Yohimbine hydrochloride, >=98% (TLC), powder

Code: Y3125-10G D2-231

Application

Yohimbine hydrochloride has been:used to study its in vitro antiviral, antibacterial and antifungal activities and cytotoxicityused as a tyramine recepto...


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€267.08 10G
€328.51 inc. VAT

Application

Yohimbine hydrochloride has been:used to study its in vitro antiviral, antibacterial and antifungal activities and cytotoxicityused as a tyramine receptor blocker to oppose the effects of increased tyramine in relation with flight initiation and maintenance deficits in experimental fliesused alone and as well as with brimonidine to study the neuroprotective effect of brimonidine in the presence of glutamate-induced neurotoxicity, oxidative stress and hypoxia on in vitro cultures of purified rat retinal ganglion cells

Biochem/physiol Actions

Yohimbine is derived from the Coryanthe yohimbe tree cortex. It is an alkaloid. Yohimbine hydrochloride is an α2-adrenergic receptor antagonist. It blocks the central α2-adrenergic receptors in the brain, thus preventing and reducing the effects of xylazine, an α2-adrenergic agonist. The sedative effects and respiratory depression that accompany xylazine administration are both antagonized and reversed by yohimbine. Yohimbine hydrochloride also produces an antidiuretic effect, and increases heart rate and blood pressure. It is useful in treating erectile dysfunction and promotes sexual functioning.

Features and Benefits

This compound is featured on the α2-Adrenoceptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

assay≥98% (HPLC)
colorwhite to off-white
formpowder
Gene Informationhuman ... ADRA2A(150), ADRA2B(151), ADRA2C(152)
InChI keyPIPZGJSEDRMUAW-VJDCAHTMSA-N
InChI1S/C21H26N2O3.ClH/c1-26-21(25)19-15-10-17-20-14(13-4-2-3-5-16(13)22-20)8-9-23(17)11-12(15)6-7-18(19)24;/h2-5,12,15,17-19,22,24H,6-11H2,1H3;1H/t12-,15-,17-,18-,19+;/m0./s1
mp288-290 °C (dec.) (lit.)
Quality Level100
SMILES stringCl.COC(=O)[C@H]1[C@@H](O)CCC2CN3CCc4c([nH]c5ccccc45)C3CC12
solubilityH2O: 10 mg/mL
Cas Number65-19-0
Hazard Class6.1
Un Number1544
Pack GroupII
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