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2,4-Dichloro-5,6-diMethylthieno[2,3-d]pyriMidine, also known as DCPT, is a thienopyrimidine derivative that functions as a potent and selective inhibitor of the enzyme PIM1 kinase. This enzyme is involved in the regulation of cell growth and survival, making DCPT a promising candidate for cancer treatment due to its unique structure and targeted mechanism of action.
Used in Pharmaceutical Industry:
2,4-Dichloro-5,6-diMethylthieno[2,3-d]pyriMidine is used as a potential anticancer agent for its ability to inhibit PIM1 kinase, which is implicated in cell growth and survival. This makes DCPT a promising candidate for the treatment of various types of cancer, particularly hematologic malignancies.
Used in Cancer Research:
In the field of cancer research, 2,4-Dichloro-5,6-diMethylthieno[2,3-d]pyriMidine serves as a valuable tool for studying the role of PIM1 kinase in cancer development and progression. Its selectivity for this enzyme allows researchers to investigate the effects of inhibiting PIM1 kinase on cancer cells and to explore the potential therapeutic benefits of DCPT in preclinical studies.

42518-42-3

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42518-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42518-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,1 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42518-42:
(7*4)+(6*2)+(5*5)+(4*1)+(3*8)+(2*4)+(1*2)=103
103 % 10 = 3
So 42518-42-3 is a valid CAS Registry Number.

42518-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dichloro-5,6-dimethylthieno[2,3-d]pyrimidine

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:42518-42-3 SDS

42518-42-3Relevant academic research and scientific papers

METHODS OF USE FOR PYRIMIDINES AS FERROPORTIN INHIBITORS

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, (2021/11/06)

The subject matter described herein is directed to ferroportin inhibitor compounds of Formula (I) and pharmaceutical salts thereof, methods of preparing the compounds, pharmaceutical compositions comprising the compounds, and methods of administering the compounds for prophylaxis and/or treatment of diseases caused by a lack of hepcidin or iron metabolism disorders, particularly iron overload states, such as thalassemia, sickle cell disease and hemochromatosis, and also kidney injuries.

THIENO PYRIMIDINES AS FERROPORTIN INHIBITORS

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Paragraph 199-200, (2021/11/06)

The subject matter described herein is directed to ferroportin inhibitor compounds of Formula I and pharmaceutical salts thereof, methods of preparing the compounds, pharmaceutical compositions comprising the compounds, and methods of administering the compounds for prophylaxis and/or treatment of diseases caused by a lack of hepcidin or iron metabolism disorders, particularly iron overload states, such as thalassemia, sickle cell disease and hemochromatosis, and also kidney injuries.

2,4-Diaminothienopyrimidines as orally active antimalarial agents

González Cabrera, Diego,Le Manach, Claire,Douelle, Frederic,Younis, Yassir,Feng, Tzu-Shean,Paquet, Tanya,Nchinda, Aloysius T.,Street, Leslie J.,Taylor, Dale,De Kock, Carmen,Wiesner, Lubbe,Duffy, Sandra,White, Karen L.,Zabiulla, K. Mohammed,Sambandan, Yuvaraj,Bashyam, Sridevi,Waterson, David,Witty, Michael J.,Charman, Susan A.,Avery, Vicky M.,Wittlin, Sergio,Chibale, Kelly

supporting information, p. 1014 - 1022 (2014/03/21)

A novel series of 2,4-diaminothienopyrimidines with potential as antimalarials was identified from whole-cell high-throughput screening of a SoftFocus ion channel library. Synthesis and structure-activity relationship studies identified compounds with potent antiplasmodial activity and low in vitro cytotoxicity. Several of these analogues exhibited in vivo activity in the Plasmodium berghei mouse model when administered orally. However, inhibition of the hERG potassium channel was identified as a liability for this series.

Facile and efficient cyclization of anthranilonitrile to 2,4-dichloroquinazoline by bis(trichloromethyl) carbonate and catalytic amount triphenylphosphine oxide

Li, Zhenhua,Wu, Danli,Zhong, Weihui

experimental part, p. 1417 - 1426 (2012/08/28)

2,4-Dichloroquinazolines were synthesized by the cyclization of anthranilonitrile using bis(trichloromethyl) carbonate (BTC) with the aid of catalytic amount of triphenylphosphine oxide (Ph3PO) at 120 °C. This method was also applied to the syn

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