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L-Glutamic acid, N-(4-amino-3-fluorobenzoyl)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126632-35-7

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126632-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126632-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,6,3 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126632-35:
(8*1)+(7*2)+(6*6)+(5*6)+(4*3)+(3*2)+(2*3)+(1*5)=117
117 % 10 = 7
So 126632-35-7 is a valid CAS Registry Number.

126632-35-7Downstream Products

126632-35-7Relevant academic research and scientific papers

Synthesis and biological activity of open-chain analogues of 5,6,7,8- tetrahydrofolic acid-potential antitumor agents

Bigham,Hodson,Mallory,Wilson,Duch,Smith,Ferone

, p. 1399 - 1410 (2007/10/02)

This study describes the synthesis and in vitro antitumor activity of inhibitors of purine de novo biosynthesis that are analogues of N-[4-[[3- (2,4-diamino-1,6-dihydro-6-oxo-5-pyrimidinyl)propyl]amino]benzoyl-L-glutamic acid (5-DACTHF). Benzene ring subs

Quinazoline antifolate thymidylate synthase inhibitors: Benzoyl ring modifications in the C2-methyl series

Marsham,Jackman,Oldfield,Hughes,Thornton,Bisset,O'Connor,Bishop,Calvert

, p. 3072 - 3078 (2007/10/02)

The synthesis of nine new 2-methyl-10-propargylquinazoline antifolates with substituents in the p-aminobenzoyl ring is described. In general the synthetic route involved the coupling of the appropriate ring-substituted diethyl N-[4-(prop-2-ynylamino)benzoyl]-L-glutamate with 6-(bromomethyl)-3,4-dihydro-2-methyl-4-oxoquinazoline (11) followed by deprotection using mild alkali. The compounds were tested as inhibitors of partially purified L1210 thymidylate synthase (TS). They were also examined for their inhibition of the growth L1210 cells in culture. Compared to the parent compound 1a the 2'-fluoro analogue 2a exhibited enhanced potency in both systems whereas the 3'-fluoro analogue 3a showed enhanced growth inhibitory properties against L1210 cells despite being a poorer inhibitor of the isolated enzyme. Chloro, hydroxy, methoxy, and nitro substituents in the 2'-position were also well tolerated by the enzyme but failed to give enhanced growth inhibition. The series was extended to cover analogues of the 2'-fluoro, 3'-fluoro, 2'-chloro, 2'-methyl, 2'-amino, 2'-methoxy, and 2'-nitro derivatives with modified alkyl substituents at N10.

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