Gallic acid (Synonyms: 3,4,5-Trihydroxybenzoic acid)

Name: Gallic acid
Brand: MedChemExpress
SKU: HY-N0523
Rating: 5.0 (16 reviews)

Cat. No.: HY-N0523 Purity: 99.99%: Data Sheet
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Gallic acid (3,4,5-Trihydroxybenzoic acid) is a natural polyhydroxyphenolic compound and an free radical scavenger to inhibit cyclooxygenase-2 (COX-2). Gallic acid has various activities, such as antimicrobial, antioxidant, antimicrobial, anti-inflammatory, and anticance activities.

For research use only. We do not sell to patients.

CAS No. : 149-91-7

Size	Stock	Quantity
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO ready for reconstitution	In-stock	Estimated Time of Arrival: December 31
Solution
10 mM * 1 mL in DMSO	In-stock	Estimated Time of Arrival: December 31
Solid
25 mg	In-stock	Estimated Time of Arrival: December 31
50 mg	In-stock	Estimated Time of Arrival: December 31
100 mg	In-stock	Estimated Time of Arrival: December 31
500 mg	In-stock	Estimated Time of Arrival: December 31
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Customer Review

Based on 16 publication(s) in Google Scholar

Other Forms of Gallic acid:

16 Publications Citing Use of MCE Gallic acid

Histological Imaging/Staining

ELISA

RT-PCR

IHC

: Gallic acid purchased from MedChemExpress. Usage Cited in: J Transl Med. 2025 Jan 8;23(1):30. [Abstract]; Hematoxylin and eosin (HE) and Sirius red staining revealed that after intervention with the ferroptosis inhibitor Fer-1 or Gallic acid (GA) (200 mg/kg/d, i.g.), the muscle fibers were more orderly arranged, and some muscle cells exhibited mild edema and a small amount of inflammatory cell infiltration.

: Gallic acid purchased from MedChemExpress. Usage Cited in: J Transl Med. 2025 Jan 8;23(1):30. [Abstract]; Detection of IL-6, TNF-α, CK, LDH, Fe2⁺ and MDA levels significantly reduced treated with Gallic acid (GA) (200 mg/kg/d, i.g.) in skeletal muscle tissue by ELISA.

: Gallic acid purchased from MedChemExpress. Usage Cited in: J Transl Med. 2025 Jan 8;23(1):30. [Abstract]; After Gallic acid (GA) (200 mg/kg/d, i.g.) intervention, both Piezo1 and COX2 were significantly decreased, and the expression of GPX4 and FTH1 was increased by Western blot.

: Gallic acid purchased from MedChemExpress. Usage Cited in: J Transl Med. 2025 Jan 8;23(1):30. [Abstract]; Detection of Piezo1, GPX4, FTH1 and COX2 mRNA levels treated with Gallic acid (GA) (200 mg/kg/d, i.g.) in skeletal muscle tissue by RT-qPCR.

: Gallic acid purchased from MedChemExpress. Usage Cited in: J Transl Med. 2025 Jan 8;23(1):30. [Abstract]; Immunohistochemical detection of Piezo1 and GPX4 expression treated with Gallic acid (GA) (200 mg/kg/d, i.g.) in skeletal muscle tissue of different groups of mice.

: Gallic acid purchased from MedChemExpress. Usage Cited in: Pharmaceutics. 2024 Jun 2;16(6):751.; A549 cells were pre-treated with active compounds (Gallic acid, Chebulagic acid, and Chebulinic acid) (0–20 µg/mL) for 24 h. Then, the cells were exposed to CoV2-SP (100 ng/mL) for 3 h. The IL-6 (A), IL-1β (B), and IL-18 secretions (C) in the culture supernatant were examined by ELISA.

: Gallic acid purchased from MedChemExpress. Usage Cited in: Pharmaceutics. 2024 Jun 2;16(6):751.; Inhibitory effects of active compounds (Gallic acid, Chebulagic acid and Chebulinic acid) on the IL-6 (A), IL-1β (B), IL-18 (C), and NLRP3 gene expressions (D) in CoV2-SP-induced A549 cells. A549 cells were pre-treated with active compounds (gallic acid, chebulagic acid and chebulinic acid) (0–20 µg/mL) for 24 h. Then, the cells were exposed to CoV2-SP (100 ng/mL) for 3 h. The mRNA expressions were determined using RT-qPCR.

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Description

Gallic acid (3,4,5-Trihydroxybenzoic acid) is a natural polyhydroxyphenolic compound and an free radical scavenger to inhibit cyclooxygenase-2 (COX-2)^[1]. Gallic acid has various activities, such as antimicrobial, antioxidant, antimicrobial, anti-inflammatory, and anticance activities^[2].

IC₅₀ & Target^[1]

COX-2

Microbial Metabolite

Human Endogenous Metabolite

Cellular Effect

Cell Line	Type	Value	Description	References
A549	IC₅₀	0.4 mM Compound: Gallic acid	Cytotoxicity against human A549 cells assessed as reduction in cell viability measured after 48 hrs by FMCA assay Cytotoxicity against human A549 cells assessed as reduction in cell viability measured after 48 hrs by FMCA assay	[PMID: 27162124]
A549	IC₅₀	0.4 mM Compound: Gallic acid	Cytotoxicity against human A549 cells assessed as reduction in cell viability measured after 48 hrs by MTT assay Cytotoxicity against human A549 cells assessed as reduction in cell viability measured after 48 hrs by MTT assay	[PMID: 27162124]
A549	IC₅₀	0.4 mM Compound: Gallic acid	Cytotoxicity against human A549 cells assessed as reduction in cell viability measured after 48 hrs by luminescence-based ATP assay Cytotoxicity against human A549 cells assessed as reduction in cell viability measured after 48 hrs by luminescence-based ATP assay	[PMID: 27162124]
A549	IC₅₀	100 μM Compound: GA, Gallic acid	Cytotoxicity against human A549 cells Cytotoxicity against human A549 cells	[PMID: 23291333]
BV-2	IC₅₀	> 50 μM Compound: 27	Inhibition of iNOS-mediated NO production in LPS-induced mouse BV2 cells Inhibition of iNOS-mediated NO production in LPS-induced mouse BV2 cells	[PMID: 18926710]
CCRF-CEM	CC₅₀	> 250 μM Compound: 1	Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation Cytotoxicity against human CEM cells assessed as inhibition of cell proliferation	[PMID: 25617695]
CCRF-CEM	EC₅₀	> 50 μM Compound: 1	Antiviral activity against HIV1 3B infected in human CEM cells assessed as reduction in virus-induced cytopathicity after 4 to 5 days by microscopy based syncytium cell formation assay Antiviral activity against HIV1 3B infected in human CEM cells assessed as reduction in virus-induced cytopathicity after 4 to 5 days by microscopy based syncytium cell formation assay	[PMID: 25617695]
CCRF-CEM	EC₅₀	> 50 μM Compound: 1	Antiviral activity against HIV2 ROD infected in human CEM cells assessed as reduction in virus-induced cytopathicity after 4 to 5 days by microscopy based syncytium cell formation assay Antiviral activity against HIV2 ROD infected in human CEM cells assessed as reduction in virus-induced cytopathicity after 4 to 5 days by microscopy based syncytium cell formation assay	[PMID: 25617695]
CCRF-CEM	IC₅₀	> 200 μM Compound: GA	Cytotoxicity against human CCRF-CEM cells after 48 hrs by neutral red assay Cytotoxicity against human CCRF-CEM cells after 48 hrs by neutral red assay	[PMID: 24568614]
CCRF-CEM	IC₅₀	> 50 μM Compound: 0, Gallic acid	Cytotoxicity against human CEM cells after 24 hrs by MTT assay Cytotoxicity against human CEM cells after 24 hrs by MTT assay	[PMID: 18295493]
CCRF-CEM	IC₅₀	> 50 μM Compound: 0, Gallic acid	Cytotoxicity against human CEM cells after 72 hrs by MTT assay Cytotoxicity against human CEM cells after 72 hrs by MTT assay	[PMID: 18295493]
Calu-6	IC₅₀	10 μM Compound: GA, Gallic acid	Cytotoxicity against human Calu6 cells Cytotoxicity against human Calu6 cells	[PMID: 23291333]
Epithelial cell	IC₅₀	> 20 μg/mL Compound: GA, Gallic acid	Cytotoxicity against rat epithelial cells Cytotoxicity against rat epithelial cells	[PMID: 23291333]
Erythrocyte	IC₅₀	0.59 mM Compound: 18	Anticomplement activity in sheep erythrocytes assessed as concentration required for 50% hemolytic inhibition by classic pathway pretreated for 10 mins with guinea pig serum followed by erythrocyte addition measured after 30 mins by spectrophotometeric method Anticomplement activity in sheep erythrocytes assessed as concentration required for 50% hemolytic inhibition by classic pathway pretreated for 10 mins with guinea pig serum followed by erythrocyte addition measured after 30 mins by spectrophotometeric method	[PMID: 29631958]
Erythrocyte	IC₅₀	0.74 mM Compound: 18	Anticomplement activity in rabbit erythrocytes assessed as concentration required for 50% hemolytic inhibition by alternative pathway pretreated for 10 mins with normal human serum followed by erythrocyte addition measured after 30 mins by spectrophotometeric method Anticomplement activity in rabbit erythrocytes assessed as concentration required for 50% hemolytic inhibition by alternative pathway pretreated for 10 mins with normal human serum followed by erythrocyte addition measured after 30 mins by spectrophotometeric method	[PMID: 29631958]
Fibroblast	IC₅₀	> 20 μg/mL Compound: GA, Gallic acid	Cytotoxicity against rat fibroblast cells Cytotoxicity against rat fibroblast cells	[PMID: 23291333]
HCT-116	IC₅₀	41.8 μg/mL Compound: Gallic acid	Anticancer activity against human HCT-116 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay Anticancer activity against human HCT-116 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay	[PMID: 32731188]
HL-60	IC₅₀	3.2 μg/mL Compound: gallic acid	Antioxidant activity in human HL60 cells assessed as reduction of cytochrome-c release Antioxidant activity in human HL60 cells assessed as reduction of cytochrome-c release	[PMID: 10650074]
HL-60	IC₅₀	300 μM Compound: GA, Gallic acid	Cytotoxicity against human HL60 cells Cytotoxicity against human HL60 cells	[PMID: 23291333]
HUVEC	IC₅₀	> 294 μM Compound: 8	Cytotoxicity against HUVEC cells assessed as inhibition of cell growth incubated for 48 hrs by fluorescence based assay Cytotoxicity against HUVEC cells assessed as inhibition of cell growth incubated for 48 hrs by fluorescence based assay	[PMID: 37122550]
HeLa	IC₅₀	26.3 μg/mL Compound: Gallic acid	Anticancer activity against human HeLa cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay Anticancer activity against human HeLa cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay	[PMID: 32731188]
HeLa	IC₅₀	358 μM Compound: GA, Gallic acid	Cytotoxicity against human HeLa cells Cytotoxicity against human HeLa cells	[PMID: 23291333]
K562	IC₅₀	33 μM Compound: GA, Gallic acid	Cytotoxicity against human K562 cells Cytotoxicity against human K562 cells	[PMID: 23291333]
K562	IC₅₀	4.75 μM Compound: GA, Gallic acid	Cytotoxicity against human imatinib-resistant K562 cells Cytotoxicity against human imatinib-resistant K562 cells	[PMID: 23291333]
KB	IC₅₀	13.2 μg/mL Compound: GA, Gallic acid	Cytotoxicity against human KB cells Cytotoxicity against human KB cells	[PMID: 23291333]
L1210	IC₅₀	50 μM Compound: 0, Gallic acid	Cytotoxicity against mouse L1210 cells after 72 hrs by MTT assay Cytotoxicity against mouse L1210 cells after 72 hrs by MTT assay	[PMID: 18295493]
L1210	IC₅₀	> 50 μM Compound: 0, Gallic acid	Cytotoxicity against mouse L1210 cells after 48 hrs by MTT assay Cytotoxicity against mouse L1210 cells after 48 hrs by MTT assay	[PMID: 18295493]
L929	IC₅₀	250 μM Compound: GA, Gallic acid	Cytotoxicity against mouse L929 cells Cytotoxicity against mouse L929 cells	[PMID: 23291333]
MCF7	IC₅₀	17.4 μM Compound: Gallic acid	Cytotoxicity against human ER-positive MCF7 cells assessed as decrease in cell proliferation at 12.5 to 100 uM incubated for 24 hrs Cytotoxicity against human ER-positive MCF7 cells assessed as decrease in cell proliferation at 12.5 to 100 uM incubated for 24 hrs	[PMID: 33711444]
P388	ED₅₀	0.7 μg/mL Compound: Gallic acid	Cytotoxicity against mouse P388 cells Cytotoxicity against mouse P388 cells	[PMID: 3404159]
P388D1	IC₅₀	282 μM Compound: GA, Gallic acid	Cytotoxicity against human P388D1 cells Cytotoxicity against human P388D1 cells	[PMID: 23291333]
PLC-PRF-5	IC₅₀	387 μM Compound: GA, Gallic acid	Cytotoxicity against human PLC/PRF/5 cells Cytotoxicity against human PLC/PRF/5 cells	[PMID: 23291333]
RAW264.7	IC₅₀	631.6 μM Compound: gallic acid	Inhibition of LPS-induced NO production in mouse RAW264.7 cells assessed as reduction in nitrite level within 24 hrs by Griess reagent method Inhibition of LPS-induced NO production in mouse RAW264.7 cells assessed as reduction in nitrite level within 24 hrs by Griess reagent method	[PMID: 22560043]
RAW264.7	IC₅₀	69.25 μM Compound: 3a	Antagonist activity at TLR2 in mouse RAW264.7 cells assessed as PAM3CSK4-induced NO production measured after 24 hrs by Griess assay Antagonist activity at TLR2 in mouse RAW264.7 cells assessed as PAM3CSK4-induced NO production measured after 24 hrs by Griess assay	[PMID: 31255924]
RAW264.7	IC₅₀	> 50 μM Compound: 13	Anti-inflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production preincubated for 2 hrs followed by LPS stimulation and measured after 24 hrs by by Griess assay Anti-inflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production preincubated for 2 hrs followed by LPS stimulation and measured after 24 hrs by by Griess assay	[PMID: 31419126]
Vero	IC₅₀	> 1 μM Compound: 0, Gallic acid	Cytotoxicity against african green monkey VERO cells Cytotoxicity against african green monkey VERO cells	[PMID: 18295493]
Vero	IC₅₀	> 299 μM Compound: 0, Gallic acid	Genotoxicity against african green monkey VERO cells Genotoxicity against african green monkey VERO cells	[PMID: 18295493]

In Vitro

Gallic acid is an antioxidant which can inhibit both COX-2^[1]. After 18 h treatment with Gallic acid, the number of viable neutrophils is dramatically decreased from 40.3% to 27.7%, highly comparable with 26.4% for untreated neutrophils. Gallic acid fails to attenuate isoproterenol-induced myocytolysis^[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

The food intake (2.6±0.08 g/day, p=0.69) and the body weight (2.5±0.69 g, p=0.76) of the Gallic acid group do not differ significantly from those of the control group (food intake; 2.41±0.14 g/day and the body weight; 2.83±0.84 g/day). The blood glucose tolerance in the Gallic acid group is significantly improved after 2 weeks of treatment. The blood glucose tolerance of the Gallic acid group after a treatment period of 2 weeks is also significantly better than that of the control group at 90 and 120 min ( p<0.05). The serum triglyceride concentration in the Gallic acid group (0.67±0.03 mM, p<0.05) is significantly reduced relative to that of the control group (1.08±0.20 mM). The total cholesterol concentration is similar in the control (3.19±0.27 mM) and Gallic acid (3.01±0.18 mM) groups^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

170.12

Formula

C₇H₆O₅

CAS No.

149-91-7

Appearance

Solid

Color

White to off-white

SMILES

O=C(O)C1=CC(O)=C(O)C(O)=C1

Structure Classification

Initial Source

Microorganisms

Endogenous metabolite

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Store at room temperature 3 years

In solvent	-80°C	2 years
	-20°C	1 year

Solvent & Solubility

In Vitro:

DMSO : ≥ 100 mg/mL (587.82 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H₂O : 8.33 mg/mL (48.97 mM; ultrasonic and warming and heat to 60°C)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions

Concentration Solvent Mass	1 mg	5 mg	10 mg

1 mM	5.8782 mL	29.3910 mL	58.7820 mL
5 mM	1.1756 mL	5.8782 mL	11.7564 mL
10 mM	0.5878 mL	2.9391 mL	5.8782 mL

View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

Molarity Calculator
Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

Volume _(final)

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (14.70 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Protocol 2

Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (14.70 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.

For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: Corn Oil
Solubility: 20 mg/mL (117.56 mM); Suspended solution; Need ultrasonic

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

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mg/kg

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μL

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Please enter your animal formula composition:

DMSO +

Tween-80 +

Saline

Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.

The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).

Calculation results:

Working solution concentration: mg/mL

Method for preparing stock solution: mg drug dissolved in μL DMSO (Stock solution concentration: mg/mL).

The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).

Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.

If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.

Purity & Documentation

Purity: 99.99%

Select Batch:

Data Sheet (281 KB) SDS (393 KB)

COA (250 KB) HNMR (109 KB) RP-HPLC (252 KB) MS (67 KB)

Handling Instructions (2659 KB)

References

[1]. Amaravani M, et al. COX-2 structural analysis and docking studies with gallic acid structural analogues. Springerplus. 2012 Dec;1(1):58. [Content Brief]

[2]. Bak EJ, et al. Gallic acid improves glucose tolerance and triglyceride concentration in diet-induced obesity mice. Scand J Clin Lab Invest. 2013 Dec;73(8):607-14. [Content Brief]

[3]. Cheng Y, et al. Plant Natural Products Calycosin and Gallic Acid Synergistically Attenuate Neutrophil Infiltration and Subsequent Injury in Isoproterenol-Induced Myocardial Infarction: A Possible Role for Leukotriene B4 12-Hydroxydehydrogenase? Oxid Med Cell Longev. 2015;2015:434052. [Content Brief]

Cell Assay ^[3]	Neutrophils are treated with 8?μg/mL Gallic acid in RPMI1640/10% FBS for 3, 6, 9, and 18?h. At the end of Gallic acid treatment, the cells are stained with Annexin V-FITC and PI according to manufacturer's instructions. Briefly, the cells are washed twice with ice-cold PBS and resuspended in 1× Binding Buffer at a concentration of 1×10⁶ cells/mL. Cell suspensions (1×10⁵ cells in 100?μL) are incubated with 5?μL of Annexin V-FITC and 10?μL PI in a 5?mL culture tube at room temperature for 20?min. The stained cells are immediately analyzed on flow cytometry system^[3]. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Administration ^[2]	Five-week-old male C57BL/6 mice are used in this study. The animals are maintained in a temperature-controlled room at 22° C on a 12 h light-dark photocycle. The mice are divided into the control vehicle group and the Gallic acid group. For 2 weeks, the mice are administered intraperitoneal treatment on a daily basis with vehicle (10% alcohol, 10% tween 80, and 80% saline) alone or with 10 mg/kg Gallic acid. After this treatment, GTTs are again conducted, and the blood samples are taken for subsequent biochemical analysis. Over the experimental period, food intake and body weight are measured on a daily basis^[2]. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
References	[1]. Amaravani M, et al. COX-2 structural analysis and docking studies with gallic acid structural analogues. Springerplus. 2012 Dec;1(1):58. [Content Brief] [2]. Bak EJ, et al. Gallic acid improves glucose tolerance and triglyceride concentration in diet-induced obesity mice. Scand J Clin Lab Invest. 2013 Dec;73(8):607-14. [Content Brief] [3]. Cheng Y, et al. Plant Natural Products Calycosin and Gallic Acid Synergistically Attenuate Neutrophil Infiltration and Subsequent Injury in Isoproterenol-Induced Myocardial Infarction: A Possible Role for Leukotriene B4 12-Hydroxydehydrogenase? Oxid Med Cell Longev. 2015;2015:434052. [Content Brief]

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

H₂O / DMSO	1 mM	5.8782 mL	29.3910 mL	58.7820 mL	146.9551 mL
	5 mM	1.1756 mL	5.8782 mL	11.7564 mL	29.3910 mL
	10 mM	0.5878 mL	2.9391 mL	5.8782 mL	14.6955 mL
	15 mM	0.3919 mL	1.9594 mL	3.9188 mL	9.7970 mL
	20 mM	0.2939 mL	1.4696 mL	2.9391 mL	7.3478 mL
	25 mM	0.2351 mL	1.1756 mL	2.3513 mL	5.8782 mL
	30 mM	0.1959 mL	0.9797 mL	1.9594 mL	4.8985 mL
	40 mM	0.1470 mL	0.7348 mL	1.4696 mL	3.6739 mL
DMSO	50 mM	0.1176 mL	0.5878 mL	1.1756 mL	2.9391 mL
	60 mM	0.0980 mL	0.4899 mL	0.9797 mL	2.4493 mL
	80 mM	0.0735 mL	0.3674 mL	0.7348 mL	1.8369 mL
	100 mM	0.0588 mL	0.2939 mL	0.5878 mL	1.4696 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

Gallic acid Related Classifications

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Keywords:

Gallic acid149-91-73,4,5-Trihydroxybenzoic acidCOXReactive Oxygen Species (ROS)ApoptosisFerroptosisEndogenous MetaboliteCyclooxygenaseInhibitorinhibitorinhibit

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Gallic acid (Synonyms: 3,4,5-Trihydroxybenzoic acid)

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Gallic acid Related Antibodies

16 Publications Citing Use of MCE Gallic acid

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References

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Complete Stock Solution Preparation Table

Gallic acid Related Classifications

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