L(-)-Tryptophan

L(-)-Tryptophan
Product Name L(-)-Tryptophan
CAS No.: 73-22-3
Catalog No.: CFN70193
Molecular Formula: C11H12N2O2
Molecular Weight: 204.2 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source:
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $30/20mg
Reference standards.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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  • Natural Product Communications2020, doi: 10.1177.
  • Front Pharmacol.2021, 12:690113.
  • Nat Commun.2019, 10(1):2745
  • Korean Journal of Pharmacognosy.2015, 46(4):352-364
  • Life Sci.2018, 209:498-506
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    Dose-response relationships between systemically administered l-tryptophan or l-5-hydroxytryptophan and raphe unit activity in the rat.[Reference: WebLink]

    METHODS AND RESULTS:
    In contrast to previous reports that l-5-hydroxytryptophan (l-5-HTP) is without effect on raphe unit activity, systemic administration of l-tryptophan(L(-)-Tryptophan) or l-5-HTP produced similar dose-dependent decreases in raphe unit activity, ranging from 0–15% at 10 mg/kg to 60–90% at 100 mg/kg doses. The dose-response curve forms a plateau for doses above 100 mg/kg of l-5-HTP or l-tryptophan. Neurochemical studies revealed that administration of varying doses of l-tryptophan or l-5-HTP (10–100 mg/kg, i.p.) under conditions simulating those of the unit recording procedure, produced dosedependent increases in forebrain serotonin of up to 42% and 353% for a 100 mg/kg dose of l-tryptophan or l-5-HTP, respectively.
    CONCLUSIONS:
    These data suggest that exogeneously administered l-5-HTP serves as an effective serotonin precursor in central serotonergic neurones. Furthermore, increases in forebrain serotonin levels within the range of normal diurnal variations dramatically depress raphe unit activity, indicating that diurnal changes in brain serotonin metabolism may significantly affect the activity of serotonin-containing neurones.
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