19387-91-8 Usage
Pharmacology and mechanism of action
Similar to metronidazole.
Indications
Infections caused by Entamoeba histolytica and Giardia lamblia. Tinidazole is more effective than metronidazole in the treatment of giardiasis.
Side effects
Different sources of media describe the Side effects of 19387-91-8 differently. You can refer to the following data:
1. Side effects are similar to but milder than those caused by metronidazole. Gastrointestinal disturbances like nausea, vomiting, anorexia and metallic taste are common. Headache, tiredness, furred tongue and itching may occur. Thrombophlebitis may occur at the site of intravenous infusion [1].
2. Tinidazole is generally well tolerated. Infrequent and transient effects include nausea, vomiting, diarrhea and a metallic taste. Disulfiram-like reactions may occur and rare neurological disturbances and transient leukopenia have been described. Rash, which may be severe, urticaria and angioneurotic edema can occur.
Contraindications
Tinidazole should not be taken together with alcohol.
Interactions
A disulfiram-like reaction might occur if tinidazole is taken together with alcohol.
Preparations
? Fasigyn? (Pfizer). Tablets 150 mg, 200 mg, 300 mg, 500 mg, 1 g. Oral suspension 200 mg per ml. Solution for injection 2 mg per ml.
? Tricolam? (Pfizer). Tablets 500 mg.
? Simplotan? (Pfizer). Tablets 1 g.
References
1. Sawyer PR, Brogden RN, Pinder RM, Speight TM, Avery GS (1976). Tinidazole: a review of its antiprotozoal activity and therapeutic efficacy. Drugs, 11, 424–440.
Chemical Properties
solid
Originator
Simplotan,Pfizer,W. Germany,1971
Uses
Different sources of media describe the Uses of 19387-91-8 differently. You can refer to the following data:
1. Antiprotozoal (Trichomonas, Giardia); antiamebic; antibacterial.
2. anticonvulsant
3. anti-ulcerative
4. For the treatment of trichomoniasis caused by T. vaginalis in both female and male patients. Also for the treatment of giardiasis caused by G. duodenalis in both adults and pediatric patients older than three years of age and for the treatment of intestin
Manufacturing Process
The preparation of ethylsulfonylethyl-p-toluenesulfonate is carried out in the
following manner: 69.0 grams (0.5 mol) ethylsulfonylethanol dissolved in 150
ml pyridine is cooled to 0°C with stirring and while maintaining the
temperature between 0° to 10°C, 95 grams (0.5 mol) p-toluenesulfonyl
chloride is added in portions over a 10 minute period. After this time, 250 ml
water is added slowly and the mixture extracted with chloroform, the organic
phase washed first with 2 N HCl, then with water, separated and dried. The
product which crystallizes on cooling is filtered and dried to give 77.5% yield
of this intermediate.
A mixture of 12.7 grams (0.1 mol) of 2-methyl-5-nitroimidazole and 58.4
grams (0.2 mol) ethylsulfonylethyl-p-toluenesulfonate is heated with stirring,
under nitrogen, at 145° to 150°C for about 4 hours. After this time, the
reaction mixture is extracted with 500 ml hot water, the aqueous portion
adjusted with 10% Na2CO3 to a pH of 9 and extracted with chloroform (3
times with 150 ml portions). The separated organic phase is washed with
water, dried with Na2SO4 and evaporated to dryness. The crude tinidazole
product is then crystallized from benzene to give 4.36 grams of product
having a MP of 127° to 128°C.
Therapeutic Function
1-[2-(Ethylsulfonyl)ethyl]-2-methyl-5-nitroimidazole
Antimicrobial activity
Its antibacterial and antiprotozoal activity is similar to that of metronidazole.The MIC against G. vaginalis is 0.2–2 mg/L; the hydroxy metabolite is significantly more active than that of metronidazole. H. pylori is inhibited by 0.5 mg/L. T. vaginalis and T. fetus at 2.5 mg/L and E. histolytica is inhibited by about 0.3–2.5 mg/L.
Pharmaceutical Applications
A 5-nitroimidazole available for oral administration and, in some countries, for intravenous infusion.
Mechanism of action
Tinidazole has a mechanism of action that parallels that of metronidazole as well
as a similar metabolic pathway leading to hydroxylation at the 2-methyl group catalyzed by
CYP3A4. Basically, tinidazole appears to mimic the actions of metronidazole, although there are
reports that it is effective against some protozoa which are resistant to metronidazole.
Pharmacokinetics
Oral absorption ：>95% Cmax 2 g oral：40 mg/L after 2 h 800 mg (30-min infusion)： 12 mg/L 6 min after end infusion Plasma half-life： 12–14 h Volume of distribution 0.64 L/kg ：Plasma protein binding 12%absorption and distribution After a 2 g oral dose, concentrations remain at c. 10 mg/L at 24 h and 2.5 mg/L at 48 h. Daily doses of 1 g maintain plasma levels in excess of 8 mg/L, irrespective of whether the dose is oral or intravenous. It is well distributed, with concentrations in bile, CSF, breast milk and saliva similar to those reached in plasma. The drug readily crosses the placenta. In women undergoing first trimester abortion, concentrations of 4.9 mg/kg (placenta) and 7.6 mg/kg (fetus) were found when the plasma concentration was 13.2 mg/L.Metabolism and excretion Metabolites include the 2-hydroxymethyl derivative, its glucuronide and two unidentified minor derivatives. In urine about half the drug remains unmetabolized.The parent drug and its metabolites are excreted primarily in the urine and to a minor extent in the feces. The clearance rate is about 0.73 mL/min per kg and the urinary excretion is about 21% of the dose. Total clearance of the drug is 51 mL/min, renal clearance 10 mL/min. In healthy volunteers given an?： intravenousinfusion of 800 mg [14C]tinidazole over 30 min, a mean of 44% of the dose was excreted in the urine during the first 24 h, increasing to 63% over 5 days： only 12% of the dose appeared in the feces. Unchanged tinidazole comprised 32% of urinary 14C in 0&ndash：12 h urine. The 2-hydroxymethyl metabolite accounted for about 9% of the urinary 14C and was also present in plasma.In renal failure the pharmacokinetics are not significantly different from those in healthy individuals. It is rapidly removed by hemodialysis and a normal dose should be given after each dialysis： if treatment precedes dialysis a half dose should be infused after the end of the procedure.
Clinical Use
Anaerobic bacterial infections(prophylaxis and treatment) Trichomoniasis Giardiasis (single dose) Amebiasis (including amebic liver abscess) Bacterial vaginosis Gastric colonization with H. pylori (in combination with other agents)
Synthesis
Tinidazole, 1-2-(ethylsulfonyl)ethyl-2-methyl-5-nitroimidazole (37.2.12), is
also made from 2-methyl-5-nitroimidazole (37.2.9), which upon being reacted with
2-ethoxysulfonyl-p-toluenesulfonate (37.2.11) transformed into the desired tinidazole.The 2-ethoxysulfonyl-p-toluenesulfonate (37.2.11) necessary for this reaction is in turn
made by tosylation of 2-ethylsulfonyl ethanol using p-toluenesulfonyl chloride.
Veterinary Drugs and Treatments
Little information is presently available on the use of tinidazole in
dogs, cats, or horses. It potentially could be useful for treating anaerobic
infections, particularly associated with dental infections in
small animals. Because of its antiprotozoal effects, it has been used
as an alternative for treating giardiasis in small animals, and it could
have efficacy against amebiasis, trichomoniasis or balantidiasis in
veterinary species, but documentation of efficacy is not available.
Tinidazole has a longer duration of action in dogs and cats than
does metronidazole.
In humans, oral tinidazole is FDA-approved for treating extraintestinal
and intestinal amebiasis, (Entamoeba histolytica), giardiasis
(Giardia duodenalis/lamblia), and trichomoniasis (T. vaginalis).
Drug interactions
Potentially hazardous interactions with other drugs
Alcohol: disulfiram-like reaction.
Metabolism
Tinidazole is excreted by the liver (up to 5%) and kidneys
as unchanged drug and metabolites. An active hydroxy
metabolite has been identified.
Check Digit Verification of cas no
The CAS Registry Mumber 19387-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,8 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19387-91:
(7*1)+(6*9)+(5*3)+(4*8)+(3*7)+(2*9)+(1*1)=148
148 % 10 = 8
So 19387-91-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H13N3O4S/c1-3-16(14,15)5-4-10-7(2)9-6-8(10)11(12)13/h6H,3-5H2,1-2H3
19387-91-8Relevant articles and documents
Preparation method of high-purity tinidazole
-
Paragraph 0021; 0022-0024; 0026-0027; 0028-0030; 0031-0032, (2020/10/04)
The invention discloses a synthetic preparation method of high-purity tinidazole, and belongs to the technical field of chemical pharmacy. The method includes: taking beta-hydroxyethyl sulfide and 2-methyl-5-nitroimidazole as the raw materials, using 4-methyl-2-pentanone as a solvent, conducting dehydration condensation under the action of concentrated sulfuric acid to obtain a condensation compound 2-methyl-1-(2-ethylthioethyl)-5-nitro-1H-imidazole, and then under the catalysis of sodium molybdate, performing oxidization to generate a tinidazole crude product; and decoloring and refining thecrude product with water to obtain a tinidazole finished product with purity of greater than or equal to 99.98%. Compared with the prior art, the raw materials are easy to obtain, reaction is simple,and operation is easy and convenient; meanwhile, the incompletely reacted 2-methyl-5-nitroimidazole and the recycled 4-methyl-2-pentanone can be directly applied mechanically, so that the production cost is effectively reduced, the reaction period is shortened, pollution is reduced, and the yield and the product quality are improved.
Selective Late-Stage Oxygenation of Sulfides with Ground-State Oxygen by Uranyl Photocatalysis
Li, Yiming,Rizvi, S. Aal-e-Ali,Hu, Deqing,Sun, Danwen,Gao, Anhui,Zhou, Yubo,Li, Jia,Jiang, Xuefeng
supporting information, p. 13499 - 13506 (2019/08/21)
Oxygenation is a fundamental transformation in synthesis. Herein, we describe the selective late-stage oxygenation of sulfur-containing complex molecules with ground-state oxygen under ambient conditions. The high oxidation potential of the active uranyl cation (UO22+) enabled the efficient synthesis of sulfones. The ligand-to-metal charge transfer process (LMCT) from O 2p to U 5f within the O=U=O group, which generates a UV center and an oxygen radical, is assumed to be affected by the solvent and additives, and can be tuned to promote selective sulfoxidation. This tunable strategy enabled the batch synthesis of 32 pharmaceuticals and analogues by late-stage oxygenation in an atom- and step-efficient manner.
External preparation for skin diseases containing nitroimidazole
-
, (2008/06/13)
An external preparation for skin disease which comprises a nitroimidazole derivative represented by the following formula (I): wherein R1, R3 and R4 may be the same or different and represent a hydrogen atom, a nitro group, a lower alkyl group, a substituted lower alkyl group, a lower alkenyl group, or a substituted lower alkenyl group; and R2 represents a hydrogen atom, a lower alkyl group, a substituted lower alkyl group and a lower alkenyl group or a substituted lower alkenyl group, provided that any one of R1, R3 and R4 is a nitro group.
