61281-03-6 Usage
Description
[(1S,3Z,4aS,11R,11aR,12S,12aR)-3-(amino-hydroxy-methylidene)-4a,6,7,12-tetrahydroxy-11-methyl-2,4,5-trioxo-11,11a,12,12a-tetrahydro-1H-tetracen-1-yl]-dimethyl-azanium chloride is a complex tetrahydroxy tetracenomycin family molecule with a positively charged dimethylazanium ion and a chloride ion, making it a salt. It features a hydroxymethylidene group, an amino group, and multiple hydroxyl and carbonyl groups, which may suggest potential pharmaceutical or biological applications due to its ability to interact with biological systems.
Uses
Used in Pharmaceutical Industry:
[(1S,3Z,4aS,11R,11aR,12S,12aR)-3-(amino-hydroxy-methylidene)-4a,6,7,12-tetrahydroxy-11-methyl-2,4,5-trioxo-11,11a,12,12a-tetrahydro-1H-tetracen-1-yl]-dimethyl-azanium chloride is used as a potential pharmaceutical compound for its possible interactions with biological systems, which may lead to the development of new drugs or therapies.
Used in Biotechnology Industry:
In the biotechnology industry, [(1S,3Z,4aS,11R,11aR,12S,12aR)-3-(amino-hydroxy-methylidene)-4a,6,7,12-tetrahydroxy-11-methyl-2,4,5-trioxo-11,11a,12,12a-tetrahydro-1H-tetracen-1-yl]-dimethyl-azanium chloride could be utilized for the development of novel bioactive molecules or as a component in the creation of biosensors or other diagnostic tools, given its complex structure and potential for specific interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 61281-03-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,8 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61281-03:
(7*6)+(6*1)+(5*2)+(4*8)+(3*1)+(2*0)+(1*3)=96
96 % 10 = 6
So 61281-03-6 is a valid CAS Registry Number.
61281-03-6Relevant articles and documents
PENTACYCLINE DERIVATIVES FOR THE TREATMENT OF INFECTIONS
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, (2020/07/02)
The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The modular synthesis of tetracyclines and tetracycline analogs described provides an efficient and enantioselective route to a variety of tetracycline analogs and polycyclines previously inaccessible via earlier tetra-cycline syntheses and semi-synthetic methods. These analogs may be used as anti-microbial agents or anti-pro liferative agents in the treatment of diseases of humans or other animals.
SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF
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Page/Page column 117-118, (2008/06/13)
The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The modular synthesis of tetracyclines and tetracycline analogs described provides an efficient and enantioselective route to a variety of tetracycline analogs and polycyclines previously inaccessible via earlier tetracycline syntheses and semi-synthetic methods. These analogs may be used as anti-microbial agents or anti-proliferative agents in the treatment of diseases of humans or other animals.
