1. GPCR/G Protein Neuronal Signaling Stem Cell/Wnt
  2. Dopamine Receptor YAP
  3. Dihydrexidine

Dihydrexidine (DAR-0100) is a high potent, selective and full efficacy D1-like dopamine receptor (D1/D5) agonist with an IC50 of 10 nM for D1 receptor. Dihydrexidine exhibits potent antiparkinsonian activity. Dihydrexidine can stimulate YAP phosphorylation.

At equivalent molar concentrations, both the salt and free forms of a compound exhibit comparable biological activity. Nevertheless, the salt form (Dihydrexidine hydrochloride) usually boasts enhanced water solubility and stability.

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Dihydrexidine

Dihydrexidine 構造式

CAS 番号 : 123039-93-0

容量 在庫状況
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Other 在庫あり Forms of Dihydrexidine:

Other Forms of Dihydrexidine:

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製品説明

Dihydrexidine (DAR-0100) is a high potent, selective and full efficacy D1-like dopamine receptor (D1/D5) agonist with an IC50 of 10 nM for D1 receptor. Dihydrexidine exhibits potent antiparkinsonian activity[1][2][3][4]. Dihydrexidine can stimulate YAP phosphorylation[5].

IC50 & Target

D1 Receptor

10 nM (IC50)

Cellular Effect
Cell Line Type Value Description References
HEK293 EC50
17 nM
Compound: DHX, 1
Activity at human dopamine D4.4 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP production
Activity at human dopamine D4.4 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP production
[PMID: 17154515]
HEK293 EC50
19 nM
Compound: DHX, 1
Activity at human dopamine D1 receptor expressed in HEK293 cells assessed as stimulation of cAMP production
Activity at human dopamine D1 receptor expressed in HEK293 cells assessed as stimulation of cAMP production
[PMID: 17154515]
HEK293 EC50
7.2 nM
Compound: 3, DHX
Agonist activity at human dopamine D1 receptor expressed in HEK293 cells assessed as cAMP accumulation after 15 mins
Agonist activity at human dopamine D1 receptor expressed in HEK293 cells assessed as cAMP accumulation after 15 mins
[PMID: 21862338]
HEK293 EC50
70 nM
Compound: DHX, 1
Activity at rat dopamine D2L receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP production
Activity at rat dopamine D2L receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP production
[PMID: 17154515]
体外実験

Dihydrexidine (DAR-0100) strongly increased YAP phosphorylation in U2OS cells[5].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

体内実験

Dihydrexidine has poor oral bioavailability and a relatively short half-life of 1 to 2 h[3].
Dihydrexidine (3 mg/kg; i.p.) produces prominent dopamine D1 receptor agonist effects in vivo[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Adult male Sprague–Dawley rats (275-300 g)[4]
Dosage: Adult male Sprague–Dawley rats (275-300 g)[4]
Administration: Intraperitoneal injection
Result: Produces prominent dopamine D1 receptor agonist effects in vivo
臨床実験
分子量

267.32

分子式

C17H17NO2

CAS 番号
SMILES

OC1=C(O)C=C(CC[C@]2([H])[C@]3([H])C4=C(C=CC=C4)CN2)C3=C1

輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件

Please store the product under the recommended conditions in the Certificate of Analysis.

純度とドキュメンテーション
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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製品名:
Dihydrexidine
製品番号:
HY-101299A
数量:
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