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2-([(4-BROMOPHENYL)SULFONYL]AMINO)ACETIC ACID, commonly known as BPSAA, is a synthetic compound that features an amino acid structure. It is composed of carbon, hydrogen, bromine, sulfur, nitrogen, and oxygen atoms, with the presence of functional groups such as phenyl, sulfonic, and carboxylic groups. The substantial presence of bromine in its structure imparts specific reactive properties, making it suitable for a variety of biochemical interactions and reactions. The exact physical properties of BPSAA, such as its melting point, boiling point, or specific gravity, can vary depending on the conditions and purity of the compound.

13029-73-7

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13029-73-7 Usage

Uses

Used in Scientific Research:
2-([(4-BROMOPHENYL)SULFONYL]AMINO)ACETIC ACID is used as a research chemical for various applications in the fields of chemistry and biochemistry. Its unique structure and reactivity make it a valuable tool for studying chemical reactions and interactions.
Used in Chemical Synthesis:
In the chemical industry, 2-([(4-BROMOPHENYL)SULFONYL]AMINO)ACETIC ACID is used as an intermediate or building block in the synthesis of more complex molecules. Its reactive bromine atom allows for further functionalization and the creation of new compounds with potential applications in various industries.
Used in Biochemical Studies:
2-([(4-BROMOPHENYL)SULFONYL]AMINO)ACETIC ACID is employed as a biochemical probe to investigate the mechanisms of enzymatic reactions and interactions with biological molecules. Its sulfonic and carboxylic groups facilitate binding to enzymes and other biomolecules, providing insights into their structure and function.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-([(4-BROMOPHENYL)SULFONYL]AMINO)ACETIC ACID is used as a potential lead compound for the development of new drugs. Its unique structure and reactivity may offer opportunities for the design of novel therapeutic agents with specific biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 13029-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13029-73:
(7*1)+(6*3)+(5*0)+(4*2)+(3*9)+(2*7)+(1*3)=77
77 % 10 = 7
So 13029-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrNO4S/c9-6-1-3-7(4-2-6)15(13,14)10-5-8(11)12/h1-4,10H,5H2,(H,11,12)/p-1

13029-73-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-bromophenyl)sulfonylamino]acetic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13029-73-7 SDS

13029-73-7Relevant academic research and scientific papers

Development of Piperazinediones as dual inhibitor for treatment of Alzheimer's disease

Kumar, Devendra,Gupta, Sukesh K.,Ganeshpurkar, Ankit,Gutti, Gopichand,Krishnamurthy, Sairam,Modi, Gyan,Singh, Sushil K.

, p. 87 - 101 (2018/03/13)

Novel multifunctional 3,6-Diphenyl-1,4-bis(phenylsulfonyl)piperazine-2,5-dione derivatives were designed and synthesized for the treatment of Alzheimer's disease (AD). The designed scaffold has blood brain barrier penetrating ability, acetylcholinesterase (AChE) and matrix metalloproteinase-2 (MMP-2) inhibition potential. Compounds 52 and 46 showed very significant inhibition against AChE, IC50 = 32.45 ± 0.044, 28.65 ± 0.029, BuChE, IC50 = 157.95 ± 0.264, 160.58 ± 0.082 and MMP-2, IC50 = 36.83 ± 0.015, 19.57 ± 0.005 (nM). In the enzyme kinetics study, lead molecule 46 showed non-competitive inhibition of AChE with Ki = 7 nM and competitive inhibition of MMP-2 with Ki = 20 nM. Compounds 52 and 46 inhibited AChE-induced Aβ aggregation at 20 μM. The compounds also exhibited in-vitro antioxidant potential in DPPH assay. Further, compound 46 was found to be a promising neuroprotective agent in MC65 cells. Lead molecule 46 significantly enhanced working memory in scopolamine induced amnesia animal model at dose of 5 mg/kg dose. The mitochondrial membrane potential was restored in animals when treated with compounds 52 and 46.

Potent arylsulfonamide inhibitors of tumor necrosis factor-α converting enzyme able to reduce activated leukocyte cell adhesion molecule shedding in cancer cell models

Nuti, Elisa,Casalini, Francesca,Avramova, Stanislava I.,Santamaria, Salvatore,Fabbi, Marina,Ferrini, Silvano,Marinelli, Luciana,La Pietra, Valeria,Limongelli, Vittorio,Novellino, Ettore,Cercignani, Giovanni,Orlandini, Elisabetta,Nencetti, Susanna,Rossello, Armando

supporting information; experimental part, p. 2622 - 2635 (2010/08/20)

Activated leukocyte cell adhesion molecule (ALCAM) plays a relevant role in tumor biology and progression. Our previous studies showed that ALCAM is expressed at the surface of epithelial ovarian cancer (EOC) cells and is released in a soluble form by ADAM-17-mediated shedding. This process is relevant to EOC cell motility and invasiveness, which is reduced by nonspecific inhibitors of ADAM-17. For this reason, ADAM-17 may represent a new useful target in anticancer therapy. Herein, we report the synthesis and biological evaluation of new ADAM-17 inhibitors containing an arylsulfonamidic scaffold. Among the new potential inhibitors, two very promising compounds 17 and 18 were discovered, with a nanomolar activity for ADAM-17 isolated enzyme. These compounds proved to be also the most potent in inhibiting soluble ALCAM release in cancer cells, showing a nanomolar activity on A2774 and SKOV3 cell lines

Acetylenic TACE inhibitors. Part 1. SAR of the acyclic sulfonamide hydroxamates

Levin,Chen,Cheung,Cole,Crago,Delos Santos,Du,Khafizova,MacEwan,Niu,Salaski,Zask,Cummons,Sung,Xu,Zhang,Xu,Ayral-Kaloustian,Jin,Cowling,Barone,Mohler,Black,Skotnicki

, p. 2799 - 2803 (2007/10/03)

The SAR of a series of potent sulfonamide hydroxamate TACE inhibitors, all bearing a butynyloxy P1′ group, was explored. In particular, compound 5j has excellent in vitro potency against isolated TACE enzyme and in cells, good selectivity over MMP-1 and MMP-9, and oral activity in an in vivo model of TNF-α production and a collagen-induced arthritis model.

Amino acids in the syntheses of heterocyclic systems: Syntheses and radiostability of novel biologically active triazoles containing the sulfonamide moiety

El-Sharief,Ghorab,El-Gaby,Mohamed,Ammar

, p. 316 - 323 (2007/10/03)

A number of novel triazoles 2a-f, 4, 9, 10, 12, 15; triazolothiadiazoles 6, 8, 11, 16; triazolothiadizine 5; and triazolotriazine 14 were synthesized and characterized by elemental analyses and spectral data. Six of the compounds showed antifungal activity compared with the fungicide Mycostatine. Radiosterilization of the biologically active compounds 4, 8, 9b, and 10 in the dry state may prove to be applicable at the sterile dose 25 kGy.

Protease inhibitors - Part 5. Alkyl/arylsulfonyl- and arylsulfonylureido-/arylureido- glycine hydroxamate inhibitors of Clostridium histolyticum collagenase

Scozzafava, Andrea,Supuran, Claudiu T.

, p. 299 - 307 (2007/10/03)

Reaction of alkyl/arylsulfonyl halides with glycine afforded a series of derivatives which were first N-benzylated by treatment with benzyl chloride, and then converted to the corresponding hydroxamic acids with hydroxylamine in the presence of carbodiimide derivatives. Other derivatives were obtained by reaction of N-benzyl-glycine with aryl isocyanates, arylsulfonyl isocyanates or benzoyl isothiocyanate, followed by conversion of their COOH group into the CONHOH moiety, as mentioned above. The 90 new compounds reported here were assayed as inhibitors of the Clostridium histolyticum collagenase (EC 3.4.24.3), a zinc enzyme which degrades triple helical regions of native collagen. The prepared hydroxamate derivatives were generally 100-500 times more active than the corresponding carboxylates. In the series of synthesized hydroxamates, substitution patterns leading to the best inhibitors were those involving perfluoroalkylsulfonyl- and substituted- arylsulfonyl moieties, such as pentafluorophenylsulfonyl, 3- and 4- carboxyphenylsulfonyl-, 3-trifluoromethyl-phenylsulfonyl or 1- and 2-naphthyl among others. Thus, it seems that similarly to the matrix metalloproteinase (MMP) hydroxamate inhibitors, Clostridium histolyticum collagenase inhibitors should incorporate hydrophobic moieties at the P1, and P2, sites, whereas the α-carbon substituent may be a small and compact moiety (such as H. for the Gly derivatives reported here). Such compounds might lead to the design of collagenase inhibitor-based drugs useful as anti-cancer, anti-arthritis or anti-bacterial agents for the treatment of corneal keratitis. (C) 2000 Editions scientifiques et medicales Elsevier SAS.

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