6"-O-Malonyldaidzin

    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 561546

CAS#: 124590-31-4

Description: 6"-O-Malonyldaidzin is a metabolite of soy isoflavones.


Price and Availability

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6"-O-Malonyldaidzin is not in stock, may be available through custom synthesis. For cost-effective reason, minimum 1 gram order is requested. The product will be characterized by NMR, HPLC and MS analysis. Purity (HPLC) is usually >98%. CoA, QC data, MSDS will be provided when product is successfully made. The estimated lead time is 2-3 months. Please send email to sales@medkoo.com to inquire quote.


Chemical Structure

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Theoretical Analysis

MedKoo Cat#: 561546
Name: 6"-O-Malonyldaidzin
CAS#: 124590-31-4
Chemical Formula: C24H22O12
Exact Mass: 502.1111
Molecular Weight: 502.42
Elemental Analysis: C, 57.37; H, 4.41; O, 38.21


Synonym: 6"-O-Malonyldaidzin; 6" O-Malonyldaidzin;

IUPAC/Chemical Name: 3-Oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxyoxan-2-yl]methoxy]propanoic acid

InChi Key: AKYASNRLFJHNQV-XQKZCQIMSA-N

InChi Code: InChI=1S/C24H22O12/c25-12-6-4-11(5-7-12)14-9-34-23-13(19(14)29)2-1-3-15(23)35-24-22(32)21(31)20(30)16(36-24)10-33-18(28)8-17(26)27/h1-7,9,16,20-22,24-25,30-32H,8,10H2,(H,26,27)/t16-,20-,21+,22-,24-/m1/s1

SMILES Code: O=C(O)CC(OC[C@H]1O[C@@H](OC2=CC=CC3=C2OC=C(C4=CC=C(O)C=C4)C3=O)[C@H](O)[C@@H](O)[C@@H]1O)=O


Technical Data

Appearance:
Solid powder

Purity:
>98% (or refer to the Certificate of Analysis)

Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition:
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility:
Soluble in DMSO

Shelf Life:
>2 years if stored properly

Drug Formulation:
This drug may be formulated in DMSO

Stock Solution Storage:
0 - 4 C for short term (days to weeks), or -20 C for long term (months).

Harmonized System Code:
293490


References

1: Farrell K, Jahan MA, Kovinich N. Distinct Mechanisms of Biotic and Chemical Elicitors Enable Additive Elicitation of the Anticancer Phytoalexin Glyceollin I. Molecules. 2017 Jul 27;22(8). pii: E1261. doi: 10.3390/molecules22081261. PubMed PMID: 28749423.

2: Tanaka T, Tang H, Yu F, Michihara S, Uzawa Y, Zaima N, Moriyama T, Kawamura Y. Kudzu (Pueraria lobata) vine ethanol extracts improve ovariectomy-induced bone loss in female mice. J Agric Food Chem. 2011 Dec 28;59(24):13230-7. doi: 10.1021/jf2031617. Epub 2011 Nov 18. PubMed PMID: 22053809.

3: Wu J, Muir AD. Isoflavone content and its potential contribution to the antihypertensive activity in soybean Angiotensin I converting enzyme inhibitory peptides. J Agric Food Chem. 2008 Nov 12;56(21):9899-904. doi: 10.1021/jf801181a. Epub 2008 Oct 15. PubMed PMID: 18921974.

4: Charron CS, Allen FL, Johnson RD, Pantalone VR, Sams CE. Correlations of oil and protein with isoflavone concentration in soybean [Glycine max (L.) Merr.]. J Agric Food Chem. 2005 Sep 7;53(18):7128-35. PubMed PMID: 16131120.

5: Lee SJ, Ahn JK, Kim SH, Kim JT, Han SJ, Jung MY, Chung IM. Variation in isoflavone of soybean cultivars with location and storage duration. J Agric Food Chem. 2003 May 21;51(11):3382-9. PubMed PMID: 12744671.

6: Wiseman H, Casey K, Clarke DB, Barnes KA, Bowey E. Isoflavone aglycon and glucoconjugate content of high- and low-soy U.K. foods used in nutritional studies. J Agric Food Chem. 2002 Mar 13;50(6):1404-10. PubMed PMID: 11879011.

7: Du Q, Lib Z, Ito Y. Preparative separation of isoflavone components in soybeans using high-speed counter-current chromatography. J Chromatogr A. 2001 Jul 20;923(1-2):271-4. PubMed PMID: 11510551.