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[(3S)-4-Oxo-4-hydroxy-3-aminobutyl]dimethylsulfonium is a complex organic compound with the chemical formula C6H14NO3S. It is a chiral molecule, with the (3S) configuration indicating that the hydroxyl group is on the left side when looking at the molecule from the perspective of the carbon chain. [(3S)-4-Oxo-4-hydroxy-3-aminobutyl]dimethylsulfonium features a 4-oxo-4-hydroxy-3-aminobutyl group, which consists of a four-carbon chain with a carbonyl group (C=O), a hydroxyl group (-OH), and an amino group (-NH2). The dimethylsulfonium part of the molecule is a positively charged sulfonium ion, which is derived from dimethylsulfide (CH3SCH3) and has a formal charge of +1. [(3S)-4-Oxo-4-hydroxy-3-aminobutyl]dimethylsulfonium is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and other chemical products.

6708-35-6

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6708-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6708-35-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6708-35:
(6*6)+(5*7)+(4*0)+(3*8)+(2*3)+(1*5)=106
106 % 10 = 6
So 6708-35-6 is a valid CAS Registry Number.

6708-35-6Relevant academic research and scientific papers

Synthesis and delivery of a stable phosphorylated ubiquitin probe to study ubiquitin conjugation in mitophagy

Mann, Guy,Satish, Gandhesiri,Sulkshane, Prasad,Mandal, Shaswati,Glickman, Michael H.,Brik, Ashraf

supporting information, p. 9438 - 9441 (2021/09/22)

Protein post-translational modifications are involved in essentially all aspects of cellular signaling. Their dynamic nature and the difficulties in installing them using enzymatic approaches limits their direct study in human cells. Reported herein is the first synthesis, delivery and cellular study of a stable phosphoubiquitin probe. Our results compare Parkin's substrate preference during mitophagyviadirect visualization of a phosphorylated ubiquitin probe in the cellular environment.

In Vitro Reconstitution of Bacterial DMSP Biosynthesis

Liao, Cangsong,Seebeck, Florian P.

supporting information, p. 3553 - 3556 (2019/02/20)

Dimethylsulfoniopropionate (DMSP) is one of the most abundant sulfur metabolites in marine environments. The biosynthesis of DMSP and its degradation to dimethylsulfide are important links in the planetary sulfur cycle. Herein, the first complete description of a DMSP biosynthetic pathway is provided by the in vitro reconstitution of four enzymes from Streptomyces mobaraensis. The isolation of DMSP from S. mobaraensis cells grown at high salinity confirmed that this actinobacterium is indeed is a DMSP-producing organism. The described DMSP biosynthesis follows the same route as that previously described for angiosperm plants. Despite this chemical congruence, limited sequence similarity between plant and bacterial enzymes suggests that the two biosynthetic activities emerged by convergent evolution.

Synthesis and biological evaluation of novel curcuminoid derivatives

Cao, Ya-Kun,Li, Hui-Jing,Song, Zhi-Fang,Li, Yang,Huai, Qi-Yong

, p. 16349 - 16372 (2015/01/08)

Curcuminoids have been reported to possess multiple bioactivities, such as antioxidant, anticancer and anti-inflammatory properties. Three novel series of curcuminoid derivatives (11a-h, 15a-h and 19a-d) with enhanced bioactivity have been synthesized. Among the synthesized compounds, 11b exhibited the most significant activity with an MIC of 0.5 μ M /mL against selected medically important Gram-positive cocci (S aureus and S viridans) and Gram-negative bacilli (E. coli and E. cloacae). The derivatives exhibited remarkable results in an antioxidant test with an IC50 2.4- to 9.3-folder smaller than curcuminoids. With respect to antiproliferative activity against Hep-G2, LX-2, SMMC7221 and MDA-MB-231, the derivatives exhibited an effect stronger than curcuminoids with an IC50 ranging from 0.18 to 4.25 μ M.

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