Dynorphin A (1-10) (TFA)


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Cat. No. : HY-P1594A
M.Wt: 1348.48
Formula: C59H92F3N19O14
Purity: >98 %
Solubility: DMSO : 100 mg/mL (ultrasonic);H2O : 50 mg/mL (ultrasonic)
Introduction of Dynorphin A (1-10) (TFA) :

Dynorphin A (1-10) (TFA), an endogenous opioid neuropeptide, binds to extracellular loop 2 of the κ-opioid receptor. Dynorphin A (1-10) (TFA) also blocks NMDA-activated current with an IC50 of 42.0 μM. IC50 & Target: κ-opioid receptor[1]
IC50: 42.0 μM (NMDA receptor)[2] In Vitro: Dynorphin A (1-10) (TFA), an endogenous opioid neuropeptide, binds in the transmembrane domain of the κ-receptor[1]. The non-opioid actions of various forms of Dynorphin A (DynA) are examined on N-methyl-D-aspartate (NMDA) receptor channels in isolated rat trigeminal neurons using the whole-cell patch recording technique. All the dynorphins tested blocked NMDA-activated currents. The blocking actions are voltage-independent. The IC50 is 42.0 μM for DynA(1-10). To determine if shorter dynorphins have the similar blocking property, we examined the action of DynA(1-10) at different membrane potentials. DynA(1-10) blocks INMDA to a similar extent as the membrane potentials changed from -80 to +60 mV. Thus, despite a 160-fold difference in the apparent affinities, DynA(1-32) and DynA(1-10) both exert voltage-independent actions on NMDA receptors[2].

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