GLPBio

Gallotannin

Catalog No.: GC43726Purity:>98.00%Synonyms: Tannic Acid

Gallotannin ist ein Polyphenol von Gallussäure, das in verschiedenen Pflanzen gefunden wurde und antioxidative, entzündungshemmende, antivirale und antiproliferative biologische Aktivitäten aufweist.

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Gallotannin
Cas No.: 1401-55-4
5gIn Stock
$30.00
1
10gIn Stock
$46.00
1
25gIn Stock
$81.00
1

Zitate (Citations)

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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Gallotannin (Tannic acid) is a natural polyphenolic compound that has been found in various plants and has antioxidant, anti-inflammatory, anti-angiogenic, antiviral and anti-tumor biological activities[1]. Gallotannin inhibits the activity of DNA polymerase α, β and κ with IC50 values of 13, 130 and 30nM, respectively [2]. Gallotannin is a novel human Ether-à-go-go-Related Gene (hERG) blocker with an IC50 value of 3.4 μM[3]. Gallotannin is a potent inhibitor of the CXCL12/CXCR4 signaling pathway[4]. Gallotannin is a direct inhibitor of poly (ADP-ribose) glycohydrolase (PARG) [5]. Gallotannin is an inhibitor of NOS3 (eNOS) and a weak inhibitor of NOS2 (iNOS) and NOS1(nNOS)[6]. Gallotannin can induce cyclooxygenase-2 (Cox-2) expression and is a free radical scavenger[7].

In vitro, Gallotannin (0-100 μM) treatment of HEK293 cells rapidly inhibited intracellular hERG channels with an IC50 of 3.4±0.8 μM, and at a concentration of 10 μM, the activation curve of hERG current was significantly shifted to a more positive potential[3]. Gallotannin (100μM) treatment of AML12 cells for 1 h significantly inhibited the intracellular NAD+ level after nicotinamide riboside (NRH) treatment [8].

In vivo, Gallotannin (25 mg/kg) was treated with intraperitoneal injection of colon cancer xenograft mice for 4 weeks, significantly inhibiting tumor growth, reducing the proliferation index (Ki67), and reducing the mRNA expression levels of IL-6, TNF-α and IL-1α and angiogenesis (VEGFA) proteins [9].

References:
[1] Fraga-Corral M, Otero P, Cassani L, et al. Traditional applications of tannin rich extracts supported by scientific data: Chemical composition, bioavailability and bioaccessibility[J]. Foods, 2021, 10(2): 251.
[2] Savelyev N, Baykuzina P, Dokudovskaya S, et al. Comprehensive analysis of telomerase inhibition by gallotannin[J]. Oncotarget, 2018, 9(27): 18712.
[3] Chu X, Guo Y, Xu B, et al. Effects of tannic acid, green tea and red wine on hERG channels expressed in HEK293 cells[J]. PLoS One, 2015, 10(12): e0143797.
[4] Chen X, Beutler J A, McCloud T G, et al. Tannic acid is an inhibitor of CXCL12 (SDF-1α)/CXCR4 with antiangiogenic activity[J]. Clinical Cancer Research, 2003, 9(8): 3115-3123.
[5] Ying W, Swanson R A. The poly (ADP-ribose) glycohydrolase inhibitor gallotannin blocks oxidative astrocyte death[J]. Neuroreport, 2000, 11(7): 1385-1388.
[6] Olmos A, Giner R M, Máñez S. Drugs modulating the biological effects of peroxynitrite and related nitrogen species[J]. Medicinal Research Reviews, 2007, 27(1): 1-64.
[7] Go J, Kim J E, Koh E K, et al. Hepatoprotective effect of gallotannin-enriched extract isolated from gall on hydrogen peroxide-induced cytotoxicity in HepG2 cells[J]. Pharmacognosy Magazine, 2017, 13(Suppl 2): S294.
[8] Giroud-Gerbetant J, Joffraud M, Giner M P, et al. A reduced form of nicotinamide riboside defines a new path for NAD+ biosynthesis and acts as an orally bioavailable NAD+ precursor[J]. Molecular metabolism, 2019, 30: 192-202.
[9] Al-Halabi R, Bou Chedid M, Abou Merhi R, et al. Gallotannin inhibits NFĸB signaling and growth of human colon cancer xenografts[J]. Cancer biology & therapy, 2011, 12(1): 59-68.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

AML12 cells

Preparation Method

AML12 cells were treated with gallotannin (100 μM) for 1 h prior to nicotinamide riboside (NRH) treatment at the doses indicated.

Reaction Conditions

100μM; 1 h 

Applications

Use of gallotannin as a NMN adenylyltransferase (NMNAT) inhibitor largely compromised the NAD+ levels after NRH treatment.
Animal experiment [2]:

Animal models

NOD/SCID female mice

Preparation Method

Mice were divided into four groups of ten mice each and maintained in Maxi-miser hepa-filtered facility. Group 1 (control) was injected with HCT116 tumor cells and received i.p. injections of 0.9% saline throughout. Group 2 (prevention) received i.p. injections of 25mg/kg body weight Gallotannin, three times per week for one week prior to tumor cell injection and three times per week after tumor inoculation. Group 3 (therapy) was implanted with tumor cells and Gallotannin(25 mg/kg) injections were started at the time the tumor reached a palpable size (one week after tumor inoculation) and continued three times per week. Group 4 (toxicity) received only 25 mg/kg Gallotannin injections three times per week over a total period of 4 weeks.

Dosage form

25mg/kg; i.p.

Applications

Gallotannin treated significantly decreased the volume of human colon cancer xenografts in mice. Gallotannin treated xenografts showed significantly lower microvessel density (CD31) as well as lower mRNA expression levels of IL-6, TNF-α and IL-1α and of the proliferation (Ki-67) and angiogenesis (VEGFA) proteins.

References:
[1] Giroud-Gerbetant J, Joffraud M, Giner M P, et al. A reduced form of nicotinamide riboside defines a new path for NAD+ biosynthesis and acts as an orally bioavailable NAD+ precursor[J]. Molecular metabolism, 2019, 30: 192-202.
[2] Al-Halabi R, Bou Chedid M, Abou Merhi R, et al. Gallotannin inhibits NFĸB signaling and growth of human colon cancer xenografts[J]. Cancer biology & therapy, 2011, 12(1): 59-68.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
1401-55-4
Synonyme
Tannic Acid
SMILES
OC1=C(O)C(O)=CC(C(OC2=CC(C(OC[C@@H]3[C@@H](OC(C4=CC(O)=C(O)C(OC(C5=CC(O)=C(O)C(O)=C5)=O)=C4)=O)[C@H](OC(C6=CC(O)=C(O)C(OC(C7=CC(O)=C(O)C(O)=C7)=O)=C6)=O)[C@@H](OC(C8=CC(O)=C(O)C(OC(C9=CC(O)=C(O)C(O)=C9)=O)=C8)=O)[C@H](OC(C%10=CC(O)=C(O)C(OC(C%11=CC(O
Summenformel
C76H52O46
Molekulargewicht
1701.2
Löslichkeit
DMF: 10 mg/ml,DMSO: 10 mg/ml,PBS (pH 7.2): 0.3 mg/ml
Lagerung
Store at-20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
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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