DREADD
Designer receptors exclusively activated by designer drugs (DREADDs) are genetically engineered GPCRs that are activated by physiologically inert synthetic small molecules (designer drugs) but not their endogenous ligand. Read our DREADDs mini-review or for practical advice on using these ligands in the lab see Stability of Water-Soluble DREADD Ligands in Solution: A Technical Review and Clozapine N-Oxide (freebase) - a technical review on stability, solubility and use in the lab).
- Description:
Inhibits α-MSH release inhibitors. Also increase dopamine levels.
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Metergoline (HB1623)
Description:5-HT1/5-HT2 antagonist. Shows affinity for 5-HT6 and 5-HT7.
Purity:>98%
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Mianserin hydrochloride (HB1658)
Description:Non-selective 5-HT2 receptor antagonist. Shows activity at other receptors.
Purity:>99%
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MK-571 sodium salt (HB3976)
Description:Selective leukotriene LTD4 receptor antagonist. Potent MRP1 inhibitor.
Purity:>97%
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MNI-caged-L-Glutamate (HB0423)
Description:Caged glutamate that rapidly and efficiently releases glutamate when photolysed
Purity:>98%
