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N-[4-(3-ethyl-2,4,4-trimethylcyclohexylmethyl)benzoyl]guanidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1609535-67-2

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1609535-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609535-67-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,5,3 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1609535-67:
(9*1)+(8*6)+(7*0)+(6*9)+(5*5)+(4*3)+(3*5)+(2*6)+(1*7)=182
182 % 10 = 2
So 1609535-67-2 is a valid CAS Registry Number.

1609535-67-2Downstream Products

1609535-67-2Relevant academic research and scientific papers

N-carbamidoyl-4-((3-ethyl-2,4,4-trimethylcyclohexyl)methyl)benzamide enhances staurosporine cytotoxic effects likely inhibiting the protective action of Magmas toward cell apoptosis

Zatelli, Maria Chiara,Gagliano, Teresa,Pelà, Michela,Bianco, Sara,Bertolasi, Valerio,Tagliati, Federico,Guerrini, Remo,Degli Uberti, Ettore,Salvadori, Severo,Trapella, Claudio

, p. 4606 - 4614 (2014)

We recently demonstrated that Magmas overexpression protects GH-secreting rat pitutitary adenoma cell lines from apoptosis by inhibiting cytochrome c release from mitochondria after treatment with staurosporine, strongly suggesting a role of Magmas in preventing apoptosis. The aim of this study was to produce a drug that, by inhibiting Tim16, may sensitize chemoresistant tumor cell to proapoptotic stimuli. We synthesized six compounds and challenged their sensitizing effects toward the proapoptotic effects of staurosporine in the TT cell line, derived from a human medullary thyroid carcinoma. We found that compound 5, devoid of the planarity in the aliphatic part of the lead 1, is not cytotoxic but enhances the proapoptotic effects of staurosporine by reducing MMP activation. Compound 5 may be useful for cancer treatment in association with chemotherapeutic drugs, possibly allowing a reduction of the chemotherapeutic agent effective dose.

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