Urolithin C

Modify Date: 2024-01-02 16:51:33

Urolithin C Structure
Urolithin C structure
Common Name Urolithin C
CAS Number 165393-06-6 Molecular Weight 244.200
Density 1.6±0.1 g/cm3 Boiling Point 605.4±55.0 °C at 760 mmHg
Molecular Formula C13H8O5 Melting Point N/A
MSDS N/A Flash Point 243.6±25.0 °C

 Use of Urolithin C


Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].

 Names

Name Urolithin C
Synonym More Synonyms

 Urolithin C Biological Activity

Description Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].
Related Catalog
Target

Insulin secretion[1] L-type Ca2+ channel[1] Reactive oxygen species (ROS)[2] Apoptosis[2]

In Vitro Urolithin C (20-100 μM; 1 hour; INS-1 cells) treatment enhances glucose-induced extracellular signal-regulated kinases 1/2 (ERK1/2) activation in INS-1 β-cells[1]. Urolithin C significantly inhibits the proliferation of PC12 cells. Urolithin C treatment actively increases the lactate dehydrogenase (LDH) release and lipid peroxidation malondialdehyde (MDA), stimulates reactive oxygen species (ROS) formation and mitochondrial membrane depolarization, and caused calcium dyshomeostasis[2]. Urolithin C treatment induces apoptosis and S phase cell cycle arrest[2]. Western Blot Analysis[1] Cell Line: INS-1 cells Concentration: 20 μM, 100 μM Incubation Time: 1 hour Result: Enhanced glucose-induced extracellular signal-regulated kinases 1/2 (ERK1/2) activation.
In Vivo The pharmacokinetics of Urolithin C (10 mg/kg; intraperitoneal administration) in male Wistar rat (140-160 g) are studied. The half-life of the terminal part is 11.3 h and the total clearance (CL/F) is 3.41 L/h/kg. The initial volume of distribution (V1/F) and the steady-state volume of distribution (Vss/F) are 0.831 L/kg and 55.6 L/kg, respectively[3].
References

[1]. Slimane Toubal, et al. Urolithin C Increases Glucose-Induced ERK Activation Which Contributes to Insulin Secretion. Fundam Clin Pharmacol. 2020 Feb 21.

[2]. Peipei Yin, et al. Urolithin C, a gut metabolite of ellagic acid, induces apoptosis in PC12 cells through a mitochondria-mediated pathway. RSC Advances. Issue 28, 2017.

[3]. Morgane Bayle, et al. Development and Validation of a Liquid Chromatography-Electrospray Ionization-Tandem Mass Spectrometry Method for the Determination of Urolithin C in Rat Plasma and Its Application to a Pharmacokinetic Study. J Pharm Biomed Anal. 2016 Nov 30;131:33-39.

 Chemical & Physical Properties

Density 1.6±0.1 g/cm3
Boiling Point 605.4±55.0 °C at 760 mmHg
Molecular Formula C13H8O5
Molecular Weight 244.200
Flash Point 243.6±25.0 °C
Exact Mass 244.037170
PSA 90.90000
LogP 1.88
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.758

 Synonyms

Urolithin C
Uro C
3,8,9-thihydroxy-6H-benzo[c]chromen-6-one
6H-Dibenzo[b,d]pyran-6-one, 3,8,9-trihydroxy-
3,8,9-Thihydroxybenzo[c]chromen-6-one
3,8,9-Trihydroxy-6H-benzo[c]chromen-6-one
3,8,9-trihydroxy-6H-dibenzo[b,d]pyran-6-one
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