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10391-09-0

Nodosin, a flavonoid compound derived from the Chinese herb Isodon rubescens, is known for its anti-inflammatory, antioxidant, and anti-cancer properties. It has demonstrated potential in inhibiting cancer cell growth and proliferation, as well as reducing inflammation and oxidative stress in the body. With its promising health benefits, nodosin is a compound of interest for further research and potential therapeutic applications.

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  • 10391-09-0 Structure

  • Basic information

    1. Product Name: Nodosin
    2. Synonyms: Nodosin;Nodosin【terpene】;dosin
    3. CAS NO:10391-09-0
    4. Molecular Formula: C20H26O6
    5. Molecular Weight: 362.4168
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10391-09-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 615.3°Cat760mmHg
    3. Flash Point: 222.1°C
    4. Appearance: /
    5. Density: 1.37g/cm3
    6. Vapor Pressure: 1.03E-17mmHg at 25°C
    7. Refractive Index: 1.601
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Nodosin(CAS DataBase Reference)
    11. NIST Chemistry Reference: Nodosin(10391-09-0)
    12. EPA Substance Registry System: Nodosin(10391-09-0)

  • 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: 10391-09-0(Hazardous Substances Data)

10391-09-0 Usage

Uses

Used in Pharmaceutical Industry:
Nodosin is used as an anti-inflammatory agent for its ability to reduce inflammation and oxidative stress in the body. Its antioxidant properties also contribute to its potential use in treating neurodegenerative disorders.
Used in Oncology:
Nodosin is used as an anti-cancer agent for its potential to inhibit the growth and proliferation of cancer cells. It has shown promise in preclinical studies, warranting further research into its mechanisms of action and potential therapeutic applications in cancer treatment.
Used in Nutraceutical Industry:
Nodosin, being a natural compound with health benefits, can be used as a nutraceutical ingredient in dietary supplements and functional foods to support overall health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 10391-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10391-09:
(7*1)+(6*0)+(5*3)+(4*9)+(3*1)+(2*0)+(1*9)=70
70 % 10 = 0
So 10391-09-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H26O6/c1-9-10-6-11(21)13-19(7-10,15(9)22)17(24)26-12-4-5-18(2,3)14-16(23)25-8-20(12,13)14/h10-14,16,21,23H,1,4-8H2,2-3H3

10391-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name NODOSIN

1.2 Other means of identification

Product number -
Other names -

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:10391-09-0 SDS

10391-09-0Downstream Products

10391-09-0Relevant articles and documents

NERVOSANIN A AND B, AND ENT- KAURANOIDS FROM ISODON NERVOSUS

Xian-rong, Wang,Hui-ping, Hu,Hong-ping, Wang,Su-qing, Wang,Ueda, Shinichi,Fujita, Tetsuro

, p. 1367 - 1370 (1994)

Two new diterpenoids nervosanin A and nervosanin B were isolated, together with the known neorabdosin, nervosin, odonicin, effusanin A and effusanin E, from the leaves of Isodon nervosus and their structures were elucidated from spectral and chemical evidence. - Key words: Isodon nervosus; Labiatae; ent-kauranoids; nervosanin A; nervosanin B.

STRUCTURES OF EFFUSANINS, ANTIBACTERIAL DITERPENOIDS FROM RABDOSIA EFFUSA

Fujita, Tetsuro,Takeda, Yoshio,Shingu, Tetsuro,Ueno, Akira

, p. 1635 - 1638 (2007/10/02)

Five new diterpenoids, effusanin A, B, C, D and E with antibacterial activity were isolated from the stem and leaves of Rabdosia effusa and their structures were deduced from chemical and spectral findings.

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