Welcome to LookChem.com Sign In|Join Free
  • or
RPI-1 is a RET kinase inhibitor, which plays a significant role in various biological studies and applications. It is particularly useful in the research and understanding of mutant Swi/Snf complexes and medullary thyroid carcinomas expressing RET germ-line mutations.
Usage:
Used in Biological Research:
RPI-1 is used as a research tool for studying the composition and function of mutant Swi/Snf complexes. Its ability to inhibit RET kinase activity makes it a valuable asset in understanding the underlying mechanisms and interactions within these complexes.
Used in Proteomics Studies:
RPI-1 is used as an inhibitor in proteomics studies of medullary thyroid carcinomas expressing RET germ-line mutations. This application aids in the identification of new signaling elements and provides insights into the molecular pathways involved in these specific types of carcinomas.
Used in Pharmaceutical Development:
As a RET kinase inhibitor, RPI-1 has potential applications in the development of targeted therapies for various cancers and diseases associated with abnormal RET kinase activity. Its use in biological studies and proteomics research can contribute to the discovery of novel therapeutic strategies and the design of more effective drugs.

269730-03-2

Post Buying Request

269730-03-2 Suppliers

Recommended suppliers

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

269730-03-2 Usage

Biological Activity

rpi-1 is an atp-dependent ret tyrosine kinase and inhibitor [1]. rpi-1 also inhibits c-met activation and expression [2].the ret proto-oncogene encodes a receptor protein tyrosine kinase involved in the etiology of human tumors. ret loss of function mutations are associated with the development of hirschsprung's disease, and gain of function mutations are associated with the development of various types of human cancer, including medullary thyroid carcinoma, multiple endocrine neoplasias, pheochromocytoma and parathyroid hyperplasia.in nih3t3 fibroblasts expressing the ret/ptc1 target tyrosine kinase (nih3t3ptc1), rpi-1 preferentially inhibited the anchorage-independent growth with ic50 value of 0.97 μm [1]. in the n592 sclc and h460 nsclc cell lines, rpi-1 dose-dependently inhibited met phosphorylation. in h460 cells, rpi-1 also inhibited hgf-induced met tyrosine phosphorylation in a dose-dependent way [2].in mice implanted s.c. with h460 cells, rpi-1 with 100 and 150 mg/kg significantly reduced the mean number of macroscopic lung metastases by 57% and 75%, respectively. in primary s.c. growing h460 tumors, rpi-1 exhibited significant antiangiogenic effect [2].

references

[1]. lanzi c, cassinelli g, pensa t, et al. inhibition of transforming activity of the ret/ptc1 oncoprotein by a 2-indolinone derivative. int j cancer. 2000 feb 1;85(3):384-90.[2]. cassinelli g, lanzi c, petrangolini g, et al. inhibition of c-met and prevention of spontaneous metastatic spreading by the 2-indolinone rpi-1. mol cancer ther. 2006 sep;5(9):2388-97.

Check Digit Verification of cas no

The CAS Registry Mumber 269730-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,7,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 269730-03:
(8*2)+(7*6)+(6*9)+(5*7)+(4*3)+(3*0)+(2*0)+(1*3)=162
162 % 10 = 2
So 269730-03-2 is a valid CAS Registry Number.

269730-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2H-?Indol-?2-?one, 1,?3-?dihydro-?3-?[(4-?hydroxyphenyl)?methylene]?-?5,?6-?dimethoxy-

1.2 Other means of identification

Product number -
Other names 3-(4-Hydroxybenzylidene)-5,6-dimethoxyindolin-2-one

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:269730-03-2 SDS

269730-03-2Downstream Products

269730-03-2Relevant academic research and scientific papers

INDOLINONE DERIVATIVES AS RECEPTOR TYROSINE KINASE IHIBITORS

-

Page/Page column 18-19, (2008/06/13)

Novel derivatives of compound (E)-1,3-dihydro-5,6-dimethoxy-3-[(4-hydroxyphenyl)methylene]-2H-indol-2-one and the use thereof for the preparation of medicaments for the treatment of tumors in which the tyrosine kinase activity proteins Met, PDGF-R, FGF-R1

Indolinone derivatives

-

Page/Page column 7, (2008/06/13)

Novel derivatives of compound (E)-1,3-dihydro-5,6-dimethoxy-3-[(4-hydroxyphenyl)methylene]-2H-indol-2-one and the use thereof for the preparation of medicaments for the treatment of tumors in which the tyrosine kinase activity proteins Met, PDGF-R, FGF-R1

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 269730-03-2