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methyl 2-(7-chloro-5-methyl-2-phenylpyrazolo[1,5-a]pyrimidin-6-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1313377-99-9

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1313377-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1313377-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,3,7 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1313377-99:
(9*1)+(8*3)+(7*1)+(6*3)+(5*3)+(4*7)+(3*7)+(2*9)+(1*9)=149
149 % 10 = 9
So 1313377-99-9 is a valid CAS Registry Number.

1313377-99-9Relevant academic research and scientific papers

Discovery and Optimization of Novel Pyrazolopyrimidines as Potent and Orally Bioavailable Allosteric HIV-1 Integrase Inhibitors

Li, Guo,Meanwell, Nicholas A.,Krystal, Mark R.,Langley, David R.,Naidu, B. Narasimhulu,Sivaprakasam, Prasanna,Lewis, Hal,Kish, Kevin,Khan, Javed A.,Ng, Alicia,Trainor, George L.,Cianci, Christopher,Dicker, Ira B.,Walker, Michael A.,Lin, Zeyu,Protack, Tricia,Discotto, Linda,Jenkins, Susan,Gerritz, Samuel W.,Pendri, Annapurna

, p. 2620 - 2637 (2020/03/05)

The standard of care for HIV-1 infection, highly active antiretroviral therapy (HAART), combines two or more drugs from at least two classes. Even with the success of HAART, new drugs with novel mechanisms are needed to combat viral resistance, improve adherence, and mitigate toxicities. Active site inhibitors of HIV-1 integrase are clinically validated for the treatment of HIV-1 infection. Here we describe allosteric inhibitors of HIV-1 integrase that bind to the LEDGF/p75 interaction site and disrupt the structure of the integrase multimer that is required for the HIV-1 maturation. A series of pyrazolopyrimidine-based inhibitors was developed with a vector in the 2-position that was optimized by structure-guided compound design. This resulted in the discovery of pyrazolopyrimidine 3, which was optimized at the 2- and 7-positions to afford 26 and 29 as potent allosteric inhibitors of HIV-1 integrase that exhibited low nanomolar antiviral potency in cell culture and encouraging PK properties.

Inhibitors of Human Immunodeficiency Virus Replication

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Paragraph 0094, (2013/09/12)

The disclosure generally relates to compounds of formula I, including compositions and methods for treating human immunodeficiency virus (HIV) infection. The disclosure provides novel inhibitors of HIV, pharmaceutical compositions containing such compounds, and methods for using these compounds in the treatment of HIV infection.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 41-42, (2012/03/27)

The disclosure generally relates to compounds of formula (I), including compositions and methods for treating human immunodeficiency virus (HIV) infection. The disclosure provides novel inhibitors of HIV, pharmaceutical compositions containing such compounds, and methods for using these compounds in the treatment of HIV infection.

NOVEL ANTIVIRAL COMPOUNDS

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Page/Page column 40, (2013/02/27)

The present invention relates to compounds of formula (A) as defined herein having antiviral activity, more specifically HIV (Human Immunodeficiency Virus) replication inhibiting properties. The invention also relates to pharmaceutical compositions comprising an effective amount of such compounds as active ingredients. This invention further relates to the use of such compounds as medicines or in the manufacture of a medicament useful for the treatment of animals suffering from viral infections, in particular HIV infection. This invention further relates to methods for the treatment of viral infections in animals by the administration of a therapeutical amount of such compounds, optionally combined with one or more other drugs having antiviral activity.

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