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2-(2-nitro-fluoren-9-ylidenemethyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

906440-37-7

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906440-37-7 Usage

Uses

SMBA 1 is a small molecule Bax agonist.

Check Digit Verification of cas no

The CAS Registry Mumber 906440-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,4,4 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 906440-37:
(8*9)+(7*0)+(6*6)+(5*4)+(4*4)+(3*0)+(2*3)+(1*7)=157
157 % 10 = 7
So 906440-37-7 is a valid CAS Registry Number.

906440-37-7 Well-known Company Product Price

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  • Sigma

  • (SML1464)  SMBA1  ≥98% (HPLC)

  • 906440-37-7

  • SML1464-5MG

  • 983.97CNY

  • Detail
  • Sigma

  • (SML1464)  SMBA1  ≥98% (HPLC)

  • 906440-37-7

  • SML1464-25MG

  • 3,970.98CNY

  • Detail

906440-37-7Relevant academic research and scientific papers

Modulation of Bax and mTOR for cancer therapeutics

Li, Rui,Ding, Chunyong,Zhang, Jun,Xie, Maohua,Park, Dongkyoo,Ding, Ye,Chen, Guo,Zhang, Guojing,Gilbert-Ross, Melissa,Zhou, Wei,Marcus, Adam I.,Sun, Shi-Yong,Chen, Zhuo G.,Sica, Gabriel L.,Ramalingam, Suresh S.,Magis, Andrew T.,Fu, Haian,Khuri, Fadlo R.,Curran, Walter J.,Owonikoko, Taofeek K.,Shin, Dong M.,Zhou, Jia,Deng, Xingming

, p. 3001 - 3012 (2017/06/20)

A rationale exists for pharmacologic manipulation of the serine (S)184 phosphorylation site of the proapoptotic Bcl2 family member Bax as an anticancer strategy. Here, we report the refinement of the Bax agonist SMBA1 to generate CYD-2-11, which has characteristics of a suitable clinical lead compound. CYD-2-11 targeted the structural pocket proximal to S184 in the C-terminal region of Bax, directly activating its proapoptotic activity by inducing a conformational change enabling formation of Bax homooligomers in mitochondrial membranes. In murine models of small-cell and non-small cell lung cancers, including patient-derived xenograft and the genetically engineered mutant KRAS-driven lung cancer models, CYD-2-11 suppressed malignant growth without evident significant toxicity to normal tissues. In lung cancer patients treated with mTOR inhibitor RAD001, we observed enhanced S184 Bax phosphorylation in lung cancer cells and tissues that inactivates the propaoptotic function of Bax, contributing to rapalog resistance. Combined treatment of CYD-2-11 and RAD001 in murine lung cancer models displayed strong synergistic activity and overcame rapalog resistance in vitro and in vivo. Taken together, our findings provide preclinical evidence for a pharmacologic combination of Bax activation and mTOR inhibition as a rational strategy to improve lung cancer treatment.

BAX AGONIST, COMPOSITIONS, AND METHODS RELATED THERETO

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Page/Page column 34, (2013/03/26)

The disclosure relates to BAX activators and therapeutic uses relates thereto. In certain embodiments, the disclosure relates to methods of treating or preventing cancer, such as lung cancer, comprising administering a therapeutically effective amount of a pharmaceutical composition comprising a compound disclosed herein or pharmaceutically acceptable salt to a subject in need thereof.

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