4,5-Dicaffeoylquinic acid
CAS No. 57378-72-0
4,5-Dicaffeoylquinic acid( Isochlorogenic acid C )
Catalog No. M18835 CAS No. 57378-72-0
Isochlorogenic acid C(4, 5) has antiviral activity, including anti-HIV-1 integrase activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 104 | In Stock |
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| 5MG | 77 | In Stock |
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| 10MG | 111 | In Stock |
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| 25MG | 182 | In Stock |
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| 50MG | 259 | In Stock |
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| 100MG | 338 | In Stock |
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| 200MG | 538 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name4,5-Dicaffeoylquinic acid
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NoteResearch use only, not for human use.
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Brief DescriptionIsochlorogenic acid C(4, 5) has antiviral activity, including anti-HIV-1 integrase activity.
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DescriptionIsochlorogenic acid C(4, 5) has antiviral activity, including anti-HIV-1 integrase activity. Isochlorogenic acid C(4, 5) shows anti-hepatotoxic activity.
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In Vitro4,5-Dicaffeoylquinic acid (0.1~100 μM; 72 h) has dose-dependent inhibitory activity against DU-145 prostate cancer cells, and induces cell cycle arrest, also induces inactivation of Bcl-2.4,5-Dicaffeoylquinic acid (1~100 μg/mL; 48 h) has anti-apoptotic effect in D-GalN-challenged HL-7702 hepatocytes, and improves significantly cell viability at concentrations of 10 to 100 μg/mL.4,5-Dicaffeoylquinic acid (1~100 μg/mL; 4 days) inhibits significantly expressions of HBsAg and HBeAg, and produces the maximum inhibition rates of 86.93 and 59.79% at 100 μg/mL on expressions of HBsAg and HBeAg, respectively. Cell Proliferation Assay Cell Line:DU-145 cells Concentration:0.1~100 μM Incubation Time:72 h Result:Exhibits dose-dependent inhibitory activity against DU-145 prostate cancer cells with an IC50 of 5 μM.Cell Cycle Analysis Cell Line:DU-145 cells Concentration:5 μMIncubation Time:72 h Result:Decreased in numbers in G0/G1 phase and increased in S phase.Apoptosis Analysis Cell Line:HL-7702 hepatocytes (exposure to 60 mM D-GalN for 6h) Concentration:1~100 μg/m L Incubation Time:48 h Result:Significantly reduced the caspase-3 and transforming growth factor β1 (TGFβ1) levels of the D-GalN-challenged hepatocytes at 10~100 μg/mL.Cell Viability Assay Cell Line:HL-7702 hepatocytes (exposure to 80 mM D-GalN for 6h) Concentration:1~100 μg/mL Incubation Time:48 h Result:Improved significantly cell viability at concentrations of 10 to 100 μg/mL, and produced a maximum protection rate of 47.28% at 100 μg/mL.
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In Vivo4,5-Dicaffeoylquinic acid enhances the expression of GLUT2, GK, and PDX-1 protein, and effectively alleviate glycaemia and insulin resistance and enhance insulin sensitivity in type 2 diabetic mice.
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SynonymsIsochlorogenic acid C
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research AreaInfection
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Indication——
Chemical Information
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CAS Number57378-72-0
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Formula Weight516.45
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Molecular FormulaC25H24O12
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Purity>98% (HPLC)
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SolubilityDMSO : 50 mg/mL 96.81 mM
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SMILESC1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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SRI-42127
SRI-42127 is a novel small molecule inhibitor of the RNA regulatory factor HuR, which inhibits tumor growth, attenuates glial activation in a lipopolysaccharide-induced neuroinflammation model, and reduces neuropathic pain after nerve injury by inhibiting the neuroinflammatory response.
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Licochalcone B
Licochalcone B (LCB) inhibits the proliferation of human malignant bladder cancer cell lines (T24 and EJ) in vitro and antitumor activity in vivo in MB49 (murine bladder cancer cell line) tumor model.
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Tridecanoic acid
Tridecanoic acid is a 13-carbon saturated fatty acid found in dairy products and also as a product of anaerobic biodegradation of n-hexadecane. It has been identified as a substrate of phospholipase A2.
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