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4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid is a complex organic compound characterized by the presence of a dihydropyridine ring, a carboxylic acid group, and a 4-fluorophenyl substituent. 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid is recognized for its potential biological activity and versatile reactivity, making it a valuable building block in the synthesis of pharmaceutical drugs and other organic compounds. Its unique structural features position it as a promising candidate for use in medicinal chemistry and pharmaceutical development.

1174046-90-2

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1174046-90-2 Usage

Uses

Used in Pharmaceutical Synthesis:
4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its structural complexity and reactivity allow for the creation of a wide range of biologically active compounds, contributing to the development of new medications with improved efficacy and selectivity.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid serves as a valuable research tool. Its potential for biological activity and chemical modification make it an ideal candidate for studying the structure-activity relationships of various drug targets, aiding in the design and optimization of novel therapeutic agents.
Used in Drug Discovery:
4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid is utilized in drug discovery processes as a potential drug candidate. Its unique properties and reactivity may offer new avenues for the treatment of various diseases and conditions, providing a foundation for the development of innovative therapeutic strategies.
Used in Organic Chemistry:
Beyond its applications in the pharmaceutical industry, 4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid also finds use in organic chemistry. Its versatile reactivity allows for the synthesis of a variety of organic compounds, contributing to the advancement of chemical research and the development of new materials and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 1174046-90-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,0,4 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1174046-90:
(9*1)+(8*1)+(7*7)+(6*4)+(5*0)+(4*4)+(3*6)+(2*9)+(1*0)=142
142 % 10 = 2
So 1174046-90-2 is a valid CAS Registry Number.

1174046-90-2Downstream Products

1174046-90-2Relevant academic research and scientific papers

BIOMARKER-BASED THERAPEUTIC COMPOSITION

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, (2021/05/13)

The present invention provides an anticancer agent for treating a patient who is resistant to a protein kinase inhibitor, the anticancer agent comprising, as an active ingredient, a thienopyridine derivative compound or a pharmaceutically acceptable salt thereof. Here, the patient may be a patient carrying active RON. In addition, the patient may be a patient carrying normal KRAS. In addition, the anticancer agent may be applied to a patient who is resistant to an EGFR inhibitor. In particular, the anticancer agent may be usefully used to treat a patient who is resistant to the therapeutic agent cetuximab.

PYRAZOLO[3,4-b]PYRIDINE COMPOUNDS AS INHIBITORS OF TAM AND MET KINASES

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, (2020/03/23)

Provided herein are compounds of the Formula (I): and stereoisomers, tautomers and pharmaceutically acceptable salts thereof, wherein R1, R2, R9, X1 and G are as defined herein, which are inhibitors of one or more TAM kinases and/or c-Met kinase, and are useful in the treatment and prevention of diseases which can be treated with a TAM kinase inhibitor and/or a c-Met kinase inhibitor.

Aromatic ring dioxane quinazoline or quinoline compound, composition and application of aromatic ring dioxane quinazoline or quinoline compound

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, (2020/06/09)

The invention relates to a novel compound serving as an inhibitor of kinase such as TRK, c-MET, AXL, MER and/or VEGFR2, a composition and application of the novel compound. Specifically, the inventionprovides a compound (as shown in formula (1)) or an isomer, a solvate, a hydrate, a pharmaceutically acceptable salt and a prodrug thereof, and a pharmaceutical composition containing the compound, wherein the compound has the activity of strongly inhibiting kinase such as TRK, c-MET, AXL, MER and/or VEGFR2. The invention further discloses application of the compound or the pharmaceutical composition in preparation of a medicine. The medicine is used for treating autoimmune diseases or cancers.

THIENOPYRIDINE DERIVATIVES AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

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, (2019/10/15)

A thienopyridine derivative compound represented by Formula 1 or pharmaceutically acceptable salts thereof have an excellent inhibitory effect on protein kinase activity, and accordingly, pharmaceutical compositions comprising same can be usefully used for the prevention or treatment of a disease associated with the activity of a protein kinase.

THIENOPYRIDINE DERIVATIVES AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

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, (2019/10/29)

Since a thienopyridine derivative compound represented by chemical formula 1 or a pharmaceutically acceptable salt thereof of the present invention has an excellent effect of inhibiting protein kinase activity, a pharmaceutical composition comprising the same can be usefully used for preventing or treating diseases related to protein kinase activity.COPYRIGHT KIPO 2020

Protein kinase inhibitors comprising a pyrrolopyridazine derivative

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, (2016/10/07)

The present invention relates to a pyrrolopyridazine derivative represented by chemical formula 1, or a pharmaceutically acceptable salt of the same. A compound according to the present invention and a pharmaceutically acceptable salt of the same can be u

PROTEIN KINASE INHIBITOR CONTAINING PYRROLOPYRIDAZINE DERIVATIVE

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, (2016/08/17)

The present invention relates to a pyrrolopyridazine derivative represented by Formula 1 of the detailed description, or a pharmaceutically acceptable salt thereof. The compound according to the present invention and a pharmaceutically acceptable salt the

Protein kinase inhibitors comprising a pyrrolopyridazine derivative

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, (2016/11/21)

The present invention relates to a pyrrolopyridazine derivative represented by Formula 1 of the detailed description, or a pharmaceutically acceptable salt thereof. The compound according to the present invention and a pharmaceutically acceptable salt the

PYRIDONE AMIDES AND ANALOGS EXHIBITING ANTI-CANCER AND ANTI-PROLIFERATIVE ACTIVITIES

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, (2014/09/29)

Compounds useful in the treatment of mammalian cancers and especially human cancers according to Formula I are disclosed. Formula (I). Pharmaceutical compositions and methods of treatment employing the compounds disclosed herein are also disclosed.

PYRIDONE AMIDES AND ANALOGS EXHIBITING ANTI-CANCER AND ANTI-PROLIFERATIVE ACTIVITIES

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, (2013/06/06)

Compounds useful in the treatment of mammalian cancers and especially human cancers according to Formula I are disclosed. Pharmaceutical compositions and methods of treatment employing the compounds disclosed herein are also disclosed.

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