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Details

Stereochemistry EPIMERIC
Molecular Formula C43H58N4O12.C8H15O2.Na
Molecular Weight 989.1335
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 10
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of RIFAMPIN SODIUM ETHYLHEXANOATE

SMILES

[Na+].CCCCC(CC)C([O-])=O.CO[C@H]1\C=C\O[C@@]2(C)OC3=C(C2=O)C4=C(O)C(\C=N\N5CCN(C)CC5)=C(NC(=O)C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)C(O)=C4C(O)=C3C

InChI

InChIKey=FDVPAXCAGKNCPH-OIXVRUHCSA-M
InChI=1S/C43H58N4O12.C8H16O2.Na/c1-21-12-11-13-22(2)42(55)45-33-28(20-44-47-17-15-46(9)16-18-47)37(52)30-31(38(33)53)36(51)26(6)40-32(30)41(54)43(8,59-40)57-19-14-29(56-10)23(3)39(58-27(7)48)25(5)35(50)24(4)34(21)49;1-3-5-6-7(4-2)8(9)10;/h11-14,19-21,23-25,29,34-35,39,49-53H,15-18H2,1-10H3,(H,45,55);7H,3-6H2,1-2H3,(H,9,10);/q;;+1/p-1/b12-11+,19-14+,22-13-,44-20+;;/t21-,23+,24+,25+,29-,34-,35+,39+,43-;;/m0../s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including: http://www.rxlist.com/rifadin-drug.htm http://www.wikidoc.org/index.php/Rifampin_(oral)

Rifampin is an antibiotic that inhibits DNA-dependent RNA polymerase activity in susceptible cells. Specifically, it interacts with bacterial RNA polymerase but does not inhibit the mammalian enzyme. It is bactericidal and has a very broad spectrum of activity against most gram-positive and gram-negative organisms (including Pseudomonas aeruginosa) and specifically Mycobacterium tuberculosis. It is FDA approved for the treatment of tuberculosis, meningococcal carrier state. Healthy subjects who received rifampin 600 mg once daily concomitantly with saquinavir 1000 mg/ritonavir 100 mg twice daily (ritonavir-boosted saquinavir) developed severe hepatocellular toxicity. Rifampin has been reported to substantially decrease the plasma concentrations of the following antiviral drugs: atazanavir, darunavir, fosamprenavir, saquinavir, and tipranavir. These antiviral drugs must not be co-administered with rifampin. Common adverse reactions include heartburn, epigastric distress, anorexia, nausea, vomiting, jaundice, flatulence, cramps.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P0A8V2
Gene ID: 948488.0
Gene Symbol: rpoB
Target Organism: Escherichia coli (strain K12)
18.5 µM [Ki]
30.2 µM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
RIFADIN

Approved Use

In the treatment of both tuberculosis and the meningococcal carrier state, the small number of resistant cells present within large populations of susceptible cells can rapidly become the predominant type. Bacteriologic cultures should be obtained before the start of therapy to confirm the susceptibility of the organism to rifampin and they should be repeated throughout therapy to monitor the response to treatment. Since resistance can emerge rapidly, susceptibility tests should be performed in the event of persistent positive cultures during the course of treatment. If test results show resistance to rifampin and the patient is not responding to therapy, the drug regimen should be modified. Tuberculosis Rifampin is indicated in the treatment of all forms of tuberculosis. A three-drug regimen consisting of rifampin, isoniazid, and pyrazinamide (e.g., RIFATER®) is recommended in the initial phase of short-course therapy which is usually continued for 2 months. The Advisory Council for the Elimination of Tuberculosis, the American Thoracic Society, and Centers for Disease Control and Prevention recommend that either streptomycin or ethambutol be added as a fourth drug in a regimen containing isoniazid (INH), rifampin, and pyrazinamide for initial treatment of tuberculosis unless the likelihood of INH resistance is very low. The need for a fourth drug should be reassessed when the results of susceptibility testing are known. If community rates of INH resistance are currently less than 4%, an initial treatment regimen with less than four drugs may be considered. Following the initial phase, treatment should be continued with rifampin and isoniazid (e.g., RIFAMATE®) for at least 4 months. Treatment should be continued for longer if the patient is still sputum or culture positive, if resistant organisms are present, or if the patient is HIV positive. RIFADIN IV is indicated for the initial treatment and retreatment of tuberculosis when the drug cannot be taken by mouth. Meningococcal Carriers Rifampin is indicated for the treatment of asymptomatic carriers of Neisseria meningitidis to eliminate meningococci from the nasopharynx. Rifampin is not indicated for the treatment of meningococcal infection because of the possibility of the rapid emergence of resistant organisms. (See WARNINGS.) Rifampin should not be used indiscriminately, and therefore, diagnostic laboratory procedures, including serotyping and susceptibility testing, should be performed for establishment of the carrier state and the correct treatment. So that the usefulness of rifampin in the treatment of asymptomatic meningococcal carriers is preserved, the drug should be used only when the risk of meningococcal disease is high. To reduce the development of drug-resistant bacteria and maintain the effectiveness of rifampin and other antibacterial drugs, rifampin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Launch Date

1971
Curative
RIFADIN

Approved Use

In the treatment of both tuberculosis and the meningococcal carrier state, the small number of resistant cells present within large populations of susceptible cells can rapidly become the predominant type. Bacteriologic cultures should be obtained before the start of therapy to confirm the susceptibility of the organism to rifampin and they should be repeated throughout therapy to monitor the response to treatment. Since resistance can emerge rapidly, susceptibility tests should be performed in the event of persistent positive cultures during the course of treatment. If test results show resistance to rifampin and the patient is not responding to therapy, the drug regimen should be modified. Tuberculosis Rifampin is indicated in the treatment of all forms of tuberculosis. A three-drug regimen consisting of rifampin, isoniazid, and pyrazinamide (e.g., RIFATER®) is recommended in the initial phase of short-course therapy which is usually continued for 2 months. The Advisory Council for the Elimination of Tuberculosis, the American Thoracic Society, and Centers for Disease Control and Prevention recommend that either streptomycin or ethambutol be added as a fourth drug in a regimen containing isoniazid (INH), rifampin, and pyrazinamide for initial treatment of tuberculosis unless the likelihood of INH resistance is very low. The need for a fourth drug should be reassessed when the results of susceptibility testing are known. If community rates of INH resistance are currently less than 4%, an initial treatment regimen with less than four drugs may be considered. Following the initial phase, treatment should be continued with rifampin and isoniazid (e.g., RIFAMATE®) for at least 4 months. Treatment should be continued for longer if the patient is still sputum or culture positive, if resistant organisms are present, or if the patient is HIV positive. RIFADIN IV is indicated for the initial treatment and retreatment of tuberculosis when the drug cannot be taken by mouth. Meningococcal Carriers Rifampin is indicated for the treatment of asymptomatic carriers of Neisseria meningitidis to eliminate meningococci from the nasopharynx. Rifampin is not indicated for the treatment of meningococcal infection because of the possibility of the rapid emergence of resistant organisms. (See WARNINGS.) Rifampin should not be used indiscriminately, and therefore, diagnostic laboratory procedures, including serotyping and susceptibility testing, should be performed for establishment of the carrier state and the correct treatment. So that the usefulness of rifampin in the treatment of asymptomatic meningococcal carriers is preserved, the drug should be used only when the risk of meningococcal disease is high. To reduce the development of drug-resistant bacteria and maintain the effectiveness of rifampin and other antibacterial drugs, rifampin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Launch Date

1971
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
21.6 mg/L
20 mg/kg 1 times / day steady-state, oral
dose: 20 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
25.1 mg/L
25 mg/kg 1 times / day steady-state, oral
dose: 25 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
33.1 mg/L
30 mg/kg 1 times / day steady-state, oral
dose: 30 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
35.2 mg/L
35 mg/kg 1 times / day steady-state, oral
dose: 35 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
7.4 mg/L
10 mg/kg 1 times / day steady-state, oral
dose: 10 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
3.3 mg/L
10 mg/kg 1 times / day steady-state, oral
dose: 10 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
6.3 mg/L
10 mg/kg 1 times / day steady-state, oral
dose: 10 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
325 μg × h/mL
600 mg single, oral
dose: 600 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIFAMPIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
113 mg × h/L
20 mg/kg 1 times / day steady-state, oral
dose: 20 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
135 mg × h/L
25 mg/kg 1 times / day steady-state, oral
dose: 25 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
190 mg × h/L
30 mg/kg 1 times / day steady-state, oral
dose: 30 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
235 mg × h/L
35 mg/kg 1 times / day steady-state, oral
dose: 35 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
26.3 mg × h/L
10 mg/kg 1 times / day steady-state, oral
dose: 10 mg/kg
route of administration: Oral
experiment type: STEADY-STATE
co-administered: ISONIAZID
RIFAMPIN serum
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
17.3 h
600 mg single, oral
dose: 600 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
25-DESACETYLRIFAMPIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
16.3 h
600 mg single, oral
dose: 600 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
RIFAMPIN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
60 g single, oral (total)
Overdose
Dose: 60 g
Route: oral
Route: single
Dose: 60 g
Sources:
unknown, 26 years
n = 1
Health Status: unknown
Age Group: 26 years
Sex: M
Population Size: 1
Sources:
Other AEs: Pruritus...
Other AEs:
Pruritus (grade 5, 1 patient)
Sources:
1200 mg 1 times / day multiple, oral
Highest studied dose
Dose: 1200 mg, 1 times / day
Route: oral
Route: multiple
Dose: 1200 mg, 1 times / day
Sources:
unhealthy, adult
n = 8
Health Status: unhealthy
Condition: rheumatoid arthritis
Age Group: adult
Population Size: 8
Sources:
1200 mg single, intravenous
Highest studied dose
Dose: 1200 mg
Route: intravenous
Route: single
Dose: 1200 mg
Sources:
unknown, adult
n = 18
Health Status: unknown
Age Group: adult
Sex: M
Population Size: 18
Sources:
AEs

AEs

AESignificanceDosePopulation
Pruritus grade 5, 1 patient
60 g single, oral (total)
Overdose
Dose: 60 g
Route: oral
Route: single
Dose: 60 g
Sources:
unknown, 26 years
n = 1
Health Status: unknown
Age Group: 26 years
Sex: M
Population Size: 1
Sources:
Overview

Overview

OverviewOther

Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no
no
no
no
no
yes [IC50 79.1 uM]
yes [Ki 18.5 uM]
yes [Ki 30.2 uM]
yes
yes
yes
yes
yes
yes (co-administration study)
Comment: induced levels of CYP1C19 apoprotein to 330% of control; coadministration with simvastatin: decrease exposure of simvastatin; coadministration with irinotecan: decrease irinotecan and active metabolite exposure; rifampicin reduced AUC of repaglinide by 57%;
Page: 12.0
yes
yes (co-administration study)
Comment: Coadministration of ertugliflozin with rifampin decreased ertugliflozin AUC0-∞ and Cmax by 39% and 15%, respectively
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
[Letter: Acute renal failure caused by rifampicin].
1975 Apr 19
[A new case of acute renal failure, with high hemolysis, after rifampicin (author's transl)].
1975 Nov-Dec
Acute renal failure after rifampicin: a case report and survey of the literature.
1976
[Tolerance of rifampicin in long-term treatment of patients with pulmonary tuberculosis].
1976 Feb
[Acute renal failure associated with rifampicin].
2000 Sep
Antibacterials for the prophylaxis and treatment of bacterial endocarditis in children.
2001
Rifampicin-induced erythema nodosum leprosum-like eruption in borderline lepromatous leprosy.
2001 Apr-Jun
Drug-induced acute interstitial nephritis.
2001 Aug
Postantibiotic effects of antituberculosis agents alone and in combination.
2001 Dec
Therapeutic efficacy of Poly(DL-lactide-Co-Glycolide)-encapsulated antitubercular drugs against Mycobacterium tuberculosis infection induced in mice.
2001 Jan
[Clinico-pathological features and possible pathogenesis of rifampicin-induced acute renal failure].
2001 Jun
Treatment of tuberculosis using a combination of sustained-release rifampin-loaded microspheres and oral dosing with isoniazid.
2001 Jun
CYP3A inductive potential of the rifamycins, rifabutin and rifampin, in the rabbit.
2001 May
[Acute renal insufficiency and interstitial nephritis caused by rifampicin. A comment on this subject].
2001 May-Jun
Acute renal failure caused by rifampicin re-exposure with 10-year of interval.
2001 Nov
Retrospective analysis of drug-induced urticaria and angioedema: a survey of 2287 patients.
2001 Nov
Antimycobacterial plant terpenoids.
2001 Nov
Bisphenol-A, an environmental estrogen, activates the human orphan nuclear receptor, steroid and xenobiotic receptor-mediated transcription.
2001 Oct
[Post-rifampicin acute renal failure--serious, but seldom recognized complication of the anti-tuberculosis treatment].
2001 Oct-Dec
Acute renal failure complicating rifampicin therapy.
2001 Sep
Optic neuropathy after treatment with anti-tuberculous drugs in a subject with Leber's hereditary optic neuropathy mutation.
2001 Sep
The drug efflux pump MRP2: regulation of expression in physiopathological situations and by endogenous and exogenous compounds.
2002
Bactericidal activities of commonly used antiseptics against multidrug-resistant mycobacterium tuberculosis.
2002
Limitations in the use of rifampicin-gelatin grafts against virulent organisms.
2002 Apr
Simple fibroblast-based assay for screening of new antimicrobial drugs against Mycobacterium tuberculosis.
2002 Aug
Receptor-dependent regulation of the CYP3A4 gene.
2002 Dec 27
In vitro activity of 11 antimicrobial agents, including gatifloxacin and GAR936, tested against clinical isolates of Mycobacterium marinum.
2002 Feb
Rifampicin inhibits CD95-mediated apoptosis of Jurkat T cells via glucocorticoid receptors by modifying the expression of molecules regulating apoptosis.
2002 Jan
Rapidly progressive glomerulonephritis due to rifampicin therapy.
2002 Jan
Induction of multidrug resistance-1 and cytochrome P450 mRNAs in human mononuclear cells by rifampin.
2002 Jan
[Specific features of acute renal failure in patients treated with rifampicin].
2002 Jan-Mar
Functional analysis of the rat bile salt export pump gene promoter.
2002 Jul
CYP3A4 induction by drugs: correlation between a pregnane X receptor reporter gene assay and CYP3A4 expression in human hepatocytes.
2002 Jul
Diffuse glomerulonephritis associated with rifampicin treatment for tuberculosis.
2002 Jun
Paraquat detoxicative system in the mouse liver postmitochondrial fraction.
2002 Jun 1
Evaluation of gene induction of drug-metabolizing enzymes and transporters in primary culture of human hepatocytes using high-sensitivity real-time reverse transcription PCR.
2002 May
Death associated with rifampin and pyrazinamide 2-month treatment of latent mycobacterium tuberculosis.
2002 May
3-[4'-bromo-(1,1'-biphenyl)-4-yl]-N, N-dimethyl-3-(2-thienyl)-2-propen-1-amine: synthesis, cytotoxicity, and leishmanicidal, trypanocidal and antimycobacterial activities.
2002 Nov
PXR-dependent induction of human CYP3A4 gene expression by organochlorine pesticides.
2002 Nov 15
Acute renal failure due to rifampicin: a study of 25 patients.
2002 Oct
A cell-based reporter gene assay for determining induction of CYP3A4 in a high-volume system.
2002 Oct
Induction of CYP3As in HepG2 cells by several drugs. Association between induction of CYP3A4 and expression of glucocorticoid receptor.
2003 Apr
Synergic activity of fluoroquinolones and linezolid against Mycobacterium tuberculosis.
2003 Apr
Comparative effects of thiazolidinediones on in vitro P450 enzyme induction and inhibition.
2003 Apr
A novel distal enhancer module regulated by pregnane X receptor/constitutive androstane receptor is essential for the maximal induction of CYP2B6 gene expression.
2003 Apr 18
Molecular basis of rifampicin-induced inhibition of anti-CD95-induced apoptosis of peripheral blood T lymphocytes: the role of CD95 ligand and FLIPs.
2003 Jan
Activities of moxifloxacin alone and in combination with other antimicrobial agents against multidrug-resistant Mycobacterium tuberculosis infection in BALB/c mice.
2003 Jan
Induction of cytochrome P450 enzymes in cultured precision-cut human liver slices.
2003 Mar
Glucocorticoid receptor enhancement of pregnane X receptor-mediated CYP2B6 regulation in primary human hepatocytes.
2003 May
Regulation of CYP3A4 expression in human hepatocytes by pharmaceuticals and natural products.
2003 May
Patents

Sample Use Guides

Tuberculosis: 10 mg/kg, in a single daily administration, not to exceed 600 mg/day, oral or intravenous. It is recommended that oral rifampin be administered once daily, either 1 hour before or 2 hours after a meal with a full glass of water. Meningococcal Carriers: it is recommended that 600 mg rifampin be administered twice daily for two days.
Route of Administration: Other
By the absolute concentration method, the MIC50 and MIC90 of rifampicin were 0.5-1 mg/L
Name Type Language
RIFAMPIN SODIUM ETHYLHEXANOATE
Common Name English
RIFAMPICIN SODIUM ETHYLHEXANOATE
Common Name English
Rifamycin sodium ethylhexanoate [WHO-DD]
Common Name English
RIFAMYCIN, 3-(((4-METHYL-1-PIPERAZINYL)IMINO)METHYL)-, MONOSODIUM SALT, MONO(2-ETHYLHEXANOATE) (SALT)
Systematic Name English
Code System Code Type Description
PUBCHEM
86278253
Created by admin on Sat Dec 16 08:06:11 GMT 2023 , Edited by admin on Sat Dec 16 08:06:11 GMT 2023
PRIMARY
EVMPD
SUB04247MIG
Created by admin on Sat Dec 16 08:06:11 GMT 2023 , Edited by admin on Sat Dec 16 08:06:11 GMT 2023
PRIMARY
CAS
67612-55-9
Created by admin on Sat Dec 16 08:06:11 GMT 2023 , Edited by admin on Sat Dec 16 08:06:11 GMT 2023
PRIMARY
FDA UNII
A9H22WY749
Created by admin on Sat Dec 16 08:06:11 GMT 2023 , Edited by admin on Sat Dec 16 08:06:11 GMT 2023
PRIMARY