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추천 제품
양식
lyophilized powder
특이 활성도
≥3 units/mg solid
저장 온도
2-8°C
단위 정의
One unit will oxidize 1.0 μmole of tyramine to p-hydroxyphenylacetaldehyde per min at pH 7.5 at 37 °C.
신호어
Danger
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Resp. Sens. 1
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Alexandra Soliman et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 32(48), 17120-17127 (2012-12-01)
Monoamine oxidase-A (MAO-A), a key brain enzyme which metabolizes monoamines, is implicated in the pathophysiology of stress-related illnesses, including major depressive disorder, addiction, and violent behavior. Chronic stressors and glucocorticoid-administration typically associate with elevated MAO-A levels/activity. However, the relationship of
Kalpana Nagpal et al.
Drug delivery, 19(8), 378-391 (2012-11-24)
Gallic acid had been reported to possess antidepressant like activity, which may be attributed to its CNS effects like increase in reduced glutathione levels, increased catalase activity and decreased malonaldehyde levels in brain. This study was designed to enhance the
M Bellani et al.
Epidemiology and psychiatric sciences, 21(4), 347-351 (2012-11-24)
In a short series of articles, we will review the evidence for genotype by environment interaction (G × E) in developmental psychopathology. We will focus specifically on the characteristics of types of exposure assessed with respect to both their methods and findings.
Omaima M Abdelhafez et al.
Neurochemistry international, 62(2), 198-209 (2012-11-28)
New series of bioactive 7-oxycoumarin derivatives were synthesized and tested for their in vitro and in vivo monoamine oxidase (MAO) A and B inhibitory effect. In vitro studies revealed exceptionally potent and selective MAO-A inhibitors with K(i) values on a
Nibha Mishra et al.
Bioorganic & medicinal chemistry letters, 23(3), 702-705 (2013-01-02)
MAO-B and AChE are the two validated targets for Alzheimer's disease. In pursuit of a single molecule hitting both the targets, we explored a set of previously reported extremely potent MAO-B selective inhibitors, for their additional AChE inhibitory activity. We
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