                                Compared with steroidal agonists for the androgen receptor (AR) (e.g.
11                                              Steroidal alkaloid analysis employed silica gel-coated T
12                                            A steroidal alkaloid batrachotoxin (BTX) causes persistent
13 terribilis frogs sequester lethal amounts of steroidal alkaloid batrachotoxin (BTX) in their skin as
14 terpenoid found in apples) and tomatidine (a steroidal alkaloid derived from green tomatoes).
15 -Cortistatin A (dCA), an analog of a natural steroidal alkaloid from a marine sponge, inhibits Tat-me
16                       Batrachotoxin (BTX), a steroidal alkaloid, and pyrethroid insecticides bind to
17 fic tropane (l-hyoscyamine, scopolamine) and steroidal alkaloids (alpha-solanine, alpha-chaconine) in
18                Batrachotoxins are neurotoxic steroidal alkaloids first isolated from a Colombian pois
19 resin acids, mefenamic acid, oxybenzone, and steroidal alkaloids in the bile or plasma, and there wer
20 samples of 2 and 3 with those of appropriate steroidal analogues [e.g., petromyzonol sulfate (PS, 1,
21 e a less detrimental effect on bone than non-steroidal anastrozole.
22                    Systemic therapy includes steroidal and non-steroidal anti-inflammatory agents, di
23                     This first comparison of steroidal and nonsteroidal classes of aromatase inhibito
24 ophore that, over some 20 years, have led to steroidal and nonsteroidal drugs in numerous preclinical
25 al function and the electronic properties of steroidal and nonsteroidal estrogens by analysis of the
26  new rational template for drug discovery of steroidal and nonsteroidal glucocorticoids that can be s
27 d work to date underlying the development of steroidal and nonsteroidal receptor ligands, including t
28     In this study, we show that although the steroidal and nonsteroidal SERDs target ERalpha for degr
29                  The LBD responds to classic steroidal and nonsteroidal small ligands; both may selec
30   We describe two structurally similar 4-aza-steroidal androgen receptor (AR) ligands, Cl-4AS-1, a fu
31             We report the synthesis of novel steroidal androgen receptor ligands comprising 11beta-al
32                                     Although steroidal antagonists such as spironolactone and epleren
33                                      The non-steroidal anti-androgen bicalutamide may offer an equiva
34                     Alcohol, exercise or non-steroidal anti-inflamatory drugs (NSAID) are frequently
35 netic pathway and uniquely revealed that non-steroidal anti-inflammatories (NSAIDs) rank just as high
36 ant concentrations of ibuprofen (IBF), a non-steroidal anti-inflammatory agent and prevalent environm
37 e-1IC50/anti-cyclooxygense-2IC50>1) than non-steroidal anti-inflammatory agent ibuprofen (0.44) descr
38 rugs can easily be conjugated to another non-steroidal anti-inflammatory agent, leading to easy synth
39                                          Non-steroidal anti-inflammatory agents (NSAIDs) are associat
40 ocognitive sequelae from irradiation and non-steroidal anti-inflammatory agents can restore neurogene
41                                          Non-steroidal anti-inflammatory agents inhibit the productio
42  Systemic therapy includes steroidal and non-steroidal anti-inflammatory agents, disease-modifying ag
43                        Treatment is with non-steroidal anti-inflammatory agents, four to six weeks of
44 urogenesis through the administration of non-steroidal anti-inflammatory agents.
45 s currently on the market, including the non-steroidal anti-inflammatory blockbuster drug celecoxib.
46    Define the effectiveness of a topical non-steroidal anti-inflammatory drug (NSAID) added to topica
47             Treatment with a NO-donating non-steroidal anti-inflammatory drug (NSAID) alleviates this
48 se (GERD), Barrett's esophagus (BE), and non-steroidal anti-inflammatory drug (NSAID) bleeding prophy
49    The unprecedented polymorphism of the non-steroidal anti-inflammatory drug (NSAID) flufenamic acid
50                                   In the non-steroidal anti-inflammatory drug (NSAID) group, patients
51                           Ibuprofen is a non-steroidal anti-inflammatory drug (NSAID) that independen
52 ow that inhibition of endogenous PGE2 by non-steroidal anti-inflammatory drug (NSAID) treatment in mi
53                                          Non-steroidal anti-inflammatory drug (NSAID) treatment suppr
54 h or standard doses compared with remote non-steroidal anti-inflammatory drug (NSAID) use or celecoxi
55 mine-gallic acid hybrid molecule against non-steroidal anti-inflammatory drug (NSAID)-induced gastrop
56                                      The non-steroidal anti-inflammatory drug aspirin and its metabol
57                Tolfenamic acid (TA) is a non-steroidal anti-inflammatory drug associated with anti-tu
58 t unlike that caused by solutions of the non-steroidal anti-inflammatory drug ibuprofen.
59  investigated potential therapy with the non-steroidal anti-inflammatory drug ibuprofen.
60                                      The non-steroidal anti-inflammatory drug sulindac decreases size
61               Flufenamic acid (FFA) is a non-steroidal anti-inflammatory drug that has been long used
62                    Pretreatment with the non-steroidal anti-inflammatory drug, 2-cyano-3,12-dioxoolea
63  lumiracoxib (59 events [0.65%]) and the non-steroidal anti-inflammatory drugs (50 events [0.55%]; ha
64 ations was 1.09% (95% CI 0.82-1.36) with non-steroidal anti-inflammatory drugs (64 events) versus 0.2
65                        Aspirin and other non-steroidal anti-inflammatory drugs (NSAID) probably decre
66 ose and regularity of aspirin use, other non-steroidal anti-inflammatory drugs (NSAID), and the effec
67                                  Certain non-steroidal anti-inflammatory drugs (NSAIDs) (e.g., rofeco
68 that underlie the antitumour activity of non-steroidal anti-inflammatory drugs (NSAIDs) against color
69                                          Non-steroidal anti-inflammatory drugs (NSAIDs) are among the
70                                          Non-steroidal anti-inflammatory drugs (NSAIDs) are among the
71 2 selective inhibitors and non-selective non-steroidal anti-inflammatory drugs (NSAIDs) are associate
72                                          Non-steroidal anti-inflammatory drugs (NSAIDs) are known gam
73                                          Non-steroidal anti-inflammatory drugs (NSAIDs) are used to m
74 As an additional pharmacologic approach, non-steroidal anti-inflammatory drugs (NSAIDs) can reduce gi
75                                          Non-steroidal anti-inflammatory drugs (NSAIDs) damage the ga
76  selective inhibitors versus traditional non-steroidal anti-inflammatory drugs (NSAIDs) has not been
77                       Zinc chelation and non-steroidal anti-inflammatory drugs (NSAIDs) have been exp
78 for reducing gastrointestinal effects of non-steroidal anti-inflammatory drugs (NSAIDs) have been sub
79                                          Non-steroidal anti-inflammatory drugs (NSAIDs) have been wid
80         Previous studies have shown that non-steroidal anti-inflammatory drugs (NSAIDs) have signific
81 sis (FASS) for the determination of five non-steroidal anti-inflammatory drugs (NSAIDs) in bovine mil
82                                          Non-steroidal anti-inflammatory drugs (NSAIDs) inhibit cyclo
83                   Topically administered non-steroidal anti-inflammatory drugs (NSAIDs) inhibit perio
84 trials demonstrate that long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) markedly redu
85 opreventive effect for aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) on colorectal
86 inically important errors: non-selective non-steroidal anti-inflammatory drugs (NSAIDs) prescribed to
87               Nitric oxide (NO)-donating non-steroidal anti-inflammatory drugs (NSAIDs) represent a p
88      Furthermore, topical application of non-steroidal anti-inflammatory drugs (NSAIDs) significantly
89                                          Non-steroidal anti-inflammatory drugs (NSAIDs) use in the ye
90                Interestingly, the use of non-steroidal anti-inflammatory drugs (NSAIDs) was not assoc
91 respectively), while anti-infectives and non-steroidal anti-inflammatory drugs (NSAIDs) were frequent
92          Activity clustering showed that non-steroidal anti-inflammatory drugs (NSAIDs) were signific
93 statin drugs, low-dose aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs), and even fis
94 al trials have suggested that the use of non-steroidal anti-inflammatory drugs (NSAIDs), including as
95                          Both the use of non-steroidal anti-inflammatory drugs (NSAIDs), such as indo
96                                          Non-steroidal anti-inflammatory drugs (NSAIDs), the most wid
97 reasing prevalence of individuals taking non-steroidal anti-inflammatory drugs (NSAIDs), there is con
98 of these drugs compared with traditional non-steroidal anti-inflammatory drugs (NSAIDs).
99 nsteroidal anti-inflammatory drugs (NSAIDs), steroidal anti-inflammatory drugs (SAIDs), immunosuppres
100 gs in four therapeutic areas: analgesia (non-steroidal anti-inflammatory drugs [NSAIDs]), diabetes (m
101     This might be a result of the use of non-steroidal anti-inflammatory drugs and rheumatoid agents
102  Although Helicobacter pylori and use of non-steroidal anti-inflammatory drugs are common causes, dem
103 optimal, but combinations of opioids and non-steroidal anti-inflammatory drugs are helpful.
104 tive blood loss after tonsillectomy when non-steroidal anti-inflammatory drugs are used.
105                                          Non-steroidal anti-inflammatory drugs are widely used for th
106 t individuals taking aspirin and related non-steroidal anti-inflammatory drugs have reduced risk of l
107                                          Non-steroidal anti-inflammatory drugs inhibit PG synthesis v
108 lation of serine 121 in cells exposed to non-steroidal anti-inflammatory drugs leads to HSP90 dissoci
109 ve consistently demonstrated that common non-steroidal anti-inflammatory drugs may protect against th
110                              A subset of non-steroidal anti-inflammatory drugs modulates the gamma cl
111 vity by the administration of PTH and/or non-steroidal anti-inflammatory drugs or COX-2 selective inh
112 e of such therapies precluded the use of non-steroidal anti-inflammatory drugs or other enzyme inhibi
113 ics, antimotility agents, narcotics, and non-steroidal anti-inflammatory drugs should not be given to
114 statin, antihypertensive medications and non-steroidal anti-inflammatory drugs therapy) as well as 4
115           Selective COX-2 inhibitors are non-steroidal anti-inflammatory drugs which directly target
116 ion in ulcer complications compared with non-steroidal anti-inflammatory drugs without an increase in
117 nesthetics, ketamine, acetaminophen, and non-steroidal anti-inflammatory drugs) analgesic drugs can m
118 diuretics, antivirals, methotrexate, and non-steroidal anti-inflammatory drugs) is organic anion tran
119 tack therapies (eg, simple analgesics or non-steroidal anti-inflammatory drugs) or specific agents wi
120                       Unlike antipyretic non-steroidal anti-inflammatory drugs, APAP elicits hypother
121 omplications compared with non-selective non-steroidal anti-inflammatory drugs, but evidence is limit
122  and analgesic properties to traditional non-steroidal anti-inflammatory drugs, but with significantl
123 cancer, and is a key molecular target of non-steroidal anti-inflammatory drugs, compounds that reduce
124     Other agents, such as aspirin, other non-steroidal anti-inflammatory drugs, COX-2 inhibitors, ret
125 tments have been suggested, ranging from non-steroidal anti-inflammatory drugs, drugs for neuropathic
126 ecretase modulators (GSMs), such as some non-steroidal anti-inflammatory drugs, is a promising therap
127 n pharmacotherapies, which have included non-steroidal anti-inflammatory drugs, must take into accoun
128  inhibitor lumiracoxib compared with two non-steroidal anti-inflammatory drugs, naproxen and ibuprofe
129 d PUD was associated with current use of non-steroidal anti-inflammatory drugs, oral steroids or acid
130  In this study we evaluate the effect of non-steroidal anti-inflammatory drugs, such as indomethacin
131 d placebo-controlled trials, traditional non-steroidal anti-inflammatory drugs, such as naproxen, dic
132                                          Non-steroidal anti-inflammatory drugs, which inhibit the cyc
133 s the principal target for the action of non-steroidal anti-inflammatory drugs.
134 a target for the development of specific non-steroidal anti-inflammatory drugs.
135 ioselective oxidation of several anionic non-steroidal anti-inflammatory drugs.
136 esults against gastric damage induced by non-steroidal anti-inflammatory drugs.
137 he potential role of these drugs as oral non-steroidal anti-inflammatory therapy for asthma and COPD
138 double endocrine targeting approach with the steroidal anti-oestrogen fulvestrant in combination with
139 therapy merits discussion as an alternative; steroidal antiandrogen monotherapy should not be offered
140               Cyproterone acetate (CPA) is a steroidal antiandrogen used clinically in the treatment
141 rapy may be discussed as an alternative, but steroidal antiandrogens should not be offered as monothe
142 tained within this class of molecules is the steroidal antiestrogen ICI182,780 (faslodex), recently a
143  cleavage of all its substrates, certain non-steroidal antiinflammatory drugs (NSAIDs) have been show
144 nd isolates at 100 mug/mL was similar to non-steroidal antiinflammatory drugs aspirin, ibuprofen and
145 ablished anticoagulants like heparin and non-steroidal antiinflammatory drugs may have a solid basis.
146 he polycyclic domain of advanced and complex steroidal architectures.
147  To compare time to progression (TTP) with a steroidal aromatase inhibitor (AI) atamestane (ATA) comb
148  double-blind clinical trial to evaluate the steroidal aromatase inhibitor exemestane as extended adj
149 omised trial that compared the switch to the steroidal aromatase inhibitor exemestane with continuati
150 e) Flutamide + ATD (androgen antagonist plus steroidal aromatase inhibitor); or (f) dihydrotestostero
151                                Exemestane, a steroidal aromatase inhibitor, reduced invasive breast c
152 ive breast cancer that has progressed on non-steroidal aromatase inhibitors (NSAIs) is unclear.
153 serves bone in postmenopausal women, but non-steroidal aromatase inhibitors accelerate bone loss and
154 renders the beta-clamshell structure of this steroidal bile acid transport protein unfolded.
155                         LCA is an endogenous steroidal bile acid, variously reported to have both car
156         Previous work has shown that certain steroidal bis-(N-phenyl)ureas, derived from cholic acid,
157 ails of the structure determination of these steroidal bis-sulfates [petromyzosterol disulfate (PSDS,
158                       New chemical entities, steroidal C-17 benzoazoles (5, 6, 9 and 10) and pyrazine
159 t of diosgenin and several structure-related steroidal compounds on the growth of faecal anaerobes is
160 nal theory (DFT) calculations to suggest non-steroidal compounds selective for CYP17A1.
161 ns of mixtures of laser dyes and mixtures of steroidal compounds were performed to illustrate the cap
162 ost important phase II metabolic reaction of steroidal compounds.
163 e two species' spores respond differently to steroidal compounds.
164 gordonii and found to have homologies to the steroidal core of cardiac glycosides.
165              The ability to quickly set this steroidal core with preinstalled functional handles and
166 electivity and fewer side effects than their steroidal counterparts.
167                      1,3-Dienes derived from steroidal D-ring C 17-ketones undergo Ni(II)-catalyzed h
168   The stereoselective construction of C20 in steroidal derivatives by a highly diastereoselective Ir-
169                            Bile salts act as steroidal detergents in the gut, and could also interact
170                                              Steroidal dexamethasone is as effective as non-steroidal
171 , fast, and reliable biochemical read out of steroidal drug pharmacodynamics could enable a rapid and
172                           We found that many steroidal drugs (such as dexamethasone and cortisone) an
173 rmones testosterone and estradiol as well as steroidal drugs.
174 straightforward access to geometrically pure steroidal enol tosylate and enol triflate intermediates
175 d applications include allylic oxidations of steroidal enones.
176    These results show that beta-LGND2, a non-steroidal ERbeta selective agonist, could be a useful th
177  halogenated estrogens made up 60-70% of the steroidal estrogen load on a molar basis.
178                                         Four steroidal estrogens (17beta-estradiol, estrone, estriol,
179 n in vitro ER activity and concentrations of steroidal estrogens after correcting for the in vitro po
180                                              Steroidal estrogens are potent endocrine-disrupting chem
181 tion reagents to enhance the sensitivity for steroidal estrogens in liquid chromatography electrospra
182                   The biological function of steroidal estrogens is related to their electronic prope
183 tipes) were exposed to solutions of singular steroidal estrogens or to the estrogenic extract of an a
184                     Of the hormone analytes, steroidal estrogens were more abundant than androgens or
185 Phytoestrogens were often more abundant than steroidal estrogens, but contributed minimally toward to
186 t known to increase in vivo potency in other steroidal estrogens, into the (17alpha,20E)-21-(trifluor
187 ed site-specific C-H oxyfunctionalization of steroidal ethers with periodate or bromate as terminal o
188 ed 1,2-dioxines along with a 1,3-dialkyl and steroidal example, with yields ranging from moderate to
189 bitors (AIs) letrozole, anastrozole, and the steroidal exemestane were approved in the U.S. in the la
190 nonsteroidal (letrozole and anastrozole) and steroidal (exemestane) aromatase inhibitors may allow tr
191 ar affinity towards other hormones of the E2 steroidal family and excellent discrimination against po
192 ng squaramide groups in axial positions on a steroidal framework.
193 tors 7E and 7Z, consisting of two androstane steroidal frameworks linked by the D rings by triple bon
194                                          The steroidal glucocorticoid antagonist mifepristone has bee
195 atory drugs may offer a safer alternative to steroidal glucocorticoids in the treatment of inflammato
196 cs in wild tomato unreveal potential role of steroidal glyco-alkaloids and phenylpropanoids during ea
197  of both acetylcholinesterase activity and a steroidal glycoalkaloid with anticholinesterase activity
198 d from alpha-tomatine, an anticholinesterase steroidal glycoalkaloid.
199 triggered metabolic changes were active from steroidal glycol-alkaloid (SGA), lignin and flavonoid bi
200                                            A steroidal glycoside with anorectic activity in animals,
201 h as vitamin D analogs and various antitumor steroidal glycosides.
202 had a profile similar to that of a classical steroidal GR agonist.
203     Trenbolone acetate (TBA) is a high-value steroidal growth promoter often administered to beef cat
204 ceptors in lung cancer progression, and this steroidal growth-stimulatory pathway may be promoted by
205 ounds-all of which are spiroketal-containing steroidal heterodimers-that inhibit the proliferation of
206                               In plants, the steroidal hormone brassinosteroid (BR) regulates numerou
207 expression induction after exposure to other steroidal hormones (11-ketotestosterone approximately te
208 n of endocrine-disrupting chemicals, such as steroidal hormones and 4-nonylphenol, that can disrupt e
209 es, personal care products, pharmaceuticals, steroidal hormones, and pesticides.
210           Small lipophilic molecules such as steroidal hormones, retinoids, and free fatty acids cont
211  important group of molecular fossils is the steroidal hydrocarbons (steranes), which are the diagene
212 alts that vary in the number and position of steroidal hydroxyl groups and the presence and type of s
213 eroidal dexamethasone is as effective as non-steroidal ibuprofen for preventing or controlling postop
214                                     Five new steroidal imidazoles, amaranzoles B-F, were isolated fro
215                                          The steroidal inhibitor exemestane is partially non-cross-re
216 ndrosta-1,4-diene-3,17-dione) is a synthetic steroidal inhibitor of the aromatase reaction that catal
217 ence of either abiraterone, a first-in-class steroidal inhibitor recently approved by the US Food and
218 cellent discrimination against potential non-steroidal interfering agents.
219 duction of these enones gave the pentacyclic steroidal ketones 2 alpha,3beta- (8) and 2 alpha,3 alpha
220             Withaferin A (WA), a C5,C6-epoxy steroidal lactone derived from a medicinal plant (Withan
221                       Withaferin A (WA) is a steroidal lactone purified from medicinal plant "Indian
222 thesize a large array of biologically active steroidal lactone triterpenoids called withanolides.
223                      Withaferin A (WFA) is a steroidal lactone with antitumor effects manifested at m
224                  28-Homobrassinolide (HB), a steroidal lactone with potent plant growth-promoting pro
225       Here we show that Withaferin A (WA), a steroidal lactone, causes a change in NEMO's interaction
226 e have purified physapubescin, a predominant steroidal lactone, from medicinal plant Physalis pubesce
227 itis elegans nuclear receptor DAF-12 and its steroidal ligand directly activate promoters of let-7 mi
228 t of dihydrotestosterone (DHT, an endogenous steroidal ligand for the AR).
229  was activated in vivo by inclusion of a non-steroidal ligand in the diet, the expression of the mRNA
230           At nanomolar concentrations, these steroidal ligands (called dafachronic acids) bind and tr
231  is a great interest in the discovery of non-steroidal ligands able to bind to the ligand-binding dom
232 ful scaffold to generate novel and selective steroidal ligands for GP-BAR1.
233 ved neuroendocrine pathways that converge on steroidal ligands of the nuclear receptor DAF-12, a homo
234 mpanies have been developing a series of non-steroidal ligands that consist of different chemical sca
235 OR7D4, and in vivo olfactory perception of 2 steroidal ligands--androstenone and androstadienone--che
236 F-12 function is regulated by bile acid-like steroidal ligands; however, tools for investigating thei
237  a series of recently published studies, the steroidal lipid, cholesterol, has emerged as a clinicall
238 teins occurred when 25-OH-cholesterol or non-steroidal LXR agonists (GW3965, TO-901317) were used.
239 gesterone acetate to mimic the decidualizing steroidal milieu of the luteal phase and early pregnancy
240                                              Steroidal mineralocorticoid receptor (MR) antagonists ar
241 he renoprotective effects of Ly, a novel non-steroidal mineralocorticoid receptor (MR) blocker, throu
242 ound to improve discrimination against other steroidal molecules and to improve colorimetric sensitiv
243 similar blood pressure (BP) reduction as the steroidal MR antagonist eplerenone, providing proof-of-c
244 entified as having comparable potency to the steroidal MR antagonist eplerenone.
245      This effect, however, was restricted to steroidal MR antagonists as a nonsteroidal MR antagonist
246                    Therefore, the endogenous steroidal Na/K-ATPase inhibitor, marinobufagenin, is syn
247 rine-derived highly potent antiproliferative steroidal natural product, and nine closely related anal
248   The total synthesis of the highly degraded steroidal natural product, aplykurodinone-1 (1), has bee
249 of new synthetic disconnections in preparing steroidal natural products.
250  a novel approach to terminate the action of steroidal neuromuscular blockers (sugammadex).
251 ms very tight complexes in a 1: 1 ratio with steroidal neuromuscular blocking agents.
252 e been designed that selectively encapsulate steroidal neuromuscular blocking agents.
253                                          The steroidal neurotoxin (-)-batrachotoxin functions as a po
254                      Sugammadex encapsulates steroidal NMBAs.
255 relationship study provided a new potent and steroidal nonestrogenic inhibitor of 17beta-HSD1 named 3
256 nd intensity variance in perception of these steroidal odours.
257                        ICI 182 780 is a pure steroidal oestrogen receptor (ER) antagonist that blocks
258 e effect profiles versus currently available steroidal oral contraceptives.
259      Here we describe GDC-0810, a novel, non-steroidal, orally bioavailable selective ER downregulato
260               This suggests a role for a non-steroidal ovarian factor on adult female VZ cell prolife
261 nkeys, but in contrast to currently approved steroidal PR agonists, it did not suppress estradiol lev
262 teroids of either enantiomeric series, these steroidal products have been selectively functionalized
263 (50) value of 0.1 nm, comparable with potent steroidal progestins such as medroxyprogesterone acetate
264 th a higher relative affinity than reference steroidal progestins.
265 lin (SHBG) is believed to play a key role in steroidal radiopharmaceutical delivery to target tissues
266             It is increasingly accepted that steroidal receptor co-regulators may also function in th
267             It is increasingly accepted that steroidal receptor coregulators may also function in the
268 orphan nuclear receptor and demonstrate that steroidal regulation of reproduction, from biology to mo
269 are more photostable but also maintain their steroidal ring structure and therefore may retain some b
270                    Containers 1a-1e bind the steroidal ring system and aromatic moieties of insoluble
271 ogues possessing a framework that mimics the steroidal ring system.
272    Collectively, these results indicate that steroidal sapogenins may be a novel class of prebiotics
273 alysis showed that the prebiotic activity of steroidal sapogenins might require structural elements o
274                                 Diosgenin, a steroidal saponin present in fenugreek (Trigonella foenu
275 Existing techniques presently used for Yucca steroidal saponin quantification remain either inaccurat
276       Our results reveal for the first time, steroidal saponins from S. paniculatum and the antiulcer
277 d does not over- or under-estimate levels of steroidal saponins.
278 andard of saponins, to quantify the group of steroidal saponins.
279 7A1 inhibitor, abiraterone, which contains a steroidal scaffold similar to the endogenous CYP17A1 sub
280 n of polycyclic molecules including modified steroidal scaffolds as well as challenging-to-synthesize
281                                    Using non-steroidal scaffolds is expected to enable the design of
282                                          Non-steroidal selective-AR modulator, GTx-026, which selecti
283 gnancy C. sordellii infections suggests that steroidal sex hormones might regulate its capacity to ge
284                                              Steroidal sex hormones play an important role in the neu
285 ology for the development of a novel A,B-cis steroidal skeleton system containing a C3-C9 single bond
286 natural products characterized by an unusual steroidal skeleton, which have been found to inhibit dif
287  signaling, we report discovery of novel non-steroidal small-molecule compounds that activate the vit
288        Our study reinforces the concept that steroidal sodium channel agonists bind in the inner pore
289                   Glucocorticoids, which are steroidal stress hormones, have a broad array of biologi
290  for hormone-independent tumors, such as the steroidal STX140 and nonsteroidal counterparts, acting i
291                        A variety of Delta(5)-steroidal substrates are selectively oxidized to the cor
292  the role of SHBG in radiotracer delivery of steroidal systems to target tissues.
293 tanyl acetate resulted in a 1:1 mixture of a steroidal tetrahydrofuran and a steroidal tetrahydropyra
294 mixture of a steroidal tetrahydrofuran and a steroidal tetrahydropyran.
295 ed defensive glands on its neck that contain steroidal toxins known as bufadienolides.
296                  Cardenolides are remarkable steroidal toxins that have become model systems, critica
297  in toad-free regions are left undefended by steroidal toxins.
298 rols, brassinosteroid phytohormones, and non-steroidal triterpenoids.
299              A key feature of the nanoporous steroidal urea (NPSU) structure is that groups at either
300 uloskeletal conditions and analgesic and non-steroidal use.

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