Roxindole hydrochloride structure
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Common Name | Roxindole hydrochloride | ||
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CAS Number | 108050-82-4 | Molecular Weight | 382.92600 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C23H27ClN2O | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Roxindole hydrochlorideRoxindole hydrochloride (EMD 38362), an indot-alkyl-pipenidine, is a potent agonist at dopamine autoreceptors, with an affinity for the D2-like subtype in the low nanomolar range. Roxindole can be used for the research of positive and negative schizophrenic symptoms. Roxindole is a 5-HT1A agonist and 5-HT uptake inhibitor with high affinity for 5-HT1A (IC50=0.9 nM). Antipsychotic and antidepressant activities[1][2][3]. |
Name | Roxindole hydrochloride |
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Synonym | More Synonyms |
Description | Roxindole hydrochloride (EMD 38362), an indot-alkyl-pipenidine, is a potent agonist at dopamine autoreceptors, with an affinity for the D2-like subtype in the low nanomolar range. Roxindole can be used for the research of positive and negative schizophrenic symptoms. Roxindole is a 5-HT1A agonist and 5-HT uptake inhibitor with high affinity for 5-HT1A (IC50=0.9 nM). Antipsychotic and antidepressant activities[1][2][3]. |
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Related Catalog | |
In Vivo | Roxindole hydrochloride inhibits apomorphine-induced climbing in mice and stereotyped behavior in rats with ED50s of 1.4 mg/kg s.c. and 0.65 mg/kg s.c., respectively, and inhibits conditioned avoidance response in rats (ED50=1.5 mg/kg s.c.)[1]. Roxindole hydrochloride (1, 3, 10 mg/kg; s.c) inhibits both effects of 8-OH-DPAT (flat body and forepaw treading) in normal rats (male Wistar 200-350g)[3]. |
References |
Molecular Formula | C23H27ClN2O |
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Molecular Weight | 382.92600 |
Exact Mass | 382.18100 |
PSA | 39.26000 |
LogP | 5.72540 |
5-hydroxy-3-[4-(1,2,3,6-tetrahydro-4-phenyl-1-pyridyl)butyl]indole hydrochloride |
3-[4-(4-Phenyl-3,6-dihydro-2H-pyridin-1-yl)-butyl]-1H-indol-5-ol |
hydrochloride |