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(5-bromo-2-(methylthio)pyrimidin-4-yl)methanamine is a pyrimidine derivative featuring a bromine substituent at the 5-position, a methylthio group at the 2-position, and a methanamine group attached to the pyrimidine ring. This chemical compound is widely recognized for its significance in organic synthesis and medicinal chemistry, particularly in the development of novel drugs and pharmaceuticals.

1823402-38-5

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1823402-38-5 Usage

Uses

Used in Pharmaceutical Industry:
(5-bromo-2-(methylthio)pyrimidin-4-yl)methanamine is used as a key intermediate for the development of new drugs and pharmaceuticals. Its unique chemical structure allows for the creation of various therapeutic agents that can potentially treat a range of diseases and conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (5-bromo-2-(methylthio)pyrimidin-4-yl)methanamine serves as a valuable building block for designing and synthesizing new chemical entities with potential therapeutic applications. Its versatility in chemical modifications makes it an attractive candidate for further research and development.
Used in Agrochemical Development:
(5-bromo-2-(methylthio)pyrimidin-4-yl)methanamine is also utilized in the development of agrochemicals, where its unique properties can be harnessed to create novel compounds with applications in agriculture, such as pesticides or herbicides.
Used in Industrial Product Development:
Beyond its applications in the pharmaceutical and agrochemical industries, (5-bromo-2-(methylthio)pyrimidin-4-yl)methanamine may also find use in the development of other industrial products, thanks to its diverse chemical properties and potential for further modification.

Check Digit Verification of cas no

The CAS Registry Mumber 1823402-38-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,2,3,4,0 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1823402-38:
(9*1)+(8*8)+(7*2)+(6*3)+(5*4)+(4*0)+(3*2)+(2*3)+(1*8)=145
145 % 10 = 5
So 1823402-38-5 is a valid CAS Registry Number.

1823402-38-5Downstream Products

1823402-38-5Relevant academic research and scientific papers

IMIDAZOPYRIMIDINES AS EED INHIBITORS AND THE USE THEREOF

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Paragraph 0464; 0471-0472, (2021/02/12)

The present disclosure provides compounds represented by Formula (I) wherein R1, R2, R3, and R4 are as defined in the specification, and the salts and solvates thereof. Compounds of Formula (I) are FED inhibitors. FED inhibitors are useful for the treatment of cancer and other diseases.

EEDi-5285: An Exceptionally Potent, Efficacious, and Orally Active Small-Molecule Inhibitor of Embryonic Ectoderm Development

Rej, Rohan Kalyan,Wang, Changwei,Lu, Jianfeng,Wang, Mi,Petrunak, Elyse,Zawacki, Kaitlin P.,McEachern, Donna,Fernandez-Salas, Ester,Yang, Chao-Yie,Wang, Lu,Li, Ruiting,Chinnaswamy, Krishnapriya,Wen, Bo,Sun, Duxin,Stuckey, Jeanne,Zhou, Yunlong,Chen, Jianyong,Tang, Guozhi,Wang, Shaomeng

, p. 7252 - 7267 (2020/07/14)

Inhibition of embryonic ectoderm development (EED) is a new cancer therapeutic strategy. Herein, we report our discovery of EEDi-5285 as an exceptionally potent, efficacious, and orally active EED inhibitor. EEDi-5285 binds to the EED protein with an IC50 value of 0.2 nM and inhibits cell growth with IC50 values of 20 pM and 0.5 nM in the Pfeiffer and KARPAS422 lymphoma cell lines, respectively, carrying an EZH2 mutation. EEDi-5285 is approximately 100 times more potent than EED226 in binding to EED and >300 times more potent than EED226 in inhibition of cell growth in the KARPAS422 cell line. EEDi-5285 has excellent pharmacokinetics and achieves complete and durable tumor regression in the KARPAS422 xenograft model in mice with oral administration. The cocrystal structure of EEDi-5285 in a complex with EED defines the precise structural basis for their high binding affinity. EEDi-5285 is the most potent and efficacious EED inhibitor reported to date.

Discovery of First-in-Class, Potent, and Orally Bioavailable Embryonic Ectoderm Development (EED) Inhibitor with Robust Anticancer Efficacy

Huang, Ying,Zhang, Jeff,Yu, Zhengtian,Zhang, Hailong,Wang, Youzhen,Lingel, Andreas,Qi, Wei,Gu, Justin,Zhao, Kehao,Shultz, Michael D.,Wang, Long,Fu, Xingnian,Sun, Yongfeng,Zhang, Qiong,Jiang, Xiangqing,Zhang, Jiangwei,Zhang, Chunye,Li, Ling,Zeng, Jue,Feng, Lijian,Zhang, Chao,Liu, Yueqin,Zhang, Man,Zhang, Lijun,Zhao, Mengxi,Gao, Zhenting,Liu, Xianghui,Fang, Douglas,Guo, Haibing,Mi, Yuan,Gabriel, Tobias,Dillon, Michael P.,Atadja, Peter,Oyang, Counde

supporting information, p. 2215 - 2226 (2017/04/03)

Overexpression and somatic heterozygous mutations of EZH2, the catalytic subunit of polycomb repressive complex 2 (PRC2), are associated with several tumor types. EZH2 inhibitor, EPZ-6438 (tazemetostat), demonstrated clinical efficacy in patients with acceptable safety profile as monotherapy. EED, another subunit of PRC2 complex, is essential for its histone methyltransferase activity through direct binding to trimethylated lysine 27 on histone 3 (H3K27Me3). Herein we disclose the discovery of a first-in-class potent, selective, and orally bioavailable EED inhibitor compound 43 (EED226). Guided by X-ray crystallography, compound 43 was discovered by fragmentation and regrowth of compound 7, a PRC2 HTS hit that directly binds EED. The ensuing scaffold hopping followed by multiparameter optimization led to the discovery of 43. Compound 43 induces robust and sustained tumor regression in EZH2MUT preclinical DLBCL model. For the first time we demonstrate that specific and direct inhibition of EED can be effective as an anticancer strategy.

IMIDAZOPYRIMIDINE COMPOUNDS USEFUL FOR THE TREATMENT OF CANCER

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Paragraph 00288, (2018/04/12)

A compound of Formula (IA), or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for treating a PRC2-mediated disease or disorder: wherein A, R3, R4, R6, and R7 are as defined herein.

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