Vue d’ensemble Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

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Why this grade

Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Protected from light,Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 823 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Gallic acid is an antiinflammatory and Cox (cyclooxygease inhibitory substance found in plants and has been shown to Induce apoptosis in human lung cancer cells. It is cytotoxic to PC14 AND MKN45 human cancer cell lines.
A cyclooxygease inhibitor substance found in plants.

Specifications

Synonymes

Spécifications et pureté

Moligand™, ≥99%

Mécanismes biochimiques et physiologiques

Phase II enzyme inducer. COX inhibitor. Carbonic anhydrase inhibitor (IC 50 = 4 μM). Shows antioxidant activity.

Conditions de stockage de stockage

Protected from light,Argon charged,Room temperature

Expédié en

Normal

Grade

Moligand™

Type d'action

INHIBITOR

Mécanisme d'action

Inhibitor of carbonic anhydrase 1

Note

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 -20°C. Generally, these will be useable for up to one month. 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. Refer to SDS for further information Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureté

≥99%

Noms et identifiants

Pubchem Sid	488179516
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488179516
Sourires canoniques	C1=C(C=C(C(=C1O)O)O)C(=O)O
IUPAC Name	3,4,5-trihydroxybenzoic acid
InChIKey	LNTHITQWFMADLM-UHFFFAOYSA-N
INCHI	1S/C7H6O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,8-10H,(H,11,12)
Isomères SMILES	C1=C(C=C(C(=C1O)O)O)C(=O)O
WGK Allemagne	2
RTECS	LW7525000
Poids moléculaire	170.12
Beilstein	2050274
Reaxy-Rn	2050274
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2050274&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Classe Benzene and substituted derivatives
    - Subclass Benzoic acids and derivatives
      - Level5 Hydroxybenzoic acid derivatives
        Level6 Gallic acid and derivatives
        Level7 Gallic acids

Kingdom	Organic compounds
Superclass	Benzenoids
Classe	Benzene and substituted derivatives
Subclass	Benzoic acids and derivatives
Intermediate Tree Nodes	Hydroxybenzoic acid derivatives - Gallic acid and derivatives
Direct Parent	Gallic acids
Alternative Parents	Pyrogallols and derivatives Benzoic acids Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Polyols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Gallic acid - Benzenetriol - Benzoic acid - Pyrogallol derivative - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Polyol - Organic oxygen compound - Organic oxide - Organooxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as gallic acids. These are organic compounds that contain a 3,4,5-trihydroxybenzoic acid moiety.
External Descriptors	Gallotannins
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

CA1 Tclin Carbonic anhydrase 1 (1 Activities)

Discover Target: CA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

FUT7 Tchem Alpha-(1,3)-fucosyltransferase 7 (1 Activities)

Discover Target: FUT7

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

GALNT2 Tchem Polypeptide N-acetylgalactosaminyltransferase 2 (1 Activities)

Discover Target: GALNT2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

Discover Target: EGFR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

F2 Tclin Thrombin (11687 Activities)

Discover Target: F2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP19A1 Tclin Cytochrome P450 19A1 (6099 Activities)

Discover Target: CYP19A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACE Tclin Angiotensin-converting enzyme (1423 Activities)

Discover Target: ACE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TYR Tclin Tyrosinase (717 Activities)

Discover Target: TYR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

Discover Target: PTGS2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AKR1B1 Tclin Aldose reductase (1404 Activities)

Discover Target: AKR1B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CXCL8 Tchem Interleukin-8 (642 Activities)

Discover Target: CXCL8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PLA2G7 Tchem LDL-associated phospholipase A2 (1338 Activities)

Discover Target: PLA2G7

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA3 Tclin Carbonic anhydrase III (753 Activities)

Discover Target: CA3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA6 Tclin Carbonic anhydrase VI (993 Activities)

Discover Target: CA6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

Discover Target: CA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDOA Tbio Fructose-bisphosphate aldolase A (1 Activities)

Discover Target: ALDOA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

APP Tclin Amyloid-beta A4 protein (8510 Activities)

Discover Target: APP

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA5B Tclin Carbonic anhydrase VB (957 Activities)

Discover Target: CA5B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA5A Tclin Carbonic anhydrase VA (1168 Activities)

Discover Target: CA5A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA14 Tclin Carbonic anhydrase XIV (1305 Activities)

Discover Target: CA14

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MET Tclin Hepatocyte growth factor receptor (10718 Activities)

Discover Target: MET

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FUT4 Tbio Fucosyltransferase 4 (41 Activities)

Discover Target: FUT4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GAPDH Tchem Glyceraldehyde-3-phosphate dehydrogenase liver (1284 Activities)

Discover Target: GAPDH

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA12 Tclin Carbonic anhydrase XII (6231 Activities)

Discover Target: CA12

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SELL Tchem Leukocyte adhesion molecule-1 (145 Activities)

Discover Target: SELL

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA9 Tclin Carbonic anhydrase IX (8255 Activities)

Discover Target: CA9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

Discover Target: TP53

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

BGC-823 (3035 Activities)

Lot Number	Certificate Type	Date	Article
F2630569	Certificate of Analysis	Jun 05, 2026	G131992
F2630570	Certificate of Analysis	Jun 05, 2026	G131992
F2630571	Certificate of Analysis	Jun 05, 2026	G131992
F2630572	Certificate of Analysis	Jun 05, 2026	G131992
F2630573	Certificate of Analysis	Jun 05, 2026	G131992
F2630574	Certificate of Analysis	Jun 05, 2026	G131992
B2602248	Certificate of Analysis	Jan 16, 2026	G131992
B2602260	Certificate of Analysis	Jan 16, 2026	G131992
B2602249	Certificate of Analysis	Jan 16, 2026	G131992
B2602247	Certificate of Analysis	Jan 16, 2026	G131992
B2602246	Certificate of Analysis	Jan 16, 2026	G131992
B2602245	Certificate of Analysis	Jan 16, 2026	G131992
I2501396	Certificate of Analysis	Aug 19, 2025	G131992
I2501409	Certificate of Analysis	Aug 19, 2025	G131992
I2501410	Certificate of Analysis	Aug 19, 2025	G131992
I2501411	Certificate of Analysis	Aug 19, 2025	G131992
J2327264	Certificate of Analysis	Aug 11, 2025	G131992
D2525209	Certificate of Analysis	Mar 04, 2025	G131992
D2525210	Certificate of Analysis	Mar 04, 2025	G131992
D2525180	Certificate of Analysis	Mar 04, 2025	G131992
D2525157	Certificate of Analysis	Mar 04, 2025	G131992
D2525181	Certificate of Analysis	Mar 04, 2025	G131992
B2303912	Certificate of Analysis	Nov 06, 2024	G131992
H2423012	Certificate of Analysis	Aug 30, 2024	G131992
I2412471	Certificate of Analysis	Aug 21, 2024	G131992
I2412470	Certificate of Analysis	Aug 21, 2024	G131992
I2412415	Certificate of Analysis	Aug 21, 2024	G131992
I2412414	Certificate of Analysis	Aug 21, 2024	G131992
I2412413	Certificate of Analysis	Aug 21, 2024	G131992
K2229832	Certificate of Analysis	Aug 20, 2024	G131992
K2229780	Certificate of Analysis	Aug 20, 2024	G131992
K2229833	Certificate of Analysis	Aug 20, 2024	G131992
K2229875	Certificate of Analysis	Aug 20, 2024	G131992
B2507109	Certificate of Analysis	Aug 20, 2024	G131992
B2513043	Certificate of Analysis	Aug 20, 2024	G131992
D2508484	Certificate of Analysis	Jul 23, 2024	G131992
D2508485	Certificate of Analysis	Jul 23, 2024	G131992
D2508486	Certificate of Analysis	Jul 23, 2024	G131992
I2222789	Certificate of Analysis	Jul 15, 2024	G131992
I2222790	Certificate of Analysis	Jul 15, 2024	G131992
D2508721	Certificate of Analysis	Jun 14, 2024	G131992
L2031357	Certificate of Analysis	Oct 21, 2022	G131992
I2222788	Certificate of Analysis	Jul 23, 2022	G131992
K22291017	Certificate of Analysis	Jul 23, 2022	G131992
I2223570	Certificate of Analysis	Jul 23, 2022	G131992
I2222791	Certificate of Analysis	Jul 23, 2022	G131992
G2313212	Certificate of Analysis	Jul 23, 2022	G131992
H2203373	Certificate of Analysis	Jun 16, 2022	G131992
I2322005	Certificate of Analysis	Jun 16, 2022	G131992
H2203378	Certificate of Analysis	Jun 16, 2022	G131992
H2203375	Certificate of Analysis	Jun 16, 2022	G131992
H2203374	Certificate of Analysis	Jun 16, 2022	G131992
B2209116	Certificate of Analysis	Apr 12, 2021	G131992
B2218027	Certificate of Analysis	Apr 12, 2021	G131992

Solubilité	Soluble in water (11.5 mg/ml), ethanol, acetone, and Alcohol. Insoluble in chloroform.
Sensibilité	Light & Moisture Sensitive.Air sensitive
Point de fusion (°C)	251 °C
Poids moléculaire	170.120 g/mol
XLogP3	0.700
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	1
Exact Mass	170.022 Da
Monoisotopic Mass	170.022 Da
Topological Polar Surface Area	98.000 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	169.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Gallic acid - Moligand™, ≥99% , Inhibitor of carbonic anhydrase 1, CAS No.149-91-7, Inhibitor of carbonic anhydrase 1

Storage & shipping

Quality documents

Literature proof

Vue d’ensemble

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avis des clients

📚 Citations by Application

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