6 Results for "

Lordosis

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "Lordosis" in MCE Product Catalog:

Cat. No.: HY-122422
CAS No.: 83928-76-1
Purity:  99.88%
Target:  

5-HT Receptor

Research Areas:  

Others

Gepirone is a selective and affinitive 5-HT1A agonist. Gepirone binds selectively to 5-HT1A receptor binding site. Gepirone acts as an antidepressant agent can be used for anxiety and major depressive disorder research .
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Cat. No.: HY-119395B
CAS No.: 36681-58-0
Purity:  99.69%
Target:  

Monoamine Oxidase

Research Areas:  

Metabolic Disease

Kynuramine, an endogenously occurring amine, is a fluorescent substrate and probe of plasma amine oxidase .
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Cat. No.: HY-119395
CAS No.: 363-36-0
Synonyms: Kynurenamine
Target:  

Monoamine Oxidase

Research Areas:  

Metabolic Disease

Kynuramine is an endogenous amine that serves as a fluorescent substrate and probe for plasma amine oxidase .
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Cat. No.: HY-119395A
CAS No.: 304-47-2
Target:  

Monoamine Oxidase

Research Areas:  

Metabolic Disease

Kynuramine dihydrobromide, an endogenously occurring amine, is a fluorescent substrate of plasma amine oxidase .
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Cat. No.: HY-122422R
CAS No.: 83928-76-1
Research Areas:  

Others

Gepirone (Standard) is the analytical standard of Gepirone. This product is intended for research and analytical applications. Gepirone is a selective and affinitive 5-HT1A agonist. Gepirone binds selectively to 5-HT1A receptor binding site. Gepirone acts as an antidepressant agent can be used for anxiety and major depressive disorder research .
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Cat. No.: HY-187614
CAS No.: 1597-68-8
Target:  

Cytochrome P450

Research Areas:  

Endocrinology

6α-Fluorotestosterone is a non-aromatizable aromatase inhibitor, with IC50 values of 115 nM and 580 nM against human and rat aromatase, respectively. 6α-Fluorotestosterone binds to the substrate site of human aromatase P450arom with a Ki of 150 nM, but is not aromatized into estrogen. In vivo, 6α-Fluorotestosterone maintains sexual behavior in castrated male rats (with an effect comparable to that of testosterone), induces defeminization of sexual development, and inhibits nuclear translocation of hypothalamic estrogen receptors; its pro-mating effect is blocked by the aromatase inhibitors ATD and Fadrozole (HY-14247A). Combined with Progesterone (HY-N0437), 6α-Fluorotestosterone induces lordosis behavior in ovariectomized female rats. 6α-Fluorotestosterone can be used in studies related to anovulatory infertility and sexual behavior regulation .
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