コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 n the pharmacological properties of Delta(9)-tetrahydrocannabinol.
2 uracy was significantly reduced after Delta9-tetrahydrocannabinol.
3 or marijuana's bioactive ingredient Delta(9)-tetrahydrocannabinol.
4 inuation of chronic heavy use of cannabis or tetrahydrocannabinol.
5 ediates the functional responses of Delta(9)-tetrahydrocannabinol.
6 and adolescent exposure to cannabis/delta-9-tetrahydrocannabinol.
7 diction for cocaine, amphetamine, and Delta9-tetrahydrocannabinol.
8 abinoid receptor 1 stimulation with Delta(9)-tetrahydrocannabinol.
10 icated by the exogenous cannabinoid Delta(9)-tetrahydrocannabinol (1 microM) nor reversed by the sele
11 rocannabinol (THC-COOH), 11-hydroxy-Delta(9)-tetrahydrocannabinol (11-OH-THC), and 11-nor-9-carboxy-D
12 lead compound, (-)-3-(1-adamantyl)-Delta(8)-tetrahydrocannabinol (1a, AM411), was found to have robu
18 al structures of human CB1 in complex with a tetrahydrocannabinol (AM11542) and a hexahydrocannabinol
19 A challenging step in the preparation of tetrahydrocannabinol analogs is an acid-catalyzed intram
20 efficacy and safety of nabilone, a synthetic tetrahydrocannabinol analogue, as a treatment for non-mo
21 imols (maximum daily dose, 86.4 mg of Delta9-tetrahydrocannabinol and 80 mg of cannabidiol) or placeb
24 Here we show that the cannabinoids Delta(9)-tetrahydrocannabinol and CP55940 decreased the power of
27 er States to monitor the content of Delta(9)-tetrahydrocannabinol and other cannabinoids in food and
28 owever, therapeutic applications of Delta(9)-tetrahydrocannabinol and other CB1 orthosteric receptor
30 was also demonstrated with CP55940, Delta(9)-tetrahydrocannabinol, and cannabidiol, thus suggesting t
31 f abuse including cocaine, ethanol, Delta(9)-tetrahydrocannabinol, and opiates; the antipsychotic dru
32 hydroxypropyl)cyclohexan-1-ol) and Delta(9)-tetrahydrocannabinol are orthosteric agonists for the re
33 t HU210, a structural analog of (-)-Delta(9)-tetrahydrocannabinol, binds to brain cannabinoid (CB1) r
34 e nucleus accumbens after exposure to Delta9-tetrahydrocannabinol, but less is known about cannabis u
36 binol, delta-9-tetrahydrocannabinol, delta-8-tetrahydrocannabinol, cannabichromene, delta-9-tetrahydr
38 wed male and female mice to consume Delta(9)-tetrahydrocannabinol, cannabidiol, or morphine ad libitu
39 ader (recreational) or more restrictive (low-tetrahydrocannabinol) cannabis laws were associated with
40 uana cigarette, a 2.5-mg dronabinol (delta-9-tetrahydrocannabinol) capsule, or a placebo capsule thre
41 0-CB1 receptor complex, and the (-)-Delta(9)-tetrahydrocannabinol-CB1 receptor complex, we found that
43 ith high affinity and specificity for delta9-tetrahydrocannabinol could be valuable immunopharmacothe
44 ion phase from 5 mg to a maximum of 25 mg of tetrahydrocannabinol daily and a 10 week maintenance pha
45 cannabinoids such as cannabidiol or delta-9-tetrahydrocannabinol decreased the expression of AW11201
46 to the determination of cannabidiol, delta 8-tetrahydrocannabinol (delta 8-THC), delta 9-tetrahydroca
48 -tetrahydrocannabinol (delta 8-THC), delta 9-tetrahydrocannabinol (delta 9-THC), and cannabinol in pu
49 (QSAR) for the side-chain region of Delta(8)-tetrahydrocannabinol (Delta(8)-THC) analogues is reporte
50 nalogue of the phytocannabinoid (-)-Delta(8)-tetrahydrocannabinol (Delta(8)-THC), was shown to have i
51 55,212 (64%), anandamide (42%), and Delta(9)-tetrahydrocannabinol (Delta(9)-THC) (44%) all initiated
53 f antisense oligodeoxynucleotide to Delta(9)-tetrahydrocannabinol (Delta(9)-THC) and other naturally
54 The memory-disruptive effects of Delta(9)-tetrahydrocannabinol (Delta(9)-THC) and the synthetic ca
55 ents following repeated exposure to Delta(9)-tetrahydrocannabinol (Delta(9)-THC) are associated with
56 nd 2 (CB1 and CB2) agonists such as Delta(9)-tetrahydrocannabinol (Delta(9)-THC) can produce toleranc
58 d the acute, dose-related effects of delta-9-tetrahydrocannabinol (Delta(9)-THC) on psychophysiologic
59 The acute, dose-related effects of Delta-9-tetrahydrocannabinol (Delta(9)-THC) on the auditory stea
60 -occurring Cannabis sativa alkaloid Delta(9)-tetrahydrocannabinol (Delta(9)-THC) or the synthetic can
61 reported that intracerebellar (ICB) Delta(9)-tetrahydrocannabinol (Delta(9)-THC) produces dose-depend
62 is, which are attributed to action of Delta9-tetrahydrocannabinol (Delta(9)-THC), a cannabis constitu
63 determined by the concentration of Delta(9)-tetrahydrocannabinol (Delta(9)-THC), a psychoactive cons
64 etween its psychoactive constituent, Delta-9-tetrahydrocannabinol (Delta(9)-THC), and CB(1) receptors
65 re sensitive to acutely administered delta-9-tetrahydrocannabinol (Delta(9)-THC), have delayed tolera
66 ychoactive ingredient of marijuana, Delta(9)-tetrahydrocannabinol (Delta(9)-THC), increased GluR2-lac
67 constituent of Cannabis sativa L., Delta(9)-tetrahydrocannabinol (Delta(9)-THC), led to the identifi
68 he naturally occurring cannabinoid, Delta(9)-tetrahydrocannabinol (Delta(9)-THC), releases dynorphin
70 widely used recreational agent, and Delta(9)-tetrahydrocannabinol (Delta(9)-THC), the major active co
72 ed in the psychotomimetic effects of delta-9-tetrahydrocannabinol (Delta(9)-THC), the principal activ
74 In contrast to marijuana, where Delta(9)-tetrahydrocannabinol (Delta(9)THC) is metabolized to onl
75 al activation under the influence of delta-9-tetrahydrocannabinol (delta-9-THC) and cannabidiol (CBD)
76 arijuana and its active constituent, delta-9-tetrahydrocannabinol (delta-9-THC), may reduce pain sens
77 investigated whether the effects of delta-9-tetrahydrocannabinol (delta-9-THC), the main psychoactiv
78 nnabigerol, cannabidiol, cannabinol, delta-9-tetrahydrocannabinol, delta-8-tetrahydrocannabinol, cann
80 sativa and its principal components, Delta9-tetrahydrocannabinol (Delta9-THC) and cannabidiol, are i
83 eatment of SIV-infected macaques with Delta9-tetrahydrocannabinol (Delta9-THC) increased survival and
84 d macaques, chronic administration of Delta9-tetrahydrocannabinol (Delta9-THC) inhibited viral replic
87 e concomitant increase in potency of delta-9-tetrahydrocannabinol (Delta9-THC) may have contributed t
88 o examine the effects of estrogen and delta9-tetrahydrocannabinol (delta9-THC) on learning and memory
89 were treated with escalating doses of Delta9-tetrahydrocannabinol (Delta9-THC) or R+-[2,3-dihydro-5-m
90 psychoactive ingredient in cannabis, Delta9-tetrahydrocannabinol (Delta9-THC), affects the brain mai
93 central hypothesis that exposure to Delta-9-tetrahydrocannabinol (Delta9-THC), the major psychoactiv
94 dysfunctional by chronic exposure to delta-9-tetrahydrocannabinol (Delta9-THC), the major psychoactiv
97 main active chemical in marijuana is delta9-tetrahydrocannabinol (delta9-THC); hence, monoclonal ant
98 ffects of intravenously administered delta-9-tetrahydrocannabinol (Delta9-THC; 1.19 mg/2 ml), the key
99 s with oral cannabis extract (n=211), Delta9-tetrahydrocannabinol (Delta9-THC; n=206), or placebo (n=
102 c syntheses of four photoswitchable Delta(9)-tetrahydrocannabinol derivatives (azo-THCs) from a centr
104 vo exposure to the phytocannabinoid Delta(9)-tetrahydrocannabinol disrupts the intrasynaptic nanoscal
106 (EC(50) = 3.7 microM), followed by Delta(9)-tetrahydrocannabinol (EC(50) = 14 microM) and cannabinol
108 ptors, such as the phytocannabinoid Delta(9)-tetrahydrocannabinol, exert a remarkable array of therap
110 active compound in herbal cannabis, Delta(9)-tetrahydrocannabinol, exerts all of its known central ef
111 ors, including CP55940, HU-210, and Delta(9)-tetrahydrocannabinol, failed to stimulate [(35)S]GTP gam
113 ychoactive ingredient in marijuana, Delta(9)-tetrahydrocannabinol, has been shown to inhibit adenylyl
115 pal bioactive component of marijuana, delta9-tetrahydrocannabinol, have been used for thousands of ye
116 of cannabinoid agonists, including Delta(9)-tetrahydrocannabinol, HU-210, CP55,940, 2-arachidonoylgl
117 6) and (-)-11-hydroxydimethylheptyl-Delta(8)-tetrahydrocannabinol (HU210) were drastically reduced (5
118 pic and appetite-inducing component Delta(9)-tetrahydrocannabinol, i.e., the endocannabinoid 2-arachi
119 hanism for the addictive effects of Delta(9)-tetrahydrocannabinol in juvenile-adolescents, by potenti
121 a novelly identified TRPV2 agonist, Delta(9)-tetrahydrocannabinol, indicating that human TRPV2 is fun
122 ntion (with trehalose), rescued the Delta(9)-tetrahydrocannabinol-induced impairment of motor coordin
124 tally induced higher cannabinoid [(-)-Delta9-tetrahydrocannabinol] levels constrain preimplantation e
125 rticipants were randomly assigned to a 3.95%-tetrahydrocannabinol marijuana cigarette, a 2.5-mg drona
126 hy the closely-related psychoactive compound tetrahydrocannabinol may not have the same effects on th
128 ceptor agonism using R(+)-WIN 55,212, delta9-tetrahydrocannabinol, methanandamide and JWH-133 quantit
129 vestigated whether oral dronabinol (Delta(9)-tetrahydrocannabinol) might slow the course of progressi
130 logs of the cyclic ether O,2-propano-delta 8-tetrahydrocannabinol (O,2-propano-delta 8-THC) point to
135 estigating effects of the eCB agonist Delta9-tetrahydrocannabinol on WM function in 17 healthy volunt
136 oyl glycerol, and the plant-derived Delta(9)-tetrahydrocannabinol, one of the main psychoactive compo
139 ychoactive constituent of cannabis, Delta(9)-tetrahydrocannabinol, produces in humans subjective resp
140 ctive constituent of marijuana, (-)-Delta(9)-tetrahydrocannabinol, produces most of its physiological
141 of 89% of the patients reported having used tetrahydrocannabinol products in e-cigarette devices, al
142 se-contingent delivery of vaporized Delta(9)-tetrahydrocannabinol-rich (CAN(THC)) or cannabidiol-rich
144 cannabinoid agonists WIN 55,212-2 and delta9-tetrahydrocannabinol shortened the modal response time,
145 drawal in mice rendered tolerant to Delta(9)-tetrahydrocannabinol, suggesting that AM1710 is not a fu
146 ated cumulative lifetime exposure of Delta-9-tetrahydrocannabinol (THC) (mean 168 +/- 45 versus 244 +
147 oses (30-240 mug/kg) of intravenous Delta(9)-tetrahydrocannabinol (THC) administration on the perform
148 ch indicates that administration of Delta(9)-tetrahydrocannabinol (THC) alters threat perception and
149 xy-substituted hexahydrocannabinol (HHC) and tetrahydrocannabinol (THC) analogues in which a seven at
150 an increase of the psychoactive compound (9)-tetrahydrocannabinol (THC) and a decrease of the potenti
152 suggests that the phytocannabinoids Delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) differe
155 ids and their synthetic derivatives, such as tetrahydrocannabinol (THC) and cannabidiol (CBD), have b
157 icinal applications of pure forms of delta-9-tetrahydrocannabinol (THC) and crude marijuana are being
158 only abused psychotropic compounds, Delta(9)-tetrahydrocannabinol (THC) and heroin, on adult zebrafis
159 ins of marijuana with high levels of delta-9-tetrahydrocannabinol (THC) and low levels of cannabidiol
160 The involvement of dynorphin on Delta-9-tetrahydrocannabinol (THC) and morphine responses has be
161 We therefore compared effects of exposure to tetrahydrocannabinol (THC) and nicotine on DNA methylati
163 antagonist, blocks acute effects of Delta-9-tetrahydrocannabinol (THC) and other CB1 cannabinoid ago
164 ne, methadone, cocaine, heroin, codeine, and tetrahydrocannabinol (THC) and their major human metabol
166 ntracellular effects resulting from Delta(9)-tetrahydrocannabinol (THC) binding without modifying beh
170 ng dose-dependent effects of chronic delta-9-tetrahydrocannabinol (THC) exposure on brain connectivit
171 Little data exists on effects of paternal tetrahydrocannabinol (THC) exposure prior to reproductio
173 tamine (MDEA), morphine, cocaine, and Delta9-tetrahydrocannabinol (THC) from a single blood spot.
175 e neural mechanisms and durability of Delta9-tetrahydrocannabinol (THC) impact on threat processing i
176 e the effects of repeated exposure to Delta9-tetrahydrocannabinol (THC) in a mouse model of surgicall
177 to investigate whether exposure to Delta(9)-tetrahydrocannabinol (THC) in adolescent rats might enha
178 ontinuously rising concentrations of delta-9-tetrahydrocannabinol (THC) in cannabis (i.e., potency),
180 ta on the expected concentration of Delta(9)-tetrahydrocannabinol (THC) in the different types of can
181 murine tumors EL-4, LSA, and P815 to delta-9-tetrahydrocannabinol (THC) in vitro led to a significant
183 maging (MRI) to study the effects of delta-9-tetrahydrocannabinol (THC) infusion on brain blood flow
184 ined the acute and delayed effects of Delta9-tetrahydrocannabinol (THC) intoxication on susceptibilit
196 emic acid (AJA) is a synthetic analog of the tetrahydrocannabinol (THC) metabolite THC-11-oic acid; T
198 ffects of the endocannabinoid agonist Delta9-tetrahydrocannabinol (THC) on executive function in 20 h
200 d the effects of repeated exposure to Delta9-tetrahydrocannabinol (THC) on performance of spatial and
201 med to investigate the effect of oral Delta9-tetrahydrocannabinol (THC) on subjective and metabolic h
202 self-administration of cannabinoids delta-9-tetrahydrocannabinol (THC) or anandamide in squirrel mon
204 ere available, 47 of 50 (94%) had detectable tetrahydrocannabinol (THC) or its metabolites in BAL flu
205 f cannabinoid CB1 receptors (CB1R) by delta9-tetrahydrocannabinol (THC) produces a variety of negativ
208 d the effects of long-term/low-dose Delta(9)-tetrahydrocannabinol (THC) supplementation in simian imm
210 cannabinoids (cannabidiol (CBD) and Delta(9)-tetrahydrocannabinol (THC)) on arrestin2-, Galpha(i/o)-,
212 bited potentiation produced by both Delta(9)-tetrahydrocannabinol (THC), a major psychoactive compone
214 ull agonist at CB(1) receptors, and Delta(9)-tetrahydrocannabinol (THC), a partial agonist, on the su
215 udy this phenomenon, we assessed how delta-9-tetrahydrocannabinol (THC), a primary psychoactive ingre
216 1 (CB1) is the principal target of Delta(9)-tetrahydrocannabinol (THC), a psychoactive chemical from
217 e effects of adolescent exposure to Delta(9)-tetrahydrocannabinol (THC), a psychoactive component of
218 e psychoactive component of cannabis, delta9-tetrahydrocannabinol (THC), activated cerebellar microgl
219 t binds the active constituent of marijuana, tetrahydrocannabinol (THC), and a postulated endogenous
220 psychoactive compound in marijuana, Delta(9)-tetrahydrocannabinol (THC), and its metabolites are emer
221 ell as exogenous cannabinoids such as Delta9-tetrahydrocannabinol (THC), are mediated by two subtypes
223 them have been determined, including delta-9 tetrahydrocannabinol (THC), cannabidiol (CBD), and canna
224 (2-AG), anandamide (AEA), CP55,940, Delta(9)-tetrahydrocannabinol (THC), cannabidiol (CBD), and THC+C
225 (UHPLC-MS/MS) for analysis of urinary Delta9-tetrahydrocannabinol (THC), cannabidiol and cannabinol,
226 ry actions of the phytocannabinoids Delta(9)-tetrahydrocannabinol (THC), cannabidiol, cannabichromene
227 may result in the incorporation of Delta(9)-tetrahydrocannabinol (THC), cannabinol (CBN), cannabidio
228 tting both detection and mapping of Delta(9)-tetrahydrocannabinol (THC), cannabinol (CBN), cannabidio
230 ure to the psychoactive cannabinoid, Delta-9-tetrahydrocannabinol (THC), cerebral organoids exhibited
231 rawal symptoms following exposure to delta-9-tetrahydrocannabinol (THC), difficulties in obtaining ob
232 sychotropic component in marijuana, Delta(9)-tetrahydrocannabinol (THC), has also been shown to media
233 ow 10(-7) Torr, such as tetryl, cocaine, and tetrahydrocannabinol (THC), have been successfully detec
234 or its main psychoactive component Delta(9)-tetrahydrocannabinol (THC), impairs working memory, i.e.
235 sychoactive component of marijuana, Delta(9)-tetrahydrocannabinol (THC), is a signaling network that
236 circumvent the narcotic effects of Delta(9)-tetrahydrocannabinol (THC), many studies have concentrat
237 (alpha7nAChRs) modulate effects of Delta(9)-tetrahydrocannabinol (THC), marijuana's main psychoactiv
238 the active ingredient of cannabis, Delta(9)-tetrahydrocannabinol (THC), on sexual behavior in female
239 chronic exposure to vehicle solution, Delta9-tetrahydrocannabinol (THC), or the cannabinoid agonist R
240 nabinoids cannabichromene (CBC) and Delta(1)-tetrahydrocannabinol (THC), respectively] is predicted i
243 ent doses and treatment regimens of Delta(9)-tetrahydrocannabinol (THC), the main active ingredient i
244 strated that adolescent exposure to Delta(9)-tetrahydrocannabinol (THC), the main psychoactive compon
245 we show that adolescent exposure to Delta(9)-tetrahydrocannabinol (THC), the main psychoactive compon
246 ow co-administration of alcohol and Delta(9)-tetrahydrocannabinol (THC), the main psychoactive consti
248 ctive component of tobacco, and (-)-Delta(9)-tetrahydrocannabinol (THC), the main psychoactive ingred
249 avioral effects similar to those of Delta(9)-tetrahydrocannabinol (THC), the main psychoactive ingred
253 binoid receptor, the main target of Delta(9)-tetrahydrocannabinol (THC), the most prominent psychoact
255 er the influence of exogenously administered tetrahydrocannabinol (THC), the primary CB found in mari
259 (1)Rs) mediate the effects of triangle up(9)-tetrahydrocannabinol (THC), the psychoactive component i
261 ngredient in chilli peppers, and by Delta(9)-tetrahydrocannabinol (THC), the psychoactive component o
262 behavior by laboratory animals with delta-9-tetrahydrocannabinol (THC), the psychoactive ingredient
263 tions of its main active ingredient, delta-9-tetrahydrocannabinol (THC), to be more harmful (in terms
264 ychoactive constituent in cannabis, Delta(9)-tetrahydrocannabinol (THC), was isolated in the mid-1960
266 DC), most patients report a history of using tetrahydrocannabinol (THC)-containing e-cigarette or vap
267 male, but not female, offspring of Delta(9)-tetrahydrocannabinol (THC)-exposed dams, a rat PCE model
275 oylecgonine (BE) and 11-nor-9-carboxy-Delta9-tetrahydrocannabinol (THC-COOH) were shown to be strongl
277 nd the metabolites 11-nor-9-carboxy-Delta(9)-tetrahydrocannabinol (THC-COOH), 11-hydroxy-Delta(9)-tet
279 The cannabinoid receptor agonist, Delta(9)-tetrahydrocannabinol (THC; dronabinol), decreases mariju
281 are mimicked by administration of (-)-Delta9-tetrahydrocannabinol (THC; the major psychoactive consti
283 C. sativa), and major cannabinoid contents (tetrahydrocannabinol, THC; and cannabidiol, CBD), along
285 endogenous cannabinoids, as well as Delta(9)-tetrahydrocannabinol, the main plant psychoactive consti
286 prenatal and adolescent exposure to delta-9-tetrahydrocannabinol, the major psychoactive component o
287 ns after the acute administration of delta-9-tetrahydrocannabinol, the primary psychoactive constitue
288 receptors also mediate the effects of Delta9-tetrahydrocannabinol, the primary psychoactive ingredien
290 rs CB(1) and CB(2) are activated by Delta(9)-tetrahydrocannabinol, the psychoactive ingredient of can
292 sulting in a change in the ratio of Delta(9)-tetrahydrocannabinol to cannabidiol from 14 times in 199
293 abinoids such as the marijuana component (9)-tetrahydrocannabinol, to heterotrimeric G12/G13 proteins
295 ore study; positive 11-nor-9-carboxy-delta-9-tetrahydrocannabinol urine levels) and cannabis naive co
296 ore study; positive 11-nor-9-carboxy-delta-9-tetrahydrocannabinol urine levels) and cannabis-naive co
298 e range of 0.05-60 mg/kg, and the content of tetrahydrocannabinol varied between 3.23 and 69.5 mg/kg.
299 in the nucleus accumbens induced by Delta(9)-tetrahydrocannabinol was blocked in mice lacking the Hcr