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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 an 100 Food and Drug Administration-approved steroidal agents are prescribed daily for indications in
6  products, are glycosides of triterpenoid or steroidal aglycones (sapogenins).
7 onally defined a novel pharmacophore for the steroidal agonist site.
8  even the best clinically approved synthetic steroidal agonists are prone to cross-reactivity and off
9                                Compared with steroidal agonists for the androgen receptor (AR) (e.g.
10 s enabled the purification of the respective steroidal alcohols in moderate to excellent yields.
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      This cluster co-localizes with a tomato steroidal alkaloid gene cluster and is syntenic to a chr
17                       Batrachotoxin (BTX), a steroidal alkaloid, and pyrethroid insecticides bind to
18 fic tropane (l-hyoscyamine, scopolamine) and steroidal alkaloids (alpha-solanine, alpha-chaconine) in
19 resin acids, mefenamic acid, oxybenzone, and steroidal alkaloids in the bile or plasma, and there wer
20                                  A series of steroidal alpha,beta-unsaturated hydrazones is presented
21 samples of 2 and 3 with those of appropriate steroidal analogues [e.g., petromyzonol sulfate (PS, 1,
22 e a less detrimental effect on bone than non-steroidal anastrozole.
23 echanisms, EDCs interfere with the action of steroidal and non-steroidal receptors, and alter enzymat
24                     This first comparison of steroidal and nonsteroidal classes of aromatase inhibito
25 ophore that, over some 20 years, have led to steroidal and nonsteroidal drugs in numerous preclinical
26 al function and the electronic properties of steroidal and nonsteroidal estrogens by analysis of the
27  new rational template for drug discovery of steroidal and nonsteroidal glucocorticoids that can be s
28 d work to date underlying the development of steroidal and nonsteroidal receptor ligands, including t
29     In this study, we show that although the steroidal and nonsteroidal SERDs target ERalpha for degr
30                  The LBD responds to classic steroidal and nonsteroidal small ligands; both may selec
31 me, the inhibitory activities of a series of steroidal and nonsteroidal sulfamate derivatives against
32 nsible for immunosuppression in serum is non-steroidal and of high molecular weight.
33   We describe two structurally similar 4-aza-steroidal androgen receptor (AR) ligands, Cl-4AS-1, a fu
34                                     Although steroidal antagonists such as spironolactone and epleren
35                     Alcohol, exercise or non-steroidal anti-inflamatory drugs (NSAID) are frequently
36 netic pathway and uniquely revealed that non-steroidal anti-inflammatories (NSAIDs) rank just as high
37                                          Non-steroidal anti-inflammatories (NSAIDs), such as meloxica
38 an interesting alternative to the use of non-steroidal anti-inflammatories and/or opioids for the con
39 ketamine, physical exercise, and certain non-steroidal anti-inflammatories have been shown to alter k
40 ritic dogs participating in a cross-over non-steroidal anti-inflammatory (meloxicam) drug trial.
41 ant concentrations of ibuprofen (IBF), a non-steroidal anti-inflammatory agent and prevalent environm
42 e-1IC50/anti-cyclooxygense-2IC50>1) than non-steroidal anti-inflammatory agent ibuprofen (0.44) descr
43 rugs can easily be conjugated to another non-steroidal anti-inflammatory agent, leading to easy synth
44                                          Non-steroidal anti-inflammatory agents (NSAIDs) are associat
45                                          Non-steroidal anti-inflammatory agents inhibit the productio
46 s currently on the market, including the non-steroidal anti-inflammatory blockbuster drug celecoxib.
47    Define the effectiveness of a topical non-steroidal anti-inflammatory drug (NSAID) added to topica
48             Treatment with a NO-donating non-steroidal anti-inflammatory drug (NSAID) alleviates this
49 se (GERD), Barrett's esophagus (BE), and non-steroidal anti-inflammatory drug (NSAID) bleeding prophy
50    The unprecedented polymorphism of the non-steroidal anti-inflammatory drug (NSAID) flufenamic acid
51                                   In the non-steroidal anti-inflammatory drug (NSAID) group, patients
52                           Ibuprofen is a non-steroidal anti-inflammatory drug (NSAID) that independen
53 ow that inhibition of endogenous PGE2 by non-steroidal anti-inflammatory drug (NSAID) treatment in mi
54                                          Non-steroidal anti-inflammatory drug (NSAID) treatment suppr
55 mine-gallic acid hybrid molecule against non-steroidal anti-inflammatory drug (NSAID)-induced gastrop
56               We used an animal model of non-steroidal anti-inflammatory drug (NSAID)-induced SI epit
57                                      The non-steroidal anti-inflammatory drug aspirin and its metabol
58                Tolfenamic acid (TA) is a non-steroidal anti-inflammatory drug associated with anti-tu
59  to 70%-80% of patients with a suspected non-steroidal anti-inflammatory drug hypersensitivity (NSAID
60  investigated potential therapy with the non-steroidal anti-inflammatory drug ibuprofen.
61                                      The non-steroidal anti-inflammatory drug sulindac decreases size
62               Flufenamic acid (FFA) is a non-steroidal anti-inflammatory drug that has been long used
63                    Pretreatment with the non-steroidal anti-inflammatory drug, 2-cyano-3,12-dioxoolea
64  (DOX) and carprofen (CPF), a veterinary non-steroidal anti-inflammatory drug, have synergistic antim
65                             Ibuprofen, a non-steroidal anti-inflammatory drug, rescued female embryos
66 andomisation was stratified by asthma or non-steroidal anti-inflammatory drug-exacerbated respiratory
67 ose and regularity of aspirin use, other non-steroidal anti-inflammatory drugs (NSAID), and the effec
68                                  Certain non-steroidal anti-inflammatory drugs (NSAIDs) (e.g., rofeco
69 that underlie the antitumour activity of non-steroidal anti-inflammatory drugs (NSAIDs) against color
70                                          Non-steroidal anti-inflammatory drugs (NSAIDs) are among the
71                                          Non-steroidal anti-inflammatory drugs (NSAIDs) are among the
72 2 selective inhibitors and non-selective non-steroidal anti-inflammatory drugs (NSAIDs) are associate
73                                          Non-steroidal anti-inflammatory drugs (NSAIDs) are known gam
74                                          Non-steroidal anti-inflammatory drugs (NSAIDs) are used to m
75                                          Non-steroidal anti-inflammatory drugs (NSAIDs) cause damage
76                                          Non-steroidal anti-inflammatory drugs (NSAIDs) damage the ga
77  selective inhibitors versus traditional non-steroidal anti-inflammatory drugs (NSAIDs) has not been
78    The progressive consumption growth of non-steroidal anti-inflammatory drugs (NSAIDs) has progressi
79                                          Non-steroidal anti-inflammatory drugs (NSAIDs) have been wid
80 sis (FASS) for the determination of five non-steroidal anti-inflammatory drugs (NSAIDs) in bovine mil
81                                          Non-steroidal anti-inflammatory drugs (NSAIDs) inhibit cyclo
82                   Topically administered non-steroidal anti-inflammatory drugs (NSAIDs) inhibit perio
83 trials demonstrate that long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) markedly redu
84 opreventive effect for aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) on colorectal
85 inically important errors: non-selective non-steroidal anti-inflammatory drugs (NSAIDs) prescribed to
86               Nitric oxide (NO)-donating non-steroidal anti-inflammatory drugs (NSAIDs) represent a p
87                                          Non-steroidal anti-inflammatory drugs (NSAIDs) use in the ye
88                Interestingly, the use of non-steroidal anti-inflammatory drugs (NSAIDs) was not assoc
89 respectively), while anti-infectives and non-steroidal anti-inflammatory drugs (NSAIDs) were frequent
90          Activity clustering showed that non-steroidal anti-inflammatory drugs (NSAIDs) were signific
91 al trials have suggested that the use of non-steroidal anti-inflammatory drugs (NSAIDs), including as
92                          Both the use of non-steroidal anti-inflammatory drugs (NSAIDs), such as indo
93                                          Non-steroidal anti-inflammatory drugs (NSAIDs), the most wid
94 an inadequate response or intolerance to non-steroidal anti-inflammatory drugs (NSAIDs).
95 of these drugs compared with traditional non-steroidal anti-inflammatory drugs (NSAIDs).
96 nsteroidal anti-inflammatory drugs (NSAIDs), steroidal anti-inflammatory drugs (SAIDs), immunosuppres
97 gs in four therapeutic areas: analgesia (non-steroidal anti-inflammatory drugs [NSAIDs]), diabetes (m
98     This might be a result of the use of non-steroidal anti-inflammatory drugs and rheumatoid agents
99  Although Helicobacter pylori and use of non-steroidal anti-inflammatory drugs are common causes, dem
100 optimal, but combinations of opioids and non-steroidal anti-inflammatory drugs are helpful.
101 tive blood loss after tonsillectomy when non-steroidal anti-inflammatory drugs are used.
102                                          Non-steroidal anti-inflammatory drugs are widely used for th
103 c drugs (DMARDs), or at least 4 weeks of non-steroidal anti-inflammatory drugs for psoriatic arthriti
104 t individuals taking aspirin and related non-steroidal anti-inflammatory drugs have reduced risk of l
105 ve consistently demonstrated that common non-steroidal anti-inflammatory drugs may protect against th
106                              A subset of non-steroidal anti-inflammatory drugs modulates the gamma cl
107 vity by the administration of PTH and/or non-steroidal anti-inflammatory drugs or COX-2 selective inh
108 e of such therapies precluded the use of non-steroidal anti-inflammatory drugs or other enzyme inhibi
109 statin, antihypertensive medications and non-steroidal anti-inflammatory drugs therapy) as well as 4
110  should consider the pharmacokinetics of non-steroidal anti-inflammatory drugs to determine the optim
111                                     Oral non-steroidal anti-inflammatory drugs versus other oral anal
112           Selective COX-2 inhibitors are non-steroidal anti-inflammatory drugs which directly target
113 diuretics, antivirals, methotrexate, and non-steroidal anti-inflammatory drugs) is organic anion tran
114 tack therapies (eg, simple analgesics or non-steroidal anti-inflammatory drugs) or specific agents wi
115 roenteritis, female sex, smoking, use of non-steroidal anti-inflammatory drugs, and Helicobacter pylo
116                       Unlike antipyretic non-steroidal anti-inflammatory drugs, APAP elicits hypother
117  and analgesic properties to traditional non-steroidal anti-inflammatory drugs, but with significantl
118 cancer, and is a key molecular target of non-steroidal anti-inflammatory drugs, compounds that reduce
119     Other agents, such as aspirin, other non-steroidal anti-inflammatory drugs, COX-2 inhibitors, ret
120 tments have been suggested, ranging from non-steroidal anti-inflammatory drugs, drugs for neuropathic
121 ecretase modulators (GSMs), such as some non-steroidal anti-inflammatory drugs, is a promising therap
122 n pharmacotherapies, which have included non-steroidal anti-inflammatory drugs, must take into accoun
123 d PUD was associated with current use of non-steroidal anti-inflammatory drugs, oral steroids or acid
124  In this study we evaluate the effect of non-steroidal anti-inflammatory drugs, such as indomethacin
125                                          Non-steroidal anti-inflammatory drugs, which inhibit the cyc
126 s the principal target for the action of non-steroidal anti-inflammatory drugs.
127 a target for the development of specific non-steroidal anti-inflammatory drugs.
128 wo or intolerance or contraindication to non-steroidal anti-inflammatory drugs.
129 adequate response or contraindication to non-steroidal anti-inflammatory drugs.
130 esults against gastric damage induced by non-steroidal anti-inflammatory drugs.
131 mmunosuppression followed by maintenance non-steroidal anti-inflammatory therapy).
132 double endocrine targeting approach with the steroidal anti-oestrogen fulvestrant in combination with
133 therapy merits discussion as an alternative; steroidal antiandrogen monotherapy should not be offered
134               Cyproterone acetate (CPA) is a steroidal antiandrogen used clinically in the treatment
135 tained within this class of molecules is the steroidal antiestrogen ICI182,780 (faslodex), recently a
136 nd isolates at 100 mug/mL was similar to non-steroidal antiinflammatory drugs aspirin, ibuprofen and
137 ablished anticoagulants like heparin and non-steroidal antiinflammatory drugs may have a solid basis.
138 he polycyclic domain of advanced and complex steroidal architectures.
139  To compare time to progression (TTP) with a steroidal aromatase inhibitor (AI) atamestane (ATA) comb
140  double-blind clinical trial to evaluate the steroidal aromatase inhibitor exemestane as extended adj
141 omised trial that compared the switch to the steroidal aromatase inhibitor exemestane with continuati
142 e) Flutamide + ATD (androgen antagonist plus steroidal aromatase inhibitor); or (f) dihydrotestostero
143                                Exemestane, a steroidal aromatase inhibitor, reduced invasive breast c
144 ive breast cancer that has progressed on non-steroidal aromatase inhibitors (NSAIs) is unclear.
145 serves bone in postmenopausal women, but non-steroidal aromatase inhibitors accelerate bone loss and
146 ent inhibitors than lead compound 1, whereas steroidal backbone (A-ring) change led to identifying pr
147             Through subtle modification to a steroidal backbone, a recently developed drug, vamorolon
148 renders the beta-clamshell structure of this steroidal bile acid transport protein unfolded.
149                         LCA is an endogenous steroidal bile acid, variously reported to have both car
150         Previous work has shown that certain steroidal bis-(N-phenyl)ureas, derived from cholic acid,
151 ails of the structure determination of these steroidal bis-sulfates [petromyzosterol disulfate (PSDS,
152                                              Steroidal C7beta alcohols and their respective esters ha
153 t of diosgenin and several structure-related steroidal compounds on the growth of faecal anaerobes is
154 nal theory (DFT) calculations to suggest non-steroidal compounds selective for CYP17A1.
155 The review deals with an expanding number of steroidal compounds that are capable of forming a metall
156 ns of mixtures of laser dyes and mixtures of steroidal compounds were performed to illustrate the cap
157 ost important phase II metabolic reaction of steroidal compounds.
158 e two species' spores respond differently to steroidal compounds.
159              The ability to quickly set this steroidal core with preinstalled functional handles and
160 electivity and fewer side effects than their steroidal counterparts.
161                      1,3-Dienes derived from steroidal D-ring C 17-ketones undergo Ni(II)-catalyzed h
162   The stereoselective construction of C20 in steroidal derivatives by a highly diastereoselective Ir-
163                            Bile salts act as steroidal detergents in the gut, and could also interact
164                                              Steroidal dexamethasone is as effective as non-steroidal
165 , fast, and reliable biochemical read out of steroidal drug pharmacodynamics could enable a rapid and
166                           We found that many steroidal drugs (such as dexamethasone and cortisone) an
167 rmones testosterone and estradiol as well as steroidal drugs.
168 s in mixture experiments and resulted in the steroidal endocrine disrupting compounds in higher K(sw)
169 straightforward access to geometrically pure steroidal enol tosylate and enol triflate intermediates
170 d applications include allylic oxidations of steroidal enones.
171    These results show that beta-LGND2, a non-steroidal ERbeta selective agonist, could be a useful th
172  halogenated estrogens made up 60-70% of the steroidal estrogen load on a molar basis.
173                                         Four steroidal estrogens (17beta-estradiol, estrone, estriol,
174 harmaceutical compounds (carbamazepine), and steroidal estrogens (estrone, 17-beta-estradiol, estriol
175 n in vitro ER activity and concentrations of steroidal estrogens after correcting for the in vitro po
176                                              Steroidal estrogens are potent endocrine-disrupting chem
177 tion reagents to enhance the sensitivity for steroidal estrogens in liquid chromatography electrospra
178                   The biological function of steroidal estrogens is related to their electronic prope
179 tipes) were exposed to solutions of singular steroidal estrogens or to the estrogenic extract of an a
180                     Of the hormone analytes, steroidal estrogens were more abundant than androgens or
181 Phytoestrogens were often more abundant than steroidal estrogens, but contributed minimally toward to
182 t known to increase in vivo potency in other steroidal estrogens, into the (17alpha,20E)-21-(trifluor
183 ed site-specific C-H oxyfunctionalization of steroidal ethers with periodate or bromate as terminal o
184 ed 1,2-dioxines along with a 1,3-dialkyl and steroidal example, with yields ranging from moderate to
185 bitors (AIs) letrozole, anastrozole, and the steroidal exemestane were approved in the U.S. in the la
186 ar affinity towards other hormones of the E2 steroidal family and excellent discrimination against po
187 example of such pollution are estrogens, the steroidal female reproductive hormones.
188 ng squaramide groups in axial positions on a steroidal framework.
189 tors 7E and 7Z, consisting of two androstane steroidal frameworks linked by the D rings by triple bon
190                                          The steroidal glucocorticoid antagonist mifepristone has bee
191 atory drugs may offer a safer alternative to steroidal glucocorticoids in the treatment of inflammato
192 cs in wild tomato unreveal potential role of steroidal glyco-alkaloids and phenylpropanoids during ea
193 and provided a genomic basis for the lack of steroidal glycoalkaloid compounds in the Capsicum genus.
194 ing 14 genes, including a previously defined steroidal glycoalkaloid gene cluster.
195                                          The steroidal glycoalkaloid mQTL was localized to a chromoso
196 antitative trait loci (mQTL) for flavonoids, steroidal glycoalkaloids and further specialized metabol
197 s (and adverse effects), of polyphenolic and steroidal glycoalkaloids in the diet there is a growing
198  Two putative mQTL for flavonols and one for steroidal glycoalkaloids were cross-validated by evaluat
199 nding of the accumulation of polyphenols and steroidal glycoalkaloids, and how this knowledge may be
200 triggered metabolic changes were active from steroidal glycol-alkaloid (SGA), lignin and flavonoid bi
201                                 Charantin, a steroidal glycoside, exists as a mixture of stigmasterol
202 ytochemicals like polyphenols, saponins, and steroidal glycosides, but its crop is greatly affected b
203 h as vitamin D analogs and various antitumor steroidal glycosides.
204 had a profile similar to that of a classical steroidal GR agonist.
205     Trenbolone acetate (TBA) is a high-value steroidal growth promoter often administered to beef cat
206 ounds-all of which are spiroketal-containing steroidal heterodimers-that inhibit the proliferation of
207                               In plants, the steroidal hormone brassinosteroid (BR) regulates numerou
208 expression induction after exposure to other steroidal hormones (11-ketotestosterone approximately te
209 n of endocrine-disrupting chemicals, such as steroidal hormones and 4-nonylphenol, that can disrupt e
210 es, personal care products, pharmaceuticals, steroidal hormones, and pesticides.
211           Small lipophilic molecules such as steroidal hormones, retinoids, and free fatty acids cont
212  important group of molecular fossils is the steroidal hydrocarbons (steranes), which are the diagene
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 thesize a large array of biologically active steroidal lactone triterpenoids called withanolides.
222                      Withaferin A (WFA) is a steroidal lactone with antitumor effects manifested at m
223                  28-Homobrassinolide (HB), a steroidal lactone with potent plant growth-promoting pro
224       Here we show that Withaferin A (WA), a steroidal lactone, causes a change in NEMO's interaction
225 e have purified physapubescin, a predominant steroidal lactone, from medicinal plant Physalis pubesce
226 itis elegans nuclear receptor DAF-12 and its steroidal ligand directly activate promoters of let-7 mi
227  was activated in vivo by inclusion of a non-steroidal ligand in the diet, the expression of the mRNA
228  is a great interest in the discovery of non-steroidal ligands able to bind to the ligand-binding dom
229 ful scaffold to generate novel and selective steroidal ligands for GP-BAR1.
230 ved neuroendocrine pathways that converge on steroidal ligands of the nuclear receptor DAF-12, a homo
231 mpanies have been developing a series of non-steroidal ligands that consist of different chemical sca
232 OR7D4, and in vivo olfactory perception of 2 steroidal ligands--androstenone and androstadienone--che
233 F-12 function is regulated by bile acid-like steroidal ligands; however, tools for investigating thei
234  a series of recently published studies, the steroidal lipid, cholesterol, has emerged as a clinicall
235 neuroactive glucocorticoid/pregnanolone-type steroidal metabolites.
236                                The future of steroidal metallogels holds a myriad of potential applic
237 hesis, characterization, and applications of steroidal metallogels.
238 gesterone acetate to mimic the decidualizing steroidal milieu of the luteal phase and early pregnancy
239                                              Steroidal mineralocorticoid receptor (MR) antagonists ar
240 he renoprotective effects of Ly, a novel non-steroidal mineralocorticoid receptor (MR) blocker, throu
241 ndothelin receptors (eg, atrasentan) and non-steroidal mineralocorticoid receptors (eg, finerenone).
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                    Diosgenin is a spiroketal steroidal natural product extracted from plants and used
248 rine-derived highly potent antiproliferative steroidal natural product, and nine closely related anal
249   The total synthesis of the highly degraded steroidal natural product, aplykurodinone-1 (1), has bee
250 of new synthetic disconnections in preparing steroidal natural products.
251  a novel approach to terminate the action of steroidal neuromuscular blockers (sugammadex).
252 ms very tight complexes in a 1: 1 ratio with steroidal neuromuscular blocking agents.
253 e been designed that selectively encapsulate steroidal neuromuscular blocking agents.
254                                          The steroidal neurotoxin (-)-batrachotoxin functions as a po
255                      Sugammadex encapsulates steroidal NMBAs.
256 relationship study provided a new potent and steroidal nonestrogenic inhibitor of 17beta-HSD1 named 3
257 nd intensity variance in perception of these steroidal odours.
258 ounds comprising bioactive glycosides with a steroidal or triterpenoid aglycone backbone.
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  stress increased members of the neuroactive steroidal pregnane molecular family; and that Test diet
263 teroids of either enantiomeric series, these steroidal products have been selectively functionalized
264 lin (SHBG) is believed to play a key role in steroidal radiopharmaceutical delivery to target tissues
265             It is increasingly accepted that steroidal receptor coregulators may also function in the
266 terfere with the action of steroidal and non-steroidal receptors, and alter enzymatic, metabolic and
267 orphan nuclear receptor and demonstrate that steroidal regulation of reproduction, from biology to mo
268 are more photostable but also maintain their steroidal ring structure and therefore may retain some b
269                    Containers 1a-1e bind the steroidal ring system and aromatic moieties of insoluble
270 ogues possessing a framework that mimics the steroidal ring system.
271    Collectively, these results indicate that steroidal sapogenins may be a novel class of prebiotics
272 alysis showed that the prebiotic activity of steroidal sapogenins might require structural elements o
273 Existing techniques presently used for Yucca steroidal saponin quantification remain either inaccurat
274       Our results reveal for the first time, steroidal saponins from S. paniculatum and the antiulcer
275 showed higher comparative peak responses for steroidal saponins.
276 andard of saponins, to quantify the group of steroidal saponins.
277 d does not over- or under-estimate levels of steroidal saponins.
278 7A1 inhibitor, abiraterone, which contains a steroidal scaffold similar to the endogenous CYP17A1 sub
279 n of polycyclic molecules including modified steroidal scaffolds as well as challenging-to-synthesize
280                                    Using non-steroidal scaffolds is expected to enable the design of
281                                 The clinical steroidal selective estrogen receptor (ER) degrader (SER
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 alogues, we explored the modification of the steroidal side chain and inserted a methylene moiety in
286 indings suggest a tumor-suppressive role for steroidal signaling by promoting postmitotic fate when l
287 ology for the development of a novel A,B-cis steroidal skeleton system containing a C3-C9 single bond
288 natural products characterized by an unusual steroidal skeleton, which have been found to inhibit dif
289  signaling, we report discovery of novel non-steroidal small-molecule compounds that activate the vit
290        Our study reinforces the concept that steroidal sodium channel agonists bind in the inner pore
291                   Glucocorticoids, which are steroidal stress hormones, have a broad array of biologi
292  for hormone-independent tumors, such as the steroidal STX140 and nonsteroidal counterparts, acting i
293                        A variety of Delta(5)-steroidal substrates are selectively oxidized to the cor
294  the role of SHBG in radiotracer delivery of steroidal systems to target tissues.
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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