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5-bromo-5'-phenyl-1,2',3,3'-tetrahydrospiro[2H-indole-3,2'-(1,3,4)-thiadiazole]-2-one is a complex organic compound characterized by its unique molecular structure. It is a derivative of spiro[2H-indole-3,2'-(1,3,4)-thiadiazole] with a bromine atom at the 5-position and a phenyl group at the 5'-position. 5-bromo-5'-phenyl-1,2',3,3'-tetrahydrospiro[2H-indole-3,2'-(1,3,4)-thiadiazole]-2-one exhibits a tetrahydro structure, which may contribute to its potential applications in various fields.

297180-15-5

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  • 5-bromo-5'-phenyl-1H,3'H-spiro[indole-3,2'-[1,3,4]thiadiazol]-2-one

    Cas No: 297180-15-5

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297180-15-5 Usage

Uses

Used in Pharmaceutical Industry:
5-bromo-5'-phenyl-1,2',3,3'-tetrahydrospiro[2H-indole-3,2'-(1,3,4)-thiadiazole]-2-one is used as a potential therapeutic agent for the treatment of various diseases. Its specific application reason is not provided in the materials, but its unique structure suggests that it may have properties that can be exploited for medicinal purposes.
Used in Chemical Research:
5-bromo-5'-phenyl-1,2',3,3'-tetrahydrospiro[2H-indole-3,2'-(1,3,4)-thiadiazole]-2-one can be used as a research compound in the field of organic chemistry. Its synthesis and properties can be studied to gain insights into the behavior of similar compounds and to develop new synthetic methods or applications.
Used in Material Science:
5-bromo-5'-phenyl-1,2',3,3'-tetrahydrospiro[2H-indole-3,2'-(1,3,4)-thiadiazole]-2-one may also find applications in the field of material science, particularly in the development of new materials with specific properties. Its unique structure could potentially be utilized to create materials with tailored characteristics for various applications.

References

1) Sandoval?et al.?(2010),?Identification and characterization of small compound inhibitors of human FATP2; Biochem. Pharmacol.?79?990 2) Ahowesso?et al.?(2015),?Chemical inhibition of fatty acid absorption and cellular uptake limits lipotoxic cell death; Biochem. Pharmacol.?98?167 3) Zhang?et al.?(2018),?Adipocyte-derived lipids mediate melanoma progression via FATP proteins; Cancer Discov.?8?1006 br />

Check Digit Verification of cas no

The CAS Registry Mumber 297180-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,8 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 297180-15:
(8*2)+(7*9)+(6*7)+(5*1)+(4*8)+(3*0)+(2*1)+(1*5)=165
165 % 10 = 5
So 297180-15-5 is a valid CAS Registry Number.

297180-15-5Downstream Products

297180-15-5Relevant articles and documents

Spiro indolone compound as well as, preparation, method and pharmaceutical composition and application thereof

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Paragraph 0158-0161; 0182-0185, (2020/01/11)

Spiro indolone compounds, a preparing method, a medicine composition and uses of the compounds are disclosed. In particular, the invention provide spiro indolone compounds shown as a formula I or II, a preparing method of the spiro indolone compounds and

Synthesis and biological evaluation of 5′-phenyl-3′H-spiro- [indoline-3,2′-[1,3,4]oxadiazol]-2-one analogs

Liu, Hua-Quan,Wang, De-Cai,Wu, Fei,Tang, Wei,Ouyang, Ping-Kai

, p. 929 - 933 (2013/09/24)

A series of 5′-phenyl-3′H-spiro[indoline-3,2′-[1,3,4] thiadiazol]-2-one analogs were synthesized and their Bcl-2 protein inhibitory activities were studied. The lead compound was originally identified using a fluorescence polarization-based competitive binding assay. Among the 10 compounds investigated, 1k showed good binding affinities to Bcl-xL and Mcl-1, with inhibition constants of 8.9 μmol/L and 3.4 μmol/L, respectively. While compound 1c achieved tight binding affinities to Bcl-xL (Ki = 0.16 μmol/L), has the potential to be a new lead compound.

Thiadiazole compounds and methods of use thereof

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Page/Page column 27, (2008/12/05)

The present invention relates to Thiadiazole Compounds; compositions comprising an effective dose of a Thiadiazole Compound; and methods treating or preventing a metalloproteinase-related disorder, such as, an arthritic disorder, osteoarthritis, cancer, r

5′-Phenyl-3′H-spiro[indoline-3,2′-[1,3,4]thiadiazol]-2-one inhibitors of ADAMTS-5 (Aggrecanase-2)

Bursavich, Matthew G.,Gilbert, Adam M.,Lombardi, Sabrina,Georgiadis, Katy E.,Reifenberg, Erica,Flannery, Carl R.,Morris, Elisabeth A.

, p. 5630 - 5633 (2008/03/14)

5′-Phenyl-3′H-spiro[indoline-3,2′-[1,3,4]thiadiazol]-2-one inhibitors of ADAMTS-5 (Aggrecanase-2) have been prepared via commercially available starting materials. Selected compounds 23, 33-35 show sub-micromolar ADAMTS-5 potency and strong SAR trends with selectivity over the related metalloproteases ADAMTS-4 (Aggrecanase-1), MMP12, and MMP13. This series of compounds represents progress toward a selective ADAMTS-5 inhibitor as a disease modifying osteoarthritis drug.

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