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Buy Pinoline powder (20315-68-8) from Wisepowder

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https://www.wisepowder.com/product-details/20315-68-8Pinoline (6-methoxy-tetrahydro-beta-carboline) powder can be formed in the mammalian body under physiological conditions from 5-hydroxytryptamine or as a tricyclic metabolite of melatonin. Both
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  www.wisepowder.com wise12@wisepowder.com1  /  3 Buy Pinoline powder (20315-68-8) fromWisepowder Overview Pinoline powder is a methoxylated tryptoline (5-methoxytryptoline) long claimed tobe produced in the pineal gland during the metabolism of melatonin, however itspineal occurrence remains controversial. Its IUPAC name is6-methoxy-1,2,3,4-tetrahydro-β-carboline, usually abbreviated as 6-MeO-THBC, andits more common name is a combination of "pineal beta-carboline". The biologicalactivity of this molecule is of interest as a potential free radical scavenger, alsoknown as an antioxidant, and as a monoamine oxidase A inhibitor.  www.wisepowder.com wise12@wisepowder.com2  /  3 Pinoline powder (20315-68-8) videoPinoline powder (20315-68-8) Base Information Name pinoline powderCAS 20315-68-8Purity 98%Chemical name 6-Methoxy-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indoleSynonyms20315-68-86-methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole6-methoxytryptoline6-Methoxy-1,2,3,4-tetrahydro-beta-carbolinepinolineMolecular Formula C12H14N2OMolecular Weight 202.257 g/molMelting Point 216- 224 ° CInChI Key QYMDEOQLJUUNOF-UHFFFAOYSA-NForm SolidAppearance  / Half Life  / Solubility  / Storage Condition  / ApplicationPinoline is a methoxylated tryptoline(5-methoxytryptoline) long claimed to be produced inthe pineal gland during the metabolism of melatonin,Testing Document Available Pinoline powder General Description Pinoline (6-methoxy-tetrahydro-beta-carboline) powder can be formed in themammalian body under physiological conditions from 5-hydroxytryptamine or as atricyclic metabolite of melatonin. Both melatonin and pinoline inhibited lipidperoxidation and showed comparable activity in a total antioxidant statustest. These results support the importance of the indolic part of the molecule and  www.wisepowder.com wise12@wisepowder.com3  /  3 the 5-methoxy group common to both compounds in terms of the ability of thesemolecules to quench the hydroxyl radicals. Pinoline powder (20315-68-8) HistoryPinoline (20315-68-8) Mechanism Of ActionPinoline (20315-68-8) ApplicationPinoline (20315-68-8) More research As pinoline has been shown to exert an antidepressant-like effect in behavioralexperiments and has been reported to have a low toxicity, this compound should befurther studied as a potential antidepressant with pronounced antioxidative effects.These results further support the importance of pineal gland in antioxidativeprotection. Pinoline (20315-68-8) Document Download COA Pinoline (20315-68-8) Reference 1.  Schiller, Erich; Bartsch, H. (2003). Free Radicals and Inhalation Pathology: RespiratorySystem, Mononuclear Phagocyte System, Hypoxia and Reoxygenation, Pneumoconioses,and Other Granulomatoses, Cancer (Google Books, page view). Springer. p. 107. ISBN978-3-540-00201-7. Retrieved 2009-02-14. 2.  Airaksinen, M. M., Huang, J. T., Ho, B. T., Taylor, D., and Walker, K. (1978). “The Uptake of 6-Methoxy-1,2,3,4-Tetrahydro-β-carboline and its Effect on 5-Hydroxytryptamine Uptakeand Release in Blood Platelets”. Acta Pharmacol Toxicol. 43 (5): 375–380.doi:10.1111/j.1600-0773.1978.tb02281.x. 3.  Bartels, S. P. (2006) U.S. Patent No. 20,060,292,202 Washington, DC: U.S. 4.  { Mario de la Fuente et al. 2015 “Neurogenic Potential Assessment and PharmacologicalCharacterization of 6-Methoxy-1,2,3,4-tetrahydro-β-carboline (Pinoline) andMelatonin–Pinoline Hybrids”http://pubs.acs.org/doi/abs/10.1021/acschemneuro.5b00041}
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