Welcome to LookChem.com Sign In|Join Free

CAS

  • or

142741-24-0

Cophylline, a naturally occurring alkaloid, is derived from various plant sources and possesses unique pharmacological properties. It has been found to play a significant role in the differentiation of stem cells, particularly in the context of regenerative medicine.

142741-24-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 142741-24-0 Structure

  • Basic information

    1. Product Name: Cophylline
    2. Synonyms: Cophylline;Vinca alkaloid III-121C
    3. CAS NO:142741-24-0
    4. Molecular Formula: C44H50N4O10
    5. Molecular Weight: 794.89
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142741-24-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cophylline(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cophylline(142741-24-0)
    11. EPA Substance Registry System: Cophylline(142741-24-0)

  • 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: 142741-24-0(Hazardous Substances Data)

142741-24-0 Usage

Uses

Used in Regenerative Medicine:
Cophylline is used as a differentiation agent for promoting the development of adipose-derived stem cells into functional islet-like cells. This application is particularly relevant in the field of diabetes research and treatment, as these islet-like cells have the potential to be used in cell replacement therapies for patients with diabetes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Cophylline is utilized for its potential to enhance the therapeutic use of stem cells. Its role in promoting the differentiation of stem cells into specific cell types makes it a valuable compound for developing novel treatments and therapies for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 142741-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 142741-24:
(8*1)+(7*4)+(6*2)+(5*7)+(4*4)+(3*1)+(2*2)+(1*4)=110
110 % 10 = 0
So 142741-24-0 is a valid CAS Registry Number.

142741-24-0SDS

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 Conophylline

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:142741-24-0 SDS

142741-24-0Upstream product

142741-24-0Downstream Products

142741-24-0Relevant articles and documents

Biologically active indole and bisindole alkaloids from Tabernaemontana divaricata

Kam, Toh-Seok,Pang, Huey-Shen,Lim, Tuck-Meng

, p. 1292 - 1297 (2003)

The ethanol extract of the leaves of Tabernaemontana divaricata (double flower variety) provided a total of 23 alkaloids, including the new aspidosperma alkaloids, taberhanine, voafinine, N-methylvoafinine, voafinidine, voalenine and the new bisindole alkaloid, conophylinine in addition to the previously known, biologically active bisindole, conophylline and its congener, confoline. The structures of the new alkaloids were established by spectroscopic methods. The preparation and characterization of the corresponding quinones of the biologically active bisindoles are also described in relation to a structure-activity study of these compounds with respect to their action in stimulating insulin expression.

Total synthesis of (-)-conophylline and (-)-conophyllidine

Han-Ya, Yuki,Tokuyama, Hidetoshi,Fukuyama, Tohru

supporting information; experimental part, p. 4884 - 4887 (2011/06/26)

Double take: The total syntheses of the title compounds were accomplished in a highly convergent manner. The approach features the regio- and diastereoselective Polonovski-Potier-type reaction for the coupling of two aspidosperma skeletons and the formation of the dihydrofuran ring. Troc=2,2,2-trichloroethoxycarbonyl. Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 142741-24-0