GLPBio

2-Hydroxymelatonin

Catalog No.: GC81601Purity:>98.00%
2-Hydroxymelatonin is a major hydroxylated metabolite of Melatonin.

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2-Hydroxymelatonin
Cas No.: 229018-17-1
50mgIn Stock
$67.00
1
100mgIn Stock
$107.00
1
250mgIn Stock
$215.00
1
500mgIn Stock
$343.00
1

Zitate (Citations)

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    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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    31, 1291–1307 (2021)

Beschreibung (Description)

2-Hydroxymelatonin is a major hydroxylated metabolite of Melatonin. It is enzymatically produced in plants by melatonin 2-hydroxylase ( M2H/AsMT ), while in animals, it is generated in trace amounts via CYP450 or spontaneous oxidation. 2-Hydroxymelatonin acts as a respiratory burst oxidase homolog (RBOH)-dependent ROS burst inducer, thereby regulating stress tolerance, seed germination and growth in plants. In animal cells, 2-Hydroxymelatonin synergizes with BMP-4 to promote osteogenesis, and exerts pro- apoptotic and anti-metastatic activities against colorectal cancer cells. 2-Hydroxymelatonin can be used in studies related to plant premature senescence, osteoporosis and colorectal cancer [1] [2] [3] [4] [5].

In Vitro, 2-Hydroxymelatonin (50-150 μM; 15 days) exerts the optimal effect on alleviating cadmium toxicity in cucumber seedlings at a concentration of 100 μM. It promotes seedling growth, increases photosynthetic and gas exchange parameters, antioxidant enzyme activities, polyamine levels, and the expression of the CS-ERS gene, while reducing cadmium uptake and the levels of oxidative stress markers[1]. 2-Hydroxymelatonin (5-20 μM; 40 h) potently promotes the germination of non-dormant and dormant seeds of Arabidopsis thaliana (L.) Heynh. Columbia-0 wild type, with the germination rate increased to 80% and 40%, respectively, after treatment with 20 μM for 40 h[3]. 2-Hydroxymelatonin (20 μM; 24 h) upregulates the expression of gibberellin (GA) biosynthesis and response genes in non-dormant *Arabidopsis thaliana* (L.) Heynh. Columbia-0 wild-type seeds after 24 h of incubation[3]. 2-Hydroxymelatonin (20 μM) promotes the production of superoxide anions (ROS) in non-dormant seeds of Arabidopsis thaliana (L.) Heynh. Columbia-0 wild type, which is confirmed by enhanced NBT staining[3]. 2-Hydroxymelatonin (20 μM; 40 h) increases the germination rate of non-dormant Arabidopsis thaliana m2h knockout mutant seeds from 20% to 80%, fully restoring it to the wild-type level after 40 h of incubation[3]. 2-Hydroxymelatonin (125-2000 μM; 48 h) potently reduces the viability of Caco2, HCT116, DLD1, and CT26 colorectal cancer cells, with IC50 values of 1010.3 μM, 1482.3 μM, 2136.5 μM, and 1036.1 μM, respectively[5]. 2-Hydroxymelatonin (1000 μM; 24 h) induces significant apoptosis and nuclear pyknosis in Caco2 colorectal cancer cells[5]. 2-Hydroxymelatonin (50-100 μM; 24 h) inhibits the invasive ability of Caco2 colorectal cancer cells[5]. 2-Hydroxymelatonin (50-100 μM; 24 h) inhibits the invasive ability of Caco2 colorectal cancer cells by downregulating the mRNA expression of EMT markers (Snail, Twist, N-cadherin) and the Wnt pathway marker β-catenin[5].

References:
[1]. Shah AA, et al. 2-Hydroxymelatonin mitigates cadmium stress in cucumis sativus seedlings: Modulation of antioxidant enzymes and polyamines. Chemosphere. 2020 Mar;243:125308.
[2]. Lee HY, et al. 2-Hydroxymelatonin, Rather Than Melatonin, Is Responsible for RBOH-Dependent Reactive Oxygen Species Production Leading to Premature Senescence in Plants. Antioxidants (Basel, Switzerland). 2021 Oct 29;10(11):1728.
[3]. Lee HY, Back K. 2-Hydroxymelatonin Promotes Seed Germination by Increasing Reactive Oxygen Species Production and Gibberellin Synthesis in Arabidopsis thaliana. Antioxidants (Basel). 2022 Apr 8;11(4):737.
[4]. Lee SH, et al. Synergistic stimulating effect of 2-hydroxymelatonin and BMP-4 on osteogenic differentiation in vitro. Biochemical and biophysical research communications. 2020 Jul 05;527(4):941-946.
[5]. Yang Y, et al. 2-Hydroxymelatonin, a Predominant Hydroxylated Melatonin Metabolite in Plants, Shows Antitumor Activity against Human Colorectal Cancer Cells. Molecules (Basel, Switzerland). 2017 Mar 14;22(3):453.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
229018-17-1
Summenformel
C13H16N2O3
Molekulargewicht
248.28
Lagerung
Store at room temperature, keep dry and cool
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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