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{4-[3-(6,7-Dimethoxy-3,4-dihydro-1H-isoquinoline-2-carbonyl)-adamantan-1-yl]-phenoxy}-acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1192322-60-3

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1192322-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1192322-60-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,3,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1192322-60:
(9*1)+(8*1)+(7*9)+(6*2)+(5*3)+(4*2)+(3*2)+(2*6)+(1*0)=133
133 % 10 = 3
So 1192322-60-3 is a valid CAS Registry Number.

1192322-60-3Relevant academic research and scientific papers

Disubstituted adamantyl derivative or pharmaceutically acceptable salt thereof, and pharmaceutical composition and kit for inhibiting the growth of cancer containing the same as an active ingredient

-

, (2021/07/20)

The present invention relates to: a disubstituted adamantyl derivative or a pharmaceutically acceptable salt thereof, and an anticancer pharmaceutical composition and a kit containing same as an active ingredient. The disubstituted adamantyl derivative according to the present invention suppresses the growth of cancer cells by targeting mitochondria ETC complex I and damaging the metabolism of cancer cells, and thus can be useful as an anticancer pharmaceutical composition that is a powerful therapeutic agent for cancer dependent on oxidative phosphorylation for producing ATP.

A novel class of highly potent multidrug resistance reversal agents: Disubstituted adamantyl derivatives

Min, Kyung Hoon,Xia, Yan,Kim, Eun Kyung,Jin, Yinglan,Kaur, Navneet,Kim, Eun Seon,Kim, Dae Kyong,Jung, Hwa Young,Choi, Yongseok,Park, Mi-Kyung,Min, Yong Ki,Lee, Kiho,Lee, Kyeong

scheme or table, p. 5376 - 5379 (2010/05/19)

Novel disubstituted adamantyl derivatives were synthesized and evaluated in a P-glycoprotein dependent multidrug resistance cancer cell line. The hit to lead optimization provided potent MDR reversal agents. Some potent adamantyl derivatives were more than 10-fold more potent than verapamil without considerable intrinsic cytotoxicity. The 3-trifluorophenyl derivative 14f did not affect the metabolism of CYP450 3A4, whereas most of MDR revertants had a weak inhibitory effect.

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