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3'-prenylnaringenin is a naturally occurring flavonoid compound found in hops, known for its potential health benefits such as anti-inflammatory and antioxidant properties. It exhibits estrogenic activity, making it a promising candidate for hormone replacement therapy and treatment of menopausal symptoms, as well as for preventing breast cancer and reducing the risk of osteoporosis.

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  • 4H-1-Benzopyran-4-one,2,3-dihydro-5,7-dihydroxy-2-[4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-, (2S)-

    Cas No: 119240-82-3

  • USD $ 1.9-2.9 / Gram

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  • 119240-82-3 Structure
  • Basic information

    1. Product Name: 3'-prenylnaringenin
    2. Synonyms: 4H-1-Benzopyran-4-one,2,3-dihydro-5,7-dihydroxy-2-[4-hydroxy-3-(3-methyl-2-butenyl)phenyl]-, (2S)-(9CI);4H-1-Benzopyran-4-one,2,3-dihydro-5,7-dihydroxy-2-[4-hydroxy-3-(3-methyl-2-butenyl)phenyl]-, (S)-;Licoflavanone;
    3. CAS NO:119240-82-3
    4. Molecular Formula: C20H20O5
    5. Molecular Weight: 340.37
    6. EINECS: N/A
    7. Product Categories: Flavanones
    8. Mol File: 119240-82-3.mol
  • Chemical Properties

    1. Melting Point: 134-135 °C
    2. Boiling Point: 579°Cat760mmHg
    3. Flash Point: 210°C
    4. Appearance: /
    5. Density: 1.351g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 7.50±0.40(Predicted)
    10. CAS DataBase Reference: 3'-prenylnaringenin(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3'-prenylnaringenin(119240-82-3)
    12. EPA Substance Registry System: 3'-prenylnaringenin(119240-82-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 119240-82-3(Hazardous Substances Data)

119240-82-3 Usage

Uses

Used in Hormone Replacement Therapy:
3'-prenylnaringenin is used as a therapeutic agent for hormone replacement therapy, leveraging its estrogenic activity to alleviate menopausal symptoms and potentially improve overall health in postmenopausal women.
Used in Menopause Management:
3'-prenylnaringenin is used as a natural alternative for managing menopausal symptoms, providing relief from hot flashes, night sweats, and other discomforts associated with hormonal changes.
Used in Cancer Prevention:
3'-prenylnaringenin is used as a preventative agent for breast cancer, with research indicating its potential to reduce the risk of developing this type of cancer.
Used in Osteoporosis Risk Reduction:
3'-prenylnaringenin is used as a supplement to reduce the risk of osteoporosis, potentially supporting bone health and density in individuals at risk.
Used in Pharmaceutical Industry:
3'-prenylnaringenin is used as a key ingredient in the development of pharmaceutical products targeting various health conditions, including menopausal symptoms, cancer prevention, and bone health.
Used in Nutraceutical Industry:
3'-prenylnaringenin is used as an active component in nutraceutical products, offering consumers natural health benefits through dietary supplements and functional foods.

Check Digit Verification of cas no

The CAS Registry Mumber 119240-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,2,4 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119240-82:
(8*1)+(7*1)+(6*9)+(5*2)+(4*4)+(3*0)+(2*8)+(1*2)=113
113 % 10 = 3
So 119240-82-3 is a valid CAS Registry Number.

119240-82-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]chromen-4-one

1.2 Other means of identification

Product number -
Other names licoflavone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:119240-82-3 SDS

119240-82-3Downstream Products

119240-82-3Relevant articles and documents

PRENYLATED FLAVONOIDS IN THE ROOTS OF YELLOW LUPIN

Tahara, Satoshi,Katagiri, Yasufumi,Ingham, John L.,Mizutani, Junya

, p. 1261 - 1272 (1994)

A further investigation of the methanol-soluble compounds in yellow lupin roots has revealed a new diprenylchromone, a new coumaronochromone (lupinalbin H), a new isoflavone 5,7,4'-trihydroxy-8,3'-di-(3,3-dimethylallyl)isoflavone (isolupalbigenin), and so

Complementary Flavonoid Prenylations by Fungal Indole Prenyltransferases

Zhou, Kang,Yu, Xia,Xie, Xiulan,Li, Shu-Ming

supporting information, p. 2229 - 2235 (2015/10/12)

Flavonoids are found mainly in plants and exhibit diverse biological and pharmacological activities, which can often be enhanced by prenylations. In plants, such reactions are catalyzed by membrane-bound prenyltransferases. In this study, the prenylation of nine flavonoids from different classes by a soluble fungal prenyltransferase (AnaPT) involved in the biosynthesis of the prenylated indole alkaloid acetylaszonalenin is demonstrated. The behavior of AnaPT toward flavonoids regarding substrate acceptance and prenylation positions clearly differs from that of the indole prenyltransferase 7-DMATS. The two enzymes are therefore complementary in flavonoid prenylations.

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