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Morpholine, 4-(3-methoxy-5-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93398-05-1

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93398-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93398-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,9 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93398-05:
(7*9)+(6*3)+(5*3)+(4*9)+(3*8)+(2*0)+(1*5)=161
161 % 10 = 1
So 93398-05-1 is a valid CAS Registry Number.

93398-05-1Relevant academic research and scientific papers

Novel pazopanib derivatives and pharmaceutical composition comprising the same

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Paragraph 0095; 0097; 0107; 0108, (2017/05/10)

The present invention relates to novel pazopanib derivatives or a salt thereof having inhibition activities of angiogenesis and epidermal growth factors at the same time, and to a pharmaceutical composition comprising the same as an active ingredient. The pazopanib derivatives have inhibition activities of angiogenesis and epidermal growth factors at the same time unlike pazopanib, thereby more effectively treating and preventing EGFR-related cancer diseases such as lung cancer, colon cancer or breast cancer through a multiple aim target, and effectively treating and preventing non-small-cell lung cancer which Iressa or Tarceva cannot have an effect on.COPYRIGHT KIPO 2017

NOVEL PYRIMIDINE DERIVATIVES 698

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Page/Page column 186, (2008/12/07)

The invention concerns compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, n, R2, R3, and R4 are as defined in the description. The present invention also relates to processes for the preparation of such compounds, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an antiproliferative agent in the prevention or treatment of tumours or other proliferative conditions which are sensitive to the inhibition of EphB4 kinases.

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