Peimine


CAS No. : 23496-41-5

(Synonyms: Verticine; Dihydroisoimperialine)

23496-41-5
Price and Availability of CAS No. : 23496-41-5
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Cat. No. : HY-N0212
M.Wt: 431.65
Formula: C27H45NO3
Purity: >98 %
Solubility: DMSO : 50 mg/mL (ultrasonic)
Introduction of 23496-41-5 :

Peimine (Verticine; Dihydroisoimperialine) is an orally active natural product. Peimine has anti-inflammatory, analgesic and cough relieving effects. Peimine can be used in cancer and inflammation related research[1][2][3][4][5][6][7]. In Vitro:Peimine (0-200 μM, 24 h) disrupts intracellular calcium homeostasis through the Ca2+/CaMKII/JNK pathway, inhibits the growth and movement of prostate cancer cells (DU-145, LNCap, and PC-3) and induces apoptosis, while having no significant effect on normal cells (RWPE-1) [3].
Peimine (0-25 mg/L, 1 h) has anti-inflammatory activity through regulating TNF-a, IL-6, IL-1b and IL-10 by suppressing the phosphorylation of MAPK and the activation of NF-kB in LPS-stimulated RAW 264.7 macrophages[6].
Peimine (10-300 μM, 0-10 ms) can block the Nav1.7 ion channel with an IC50 value of 47.2 μM, and can also inhibit the Kv1.3 ion channel with an IC50 value of 354.4 μM[7].
In Vivo:Peimine (32.5 μM/kg/day for 7days,i.g.) can effectively alleviate LPS-induced acute lung injury in mice, inhibit the expression levels of inflammatory factors TNF-α, IL-6, and IL-1 in mouse models, and has a synergistic effect when combined with Peiminine (HY-N0213) and Forsythoside. It can effectively improve its anti-inflammatory activity[4].
The drug level of Peimine (single oral 4.25 g/kg) in the blood and tissue of male rats is significantly higher than that of female rats (Reference 3)[5].

Pharmacokinetic Analysis in male and female SD Rats[5]
Gender Route Dose (g/kg) Cmax (ng/mL) Tmax (h) t1/2 (h) MRT0-t (h) MRT0-∞ (h) AUC0-t (ng·h/mL) AUC0-∞ (ng·h/mL) CL/F (L/kg/h) V/F (L/kg)
Female p.o. 4.25 43.7 1.5 4.2 7.8 7.9 214.2 214.3 128.9 781.3
Male p.o. 4.25 57.6 2.9 6.2 7.2 7.4 662.4 665.3 41.5 374.1

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