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CAS

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79498-31-0

Glaucocalyxin A is a diterpenoid compound derived from the traditional Chinese medicinal herb Isodon rubescens. It possesses a range of biological activities, such as anti-inflammatory, anti-tumor, and anti-malarial properties. Its ability to inhibit cancer cell growth and proliferation, induce apoptosis, and cause cell cycle arrest, along with its anti-inflammatory and anti-malarial effects, makes it a promising natural compound with therapeutic potential for various diseases.

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  • 79498-31-0 Structure

  • Basic information

    1. Product Name: glaucocalyxin A
    2. Synonyms: glaucocalyxin A;LeukaMenin F;Wangzaozin B;Leucamenin F
    3. CAS NO:79498-31-0
    4. Molecular Formula: C20H28O4
    5. Molecular Weight: 332.437
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79498-31-0.mol

  • Chemical Properties

    1. Melting Point: 219.5-220.5℃ (ethyl ether )
    2. Boiling Point: 513.4°C at 760 mmHg
    3. Flash Point: 278.4°C
    4. Appearance: /
    5. Density: 1.22±0.1 g/cm3 (20 ºC 760 Torr)
    6. Vapor Pressure: 1.1E-12mmHg at 25°C
    7. Refractive Index: 1.574
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 13.15±0.70(Predicted)
    11. CAS DataBase Reference: glaucocalyxin A(CAS DataBase Reference)
    12. NIST Chemistry Reference: glaucocalyxin A(79498-31-0)
    13. EPA Substance Registry System: glaucocalyxin A(79498-31-0)

  • 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: 79498-31-0(Hazardous Substances Data)

79498-31-0 Usage

Uses

Used in Pharmaceutical Industry:
Glaucocalyxin A is used as an anti-tumor agent for its ability to inhibit the growth and proliferation of cancer cells, induce apoptosis, and cause cell cycle arrest. It is particularly effective against various types of cancer.
Glaucocalyxin A is used as an anti-inflammatory agent for its ability to suppress the production of inflammatory mediators, making it a potential candidate for the treatment of inflammatory diseases.
Used in Antimalarial Drug Development:
Glaucocalyxin A is used as a potential antimalarial drug candidate due to its potent anti-malarial activity, offering a new avenue for the development of treatments for malaria.

Check Digit Verification of cas no

The CAS Registry Mumber 79498-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,9 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79498-31:
(7*7)+(6*9)+(5*4)+(4*9)+(3*8)+(2*3)+(1*1)=190
190 % 10 = 0
So 79498-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O4/c1-10-11-5-6-12-19(4)8-7-14(21)18(2,3)13(19)9-15(22)20(12,16(10)23)17(11)24/h11-13,15,17,22,24H,1,5-9H2,2-4H3/t11?,12-,13+,15+,17?,19-,20?/m0/s1

79498-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ent-7β,14α-Dihydroxy-16-kauren-3,15-dione

1.2 Other means of identification

Product number -
Other names glaucocalyxinA 79498-31-0

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:79498-31-0 SDS

79498-31-0Upstream product

79498-31-0Downstream Products

79498-31-0Relevant articles and documents

Total Synthesis of (?)-Glaucocalyxin A

Guo, Jiuzhou,Jia, Yanxing,Li, Bo,Ma, Weihao,Pitchakuntla, Mallesham

, p. 15195 - 15198 (2020)

A practically useful method for the formation of the highly oxygenated bicyclo[3.2.1]octane ring system through Mn(OAc)3-mediated radical cyclization of alkynyl ketones was developed, which opens up a new avenue for the total synthesis of a number of highly oxidized diterpenoids. Application of this method enabled the first total synthesis of (?)-glaucocalyxin A. Other salient features of the synthesis include a highly enantioselective conjugate addition/acylation cascade reaction, a Yamamoto aldol reaction, and an intramolecular Diels–Alder reaction to assemble the A/B ring system.

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