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O6-[3-(aminomethyl)benzyl]guanine hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1348285-25-5

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1348285-25-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1348285-25-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,8,2,8 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1348285-25:
(9*1)+(8*3)+(7*4)+(6*8)+(5*2)+(4*8)+(3*5)+(2*2)+(1*5)=175
175 % 10 = 5
So 1348285-25-5 is a valid CAS Registry Number.

1348285-25-5Downstream Products

1348285-25-5Relevant academic research and scientific papers

Substitution of aminomethyl at the meta-position enhances the inactivation of O6-alkylguanine-DNA alkyltransferase by O6- benzylguanine

Pauly, Gary T.,Loktionova, Natalia A.,Fang, Qingming,Vankayala, Sai Lakshmana,Guida, Wayne C.,Pegg, Anthony E.

experimental part, p. 7144 - 7153 (2009/11/30)

O6-Benzylguanine is an irreversible inactivator of O 6-alkylguanine-DNA alkyltransferase currently in clinical trials to overcome alkyltransferase-mediated resistance to certain cancer chemotherapeutic alkylating agents. In order to produce more soluble alkyltransferase inhibitors, we have synthesized three aminomethyl-substituted O 6-benzylguanines and the three methyl analogs and found that the substitution of aminomethyl at the meta-position greatly enhances inactivation of alkyltransferase, whereas para-substitution has little effect and ortho-substitution virtually eliminates activity. Molecular modeling of their interactions with alkyltransferase provided a molecular explanation for these results. The square of the correlation coefficient (R2) obtained between E-model scores (obtained from GLIDE XP/QPLD docking calculations) vs log(ED50) values via a linear regression analysis was 0.96. The models indicate that the ortho-substitution causes a steric clash interfering with binding, whereas the meta-aminomethyl substitution allows an interaction of the amino group to generate an additional hydrogen bond with the protein.

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