「potent」の共起表現一覧(1語右で並び替え)
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It is around 5x more | potent a stimulant than cocaine, but is relatively un |
Methane is twenty times more | potent a greenhouse gas than carbon dioxide. |
Ranitidine is not as | potent a CYP inhibitor as cimetidine, although it sti |
e source regarding neurotixicity states its as | potent a neurotoxin as mdma. |
Laetiporus sulphureus has | potent ability to inhibit staph bacteria (Staphylococ |
It is a | potent acetylcholinesterase inhibitor with properties |
procoagulant properties and instead becomes a | potent activator of protein C. Activated protein C (A |
ere it is needed, rendering the drug much more | potent, actively longer in duration, and therefore re |
Stories allege that a | potent Afghan strain was most likely the basis for G- |
They are highly | potent against problematic Gram-positive hospital pat |
antity of this mixture, which he regarded as a | potent agent in the causation of volcanic action. |
It is highly | potent agent, capable of damage cancer cells in very |
AMG-36 is a | potent agonist at both CB1 and CB2 with moderate sele |
This metabolite of paracetamol is a | potent agonist at the TRPV1 vanilloid receptor, a wea |
AM-1248 is a drug which acts as a moderately | potent agonist for both the cannabinoid receptors CB1 |
oflavone, also known as 5,6-benzoflavone, is a | potent agonist of the aryl hydrocarbon receptor and a |
Bromocriptine is a | potent agonist at dopamine D2 receptors and various s |
It is a | potent agonist at both the CB1 and CB2 receptors, wit |
AMG-41 is a | potent agonist at both CB1 and CB2, with a Ki of 0.4n |
degree of selectivity, so while it is still a | potent agonist at both CB1 and CB2, it is reasonably |
AM-679 is a drug which acts as a moderately | potent agonist for the cannabinoid receptors, with a |
AS-19 is a substance which acts as a | potent agonist at the 5HT7 receptor, with an IC50 of |
25I-NBOMe acts as a highly | potent agonist for the human 5-HT2A receptor, with a |
AMG-3 is a | potent agonist at both CB1 and CB2 receptors with a K |
It acts as a | potent agonist for the 5HT2A receptor, with a Ki of 0 |
s the more active enantiomer, functioning as a | potent agonist of the serotonin 5-HT family of recept |
teahouse instead, and when Fisby discovers the | potent alcoholic beverage they brew is popular with t |
Cuscohygrine usually comes with other, more | potent alkaloids like atropine or cocaine. |
ompounds known as halocarbons, which are often | potent alkylating agents which may be toxic to indivi |
be immunosuppressive, hepatoprotective, and a | potent alpha-glucosidase inhibitor, a human gut enzym |
018, the hexyl homologue is only slightly less | potent, although extending the chain one carbon longe |
ibious ships, she provides a much-improved and | potent amphibious capability for the Royal Navy. |
It is much more | potent an antagonist, and more selective for the CB1 |
It was found to be twice as | potent an anorectic as fenfluramine. |
d derivative of trenbolone, and is a similarly | potent anabolic steroid, but with high potential for |
h efficacy 5-HT1A agonist befiradol results in | potent analgesia following an initial period of hyper |
from the skin of the African clawed frog and a | potent analgesic compound called epibatidine was obta |
d morphine-6-glucuronide (M6G),, which is more | potent analgesic than morphine. |
Dihydroetorphine is a | potent analgesic drug (painkiller), which is used mai |
l (β-hydroxy-3-methylfentanyl) is an extremely | potent analgesic drug which selectively binds to the |
It is a | potent analgesic with around the same potency as morp |
It has | potent analgesic effects and is around 10x more poten |
e Tormosyl) is a quinazolinone derivative with | potent analgesic and antipyretic effects and also ant |
and easily reversible, and it produces fairly | potent analgesic effects mediated through the μ-opioi |
It has | potent analgesic effects in animal studies comparable |
Like epibatidine, tebanicline showed | potent analgesic activity against neuropathic pain in |
Unlike dextromoramide, which is a | potent analgesic with high abuse potential, levomoram |
is more likely Cortex will use newer and more | potent analogues such as CX-1739 or CX-1763 which are |
leading to the development of a number of more | potent analogues, derived by cyclisation around the i |
ican Nickelodeon network, where it serves as a | potent analogy for the injustices of apartheid. |
ne from mast cells; C5a des-Arg is a much less | potent anaphylatoxin. |
ition, OSCS induced generation of C3a and C5a, | potent anaphylatoxins derived from complement protein |
As a medicine it is among the most | potent, and in Japan only it has been used against li |
ust by its code number 302196) is a moderately | potent and relatively short lasting anticholinergic d |
It acts as a | potent and selective agonist for the nociceptin recep |
is an indazole derivative drug which acts as a | potent and selective 5-HT2C receptor agonist, with an |
r than morphine, it can be expected to be more | potent and longer lasting, and also have higher bioav |
(-)-2β-(3-methyl-5-isoxazolyl)nortropane is a | potent and selective agonist for nicotinic acetylchol |
LGD-2226 is an orally active, | potent and selective agonist for androgen receptors w |
It acts as a | potent and highly selective norepinephrine reuptake i |
ICI-204,448 is a drug which acts as a | potent and periperhally selective κ-opioid agonist, w |
ug used in scientific research which acts as a | potent and selective antagonist for both the Neuropep |
RS-56812 is a | potent and selective partial agonist at the 5HT3 rece |
CGS-15943 is a drug which acts as a | potent and reasonably selective antagonist for the ad |
CGS-12066A is a drug which acts as a | potent and selective agonist for the 5-HT1B receptor |
AM-1221 is a drug which acts as a | potent and selective agonist for the cannabinoid rece |
pane-2β-pyrrolidine carboxamide (RTI-229) is a | potent and long-lasting stimulant drug which was deve |
g used in scientific research, which acts as a | potent and subtype-selective agonist for the metabotr |
ug used in scientific research which acts as a | potent and selective antagonist for the Neuropeptide |
-ethoxy homologues were all several times less | potent and somewhat shorter acting than the parent co |
vel chemical entities; some of them are highly | potent, and one of them has been reported as lasting |
MTEP is both more | potent and more selective than MPEP as a mGluR5 antag |
50A is a tryptamine derivative which acts as a | potent and selective agonist for the serotonin recept |
SR144528 is a drug which acts as a | potent and highly selective CB2 receptor inverse agon |
EA-3167 is a | potent and long lasting anticholinergic deliriant dru |
Tetrazolylglycine (Tet-Gly, LY-285,265) is a | potent and selective NMDA receptor agonist, stimulati |
CP-94,253 is a drug which acts as a | potent and selective serotonin 5-HT1B receptor agonis |
Doxanthrine is a synthetic compound which is a | potent and selective full agonist for the dopamine D1 |
Thioperamide is a | potent and selective histamine H3 antagonist that is |
Sildenafil is a | potent and selective inhibitor of cGMP-specific phosp |
oltidine (USAN, BAN) or AH-23,844, is a highly | potent and selective H2 receptor antagonist which was |
ich is used in scientific research, which is a | potent and selective δ-opioid agonist, selective for |
on American Tragedy," while still telling, "a | potent and poignant tale of longing for suicide." |
It is a | potent and long-acting neuroleptic, used as an antips |
is a phenyltropane derivative which acts as a | potent and selective dopamine reuptake inhibitor and |
SB-271,046 was found to be | potent and selective in vitro and had good oral bioav |
ger acting than hydromorphone, metopon is less | potent and its oral bioavailability, while higher tha |
Naltriben is a | potent and selective antagonist for the delta opioid |
odest but it was unexpectedly found to produce | potent and rapid antidepressant and anxiolytic effect |
P-7941 is as the lead compound from which more | potent and selective antagonists such as SNAP-94847 w |
N-Ethyl-3-piperidyl benzilate is less | potent and shorter acting than 3-quinuclidyl benzilat |
m the aminoalkylindole family, which acts as a | potent and selective agonist for the cannabinoid rece |
L-765,314 is a drug which acts as a | potent and selective antagonist for the Alpha-1 adren |
RTI-121 is a | potent and long-lasting stimulant, producing stimulan |
ICI-199,441 is a drug which acts as a | potent and selective κ-opioid agonist, and has analge |
ntly, it was determined that fenobam acts as a | potent and selective negative allosteric modulator of |
It is a | potent and reasonably selective agonist for the CB1 c |
loped by EPIX Pharmaceuticals, which acts as a | potent and selective antagonist at the serotonin 5-HT |
n more widely used and are presumed to be more | potent and addictive than α-PPP itself. |
LPK-26 is a drug which acts as a | potent and selective κ-opioid agonist, and has analge |
ug used in scientific research which acts as a | potent and highly selective CB1 antagonist. |
Most medications are | potent and safe after the expiration date. |
s men for whose teachings and methods he had a | potent and stimulating antipathy. |
the first compounds discovered that acts as a | potent and selective antagonist at the serotonin 5-HT |
Heroin stamps and bags, making them much more | potent and profitable when sold as Heroin alone due t |
at muscarinic acetylcholine receptors, being a | potent and selective agonist for the M1 and M4 subtyp |
s a drug developed by Organon, which acts as a | potent and selective agonist for the 5-HT2 receptor f |
GR-159,897 is a | potent and selective NK2 receptor antagonist drug. |
So they decided to find a more | potent and stable alternative, one that would be more |
eria Streptomyces toyacaensis, which acts as a | potent and irreversible GABA transaminase inhibitor, |
Ifetroban is a | potent and selective thromboxane receptor antagonist. |
RH-34 is a compound which acts as a | potent and selective partial agonist for the 5-HT2A s |
tipsychotic effects in animal models, and more | potent and selective PDE10A inhibitors are a current |
PHA-543,613 is a drug that acts as a | potent and selective agonist for the α7 subtype of ne |
Since TNF-α is a | potent and pivotal mediator in the inflammatory proce |
Like lopinavir and atazanavir, it is very | potent and is effective in salvage therapy for patien |
nity than the N-methyl analogue and so is less | potent and not so widely used for this application. |
s a drug developed by Organon, which acts as a | potent and selective agonist for the 5-HT2 receptor f |
plications in scientific research, acting as a | potent and selective antagonist for both the 5-HT6 an |
EA-3443 is a | potent and long lasting anticholinergic deliriant dru |
used as a lead compound to develop a range of | potent and selective mGluR1 positive modulators. |
IAP acts as a | potent and weakly selective serotonin releasing agent |
Fluparoxan (GR-50,360) is a | potent and highly selective α2-adrenergic receptor an |
12,111 is an opioid receptor ligand which is a | potent and selective antagonist for the nociceptin re |
Org 27569 is a drug which acts as a | potent and selective allosteric modulator of the cann |
EP has been as a lead compound to develop more | potent and selective mGluR5 antagonists such as MTEP, |
CP-154,526 is a | potent and selective antagonist of the corticotropin |
PF-03654746 is a | potent and selective histamine H3 receptor antagonist |
It acts as a moderately | potent and selective agonist for the 5-HT2A and 5-HT2 |
CP-93,129 is a drug which acts as a | potent and selective serotonin 5-HT1B receptor agonis |
pyran "classical" cannabinoid drug, which is a | potent and selective CB2 receptor agonist, with a Ki |
has identical effects to QNB, but is even more | potent and longer lasting, with an effective dose whe |
he impact and purpose of the film, writing, "A | potent and magnificent documentary, Gallipoli impacts |
F-15,599 is a very | potent and highly selective 5-HT1A receptor full agon |
icodeine can be expected to be marginally more | potent and longer acting than nicocodeine. |
It acts as a | potent and selective agonist for the nociceptin recep |
RS-127,445 is a drug which acts as a | potent and selective antagonist at the serotonin 5-HT |
s at the 4 position, usually resulting in more | potent and more metabolically stable and longer actin |
It is very | potent and has an extremely long duration of action, |
from twenty-carbon essential fatty acids, have | potent and often opposing effects on e.g. |
PNU-282,987 is a drug that acts as a | potent and selective agonist for the α7 subtype of ne |
licylhydroxamic acid (SHA) is a drug that is a | potent and irreversible inhibitor of bacterial and pl |
ted propylamphetamine to be only slightly less | potent and active than amphetamine. |
GSK-789,472 is a drug which acts as both a | potent and selective partial agonist at the dopamine |
colate or just by its code number 301060) is a | potent and long lasting anticholinergic deliriant dru |
Urocortin is also a | potent and long-lasting hypotensive agent and increas |
It acts as a | potent and selective 5-HT6 receptor agonist, with a K |
lyph associated with that character is a cross | potent, and not a Jerusalem cross. |
gonists, while XCT790 has been identified as a | potent and selective inverse agonist of ERR-α. |
enabant (CP-945,598) is a drug which acts as a | potent and highly selective CB1 antagonist. |
DAA-1106 is a drug which acts as a | potent and selective agonist at the peripheral benzod |
RS-56812: | potent and selective 5-HT3 partial agonist, 1000x sel |
SSR-180,711 is a drug that acts as a | potent and selective partial agonist for the α7 subty |
XCT790 is a | potent and selective inverse agonist ligand of the es |
lgesia and respiratory depression, but is more | potent and has a steeper dose-response curve and long |
scientific research which acts as an extremely | potent and selective antagonist of the cannabinoid re |
-oyl)-6-nitroindole) is a drug which acts as a | potent and reasonably selective agonist for the canna |
It is a | potent and selective positive allosteric modulator of |
The liquid is very | potent and is usually dropped under one's tongue or i |
a drug developed by Lundbeck, which acts as a | potent and highly selective antagonist for the Neurop |
SB-215,505 is a drug which acts as a | potent and selective antagonist at the serotonin 5-HT |
Y-317,538 (SEN-12333) is a drug that acts as a | potent and selective full agonist for the α7 subtype |
Since fentanyl itself is highly | potent and notorious for causing fatal overdoses when |
placed by more powerful weapons, it remained a | potent and useful weapon and remained in service with |
Notably, NDMC has also been shown to act as a | potent and efficacious agonist at the M1 and δ-opioid |
It acts as a | potent and selective receptor antagonist for the 5-HT |
It acts as a | potent and selective agonist for both the 5-HT2B and |
ative which is mentioned in PIHKAL as a fairly | potent and long-lasting stimulant drug, but with litt |
Desipramine is one of the most | potent and selective medications in this respect. |
is a drug developed by Pfizer which acts as a | potent and highly selective agonist for the dopamine |
SER-601 is a drug which acts as a | potent and selective cannabinoid CB2 receptor agonist |
Pazopanib (trade name Votrient) is a | potent and selective multi-targeted receptor tyrosine |
t least some species of Buthacus is relatively | potent and can be of medical importance to humans. |
It acts as a | potent and selective agonist for the 5-HT2 family of |
N-methyl-3-piperidyl benzilate is less | potent and shorter acting than 3-quinuclidyl benzilat |
It acts as a | potent and selective 5-HT1A receptor full agonist. |
ug synthesised from tropinone, which acts as a | potent and selective dopamine reuptake inhibitor. |
Oxeladin is a cough suppressant.It is a highly | potent and effective drug used to treat all types of |
-iodobenzoyl)indole) is a drug which acts as a | potent and selective agonist for the cannabinoid rece |
R-12909) is a piperazine derivative which is a | potent and selective DRI. |
e has also subsequently been found to act as a | potent and selective antagonist for the neurotensin r |
U-69,593 is a drug which acts as a | potent and selective κ1-opioid receptor agonist. |
Since it is already a very | potent androgen, many users will only use it for the |
It has | potent anorectic effects in animals, and was research |
It has | potent anorectic effects in animal studies. |
Urocortin is a | potent anorexigenic peptide of 40 amino acids that in |
They do not cause as | potent antagonism of GABA function as fluoroquinolone |
Preclinically, aclidinium showed | potent antagonism of human muscarinic receptors, with |
It acts as a | potent antagonist of the glycine receptor, and has po |
Nefazodone acts primarily as a | potent antagonist at the 5-HT2A receptors (Kd 26 nM). |
ananserin (RP-62204) is a drug which acts as a | potent antagonist at both the 5HT2A receptor, and the |
ug used in scientific research which acts as a | potent antagonist for the Neuropeptide Y / Pancreatic |
Zacopride is a | potent antagonist at the 5HT3 receptor and an agonist |
Nociceptin is a | potent anti-analgesic. |
d a meningitis patient erroneously receiving a | potent anti-cancer drug for four days. |
Because of its various | potent anti-cancer properties, the National Cancer In |
vanadium, bis(allixinato)oxovanadium(IV), is a | potent anti-diabetic agent. |
ly limited analgesic effects, although it is a | potent anti-diarrheal drug. |
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