Powder: -20°C for 3 years | In solvent: -80°C for 1 year
(+)-Dihydrexidine hydrochloride is an agonist of dopamine D1 receptor(EC50 of 72± 21 nM).
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
25 mg | 8-10 weeks | $ 1,970.00 | |
50 mg | 8-10 weeks | $ 2,580.00 | |
100 mg | 8-10 weeks | $ 3,400.00 |
Description | (+)-Dihydrexidine hydrochloride is an agonist of dopamine D1 receptor(EC50 of 72± 21 nM). |
Targets&IC50 | D1 receptor:(EC50)72±21 nM |
In vitro | (+)-Dihydrexidine hydrochloride (DHX) is a high-potency, bioavailable agonist of D1 dopamine receptor. (+)-Dihydrexidine is screened for activity against 40 other binding sites, and is inactive (IC50 > 10 microM) against all except D2 dopamine receptors with IC50 of 130 nM and alpha 2 adrenoreceptors (IC50=230 nM). Dihydrexidine competes stereoselectively and potently for D1 binding sites in rat striatal membranes labeled with [3H]SCH23390 with an IC50 of about 10 nM compared to about 30 nM for the prototypical D1 agonist SKF38393[2]. |
In vivo | To check the functional status of striatum neurons in response to D1 receptor activation, AC5+/+ and AC5-/- mice are injected with the D1 agonist (+)-Dihydrexidine (30 mg/kg, i.p.) and obtained the dorso-lateral striatum and NAc, separately, 45 min later for RT-PCR analysis. These experiments reveal that (+)-Dihydrexidine -triggered induction of the immediate early genes, c-fos, egr-1, and junB, in the NAc is markedly enhanced in AC5-/- mice compared with that in AC5+/+ mice, while the induction in the dorso-lateral striatum is suppressed in AC5-/- mice[3]. |
Synonyms | (+)-DAR-0100 (hydrochloride) |
Molecular Weight | 303.78 |
Formula | C17H18ClNO2 |
CAS No. | 158704-02-0 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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(+)-Dihydrexidine hydrochloride 158704-02-0 Others (+)Dihydrexidine hydrochloride Dihydrexidine Hydrochloride DAR-0100 (+)-DAR-0100 (hydrochloride) DAR0100 (+) Dihydrexidine hydrochloride DAR 0100 inhibitor inhibit