- Isochlorogenic acid A
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- $59.00 / 5mg
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2026-01-23
- CAS:2450-53-5
- Min. Order:
- Purity: 99.71%
- Supply Ability: 10g
- Isochlorogenic acid A
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- $1.00 / 1KG
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2019-07-14
- CAS:2450-53-5
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 25kg
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| | Isochlorogenic acid A Basic information |
| Product Name: | Isochlorogenic acid A | | Synonyms: | 3,5-Dicaffeoylquinic acid;Isochlorogenic acid A;Isochlorogenic acid A，3,5-Dicaffeoylquinic acid;3α,5β-Bis[[1-oxo-3-(3,4-dihydroxyphenyl)-2-propenyl]oxy]-1α,4α-dihydroxycyclohexane-1-carboxylic acid;1α,4α-Dihydroxy-3β,5α-bis[3-(3,4-dihydroxyphenyl)propenoyloxy]cyclohexanecarboxylic acid;1β,4β-Dihydroxy-3β,5α-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-1α-cyclohexanecarboxylic acid;1β,4β-Dihydroxy-3β,5α-bis[3-(3,4-dihydroxyphenyl)acryloyloxy]cyclohexane-1-carboxylic acid;1β,4β-Dihydroxy-3β,5α-bis[3-(3,4-dihydroxyphenyl)propenoyloxy]cyclohexanecarboxylic acid | | CAS: | 2450-53-5 | | MF: | C25H24O12 | | MW: | 516.46 | | EINECS: | | | Product Categories: | The group of Chlorogenic acid;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Aromatic Phenols | | Mol File: | 2450-53-5.mol |  |
| | Isochlorogenic acid A Chemical Properties |
| Melting point | >175°C (dec.) | | Boiling point | 826.2±65.0 °C(Predicted) | | density | 1?+-.0.1 g/cm3(Predicted) | | storage temp. | -20°C | | solubility | DMSO (Slightly), Methanol (Slightly) | | pka | 3.54±0.50(Predicted) | | form | Off-white to yellow/brown crystalline solid. | | color | Off-White to Pale Yellow | | Stability: | Hygroscopic | | Major Application | metabolomics
vitamins, nutraceuticals, and natural products | | InChIKey | KRZBCHWVBQOTNZ-PSEXTPKNSA-N | | SMILES | O([C@@H]1C[C@](O)(C(=O)O)C[C@@H](OC(=O)C=CC2C=CC(O)=C(O)C=2)[C@H]1O)C(=O)C=CC1C=CC(O)=C(O)C=1 |&1:1,3,9,23,r| |
| Safety Statements | 24/25 | | WGK Germany | 3 | | RTECS | GU8403966 | | HS Code | 29189900 | | Storage Class | 11 - Combustible Solids |
| | Isochlorogenic acid A Usage And Synthesis |
| Description | 3,5-Dicaffeoylquinic acid (3,5-DCQA) is a natural phenolic compound that has been found in L. japonica, I. kaushue, and other plants. It has antioxidant, anti-inflammatory, and antiviral biological activities. 3,5-DCQA scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; ) radicals in a cell-free assay (IC50 = 71.8 μM) and inhibits superoxide production in human neutrophils activated by N-formyl-Met-Leu-Phe (fMLF) and cytochalasin B (IC50 = 1.92 μM). It inhibits HIV-1 integrase 3''-end processing, strand transfer, and disintegration in a cell-free assay (IC50s = 0.33, 0.34, and 0.66 μg/ml, respectively) and inhibits HIV-1-induced cytotoxicity in MT-2 cells (ED50 = 1 μg/ml). In vivo, 3,5-DCQA (25 mg/kg) protects mice from acute lung injury induced by LPS and decreases neutrophil count in bronchoalveolar lavage fluid (BALF). | | Chemical Properties | Off-white crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from honeysuckle, honeysuckle, eucommia, and chrysanthemum. | | Uses | Isochlorogenic Acid A is a phenolic compound shown to provide protection against oxidative stress cells. DNA protective agent. | | Definition | ChEBI: 3,5-di-O-caffeoyl quinic acid is a carboxylic ester that is the diester obtained by the condensation of the hydroxy groups at positions 3 and 5 of (-)-quinic acid with the carboxy group of trans-caffeic acid. Isolated from Brazilian propolis and Suaeda glauca, it exhibits hepatoprotective and cytotoxic activities. It has a role as a metabolite, a hepatoprotective agent and an antineoplastic agent. It is a cyclitol carboxylic acid and a carboxylic ester. It is functionally related to a (-)-quinic acid and a trans-caffeic acid. | | in vivo | Isochlorogenic acid A (5?and 10 mg/kg, p.o., once a day for 3 weeks) ameliorates cognitive impairment induced by TMT in ICR male mice[5].
| Animal Model: | TMT-induced ICR male mice[5] | | Dosage: | 5?and 10 mg/kg | | Administration: | p.o., once a day for 3 weeks | | Result: | Improved spatial memory and learning ability of mice in MWM test.
Reduced the TMT-induced increased AChE activity.
Reduced the MDA content compared to the TMT group. |
| | References | [1] LI-YAN PENG. Constituents from Lonicera japonica[J]. Fitoterapia, 2000, 71 6: Pages 713-715. DOI: 10.1016/s0367-326x(00)00212-4
[2] KRISS DAYANA PANTOJA PULIDO José H I M Ana Julia Colmenares Dulcey. New caffeic acid derivative from Tithonia diversifolia (Hemsl.) A. Gray butanolic extract and its antioxidant activity[J]. Food and Chemical Toxicology, 2017, 109: Pages 1079-1085. DOI: 10.1016/j.fct.2017.03.059
[3] W E ROBINSON. Inhibitors of HIV-1 replication [corrected; erratum to be published] that inhibit HIV integrase.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1996, 93 13: 6326-6331. DOI: 10.1073/pnas.93.13.6326 |
| | Isochlorogenic acid A Preparation Products And Raw materials |
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