14953-63-0 Usage
Class of organic compounds
nitroimidazoles 1-methyl-5-nitro-4-phenyl-1H-imidazole belongs to a group of compounds derived from imidazole with a nitro group attached at the 5-position.
Common use
antiprotozoal and antibacterial agent This compound is used to treat infections caused by various types of bacteria and parasites.
Specific infections treated
amebiasis, trichomoniasis, and giardiasis The compound is effective against these particular infections, which are caused by different parasites and bacteria.
Mechanism of action
disrupting the DNA of microorganisms and inhibiting their growth The compound works by interfering with the genetic material of the targeted pathogens, preventing them from multiplying and allowing the body to fight off the infection.
Potential side effects
possible side effects It is important to be aware that 1-methyl-5-nitro-4-phenyl-1H-imidazole can have potential side effects, and its use should be monitored by a healthcare professional.
Usage guidance
under the guidance of a healthcare professional To ensure safe and effective treatment, it is recommended that 1-methyl-5-nitro-4-phenyl-1H-imidazole be used under the supervision of a medical professional.
Check Digit Verification of cas no
The CAS Registry Mumber 14953-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14953-63:
(7*1)+(6*4)+(5*9)+(4*5)+(3*3)+(2*6)+(1*3)=120
120 % 10 = 0
So 14953-63-0 is a valid CAS Registry Number.
14953-63-0Relevant articles and documents
Nitrosoimidazoles: Highly Bactericidal Analogues of 5-Nitroimidazole Drugs
Ehlhardt, William J.,Beaulieu, Bernard B.,Goldman, Peter
, p. 323 - 329 (2007/10/02)
It is believed that metronidazole and related 5-nitroimidazoles are activated by reduction of the nitro group and that the active species has a nitrogen functionality of intermediate oxidation state.However, the preparation and isolation of the active for
