Welcome to LookChem.com Sign In|Join Free
  • or
Celaphal A, a guanidine-containing alkaloid, is a chemical compound derived from the marine sponge Smenospongia cerebriformis. It has demonstrated cytotoxic and antitumor activities, making it a promising candidate for the development of therapeutic agents for cancer and inflammatory diseases.

244204-40-8

Post Buying Request

244204-40-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

244204-40-8 Usage

Uses

Used in Pharmaceutical Industry:
Celaphal A is used as a cytotoxic and antitumor agent for its ability to inhibit cancer cell growth by interfering with cell division and inducing apoptosis.
Used in Anti-inflammatory Applications:
Celaphal A is used as an anti-inflammatory agent for its potential to inhibit the production of pro-inflammatory cytokines, suggesting its use in the treatment of inflammatory diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 244204-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,2,0 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 244204-40:
(8*2)+(7*4)+(6*4)+(5*2)+(4*0)+(3*4)+(2*4)+(1*0)=98
98 % 10 = 8
So 244204-40-8 is a valid CAS Registry Number.

244204-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,12,13-Trihydroxypodocarpa-5,8,11,13-tetraen-7-one

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:244204-40-8 SDS

244204-40-8Downstream Products

244204-40-8Relevant academic research and scientific papers

First total synthesis of (±)-celaphanol A

Bie, Pingyan,Zhang, Chenglu,Li, Anpai,Peng, Xuanjia,Wu, Tongxing,Pan, Xinfu

, p. 581 - 583 (2002)

The first total synthesis of (±)-Celaphanol A was accomplished starting from α-cyclocitral and 3,4-dimethoxy benzyl chloride in six steps. The intramolecular cyclization with BF3·Et2O and enolization in t-BuOK/t-BuOH were the key steps. The process of intramolecular cyclization afforded an all-cis isomer intermediate for synthesis of aromatic tricyclic diterpenes.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 244204-40-8