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N-(4-IODOPHENYL)-6,7-DIMETHOXY-4-QUINAZOLINAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

168835-91-4

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168835-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168835-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,8,3 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 168835-91:
(8*1)+(7*6)+(6*8)+(5*8)+(4*3)+(3*5)+(2*9)+(1*1)=184
184 % 10 = 4
So 168835-91-4 is a valid CAS Registry Number.

168835-91-4Relevant academic research and scientific papers

Quinazoline compounds and pharmaceutical compositions containing them

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Page/Page column 37, (2008/06/13)

The use of a compound of formula (I) or a salt, ester or amide thereof; where X is O, or S, S(O) or S(O)2, NH or NR8 where R8 is hydrogen or C1-6alkyl; Ra is a 3-quinoline group or a group of sub-formula (i) where R5, R6 and R7 are various specific organic groups, in the preparation of a medicament for use in the inhibtion of aurora 2 kinase. Novel compounds of formula (I) and pharmaceutical compositions useful in the treatment of cancer are also described and claimed.

Synthesis and biological evaluation of allenic quinazolines using palladium-catalyzed hydride-transfer reaction

Nakamura, Hiroyuki,Onagi, Shinya

, p. 2539 - 2542 (2007/10/03)

Allenic quinazolines 13a-h were designed as mimics of Tarceva, which is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, and synthesized from the corresponding 4-(iodoanilino)quinazolines or 4-(iodophenoxy)quinazolines with N,N-dicyclohexylprop-2-ynylamine by the Sonogashira coupling followed by palladium-catalyzed hydride-transfer reaction. Cell growth inhibition of 13a-h toward A431, Kato III, SKBR3, and HepG2 was examined. Among the compounds synthesized, 13a showed a similar cell growth inhibition to Tarceva. Moreover, 13d and 13h exhibited a specific growth inhibition toward Kato III cells (IC50 = 12 and 4.7 μM, respectively), although a significant inhibition toward other three cell lines was not observed at a 100 μM concentration of compounds.

QUINAZOLINE DERIVATIVES

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Page/Page column 14, (2008/06/13)

A compound of formula (I) or a salt, ester or amide thereof; where X is O, or S, S(O) or S(O)2 or NR10 where R10 is hydrogen or C1-6 alkyl, and R1, R2, R3, R4, R5, R6, R7, R8 and R9 are various specified organic groups. These compounds are inhibitors of aurora 2 kinase, and are useful in the treatment of cancer.

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