orthosteric binding
正位點結合
orthosteric site
正位點
orthosterically activated
正位點活化
orthosteric modulation
正位點調節
orthosteric effect
正位點效應
orthosteric ligand
正位點配體
orthosteric agonist
正位點激動劑
orthosteric antagonist
正位點拮抗劑
orthosteric mechanism
正位點機制
orthosteric action
正位點作用
the orthosteric site of the receptor is crucial for ligand binding.
受體的正構位點對於配體結合至關重要。
orthosteric modulators can enhance or inhibit receptor activity.
正構調節劑可以增強或抑制受體的活性。
we investigated the orthosteric binding pocket using computational modeling.
我們使用計算機模擬來研究正構結合口袋。
orthosteric agonists activate the receptor in a canonical manner.
正構激動劑以一種典型的途徑活化受體。
the orthosteric ligand occupies the primary binding site.
正構配體佔據主要的結合位點。
developing orthosteric drugs can be a challenging process.
開發正構藥物可能是一個具有挑戰性的過程。
orthosteric allosteric modulators are a novel class of compounds.
正構變構調節劑是一類新型化合物。
the orthosteric effect was observed in the presence of the agonist.
在存在激動劑的情況下觀察到正構效應。
site-directed mutagenesis revealed key residues in the orthosteric region.
位點導向的突變分析揭示了正構區域中的關鍵殘基。
orthosteric compounds often exhibit high receptor selectivity.
正構化合物通常表現出高的受體選擇性。
we analyzed the orthosteric binding affinity of several candidate drugs.
我們分析了幾種候選藥物的正構結合親和力。
orthosteric binding
正位點結合
orthosteric site
正位點
orthosterically activated
正位點活化
orthosteric modulation
正位點調節
orthosteric effect
正位點效應
orthosteric ligand
正位點配體
orthosteric agonist
正位點激動劑
orthosteric antagonist
正位點拮抗劑
orthosteric mechanism
正位點機制
orthosteric action
正位點作用
the orthosteric site of the receptor is crucial for ligand binding.
受體的正構位點對於配體結合至關重要。
orthosteric modulators can enhance or inhibit receptor activity.
正構調節劑可以增強或抑制受體的活性。
we investigated the orthosteric binding pocket using computational modeling.
我們使用計算機模擬來研究正構結合口袋。
orthosteric agonists activate the receptor in a canonical manner.
正構激動劑以一種典型的途徑活化受體。
the orthosteric ligand occupies the primary binding site.
正構配體佔據主要的結合位點。
developing orthosteric drugs can be a challenging process.
開發正構藥物可能是一個具有挑戰性的過程。
orthosteric allosteric modulators are a novel class of compounds.
正構變構調節劑是一類新型化合物。
the orthosteric effect was observed in the presence of the agonist.
在存在激動劑的情況下觀察到正構效應。
site-directed mutagenesis revealed key residues in the orthosteric region.
位點導向的突變分析揭示了正構區域中的關鍵殘基。
orthosteric compounds often exhibit high receptor selectivity.
正構化合物通常表現出高的受體選擇性。
we analyzed the orthosteric binding affinity of several candidate drugs.
我們分析了幾種候選藥物的正構結合親和力。
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