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N-hydroxy-6-[(5-phenylpentanoyl)amino]hexanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

408356-18-3

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408356-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 408356-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,8,3,5 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 408356-18:
(8*4)+(7*0)+(6*8)+(5*3)+(4*5)+(3*6)+(2*1)+(1*8)=143
143 % 10 = 3
So 408356-18-3 is a valid CAS Registry Number.

408356-18-3Downstream Products

408356-18-3Relevant academic research and scientific papers

Novel amide derivatives as inhibitors of histone deacetylase: Design, synthesis and SAR

Andrianov, Victor,Gailite, Vija,Lola, Daina,Loza, Einars,Semenikhina, Valentina,Kalvinsh, Ivars,Finn, Paul,Petersen, Kamille Dumong,Ritchie, James W.A.,Khan, Nagma,Tumber, Anthony,Collins, Laura S.,Vadlamudi, Sree M.,Bjoerkling, Fredrik,Sehested, Maxwell

, p. 1067 - 1085 (2009)

Enzymatic inhibition of histone deacetylase (HDAC) activity is emerging as an innovative and effective approach for the treatment of cancer. A series of novel amide derivatives have been synthesized and evaluated for their ability to inhibit human HDACs. Multiple compounds were identified as potent HDAC inhibitors (HDACi), with IC50 values in the low nanomolar (nM) range against enzyme activity in HeLa cell extracts and sub-μM for their in vitro anti-proliferative effect on cell lines. The introduction of an unsaturated linking group between the terminal aryl ring and the amide moiety was the key to obtain good potency. This approach yielded compounds such as (E)-N-[6-(hydroxyamino)-6-oxohexyl]-3-(7-quinolinyl)-2-propenamide (27) (HDAC IC50 8 nM) which showed potent in vivo activity in the P388 mouse leukemia syngeneic model (an increased lifespan (ILS) of 111% was obtained).

Carbamic acid compounds comprising an amide linkage as hdac inhibitors

-

, (2008/06/13)

This invention pertains to certain active carbamic acid compounds which inhibit HDAC activity and which have the formula (1) wherein: A is an aryl group; Q1 is an aryl leader group having a backbone of at least 2 carbon atoms; J is an amide linkage selected from: —NR1C(═O)—and —C(═O)NR1—; R1 is an amido substituent; and, Q2 is an acid leader group; and pharmaceutically acceptable salts, solvates, amides, esters, ethers, chemically protected forms, and prodrugs thereof. The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit HDAC, and, e.g., to inhibit proliferative conditions, such as cancer and psoriasis.

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