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N-biotinyl-4-aminobenzoic acid is a chemical compound that serves as a biotinylated derivative of 4-aminobenzoic acid. It is widely used in various applications, including molecular biology and biochemistry, due to its ability to form stable covalent bonds with proteins and other molecules. N-biotinyl-4-aminobenzoic acid is particularly valuable for labeling and detection purposes, as it can be easily conjugated to antibodies or other biomolecules, allowing for the tracking and identification of specific targets within complex biological systems. The biotin group in the molecule provides a high-affinity binding site for the protein streptavidin, which is commonly used in assays and other diagnostic tools. N-biotinyl-4-aminobenzoic acid is also employed in the synthesis of biotinylated compounds for various research and commercial applications, such as in drug development and the creation of biosensors.

3672-04-6

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3672-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3672-04-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3672-04:
(6*3)+(5*6)+(4*7)+(3*2)+(2*0)+(1*4)=86
86 % 10 = 6
So 3672-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H21N3O4S/c21-14(18-11-7-5-10(6-8-11)16(22)23)4-2-1-3-13-15-12(9-25-13)19-17(24)20-15/h5-8,12-13,15H,1-4,9H2,(H,18,21)(H,22,23)(H2,19,20,24)/t12-,13-,15-/m0/s1

3672-04-6Downstream Products

3672-04-6Relevant academic research and scientific papers

Synthesis and in?vitro anticancer activities of biotinylated derivatives of glaucocalyxin A and oridonin

Huang, Xiao-Lei,Chen, Jing-Lei,Li, Xian-Lun,Zhao, Lei,Cui, Ya-Dong,Liu, Jiang-Yun,Morris-Natschke, Susan L.,Masuo, Goto,Cheng, Yung-Yi,Lee, Kuo-Hsiung,Chen, Dao-Feng,Zhang, Jian

, p. 703 - 711 (2020/06/03)

Fourteen glaucocalyxin A biotinylated derivatives, one glaucocalyxin C biotinylated derivative, and two oridonin biotinylated derivatives were designed and synthesized. Their structures were confirmed from 1H NMR, 13C NMR and HRMS data. The derivatives were evaluated for cytotoxic activities against lung (A549), cervical cancer cell line HeLa derivative (KB), multidrug-resistant KB subline (KB-VIN), triple-negative breast (MDA-MB-231), and estrogen receptor-positive breast (MCF-7) cancer cell lines. (Figure presented.).

CHEMOENZYMATIC SYNTHESIS OF HEPARIN AND HEPARAN SULFATE ANALOGS

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Paragraph 0400; 0401; 0408; 0409, (2014/09/03)

The present invention provides a one-pot multi-enzyme method for preparing UDP-sugars from simple sugar starting materials. The invention also provides a one-pot multi-enzyme method for preparing oligosaccharides from simple sugar starting materials.

Design and synthesis of ATP-based nucleotide analogues and profiling of nucleotide-binding proteins

Wolters, Justina C.,Roelfes, Gerard,Poolman, Bert

experimental part, p. 1345 - 1353 (2012/06/16)

Two nucleotide-based probes were designed and synthesized in order to enrich samples for specific classes of proteins by affinity-based protein profiling. We focused on the profiling of adenine nucleotide-binding proteins. Two properties were considered in the design of the probes: the bait needs to bind adenine nucleotide-binding proteins with high affinity and carry a second functional group suitable and easily accessible for coupling to a chromatography resin. For this purpose, we synthesized p-biotinyl amidobenzoic acid-ATP (p-BABA-ATP) and p-biotinyl aminomethylbenzoic acid-ATP (p-BAMBA-ATP). p-BABA-ATP and p-BAMBA-ATP both bind to ATP-binding cassette (ABC) proteins with at least 10-fold higher affinity than ATP. Several ABC transporters could be enriched using p-BABA-ATP or p-BAMBA-ATP.

Synthesis of chemiluminescent biotinyl naphtho[1,8-de][1,2]diazepine-1,4- diones

Krishna Murthy,Ram Reddy

, p. 2512 - 2522 (2007/10/03)

A new chemiluminescent seven numbered cyclic peri hydrazide, 6-amino-2,3-dihydronaphtho[1,8-de][1,2]diazepine-1,4-dione (AH, 4), and five of its biotin conjugates with various spacer groups are synthesized. The total framework of the chemiluminescent biot

Artificial metalloenzymes: (Strept)avidin as host for enantioselective hydrogenation by achiral biotinylated rhodium-diphosphine complexes

Skander, Myriem,Humbert, Nicolas,Collot, Jerome,Gradinaru, Julieta,Klein, Gerard,Loosli, Andreas,Sauser, Jerome,Zocchi, Andrea,Gilardoni, Francois,Ward, Thomas R.

, p. 14411 - 14418 (2007/10/03)

We report on the generation of artificial metalloenzymes based on the noncovalent incorporation of biotinylated rhodium-diphosphine complexes in (strept)avidin as host proteins. A chemogenetic optimization procedure allows one to optimize the enantioselectivity for the reduction of acetamidoacrylic acid (up to 96% ee (R) in streptavidin S112G and up to 80% ee (S) in WT avidin). The association constant between a prototypical cationic biotinylated rhodium-diphosphine catalyst precursor and the host proteins was determined at neutral pH: log Ka = 7.7 for avidin (pl = 10.4) and log Ka = 7.1 for streptavidin (pl = 6.4). It is shown that the optimal operating conditions for the enantioselective reduction are 5 bar at 30 °C with a 1% catalyst loading.

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