Jaceidin

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

MedKoo CAT#: 596091

CAS#: 10173-01-0

Description: Jaceidin is an O-methylated flavonol. It can be found in Chamomilla recutita, and in Centaurea jacea.


Chemical Structure

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Jaceidin
CAS# 10173-01-0

Theoretical Analysis

MedKoo Cat#: 596091
Name: Jaceidin
CAS#: 10173-01-0
Chemical Formula: C18H16O8
Exact Mass: 360.0845
Molecular Weight: 360.31
Elemental Analysis: C, 60.00; H, 4.48; O, 35.52

Size Price Shipping out time Quantity
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Pricing updated 2021-03-05. Prices are subject to change without notice.

Jaceidin 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.

Synonym: Jaceidin;

IUPAC/Chemical Name: 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-4H-chromen-4-one

InChi Key: XUWTZJRCCPNNJR-UHFFFAOYSA-N

InChi Code: InChI=1S/C18H16O8/c1-23-11-6-8(4-5-9(11)19)16-18(25-3)15(22)13-12(26-16)7-10(20)17(24-2)14(13)21/h4-7,19-21H,1-3H3

SMILES Code: O=C1C(OC)=C(C2=CC=C(O)C(OC)=C2)OC3=CC(O)=C(OC)C(O)=C13

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).

HS Tariff Code:
2934.99.9001

Handling Instructions:

Preparing Stock Solutions

The following data is based on the product molecular weight 360.31 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL

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Reconstitution Calculator

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1: Allison BJ, Allenby MC, Bryant SS, Min JE, Hieromnimon M, Joyner PM. Antibacterial activity of fractions from three Chumash medicinal plant extracts and in vitro inhibition of the enzyme enoyl reductase by the flavonoid jaceosidin. Nat Prod Res. 2017 Mar;31(6):707-712. doi: 10.1080/14786419.2016.1217201. Epub 2016 Aug 2. PubMed PMID: 27482826.

2: Tahtah Y, Wubshet SG, Kongstad KT, Heskes AM, Pateraki I, Møller BL, Jäger AK, Staerk D. High-resolution PTP1B inhibition profiling combined with high-performance liquid chromatography-high-resolution mass spectrometry-solid-phase extraction-nuclear magnetic resonance spectroscopy: Proof-of-concept and antidiabetic constituents in crude extract of Eremophila lucida. Fitoterapia. 2016 Apr;110:52-8. doi: 10.1016/j.fitote.2016.02.008. Epub 2016 Feb 14. PubMed PMID: 26882973.

3: Taamalli A, Arráez-Román D, Abaza L, Iswaldi I, Fernández-Gutiérrez A, Zarrouk M, Segura-Carretero A. LC-MS-based metabolite profiling of methanolic extracts from the medicinal and aromatic species Mentha pulegium and Origanum majorana. Phytochem Anal. 2015 Sep-Oct;26(5):320-30. doi: 10.1002/pca.2566. Epub 2015 May 15. PubMed PMID: 25982347.

4: Kanazawa K, Hashimoto T, Yoshida S, Sungwon P, Fukuda S. Short photoirradiation induces flavonoid synthesis and increases its production in postharvest vegetables. J Agric Food Chem. 2012 May 2;60(17):4359-68. doi: 10.1021/jf300107s. Epub 2012 Apr 20. PubMed PMID: 22506664.

5: Aljancić I, Stanković M, Tesević V, Vujisić L, Vajs V, Milosavljević S. Protective effect on human lymphocytes of some flavonoids isolated from two Achillea species. Nat Prod Commun. 2010 May;5(5):729-32. PubMed PMID: 20521537.

6: Hussain J, Khan FU, Ur Rehman N, Ullah R, Mohmmad Z, Tasleem S, Naeem A, Shah MR. One new triterpene ester from Nepeta suavis. J Asian Nat Prod Res. 2009 Dec;11(12):997-1000. doi: 10.1080/10286020903264085. PubMed PMID: 20183267.

7: Afifi FU, Aburjai T. Antiplatelet activity of Varthemia iphionoides. Fitoterapia. 2004 Dec;75(7-8):629-33. PubMed PMID: 15567236.

8: Long C, Sauleau P, David B, Lavaud C, Cassabois V, Ausseil F, Massiot G. Bioactive flavonoids of Tanacetum parthenium revisited. Phytochemistry. 2003 Sep;64(2):567-9. PubMed PMID: 12943776.

9: Fukui K, Matsumoto T, Nakamura S, Nakayama M, Horie T. The synthesis of jaceidin. Experientia. 1968 Feb 15;24(2):108-9. PubMed PMID: 5643784.