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Listado de productos por fabricante AbMole
Trans-crocetin
Trans-crocetin (Croceic Acid) is a blood-brain barrier-permeable NMDA receptor antagonist with high affinity, extracted from saffron (Crocus sativus L.). *The compound is unstable in solutions, freshly prepared is recommended
Trans-Farnesol
Trans-Farnesol is a signaling molecule that is derived from farnesyl diphosphate, an intermediate in the isoprenoid/cholesterol biosynthetic pathway.
trans-ISRIB
trans-ISRIB is a integrated stress response (ISR) inhibitor.
trans-ISRIB
trans-ISRIB is a integrated stress response (ISR) inhibitor.
trans-ISRIB
trans-ISRIB is a integrated stress response (ISR) inhibitor.
trans-Zeatin
trans-Zeatin is a plant cytokinin, which plays an important role in cell growth, differentiation, and division.
trans-Zeatin
trans-Zeatin is a plant cytokinin, which plays an important role in cell growth, differentiation, and division.
trans-Zeatin-riboside
trans-Zeatin-riboside is a type of cytokinin precursor, acts as a major long-distance signalling form in xylem vessels, regulates leaf size and meristem activity-related traits.
trans-Zeatin-riboside
trans-Zeatin-riboside is a type of cytokinin precursor, acts as a major long-distance signalling form in xylem vessels, regulates leaf size and meristem activity-related traits.
trans-Zeatin-riboside
trans-Zeatin-riboside is a type of cytokinin precursor, acts as a major long-distance signalling form in xylem vessels, regulates leaf size and meristem activity-related traits.
Tranylcypromine (2-PCPA) HCl
Tranylcypromine HCl is a monoamine oxidase inhibitor, which inhibits CYP2A6 with Ki of 0.08 μM and 0.2 μM in cDNA-expressing microsomes and Human Liver Microsomes, respectively. Tranylcypromine hydrochloride inhibits LSD1, MAO A and MAO B with IC50s of 20.7, 2.3 and 0.95 μM, respectively.
Tranylcypromine (2-PCPA) HCl
Tranylcypromine HCl is a monoamine oxidase inhibitor, which inhibits CYP2A6 with Ki of 0.08 μM and 0.2 μM in cDNA-expressing microsomes and Human Liver Microsomes, respectively. Tranylcypromine hydrochloride inhibits LSD1, MAO A and MAO B with IC50s of 20.7, 2.3 and 0.95 μM, respectively.