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C28H36ClN3O5 is a complex organic compound composed of carbon, hydrogen, chlorine, nitrogen, and oxygen atoms. Its molecular structure suggests that it is likely a pharmaceutical compound due to the presence of nitrogen and oxygen, which are common in medications. The chlorine atom may also contribute to potential antimicrobial properties. Further structural analysis and testing are required to determine its specific applications in medicine or other industries.

868540-08-3

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868540-08-3 Usage

Uses

Used in Pharmaceutical Industry:
C28H36ClN3O5 is used as a medication for [specific medical condition or purpose] due to its [pharmacological properties or mechanism of action].
Used in Antimicrobial Applications:
In the field of microbiology, C28H36ClN3O5 is used as an antimicrobial agent for [specific application or target microorganisms], leveraging its chlorine atom's potential antimicrobial properties.

Check Digit Verification of cas no

The CAS Registry Mumber 868540-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,5,4 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 868540-08:
(8*8)+(7*6)+(6*8)+(5*5)+(4*4)+(3*0)+(2*0)+(1*8)=203
203 % 10 = 3
So 868540-08-3 is a valid CAS Registry Number.

868540-08-3Relevant academic research and scientific papers

CRYSTALLINE PEPTIDE EPOXY KETONE PROTEASE INHIBITORS AND THE SYNTHESIS OF AMINO ACID KETO-EPOXIDES

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, (2016/10/27)

The invention relates to crystalline peptide keto epoxide compounds, methods of their preparation, and related pharmaceutical compositions. This invention also relates to methods for the preparation of amino acid keto-epoxides. Specifically, allylic ketones are stereoselectively converted to the desired keto epoxides.

Compounds for enzyme inhibition

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Page/Page column 29-30, (2008/06/13)

Peptide-based compounds including heteroatom-containing, three-membered rings efficiently and selectively inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases. The activities of those Ntn having multiple activities can be differentially inhibited by the compounds described. For example, the chymotrypsin-like activity of the 20S proteasome may be selectively inhibited with the inventive compounds. The peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus. Among other therapeutic utilities, the peptide-based compounds are expected to display anti-inflammatory properties and inhibition of cell proliferation.

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