SMB01076

Glycycoumarin

≥90% (LC/MS-ELSD)

Manufacturer: Sigma Aldrich

CAS Number: 94805-82-0

Synonym(S): 3-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-6-(3-methylbut-2-enyl)chromen-2-one

Select a Size

Pack Size SKU Availability Price
1 MG SMB01076-1-MG In Stock ₹ 41,005.10

SMB01076 - 1 MG

₹ 41,005.10

In Stock

Quantity

1

Base Price: ₹ 41,005.10

GST (18%): ₹ 7,380.918

Total Price: ₹ 48,386.018

biological source

plant

Assay

≥90% (LC/MS-ELSD)

form

solid

mol wt

368.38

application(s)

metabolomicsvitamins, nutraceuticals, and natural products

storage temp.

−20°C

InChI

1S/C21H20O6/c1-11(2)4-6-14-18(24)10-19-16(20(14)26-3)9-15(21(25)27-19)13-7-5-12(22)8-17(13)23/h4-5,7-10,22-24H,6H2,1-3H3

InChI key

NZYSZZDSYIBYLC-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
50-197-0422
Medchemexpress LLC HY-N4113 5mg Medchemexpress, Glycycoumarin CAS:94805-82-0 Purity:>98%
Medchemexpress LLC ₹ 8,085.42
AI63658
94805-82-0 | Glycycoumarin
A2B Chem ₹ 11,122.80 - ₹ 29,946.00

Description

  • General description: Glycycoumarin, a major bioactive coumarin, is an aromatic ether and a member of resorcinols. This bioactive natural product is commonly derived from Glycyrrhiza Sp. (G. glabra, G. uralensis and G. radix) plants. Existing research suggests that this plant-derived metabolite exerts various biological activities, including anti-spasmodic, hepatoprotective, anticancer, neuroprotective, antioxidant and anti-inflammatory activities.
  • Application: It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.
  • Biochem/physiol Actions: According to the existing research, Glycycoumarin serves as an estrogen agonist while also exhibiting moderate inhibitory effects on enzymes CYP1A2 and CYP2B6. Notably, Glycycoumarin demonstrates potent anti-hepatitis C virus (HCV) activity, with an IC(50) value of 8.8 µg/mL. Furthermore, it effectively inhibits smooth muscle contraction induced by various stimuli by targeting PDEs, especially isozyme 3, which leads to the accumulation of intracellular cAMP, a vital component of cellular signaling. Additionally, Glycycoumarin acts as a potent antispasmodic through the inhibition of phosphodiesterase 3, further underscoring its significance in modulating cellular responses and health. Moreover, it plays a crucial role in inhibiting hepatocyte lipoapoptosis by activating autophagy and inhibiting the ER stress/GSK-3-mediated mitochondrial pathway, showcasing its importance in cellular function.
  • Features and Benefits: High quality compound suitable for multiple research applicationsCompatible with HPLC and mass spectrometry techniques
  • Other Notes: For additional information on our range of Biochemicals, please complete this form.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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SMB01076

≥90% (LC/MS-ELSD)...


biological source:
plant

Assay:
≥90% (LC/MS-ELSD)

form:
solid

mol wt:
368.38

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

storage temp.:
−20°C

InChI:
1S/C21H20O6/c1-11(2)4-6-14-18(24)10-19-16(20(14)26-3)9-15(21(25)27-19)13-7-5-12(22)8-17(13)23/h4-5,7-10,22-24H,6H2,1-3H3

InChI key:
NZYSZZDSYIBYLC-UHFFFAOYSA-N

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plant

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metabolomicsvitamins, nutraceuticals, and natural products

storage temp.:
−20°C

InChI:
1S/C20H22O9/c21-9-12-8-13(22)6-7-14(12)28-20-18(25)17(24)16(23)15(29-20)10-27-19(26)11-4-2-1-3-5-11/h1-8,15-18,20-25H,9-10H2/t15-,16-,17+,18-,20-/m1/s1

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FLROYCKIIJCTDY-BFMVXSJESA-N

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plant

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1S/C17H24O5/c1-9(6-5-7-21-12(4)18)14-10(2)8-13-15(16(14)19)11(3)17(20)22-13/h9,13,15-16,19H,3,5-8H2,1-2,4H3/t9-,13+,15+,16+/m0/s1

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QKUFZFLZBUSEHN-CZLJMHDISA-N

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biological source:
plant

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metabolomicsvitamins, nutraceuticals, and natural products

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InChI:
1S/C21H22O4/c1-14(2)4-11-18-20(24)13-8-16(21(18)25-3)7-12-19(23)15-5-9-17(22)10-6-15/h4-10,12-13,22,24H,11H2,1-3H3/b12-7+

InChI key:
WBDNTJSRHDSPSR-KPKJPENVSA-N