An isoquinoline alkaloid with diverse biological activities
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Dauricine

Item No. 42364

Technical Information
Formal Name
4-[[(1R)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl]methyl]-2-[4-[[(1R)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl]methyl]phenoxy]-phenol
CAS Number
524-17-4
Synonyms
  • NSC 36413
Molecular Formula
C38H44N2O6
Formula Weight
Purity
≥98%
Formulation
A solid
PBS (pH 7.2): Slightly Soluble: 0.1-1 mg/ml
SMILES
CN1[C@@H](C(C(CC1)=C2)=CC(OC)=C2OC)CC(C=C3)=CC(OC(C=C4)=CC=C4C[C@@H](N(CC5)C)C(C5=C6)=CC(OC)=C6OC)=C3O
InChi Code
InChI=1S/C38H44N2O6/c1-39-15-13-26-20-35(42-3)37(44-5)22-29(26)31(39)17-24-7-10-28(11-8-24)46-34-19-25(9-12-33(34)41)18-32-30-23-38(45-6)36(43-4)21-27(30)14-16-40(32)2/h7-12,19-23,31-32,41H,13-18H2,1-6H3/t31-,32-/m1/s1
InChi Key
AQASRZOCERRGBL-ROJLCIKYSA-N
Origin
Plant/Menispermum dauricum DC
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Dauricine is an isoquinoline alkaloid that has been found in M. dauricum and has diverse biological activities.1,2,3 It inhibits IL-1β-induced THP-1 monocyte adhesion to human umbilical vein endothelial cells (HUVECs) when used at concentrations of 20 or 40 µM.1 Dauricine (40 µM) inhibits IL-1β-induced increases in intracellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and E-selectin levels and activation of NF-κB in HUVECs. It inhibits slowly activating delayed rectifier- (IKs) and rapidly activating delayed rectifier potassium currents (IKr) in whole-cell patch-clamp assays using isolated guinea pig ventricular myocytes (IC50s = 16 and 33 µM, respectively).2 Dauricine (20 µM) inhibits inward rectifying potassium channel (Kir) currents in the same cells. It also inhibits copper-induced paralysis and decreases in survival in C. elegans when used at a concentration of 6.4 µM.3 Dauricine (20 mg/kg) increases survival in a mouse model of LPS-induced acute lung injury.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Hu, J., Chen, R., An, J., et alDauricine attenuates vascular endothelial inflammation through inhibiting NF-κB pathway. Front. Pharmacol. 12, 758962 (2021).

    2. Xia, J.-S., Guo, D.-L., Zhang, Y., et alInhibitory effects of dauricine on potassium currents in guinea pig ventricular myocytes. Acta. Pharmacol. Sin. 21(1), 60-64 (2000).

    3. Wang, L., Pu, Z., Li, M., et alAntioxidative and antiapoptosis: Neuroprotective effects of dauricine in Alzheimer’s disease models. Life Sci. 243, 117237 (2020).