An indole alkaloid
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Corynoxine (hydrochloride)

Item No. 28496

Technical Information
Formal Name
(αE,1′S,6′S,7′S,8′aS)-6′-ethyl-1,2,2′,3′,6′,7′,8′,8′a-octahydro-α-(methoxymethylene)-2-oxo-spiro[3H-indole-3,1'(5′H)-indolizine]-7′-acetic acid, methyl ester, monohydrochloride
Molecular Formula
C22H28N2O4 • HCl
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlDMSO:PBS (pH 7.2) (1:4): 0.25 mg/mlEthanol: 3 mg/ml
λmax
242 nm
SMILES
CO/C=C(C(OC)=O)\[C@@H]1[C@H](CC)CN2[C@@]([C@@]3(C(C=CC=C4)=C4NC3=O)CC2)([H])C1.Cl
InChi Code
InChI=1S/C22H28N2O4.ClH/c1-4-14-12-24-10-9-22(17-7-5-6-8-18(17)23-21(22)26)19(24)11-15(14)16(13-27-2)20(25)28-3;/h5-8,13-15,19H,4,9-12H2,1-3H3,(H,23,26);1H/b16-13+;/t14-,15+,19+,22+;/m1./s1
InChi Key
YZEHFWIJWUTTOF-UXWWZSLJSA-N
Origin
Plant/Uncaria sp.
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Corynoxine is an indole alkaloid that has been found in U. macrophylla and has neuroprotective activity.1,2 It increases levels of the autophagy marker LC3-II in Neuro2a and SH-SY5Y neuronal cells when used at concentrations ranging from 6.25 to 25 µM.1 Corynoxine (25 µM) increases degradation of wild-type and A53T mutant α-synuclein, a major component of Lewy bodies in the brain of Parkinson’s disease patients, in PC12 cells, an effect that can be reversed by the autophagy inhibitors 3-methyladenine (Item No. 13242) and chloroquine (Item No. 14194). It reduces increases in methamphetamine-induced locomotor activity in rats when administered at doses of 30 and 100 mg/kg.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Chen, L.-L., Song, J.-X., Lu, J.-H., et alCorynoxine, a natural autophagy enhancer, promotes the clearance of alpha-synuclein via Akt/mTOR pathway. J. Neuroimmune Pharmacol. 9(3), 380-387 (2014).

    2. Sakakibara, I., Terabayashi, S., Kubo, M., et alEffect on locomotion of indole alkaloids from the hooks of Uncaria plants. Phytomedicine 6(3), 163-168 (1999).

    Product Citations

    Lei, S., Lu, J., Cheng, A., et alIdentification of PXR activators from Uncaria rhynchophylla (Gou Teng) and Uncaria tomentosa (cat’s claw). Drug Metab. Dispos. 51(5), 629-636 (2023).