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Find link is a tool written by Edward Betts .
searching for Pic50 11 found (11 total)
alternate case: pic50
IC50
(1,062 words)
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the pIC50 scale. pIC50 =−log10(IC50){\displaystyle {\ce {pIC_{50}}}=-\log _{10}{\ce {(IC_{50})}}} Due to the minus sign, higher values of pIC50 indicate
Lipophilic efficiency
(645 words)
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is defined as the pIC50 (or pEC50) of interest minus the LogP of the compound. LiPE=pIC50 −logP{\displaystyle {\ce {LiPE}}={\ce {pIC50 }}-\log P} In practice
Ligand efficiency
(481 words)
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kDa) BEI = (pKi, pKd, or pIC50 ) / (molecular weight, kDa) SEI = (pKi, pKd, or pIC50 ) / (PSA/100 Å) where pKi, pKd and pIC50 is defined as −log(Ki), −log(Kd)
Druglikeness
(890 words)
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instead. Potency at the biological target. High potency (high value of pIC50 ) is a desirable attribute in drug candidates, as it reduces the risk of
Belotecan
(260 words)
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Dang Pharmaceuticals since 2003. Belotecan blocks topoisomerase I with a pIC50 of 6.56, stabilizing the cleavable complex of topoisomerase I-DNA, which
List of benzodiazepines
(3,088 words)
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agonists (e.g. flumazenil). Low IC50 or high pIC50 values indicate tighter binding (pIC50 of 8.0 = IC50 of 10nM, pIC50 of 9.0 = IC50 of 1nM, etc.) These are
Synephrine
(9,894 words)
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preparation from rat cerebral cortex, l-synephrine had pIC50 = 3.35, and d-synephrine had pIC50 = 2.42 in competition against [3H]-prazosin (standard α1
Adenosine diphosphate receptor inhibitor
(5,282 words)
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Compound pIC50 R1 R2 R3 ATP 3.6 O C C-NH2 1A 3.5 C C-NH2 1B 8.6 C-NH2 1C 9.1 Cangrelor 9.4
Dezocine
(1,803 words)
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found to act as a serotonin–norepinephrine reuptake inhibitor (SNRI), with pIC50 values of 5.86 for the serotonin transporter (SERT) and 5.68 for the norepinephrine
Partition coefficient
(6,301 words)
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efficiency for a compound is defined as its potency, via measured values of pIC50 or pEC50, minus its value of log P. In the context of pharmacokinetics (how
Trimipramine
(4,676 words)
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2-Hydroxytrimipramine >30 μM 4.960 4.585 Trimipramine-N-oxide 5.445 4.930 5.027 Values are pIC50 . The higher the value, the more strongly the drug binds to the site.