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Rifapentine

Rifapentine Structure
CAS No.
61379-65-5
Chemical Name:
Rifapentine
Synonyms
ktc1;dl473;r-773;mdl473;Priftin;Prifitin;Rifapenti;Rifapentin;PIFAPENTINE;RIFAPENTINE
CBNumber:
CB6381080
Molecular Formula:
C47H64N4O12
Molecular Weight:
877.03
MOL File:
61379-65-5.mol
Modify Date:
2024/4/24 17:21:45

Rifapentine Properties

Melting point 179-1800C
Boiling point 969.3±65.0 °C(Predicted)
Density 1.35±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility methanol: soluble2mg/mL, clear, red to red-brown
form powder
pka 4.81±0.70(Predicted)
color Red

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26
WGK Germany  3
RTECS  JQ0902000
HS Code  2941.90.3000
Toxicity LD50 in mice (mg/kg): >2000 orally; 750 i.p. (Cricchio); LD50 in mice (mg/kg): 3300 orally; 710 i.p. (Aroli)
NFPA 704
0
2 0

Rifapentine price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) R0533 Rifapentine 61379-65-5 25MG ₹23262.93 2022-06-14 Buy
Sigma-Aldrich(India) R0533 Rifapentine 61379-65-5 100MG ₹72094.5 2022-06-14 Buy
TCI Chemicals (India) R0198 Rifapentine 61379-65-5 100MG ₹4800 2022-05-26 Buy
TCI Chemicals (India) R0198 Rifapentine 61379-65-5 500MG ₹14800 2022-05-26 Buy
ottokemi R 4788 Rifapentine, ≥98% (HPLC) 61379-65-5 100mg ₹4779 2022-05-26 Buy
Product number Packaging Price Buy
R0533 25MG ₹23262.93 Buy
R0533 100MG ₹72094.5 Buy
R0198 100MG ₹4800 Buy
R0198 500MG ₹14800 Buy
R 4788 100mg ₹4779 Buy

Rifapentine Chemical Properties,Uses,Production

Description

Rifapentine is a broad spectrum antibiotic highly active against Gram-positive bacteria and Neisseria gonorrhoea. It is reported to be 10 times more active than the structurally related rifampicin against Mycobacrerim fuberculosis. Unlike rifampicin the bioavailability of rifapentine is significantly increased when administered after a meal.

Chemical Properties

Crystalline Solid

Uses

Semi-synthetic rifamycin. Antibacterial (tuberculostatic)

Indications

Rifapentine is an analogue of rifampin that is active against M. tuberculosis and M. avium. Rifapentine’s mechanism of action, cross-resistance, hepatic induction of P450 enzymes, drug interactions, and toxic profile are similar to those of rifampin. It has been used in the treatment of tuberculosis caused by rifampinsusceptible strains.

Antimicrobial activity

Activity is similar to that of rifampicin, but it is more active against atypical mycobacteria, especially the M. avium complex (MIC <0.06–0.5 mg/L). It has good activity on staphylococci and streptococci (MIC 0.01–0.5 mg/L), L. monocytogenes and Brucella spp.; less against Enterococcus faecalis (MIC 1–4 mg/L). Bacteroides spp. are inhibited by 0.5–2 mg/L. Gram-negative cocci are susceptible and, although some Gram-negative bacilli are inhibited by 4–32 mg/L, most are resistant.

Hazard

Moderately toxic by ingestion.

Pharmaceutical Applications

An analog of rifampicin in which a cyclopentyl group is substituted for a methyl group on the piperazine ring. It is available for oral administration.

Mechanism of action

Because relapse and the emergence of resistant strains of bacteria are associated with poor patient compliance, reduced dosing is expected to increase compliance. Initial clinical studies actually showed that the relapse rates in patients treated with rifapentine (10%) were higher than those in the patients treated with RIF (5%). It was found that poor compliance with the nonrifamycin antituberculin agents was responsible for the increased relapse.

Pharmacokinetics

Oral absorption:c. 70%
Cmax600 mg oral :12 mg/L after 5 h
Plasma half-life:13 h
Volume of distribution:1.5 L/kg
Plasma protein binding:97%
absorption
The absolute oral bioavailability of rifapentine has not been determined. The relative bioavailability of capsules (with an oral solution as reference) is 70%. Food increases absorption: a 600 mg dose taken after a meal gives Cmax and AUC values 44% higher than under fasting conditions. The extended halflife provides therapeutic concentrations for at least 72 h after administration, allowing less frequent dosing.
Distribution
Animal data suggest that it is well distributed in the body, with tissue concentrations exceeding the plasma concentration, except in bone, testes and brain. The ratio of intracellular:extracellular concentration in macrophages was estimated as 24:1.
Metabolism
The main metabolite is an antimicrobially active 25-desacetyl derivative. Although it induces liver cytochromes it is not an inducer of its own metabolism, which is mediated by an esterase. The peak concentration of 25-desacetyl rifapentine is about one-third of that of the unchanged drug, and is attained after about 11 h.
excretion
The main route of elimination is through the bile. In healthy volunteers about 70% of a 600 mg dose of 14C rifapentine was recovered in the feces, and less than 17% in the urine. There is evidence of enterohepatic recycling in humans.

Clinical Use

Tuberculosis (in combination with other antituberculosis drugs)

Side effects

Signs of teratogenic effects and fetal toxicity have been observed when administered during pregnancy to rats and rabbits. Rifapentine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
The most common adverse effect observed in combinations with other antimycobacterial agents was hyperuricemia, most probably due to pyrazinamide. Effects likely to be due to rifapentine were neutropenia (3.7% of patients) and hepatitis (increased transaminases in 1.6% of patients).

Rifapentine Preparation Products And Raw materials

Global( 291)Suppliers
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AVD pharmaceuticals Pvt Ltd +919860835260 Pune, India 102 58 Inquiry
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Rxn Chemicals Pvt Ltd +91 (80) 5535-9566 New Delhi, India 88 0 Inquiry
Euroasia Trans Continental +91 22 56349035-36 New Delhi, India 519 47 Inquiry

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rifamycinaf/acpp 3{[(4-cyclopentyl-1-piperazinyl)imino]methyl}rifamycin Rifapentine(Priftin) PIFAPENTINE antibioticdl473it dl473 ktc1 mdl473 r-773 3-(((4-cyclopentyl-1-piperazinyl)imino)methyl)-rifamyci 3-(4-cyclopentyl-1-piperazinyl)iminomethylrifamycinsv RIFAPENTINE Rifapention 3 & 4-NONENES & 4-NONANOL Cyclopentylrifampicin Prifitin Priftin Rifapenti 3-[[(4-Cy-dopentyl-1piperazinyl)imino]methyl]rifamycin Rifapentin Rifamycin, 3-(((4-cyclopentyl-1-piperazinyl)imino)methyl) 3-[(4-Cyclopentylpiperazino)iminomethyl]rifamycin Rifapentinum Rifapentina (2S,12Z,14E,16S,17S,18R,19R,20R,21S,22R,23S,24E)-3-(((4-Cyclopentyl-1-piperazinyl)imino)methyl)-21-(Acetyloxy)-5,6,9,17,19-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-2,7-(epoxypentadeca[1,11,13]trienimino)naphtho[2,1-b]furan-1,11(2H)-dione Rifapentine USP/EP/BP Rifapentine (DL 473) Rifapentine, ≥98% (HPLC) 61379-65-5 6167-65-5 C47H64N4O12 API Priftin Antibiotics Chiral Reagents Active Pharmaceutical Ingredients Rifapentine Intermediates & Fine Chemicals Pharmaceuticals 61379-65-5