70050

Myricetin

≥96.0% (HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 529-44-2

Synonym(S): 3,3′,4′,5,5′,7-Hexahydroxyflavone, Cannabiscetin, Myricetol

Select a Size

Pack Size SKU Availability Price
25 MG 70050-25-MG In Stock ₹ 17,092.68
100 MG 70050-100-MG In Stock ₹ 54,265.73

70050 - 25 MG

₹ 17,092.68

In Stock

Quantity

1

Base Price: ₹ 17,092.68

GST (18%): ₹ 3,076.682

Total Price: ₹ 20,169.362

Quality Level

200

Assay

≥96.0% (HPLC)

form

powder

mp

≥300 °C>300 °C (lit.)

solubility

ethanol: 10 mg/mL, clear to very faintly turbid, yellow to very deep greenish-yellow

application(s)

metabolomicsvitamins, nutraceuticals, and natural products

SMILES string

Oc1cc(O)c2C(=O)C(O)=C(Oc2c1)c3cc(O)c(O)c(O)c3

InChI

1S/C15H10O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,16-20,22H

InChI key

IKMDFBPHZNJCSN-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544) mouse ... Hexa(15211) rat ... Il4(287287) , Tnf(24835)

Other Options

Image Product Name Manufacturer Price Range
11-101-4474
Myricetin, ≥98% (HPLC), MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 22,930.08
50-575-0
Selleck Chemical LLC Myricetin 100mg 529-44-2 Cannabiscetin
Selleck Chemical LLC ₹ 21,253.10
50-188-2069
Sigma Aldrich Fine Chemicals Biosciences Myricetin >=96.0% (HPLC) | 529-44-2 | MFCD00006827 | 25MG
Sigma Aldrich Fine Chemicals Biosciences ₹ 19,285.22
PHL89252
Myricetin
Sigma Aldrich ₹ 36,772.53
72576
Myricetin
Supelco ₹ 17,449.90
89013
Myricetin
Supelco ₹ 27,116.63
CS-6221
Myricetin
ChemScene ₹ 941.16 - ₹ 17,539.80
AB46611
529-44-2 | Myricetin
A2B Chem ₹ 941.16 - ₹ 43,122.24

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Description

  • General description: Myricetin (MYR) is a natural polyhydroxyflavonol compound, first isolated from the bark of Morella rubra (Myrica rubra) tree.[1]
  • Application: Myricetin has been used:to study its preventive effect as an antioxidant on noise-induced hearing loss (NIHL) in rats[2]as a flavonoid compound to test antiviral activity of Bourbon virus (BRBV) and in inhibition of RNA-dependent RNA polymerase (RdRP)[3]to study its effect as a treatment on biofilms of Streptococcus mutans and Candida albicans[4]as a reference standard for the quantification of phenolic compounds from Juniperus species[5]
  • Biochem/physiol Actions: Myricetin exerts anti-oxidant effects[6], and anti-inflammatory effects by regulating multiple signal pathways.[1] It also displays anti-diabetic[1] and hepatoprotective effects.[6] Myricetin strongly inhibits yeast α-glucosidase,[7] glyoxalase I in vitro,[8] and bovine milk xanthine oxidase.[9] It also promotes complex formation between DNA and both topoisomerase I and II, an effect that may have implications in cancer chemotherapy.[10] Myricetin also has various nutraceuticals values and therapeutic effects.[1][6]

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Quality Level:
200

Assay:
≥96.0% (HPLC)

form:
powder

mp:
≥300 °C>300 °C (lit.)

solubility:
ethanol: 10 mg/mL, clear to very faintly turbid, yellow to very deep greenish-yellow

application(s):
metabolomicsvitamins, nutraceuticals, and natural products

SMILES string:
Oc1cc(O)c2C(=O)C(O)=C(Oc2c1)c3cc(O)c(O)c(O)c3

InChI:
1S/C15H10O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,16-20,22H

InChI key:
IKMDFBPHZNJCSN-UHFFFAOYSA-N

Gene Information:
human ... CYP1A2(1544) mouse ... Hexa(15211) rat ... Il4(287287) , Tnf(24835)

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__

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CCCC\C=C\CCCCCCCC(=O)OC

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__

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__

Gene Information:
__

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OC(=O)c1ccc(cn1)C(F)(F)F

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1S/C7H4F3NO2/c8-7(9,10)4-1-2-5(6(12)13)11-3-4/h1-3H,(H,12,13)

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NJHGVAYLDHROPT-UHFFFAOYSA-N

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__

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FC(F)(F)c1cc(Cl)nc(Cl)c1

InChI:
1S/C6H2Cl2F3N/c7-4-1-3(6(9,10)11)2-5(8)12-4/h1-2H

InChI key:
KVNQWVYYVLCZKK-UHFFFAOYSA-N

Gene Information:
__