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Acetic acid, [3-[[(1,1-dimethylethoxy)carbonyl]amino]propoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144367-00-0

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144367-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144367-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,3,6 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144367-00:
(8*1)+(7*4)+(6*4)+(5*3)+(4*6)+(3*7)+(2*0)+(1*0)=120
120 % 10 = 0
So 144367-00-0 is a valid CAS Registry Number.

144367-00-0Downstream Products

144367-00-0Relevant academic research and scientific papers

ANTIPROLIFERATION COMPOUNDS AND USES THEREOF

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Paragraph 1150, (2019/11/11)

The present invention provides compounds of Formula I′, or pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof, and methods of use thereof for treating cellular proliferative disorders (e.g., cancer).

CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION

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Paragraph 1171-1173, (2015/11/18)

The present invention relates to a hydroxyalkyl starch conjugate and a method for preparing the same, said hydroxyalkyl starch conjugate comprising a hydroxyalkyl starch derivative and a cytotoxic agent, the cytotoxic agent comprising at least one secondary hydroxyl group, wherein the hydroxyalkyl starch is linked via said secondary hydroxyl group to the cytotoxic agent. The conjugate according to the present invention has a structure according to the following formula HAS′(-L-M)n wherein M is a residue of the cytotoxic agent, L is a linking moiety, HAS′ is the residue of the hydroxyalkyl starch derivative, and n is greater than or equal to 1, and wherein the hydroxyalkyl starch derivative has a mean molecular weight (MW) above the renal threshold.

SUBSTITUTED IMIDAZOHETEROCYCLE DERIVATIVES

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Page/Page column 33-34, (2010/07/02)

The present invention provides substituted imidazoheterocycles having the general structure of formula (I), wherein Y is chosen from -O-, -OCRgRh-, -CRgRhO-, -CRgRh-, -(CRgRh)2-, -NRi-, -CRgRhNRi- and -NRiCRgRh-. Also provided are pharmaceutically acceptable salts, acid salts, hydrates, solvates and stereoisomers of the compounds of formula I. The compounds are useful as modulators of cannabinoid receptors and for the prophylaxis and treatment of cannabinoid receptor-associated diseases and conditions, such as pain, inflammation and pruritis.

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