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Monomethyl Fumarate - >98.0%(GC), high purity , CAS No.2756-87-8, Agonist of HCA 2 receptor

  • Moligand™
  • ≥98%(GC)
Item Number
M158861
Grouped product items
SKUSizeAvailabilityPrice Qty
M158861-1g
1g
In stock
$9.90
M158861-5g
5g
In stock
$31.90
M158861-10g
10g
In stock
$56.90
M158861-25g
25g
In stock
$144.90
M158861-100g
100g
In stock
$519.90

Activator of Nrf2 pathway; primary metabolite ofDMF(Cat. No. 4512)

View related series
HCA2 receptor Agonist

Basic Description

SynonymsMonomethyl fumarate|2756-87-8|4-methoxy-4-oxobut-2-enoic acid|mono-Methyl fumarate|Methyl hydrogen fumarate|Fumaric acid monomethyl ester|(E)-4-methoxy-4-oxobut-2-enoic acid|Bafiertam|(2E)-4-Methoxy-4-oxobut-2-enoic acid|UNII-45IUB1PX8R|45IUB1PX8R|monomet
Specifications & PurityMoligand™, ≥98%(GC)
Biochemical and Physiological MechanismsNuclear factor (erythroid-derived-2)-like 2 (Nrf2) pathway activator. Also exhibits agonist activity at GPR109A. Primary metabolite ofDMF.
Storage TempArgon charged
Shipped InNormal
GradeMoligand™
Action TypeAGONIST
Mechanism of actionAgonist of HCA 2 receptor
Product Description

mono-Methyl fumarate can be used as a reactant to synthesize: · Jumonji C domain-containing histone demethylases (JCHDMs) inhibitor. · (-)-Xylariamide A, a fungal metabolite. · (±)-Methoxyfumimycin ethyl ester, a potential bacterial peptide deformylase inhibitor. It is also a wide spectrum antibacterial agent with a powerful antioxidant activity.

Product Properties

ALogP0.4

Associated Targets

CA5A Tclin Carbonic anhydrase 5A, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HCAR2 Tclin Hydroxycarboxylic acid receptor 2 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA5B Tclin Carbonic anhydrase 5B, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA1 Tclin Carbonic anhydrase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488195478
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488195478
IUPAC Name (E)-4-methoxy-4-oxobut-2-enoic acid
INCHI InChI=1S/C5H6O4/c1-9-5(8)3-2-4(6)7/h2-3H,1H3,(H,6,7)/b3-2+
InChi Key NKHAVTQWNUWKEO-NSCUHMNNSA-N
Canonical SMILES COC(=O)C=CC(=O)O
Isomeric SMILES COC(=O)/C=C/C(=O)O
WGK Germany 3
PubChem CID 5369209
Molecular Weight 130.1

Certificates

Certificate of Analysis(COA)

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6 results found

Lot NumberCertificate TypeDateItem
D2320331Certificate of AnalysisOct 28, 2022 M158861
K2215282Certificate of AnalysisOct 28, 2022 M158861
K2215309Certificate of AnalysisOct 28, 2022 M158861
K2215316Certificate of AnalysisOct 28, 2022 M158861
K2215318Certificate of AnalysisOct 28, 2022 M158861
K2215349Certificate of AnalysisOct 28, 2022 M158861

Chemical and Physical Properties

SolubilitySolvent:DMSO, Max Conc. mg/mL: 13.01, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 13.01, Max Conc. mM: 100
Melt Point(°C)145-149°C

Safety and Hazards(GHS)

Pictogram(s) GHS05
Signal Danger
Hazard Statements

H318:Causes serious eye damage

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P317:Get emergency medical help.

WGK Germany 3

Related Documents

Solution Calculators