Isotanshinone I

Isotanshinone I
Product Name Isotanshinone I
CAS No.: 20958-17-2
Catalog No.: CFN90356
Molecular Formula: C18H12O3
Molecular Weight: 276.29 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Red powder
Targets: p38MAPK | NF-kB | p65
Source: The roots of Salvia miltiorrhiza Bge.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Isotanshinone I ,neotanshinone A and cryptotanshinone have different effects on inhibiting proteic activity of P38 and NF-κB signaling pathway,and this effect may be one of main mechanisms of inhibitive inflammation reaction by salvia miltiorrhiza bunge in liver.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

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The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    《Journal of Clinical Hepatology》 2012-11
    Influence of the chemical constituents of Salvia miltiorrhiza Bunge on lipopolysaccharide-induced activation of Kupffer cells[Reference: WebLink]
    To survey the chemical constituents of Salvia miltiorrhiza bunge and characterize their abilities to influence lipopolysaccharide(LPS)-induced activation of Kupffer cells(KCs).
    METHODS AND RESULTS:
    After culturing KCs with 60 ng/ml of LPS for 12 h,the supernatant medium was collected and divided for respective mixing with 100 μg/ml each of the isolated constituents of Salvia miltiorrhiza bunge: neotanshinone B,miltionone,tanshinol A,tanshinone I,Isotanshinone I,neotanshinone A,cryptotanshinone,tanshinone IIA,and salvianolie acid B.Untreated supernatant was used as control.The mixtures and control were added to fresh cultures of KCs,respectively,and incubated for 12 h.Effects on cellular proliferation were assessed by MTT assay,on secreted levels of cytokines(TNF α,IL-6,and IL-8) were measured by enzyme linked immunosorbent assay(ELISA),and on protein expressions of immunity-related receptors(CD14,TLR2,and TLR4) were detected by Western blot. Except for neotanshinone B,the Salvia miltiorrhiza bunge chemical constituents inhibited proliferation of KCs.The extent of inhibition varied for each constituent,but tanshinone I,neotanshinone A,and miltionone produced the highest inhibitory rates.LPS stimulation of KCs led to enhanced TNFα,IL-6,and IL-8 expression.Subsequent treatment with neotanshinone B,salvianolie acid B,or tanshinone IIA had no detectable effect on the LPS-induced expression of IL-8.The other constituents,however,inhibited the ability of KCs to secret cytokines,to various degrees.In addition,LPS stimulation of KCs led to increased expression of CD14,TLR2 and TLR4 proteins.Subsequent treatment with neotanshinone B and salvianolie acid B had no effect on LPS-induced CD14;neotanshinone B and miltionone had no effect on LPS-induced TLR2;and neotanshinone B,tanshinone IIA,and salvianolie acid B had no effect on LPS-induced TLR4.The other constituents,however,significantly down-regulated the expression levels of these three receptors.
    CONCLUSIONS:
    With the exception of neotanshinone B,the full panel of Salvia miltiorrhiza burge's chemical constituents can inhibit LPS-induced activation,proliferation,and cytokine secretion of KCs.These effects may be related to the ability of the chemical constituents to decrease LPS-induced protein expression of CD14,TLR2,and TLR4.
    《Acta Pharmaceutica Sinica》 2011-07
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    The investigation on Salvia przewalskii Maxim was carried out to find the relationship of the constituents and their pharmacological activities.
    METHODS AND RESULTS:
    The isolation and purification were performed by various chromatographies such as silica gel,Sephadex LH-20,RP-C18 column chromatography,etc.Further investigation on the fraction of the 95% ethanol extract of Salvia przewalskii Maxim yielded przewalskin Y-1(1),anhydride of tanshinone-ⅡA(2),sugiol(3),epicryptoacetalide(4),cryptoacetalide(5),arucadiol(6),1-dehydromiltirone(7),miltirone(8),cryptotanshinone(9),tanshinone ⅡA(10) and Isotanshinone I(11).Their structures were elucidated by the spectral analysis such as NMR(Nuclear Magnetic Resonance) and MS(Mass Spectrometry).
    CONCLUSIONS:
    Compound 1 is a new compound.Compounds 4 and 5 are mirror isomers(1∶3).Compounds 4,5,6,8,11 were isolated from Salvia przewalskii Maxim for the first time.
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