orthosteric binding
正性位结合
orthosteric site
正性位位点
orthosterically activated
正性位激活
orthosteric modulation
正性位调节
orthosteric effect
正性位效应
orthosteric ligand
正性位配体
orthosteric agonist
正性位激动剂
orthosteric antagonist
正性位拮抗剂
orthosteric mechanism
正性位机制
orthosteric action
正性位作用
the orthosteric site of the receptor is crucial for ligand binding.
受体的正定位位点对于配体结合至关重要。
orthosteric modulators can enhance or inhibit receptor activity.
正定位调节剂可以增强或抑制受体活性。
we investigated the orthosteric binding pocket using computational modeling.
我们使用计算建模研究了正定位结合位点。
orthosteric agonists activate the receptor in a canonical manner.
正定位激动剂以经典方式激活受体。
the orthosteric ligand occupies the primary binding site.
正定位配体占据主要的结合位点。
developing orthosteric drugs can be a challenging process.
开发正定位药物可能是一个具有挑战性的过程。
orthosteric allosteric modulators are a novel class of compounds.
正定位非经典调节剂是一类新型化合物。
the orthosteric effect was observed in the presence of the agonist.
在激动剂存在的情况下观察到正定位效应。
site-directed mutagenesis revealed key residues in the orthosteric region.
定点诱变突变揭示了正定位区域的关键残基。
orthosteric compounds often exhibit high receptor selectivity.
正定位化合物通常表现出很高的受体选择性。
we analyzed the orthosteric binding affinity of several candidate drugs.
我们分析了几个候选药物的正定位结合亲和力。
orthosteric binding
正性位结合
orthosteric site
正性位位点
orthosterically activated
正性位激活
orthosteric modulation
正性位调节
orthosteric effect
正性位效应
orthosteric ligand
正性位配体
orthosteric agonist
正性位激动剂
orthosteric antagonist
正性位拮抗剂
orthosteric mechanism
正性位机制
orthosteric action
正性位作用
the orthosteric site of the receptor is crucial for ligand binding.
受体的正定位位点对于配体结合至关重要。
orthosteric modulators can enhance or inhibit receptor activity.
正定位调节剂可以增强或抑制受体活性。
we investigated the orthosteric binding pocket using computational modeling.
我们使用计算建模研究了正定位结合位点。
orthosteric agonists activate the receptor in a canonical manner.
正定位激动剂以经典方式激活受体。
the orthosteric ligand occupies the primary binding site.
正定位配体占据主要的结合位点。
developing orthosteric drugs can be a challenging process.
开发正定位药物可能是一个具有挑战性的过程。
orthosteric allosteric modulators are a novel class of compounds.
正定位非经典调节剂是一类新型化合物。
the orthosteric effect was observed in the presence of the agonist.
在激动剂存在的情况下观察到正定位效应。
site-directed mutagenesis revealed key residues in the orthosteric region.
定点诱变突变揭示了正定位区域的关键残基。
orthosteric compounds often exhibit high receptor selectivity.
正定位化合物通常表现出很高的受体选择性。
we analyzed the orthosteric binding affinity of several candidate drugs.
我们分析了几个候选药物的正定位结合亲和力。
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