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2-cyclohex-1-enyl-4-isopropyl-phenylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

915006-03-0

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915006-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 915006-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,0,0 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 915006-03:
(8*9)+(7*1)+(6*5)+(5*0)+(4*0)+(3*6)+(2*0)+(1*3)=130
130 % 10 = 0
So 915006-03-0 is a valid CAS Registry Number.

915006-03-0Relevant academic research and scientific papers

A novel GPER antagonist protects against the formation of estrogen-induced cholesterol gallstones in female mice

Arnatt, Christopher K.,Arnett, Stacy,Cole, Aidan,DeLeon, Chelsea,Gunn, Joseph,Wang, David Q.-H.,Wang, Helen H.,Wilhelm, McKenna

, p. 767 - 777 (2020/06/01)

Many clinical studies and epidemiological investigations have clearly demonstrated that women are twice as likely to develop cholesterol gallstones as men, and oral contraceptives and other estrogen therapies dramatically increase that risk. Further, anim

COMPOUNDS AND METHODS TARGETING GPER FOR TREATMENT OF DISEASES ASSOCIATED WITH CALCIUM

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Page/Page column 65, (2019/11/19)

In one aspect, the present disclosure provides compounds of the formula (I): In other aspects, the present disclosure provides compositions and methods of targeting GPER for the treatment of cancers, such as breast cancers and leukemias, gallstone disease

COMPOUNDS AND METHODS TARGETING GPER IN CALCIUM DISORDERS

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Page/Page column 7; 57; 58, (2018/10/25)

The present disclosure provides compositions and method targeting GPER for the treatment of cancers, such as breast cancers and leukemias, gallstone disease, and for conferring of neuroprotection on a subject. Also disclosed are high throughput assays for identifying antagonists of GPER.

C-FMS KINASE INHIBITORS

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Page/Page column 57-58, (2008/06/13)

The invention is directed to compounds of Formula II: wherein A, R1, R2, R3, R4, X, Y and W are set forth in the specification, as well as solvates, hydrates, tautomers or pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase.

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