kakkalide
- CAS No.
- 58274-56-9
- Chemical Name:
- kakkalide
- Synonyms
- kakkalide;CID 14037245;kakkalide USP/EP/BP;Kakkalide,Inhibitor,inhibit;4H-1-Benzopyran-4-one, 5-hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-[(6-O-β-D-xylopyranosyl-β-D-glucopyranosyl)oxy]-;5-Hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-[(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy]-4H-1-benzopyran-4-one;5-Hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one
- CBNumber:
- CB81377280
- Molecular Formula:
- C28H32O15
- Molecular Weight:
- 608.54
- MDL Number:
- MFCD09970384
- MOL File:
- 58274-56-9.mol
- MSDS File:
- SDS
- TDS File:
- TDS
kakkalide price
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| ChemScene | CS-0032520 | Kakkalide 99.80% | 58274-56-9 | 1mg | $260 | 2026-06-04 | Buy |
| ChemScene | CS-0032520 | Kakkalide 99.80% | 58274-56-9 | 5mg | $546 | 2026-06-04 | Buy |
| ChemScene | CS-0032520 | Kakkalide 99.80% | 58274-56-9 | 10mg | $928 | 2026-06-04 | Buy |
| aablocks | AA00EGKB | 5-Hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one >98% | 58274-56-9 | 1mg | $302 | 2026-05-28 | Buy |
| aablocks | AA00EGKB | 5-Hydroxy-6-methoxy-3-(4-methoxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one >98% | 58274-56-9 | 5mg | $595 | 2026-05-28 | Buy |
kakkalide Chemical Properties, Uses, Production
Uses
Kakkalide is an isoflavone derived from the flowers of Pueraria lobata. Kakkalide ameliorates endothelial insulin resistance by suppressing reactive oxygen species (ROS)-associated inflammation[1].
Synthesis
Kudzu flowers were crushed and weighed 300g, respectively, extracted with 900 mL of methanol in cold soak for three times, and the combined extracts were concentrated under reduced pressure. The methanol extract was suspended in appropriate amount of distilled water, firstly extracted with benzene to degrease, then extracted with n-butanol, the n-butanol extract was concentrated to dryness, eluted by silica gel column chromatography with CHCl3:CH3OH ( 10:1), and obtained light yellow snowflake crystals (methanol recrystallization), that is, to obtain the kudzuoside.
References
[1] Zhang D, et al. Kakkalide ameliorates endothelial insulin resistance by suppressing reactive oxygen species-associated inflammation. J Diabetes. 2013 Mar;5(1):13-24. DOI:10.1111/1753-0407.12017
kakkalide Preparation Products And Raw materials
Raw materials
Preparation Products
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Chengdu Biopurify Phytochemicals Ltd. | +86-028-82633397 18982077548 | cwb1@biopurify.cn | China | 2376 | 60 |
| Shanghai Winherb Medical Technology Co., Ltd. | 17301719108 13341702378 | winherb@126.com | China | 1245 | 58 |
| Shanghai Tauto Biotech Co., Ltd. | 021-51320588 | tauto@tautobiotech.com | China | 3984 | 66 |
| Cheng Du Pufeide Biotechnology Co., Ltd. | 028-82610909 13388174823 | scglp@glp-china.com | China | 1064 | 58 |
| Shanghai Aspire Biological Technology Co., Ltd. | 021-61317773 | sales@aspirebio.com | China | 2880 | 58 |
| Wuhan ChemFaces Biochemical Co., Ltd. | 18607101326 15172504745 | aileen@chemfaces.com | China | 6904 | 55 |
| Shanghai YuanYe Biotechnology Co., Ltd. | 15026964105 | 2881489226@qq.com | China | 89667 | 60 |
| Shandong Xiya Chemical Co., Ltd. | 4009903999 13395398332 | sales@xiyashiji.com | China | 20788 | 60 |
| Shanghai Yihe Biological Technology Co., Ltd. | 021-68882955 17721395025 | 2423903095@qq.com | China | 5000 | 58 |
| Shanghai Uteam Biotechnology Co., Ltd. | 021-36031160 13311776681 | 3338195766@QQ.com | China | 5091 | 55 |
