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| Product | Description | |
|---|---|---|
| Sinomenine | Sinomenine, an alkaloid extracted from Sinomenium acutum , is a blocker of the NF-κB activation [1]. Sinomenine also is an activator of μ-opioid receptor [2]. Uses: Scientific research. Group: Natural products. CAS No. 115-53-7. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-15122. |  |
| Sinomenine | Sinomenine. Group: Biochemicals. Grades: Highly Purified. CAS No. 115-53-7. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. US Biological Life Sciences. |  Worldwide |
| Sinomenine Extract (Ratio) | Sinomenine Extract (Ratio). Group: Others. Purity: 4:1~20:1. Sinomenine Extract (Ratio). Cat No: EXTW-060. |  |
| Sinomenine hydrochloride | Sinomenine HCl could improve survival, reduce organ damage, and attenuate the release of inflammatory cytokines induced by CLP, at least in part through regulating autophagy activities. Uses: Anti-tumor and anti-metastasis. Synonyms: SINOMENINE HYDROCHLORIDE; SINOMENINE HCL; Tuduranine Hydrochloride; (9α,13α,14α)- 7,8-Didehydro-4- hydroxy-3,7-diMet; 7,8-Didehydro-4-hydroxy-3,7-diMethoxy-17-Methyl- 9α,13α,14α-Morphinan-6-one Hydrochloride. Grade: >98%. CAS No. 6080-33-7. Molecular formula: C19H23NO4.HCl. Mole weight: 365.85. |  |
| Sinomenine hydrochloride | Sinomenine hydrochloride (Cucoline hydrochloride), an alkaloid extracted from Sinomenium acutum , is a blocker of the NF-κB activation [1]. Sinomenine also is an activator of μ-opioid receptor [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Cucoline hydrochloride. CAS No. 6080-33-7. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-15122A. | |
| Sinomenine Hydrochloride | Sinomenine is an optical isomer of Methoxythebainone. Sinomenine was extracted from root of Sinomenium acutum. Sinomenine has anti-inflammatory and analgesic effect. Group: Biochemicals. Alternative Names: (9α, 13α, 14α)-7, 8-Didehydro-4-hydroxy-3, 7-dimethoxy-17-methylmorphinan-6-one Hydrochloride; 7, 8-Didehydro-4-hydroxy-3, 7-dimethoxy-17-methyl-9α, 13α, 14α-morphinan-6-one Hydrochloride; (9α, 13α, 14α)- 7,8-Didehydro-4-hydroxy-3,7-dimethoxy-17-methylmorphinan-6-one Hydrochloride; Cucoline Hydrochloride; NSC 76021; Sinomenin Hydrochloride. Grades: Highly Purified. CAS No. 6080-33-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tetrandrine | analytical standard, for drug analysis. Group: Additional drugseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Tetrandrine (6CI,7CI,8CI), (+)-Tetrandrine, Sinomenine A, S,S-(+)-Tetrandrine, TTD, 16H-1,24:6,9-Dietheno-11,15-metheno-2H-pyrido[2',3':17,18][1,11]dioxacycloeicosino[2,3,4-ij]isoquinoline, 3,4,4a,5,16a,17,18,19-octahydro-12,21,22,26-tetramethoxy-4,17-dimethyl-, [4aS-(4aR*,16aR*)]-, NSC 77037, Berbaman, 6,6',7,12-tetramethoxy-2,2'-dimethyl-, (1beta)-,16H-1,24:6,9-Dietheno-11,15-metheno-2H-pyrido[2',3':17,18][1,11]dioxacycloeicosino[2,3,4-ij]isoquinoline, 3,4,4a,5,16a,17,18,19-octahydro-12,21,22,26-tetramethoxy-4,17-dimethyl-, (4aS,16aS)-, d-Tetrandrine, Fanchinine, Hanfangchin A, Tetrandrin, (S,S)-Tetrandrine. |  |
| Tetrandrine | Tetrandrine is a bisbenylisoquinoline alkaloid isolated from the dried root of Stephenia tetrandra S Moore. Tetrandrine exhibits very broad pharmacological actions, including anti-tumor activity. The beneficial effects of tetrandrine on tumor cell cytotoxicity and radiosensitization, multidrug resistance, normal tissue radioprotection, and angiogenesis are most promising and deserve great attention. Tetrandrine has the potential either as a tumoricidal agent or as an adjunct to chemotherapy and radiotherapy. Uses: Nti-inflammatory, immunologic and antiallergenic. Synonyms: Isotetrandrine; Tetrandrin; Fanchinine; (+)-Tetrandrine; Sinomenine A. Grade: ≥ 98%. CAS No. 518-34-3. Molecular formula: C38H42N2O6. Mole weight: 622.762. | |
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