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14346-25-9

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14346-25-9 Usage

Chemical Properties

Off-white solid

Check Digit Verification of cas no

The CAS Registry Mumber 14346-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,4 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14346-25:
(7*1)+(6*4)+(5*3)+(4*4)+(3*6)+(2*2)+(1*5)=89
89 % 10 = 9
So 14346-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2OS/c12-8-7-5-2-1-3-6(5)13-9(7)11-4-10-8/h4H,1-3H2,(H,10,11,12)

14346-25-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H32647)  3,5,6,7-Tetrahydro-4H-cyclopenta[b]thieno[2,3-d]pyrimidin-4-one, 96%   

  • 14346-25-9

  • 1g

  • 896.0CNY

  • Detail
  • Alfa Aesar

  • (H32647)  3,5,6,7-Tetrahydro-4H-cyclopenta[b]thieno[2,3-d]pyrimidin-4-one, 96%   

  • 14346-25-9

  • 5g

  • 2982.0CNY

  • Detail

14346-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6,7,8-tetrahydrocyclopenta[2,3]thieno[2,4-d]pyrimidin-1-one

1.2 Other means of identification

Product number -
Other names 3,5,6,7-Tetrahydro-4H-cyclopenta[b]thieno[2,3-d]pyrimidin-4-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:14346-25-9 SDS

14346-25-9Relevant articles and documents

Discovery of novel akt1 inhibitor induces autophagy associated death in hepatocellular carcinoma cells

Yu, Meng,Zeng, Minghui,Pan, Zhaoping,Wu, Fengbo,Guo, Li,He, Gu

supporting information, (2020/02/03)

In this study, a series of thieno [2,3-d]pyrimidine derivatives were designed, synthesized and evaluated as novel AKT1 inhibitors. In vitro antitumor assay results showed that compounds 9d-g and 9i potently suppressed the enzymatic activities of AKT1 and

Identification of 4-methoxythieno[2,3-d]pyrimidines as FGFR1 inhibitors

Balanda, A. O.,Bdzhola, V. G.,Kotey, I. M.,Pletnova, L. V.,Protopopov, M. V.,Prykhod’ko, A. O.,Starosyla, S. A.,Yarmoluk, S. M.

, p. 152 - 162 (2020/06/02)

Aim. To identify novel FGFR1 inhibitors using virtual screening approach. Methods. We used methods of organic synthesis, molecular docking via the Autodock 4.2.6 program package and in vitro biochemical tests with γ-32P. Results. In vitro experiments showed that 9 of 23 tested compounds possess inhibitory activity against FGFR1 with IC50 values in the range from 0.9 to 5.6 μM. Conclusions. Nine FGFR1 inhibitors were developed. The mode of compounds binding with the ATP-acceptor site was determined using molecular docking methods and the dependence of the compounds’ activity on the substituents R1, R4 and R5 was evaluated.

Structure based design of selective SHP2 inhibitors by De novo design, synthesis and biological evaluation

Liu, Wen-Shan,Jin, Wen-Yan,Zhou, Liang,Lu, Xing-Hua,Li, Wei-Ya,Ma, Ying,Wang, Run-Ling

, p. 759 - 774 (2019/07/17)

SHP2 phosphatase, encoded by the PTPN11 gene, is a non-receptor PTP, which plays an important role in growth factor, cytokine, integrin, hormone signaling pathways, and regulates cellular responses, such as proliferation, differentiation, adhesion migrati

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