
Coronarin A
- Product NameCoronarin A
- CAS119188-33-9
- CBNumberCB61469842
- MFC20H28O2
- MW300.44
- MDL NumberMFCD17214879
- MOL File119188-33-9.mol
Chemical Properties
form | Solid |
color | White to off-white |
Coronarin A Chemical Properties,Usage,Production
Uses
Coronarin A is an orally active natural compound that inhibits mTORC1 and S6K1 to increase IRS1 activity. Coronarin A shows anti-inflammatory activity and can also be used for type 2 diabetes mellitus research[1].in vivo
Coronarin A (30 or 100 mg/kg; i.p. or p.o.; once daily for 22 days) ameliorates hyperglycemia in mice[1].
Coronarin A (100 mg/kg; p.o.; once daily for 22 days) inhibits the mTOR/S6K1 pathway to activate PI3K/Akt and ERK/β-catenin signaling in livers of ob/ob mice[1].
Pharmacokinetic properties of Coronarin A after single administrationa in ob/ob mice[1].
Coronarin A | t1/2 (h) | tmax (h) | Cmax (ng/mL) | AUC0-t (ng·h/mL) | AUC0-∞ (ng·h/mL) | MRT (h) |
i.p. | 14.8 | 1.0 | 1073 | 4571 | 11045 | 21.7 |
p.o. | 3.01 | 1.0 | 388 | 1694 | 1856 | 4.88 |
Data are presented as the mean of three mice.
aCoronarin A was intraperitoneally or orally administered at 30 mg/kg to ob/ob mice.
Animal Model: | Male ob/ob mice[1] |
Dosage: | 30 mg/kg (IP) or 100 mg/kg (PO) |
Administration: | Oral or intraperitoneal administration, once daily for 22 days |
Result: | Significantly decreased the non-fasting and fasting blood glucose. Significantly reduced the serum insulin concentration at 15 min after glucose loading, reduced the average daily food intake while the body weight was unaffected. Increased hepatic glycogen content and the expression levels of gluconeogenic gene Pck1 and G6pc were significantly decreased. |
Animal Model: | Female ob/ob mice[1] |
Dosage: | 30 mg/kg |
Administration: | Intraperitoneal or oral administration (Pharmacokinetic Analysis) |
Result: | Intraperitoneal injection exhibited higher plasma exposure than oral gavage at the same dose of 30 mg/kg, with Cmax value of 1073 and 388 ng/mL, respectively. |
IC 50
mTORC1; S6K1References
[1] Huang SL, et al. Coronarin A modulated hepatic glycogen synthesis and gluconeogenesis via inhibiting mTORC1/S6K1 signaling and ameliorated glucose homeostasis of diabetic mice. Acta Pharmacol Sin. 2022 Sep 9. DOI:10.1038/s41401-022-00985-5Preparation Products And Raw materials
Coronarin A Suppliers
Global(49)Suppliers
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
18871490254 | linda@hubeijusheng.com | CHINA | 28172 | 58 | |
+1-631-485-4226 | inquiry@bocsci.com | United States | 19552 | 58 | |
+86-27-50766799 +8618062016861 |
contact@labnetwork.com | China | 19987 | 58 | |
support@targetmol.com | United States | 38665 | 58 | ||
+86-852-30606658 | market18@leapchem.com | China | 43340 | 58 | |
+86-18621343501; +undefined18621343501 |
product@acmec-e.com | China | 33338 | 58 | |
+8613817748580 | cooperation@kean-chem.com | China | 40066 | 58 | |
+86-88938639 +86-17705817739 |
info@dycnchem.com | China | 53900 | 58 | |
+86-21-20908456 | sales@BioChemBest.com | China | 6005 | 61 | |
0871-65217109 13211707573; |
y.liu@mail.biobiopha.com | China | 5653 | 65 |
119188-33-9, Coronarin ARelated Search
PROMPT×
PROMPT
The What'sApp is temporarily not supported in mainland China
The What'sApp is temporarily not supported in mainland China
Cancel
Determine