Welcome to LookChem.com Sign In|Join Free
  • or
Illudin S is a potent antitumor sesquiterpene derived from the fungus Clitocybe illudens, characterized by its unique DNA alkylating actions and cytotoxic properties. It is metabolically activated to reactive intermediates that bind to DNA, causing a complete block of cell cycling at the G1-S phase interface, particularly in myeloid and T-lymphocyte leukemia cells. Illudin S metabolites induce DNA damage that is not repaired by the processes that counter conventional DNA alkylating agents.

1149-99-1

Post Buying Request

1149-99-1 Suppliers

Recommended suppliers

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

1149-99-1 Usage

Uses

Used in Anticancer Applications:
Illudin S is used as an anticancer agent for its potent activity against multi-drug resistant tumors. It is particularly effective against myeloid and T-lymphocyte leukemia cells, even in cases where the cells display resistance to other chemotherapeutic agents. Illudin S's unique DNA damage mechanism makes it a valuable compound in the fight against cancer.
Used in Pharmaceutical Research:
Illudin S is used as a research compound for understanding the mechanisms of DNA alkylation and cell cycle inhibition. Its unique mode of action provides insights into the development of new anticancer drugs and potential strategies for overcoming drug resistance in cancer treatment.
Used in Drug Development:
Illudin S is used as a lead compound in the development of new antitumor drugs. Its potent activity against multi-drug resistant tumors and unique DNA damage mechanism make it an attractive candidate for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1149-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1149-99:
(6*1)+(5*1)+(4*4)+(3*9)+(2*9)+(1*9)=81
81 % 10 = 1
So 1149-99-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O4/c1-8-10-9(6-13(2,7-16)12(10)18)11(17)14(3,19)15(8)4-5-15/h6,12,16,18-19H,4-5,7H2,1-3H3/t12-,13+,14+/m1/s1

1149-99-1SDS

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 Illudin S

1.2 Other means of identification

Product number -
Other names Lampterol

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:1149-99-1 SDS

1149-99-1Relevant academic research and scientific papers

AFFINITY ILLUDOFULVENE CONJUGATES

-

Paragraph 0346, (2021/05/29)

In an embodiment of the invention, a composition for treating a cell population comprises a medicant. The medicant moiety can be an illudofulvene analog. In an embodiment of the invention, a composition for treating a cell population comprises an Affinity Medicant Conjugate (AMC). The affinity moiety can be an antibody, an antibody fragment, a receptor protein, a peptidic growth factor, an anti-angiogenic protein, a specific binding peptide, protease cleavable peptide, a glycopeptide, a peptide, a peptidic toxin, a protein toxin and an oligonucleotide. The affinity moiety can be covalently bound to the medicant via a linker.

Synthesis of [3H]-illudin S, [3H]-acylfulvene, [3H]and[14C]- hydroxymethylacylfulvene (MGI 114)

McMorris, Trevor C.,Yu, Jian,Herman, David M.,Kelner, Michael J.,Dawe, Robin,Minamida, Akira

, p. 279 - 285 (2007/10/03)

Tritiated derivatives of the toxic sesquiterpene illudin S (1) have been prepared by fermentation of Omphalotus illudens in the presence of [3H]- sodium acetate. [3H]-illudin S was converted to antitumor [3H]-acylfulvene (4) by treatment with dilute sulfuric acid. Antitumor [14C]- hydroxymethylacylfulvene (5) was best prepared by reacting acylfulvene with [14C]-paraformaldehyde in dilute sulfuric acid.

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 1149-99-1