Fumarate hydratase-IN-1

Modify Date: 2024-01-02 17:59:45

Fumarate hydratase-IN-1 Structure
Fumarate hydratase-IN-1 structure
Common Name Fumarate hydratase-IN-1
CAS Number 1644060-37-6 Molecular Weight 446.538
Density 1.2±0.1 g/cm3 Boiling Point 693.0±55.0 °C at 760 mmHg
Molecular Formula C27H30N2O4 Melting Point N/A
MSDS N/A Flash Point 372.9±31.5 °C

 Use of Fumarate hydratase-IN-1


Fumarate hydratase-IN-1, an enzyme of the TCA cycle. Inhibition of fumarate hydratase-IN-1 can contribute to tumorigenicity in some cells. The use of a photoaffinity labeling strategy identified fumarate hydratase as the principal pharmacological target.[1]In vitro: The activity of this enzyme was measured using a well-established assay that monitored the conversion of fumarate into L-malate and subsequent oxidation of L-malate to oxaloacetate by malate dehydrogenase. Initial controls established that neither the carboxylic acid 3 nor ester 2 inhibited malate dehydrogenase Using this two-enzyme protocol we found that carboxylic acid 3 inhibited fumarate hydratase in a dose-dependent fashion in vitro. Besides, inhibition of fumarate hydratase can contribute to tumorigenicity in some cells.[1]

 Names

Name Fumarate hydratase-IN-1
Synonym More Synonyms

 Fumarate hydratase-IN-1 Biological Activity

Description Fumarate hydratase-IN-1, an enzyme of the TCA cycle. Inhibition of fumarate hydratase-IN-1 can contribute to tumorigenicity in some cells. The use of a photoaffinity labeling strategy identified fumarate hydratase as the principal pharmacological target.[1]In vitro: The activity of this enzyme was measured using a well-established assay that monitored the conversion of fumarate into L-malate and subsequent oxidation of L-malate to oxaloacetate by malate dehydrogenase. Initial controls established that neither the carboxylic acid 3 nor ester 2 inhibited malate dehydrogenase Using this two-enzyme protocol we found that carboxylic acid 3 inhibited fumarate hydratase in a dose-dependent fashion in vitro. Besides, inhibition of fumarate hydratase can contribute to tumorigenicity in some cells.[1]
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References

[1]. Takeuchi T et al. Identification of Fumarate Hydratase Inhibitors with Nutrient-Dependent Cytotoxicity. J Am Chem Soc, 2015 Jan 21, 137(2): 564-567.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 693.0±55.0 °C at 760 mmHg
Molecular Formula C27H30N2O4
Molecular Weight 446.538
Flash Point 372.9±31.5 °C
Exact Mass 446.220551
LogP 4.77
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.616
Storage condition 2-8℃

 Synonyms

Ethyl (3S,3aR)-1-(4-biphenylylmethyl)-3-[2-(methylamino)-2-oxoethyl]-2-oxo-1,2,3,4,5,6-hexahydro-3aH-indole-3a-carboxylate
3aH-Indole-3a-carboxylic acid, 1-([1,1'-biphenyl]-4-ylmethyl)-1,2,3,4,5,6-hexahydro-3-[2-(methylamino)-2-oxoethyl]-2-oxo-, ethyl ester, (3S,3aR)-
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