105970-04-5 Usage
Chemical compound
1-Mmofg is a chemical compound with a specific molecular structure.
Molar mass
The molar mass of 1-Mmofg is 312.13 g/mol, representing the mass of one mole of the compound.
Derivative of chloramphenicol
1-Mmofg is a derivative of the antibiotic chloramphenicol, meaning it has a similar chemical structure and properties.
Broad-spectrum antibiotic
1-Mmofg is used as a broad-spectrum antibiotic in veterinary medicine, effective against a wide range of bacteria.
Potent antibacterial activity
1-Mmofg exhibits potent antibacterial activity against both gram-positive and gram-negative bacteria.
Inhibition of protein synthesis
The mechanism of action of 1-Mmofg involves the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit.
Disruption of peptide bond formation
1-Mmofg disrupts the formation of peptide bonds, which are essential for the growth and replication of bacteria.
Control of bacterial infections
1-Mmofg is an important antibiotic agent with significant potential for controlling bacterial infections in veterinary practice.
Check Digit Verification of cas no
The CAS Registry Mumber 105970-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,7 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105970-04:
(8*1)+(7*0)+(6*5)+(5*9)+(4*7)+(3*0)+(2*0)+(1*4)=115
115 % 10 = 5
So 105970-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N5O3/c1-6-3-12(2,20-10(6)19)4-17-9(18)7-8(15-5-14-7)16-11(17)13/h5H,1,3-4H2,2H3,(H2,13,16)(H,14,15)
105970-04-5Relevant articles and documents
Antitumor Agents. 86. Synthesis and Cytotoxicity of α-Methylene-γ-lactone-Bearing Purines
Lee, Kuo-Hsiung,Rice, Gregory K.,Hall, Iris H.,Amarnath, Venkataraman
, p. 586 - 588 (2007/10/02)
α-Methylene-γ-lactones covalently linked to adenine (3), hypoxantine (4), and guanine (5) were synthesized by using the convenient Reformatsky-type reaction between ethyl α-(bromomethyl)acrylate and the proper purine ketones.In vitro cytotoxicity data demonstrated that these compounds were active against L-1210 tissue culture cells with 3 being most potent (ED50 = 0.3 μg/mL).
