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3-(4-chlorophenyl)adamantane-1-carboxylic acid is a complex organic compound with the molecular formula C17H19ClO2. It is characterized by an adamantane core, which is a rigid, cage-like structure consisting of ten carbon atoms arranged in a fused cyclohexane pattern. One of the carbon atoms in this structure is substituted with a carboxylic acid group (-COOH), while another is connected to a 4-chlorophenyl group, which is a benzene ring with a chlorine atom at the 4th position. 3-(4-chlorophenyl)adamantane-1-carboxylic acid is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. Its unique structure and properties make it a valuable component in the development of new therapeutic agents.

56531-62-5

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56531-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56531-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,3 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56531-62:
(7*5)+(6*6)+(5*5)+(4*3)+(3*1)+(2*6)+(1*2)=125
125 % 10 = 5
So 56531-62-5 is a valid CAS Registry Number.

56531-62-5Relevant academic research and scientific papers

Discovery of Adamantane Carboxamides as Ebola Virus Cell Entry and Glycoprotein Inhibitors

Plewe, Michael B.,Sokolova, Nadezda V.,Gantla, Vidyasagar Reddy,Brown, Eric R.,Naik, Shibani,Fetsko, Alexandra,Lorimer, Donald D.,Lorimer, Donald D.,Dranow, David M.,Dranow, David M.,Smutney, Hayden,Smutney, Hayden,Bullen, Jameson,Bullen, Jameson,Sidhu, Rana,Sidhu, Rana,Master, Arshil,Master, Arshil,Wang, Junru,Wang, Junru,Kallel, E. Adam,Zhang, Lihong,Kalveram, Birte,Freiberg, Alexander N.,Henkel, Greg,McCormack, Ken

supporting information, p. 1160 - 1167 (2020/05/14)

We identified and explored the structure-activity-relationship (SAR) of an adamantane carboxamide chemical series of Ebola virus (EBOV) inhibitors. Selected analogs exhibited half-maximal inhibitory concentrations (EC50 values) of ~10-15 nM in vesicular s

ADAMANTANE DERIVATIVES FOR THE TREATMENT OF FILOVIRUS INFECTION

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Paragraph 0898-0899; 0902-0903, (2020/02/05)

Compounds of structural Formula I were developed for the treatment of infections by filoviruses including Ebolavirus and Marburgvirus, wherein, R1, R2, R3, X and Y are defined in the specification.

SPHINGOSINE KINASE INHIBITOR PRODRUGS

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Page/Page column 36-37, (2010/10/03)

The invention relates to prodrugs of hydroxyl-substituted adamantane compounds, pharmaceutical compositions thereof, and methods for inhibiting sphingosine kinase and for treating or preventing hyperproliferative disease, inflammatory disease, or angiogenic disease

SPHINGOSINE KINASE INHIBITORS

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Page/Page column 34-35, (2008/06/13)

The invention relates to substituted adamantane compounds, pharmaceutical compositions thereof, processes for their preparation, and methods for inhibiting sphingosine kinase and for treating or preventing hyperproliferative disease, inflammatory disease, or angiogenic disease.

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