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Chemistry

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Also known as: 269055-15-4, Intelence, Tmc-125, Tmc125, Etravirine (tmc125), Tmc 125
Molecular Formula
C20H15BrN6O
Molecular Weight
435.3  g/mol
InChI Key
PYGWGZALEOIKDF-UHFFFAOYSA-N
FDA UNII
0C50HW4FO1

Etravirine
Etravirine is a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor. Etravirine is designed to be active against HIV isolates with mutations that confer resistance to the two most commonly prescribed first-generation NNRTIs. It can bind the enzyme reverse transcriptase (RT) in multiple conformations, both for native and mutant RT, thereby blocking the enzymatic activity of RT.
Etravirine is a Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor. The mechanism of action of etravirine is as a Non-Nucleoside Reverse Transcriptase Inhibitor, and Cytochrome P450 3A Inducer, and Cytochrome P450 2C9 Inhibitor, and Cytochrome P450 2C19 Inhibitor, and P-Glycoprotein Inhibitor.
1 2D Structure

Etravirine

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
4-[6-amino-5-bromo-2-(4-cyanoanilino)pyrimidin-4-yl]oxy-3,5-dimethylbenzonitrile
2.1.2 InChI
InChI=1S/C20H15BrN6O/c1-11-7-14(10-23)8-12(2)17(11)28-19-16(21)18(24)26-20(27-19)25-15-5-3-13(9-22)4-6-15/h3-8H,1-2H3,(H3,24,25,26,27)
2.1.3 InChI Key
PYGWGZALEOIKDF-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CC1=CC(=CC(=C1OC2=NC(=NC(=C2Br)N)NC3=CC=C(C=C3)C#N)C)C#N
2.2 Other Identifiers
2.2.1 UNII
0C50HW4FO1
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 4-((6-amino-5-bromo-2-((4-cyanophenyl)amino)-4-pyrimidinyl)oxy)-3,5-dimethyl-benzonitrile

2. Benzonitrile, 4-((6-amino-5-bromo-2-((4-cyanophenyl)amino)-4-pyrimidinyl)oxy)-3,5-dimethyl-

3. Intelence

4. R165335

5. Tmc 125

6. Tmc-125

7. Tmc125 Cpd

2.3.2 Depositor-Supplied Synonyms

1. 269055-15-4

2. Intelence

3. Tmc-125

4. Tmc125

5. Etravirine (tmc125)

6. Tmc 125

7. R165335

8. R-165335

9. 4-((6-amino-5-bromo-2-((4-cyanophenyl)amino)pyrimidin-4-yl)oxy)-3,5-dimethylbenzonitrile

10. 4-({6-amino-5-bromo-2-[(4-cyanophenyl)amino]pyrimidin-4-yl}oxy)-3,5-dimethylbenzonitrile

11. 4-[[6-amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethylbenzonitrile

12. 0c50hw4fo1

13. Chembl308954

14. Chebi:63589

15. Etravirine-d8

16. 4-((6-amino-5-bromo-2-((4-cyanophenyl)amino)-4-pyrimidinyl)oxy)-3,5-dimethyl-benzonitrile

17. 4-(6-amino-5-bromo-2-(4-cyanoanilino)pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

18. Benzonitrile, 4-((6-amino-5-bromo-2-((4-cyanophenyl)amino)-4-pyrimidinyl)oxy)-3,5-dimethyl-

19. Benzonitrile, 4-[[6-amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethyl-

20. Benzonitrile,4-[[6-amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethyl-

21. 65b

22. Intelence(tm)

23. Dapy Deriv

24. 4-(6-amino-5-bromo-2-(4-cyanophenylamino)pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

25. Intelence (tn)

26. Diaminopyrimidine Deriv

27. Tmc125 Cpd

28. Unii-0c50hw4fo1

29. Etravirine (jan/usan/inn)

30. Etravirine [usan:inn:ban:jan]

31. Etravirine [inn]

32. Etravirine- Bio-x

33. R 165335

34. Etravine; Etravirine

35. 4-[6-amino-5-bromo-2-(4-cyanoanilino)pyrimidin-4-yl]oxy-3,5-dimethylbenzonitrile

36. R165335-tmc125

37. 3m8p

38. Etravirine [mi]

39. Tmc-125/r-165335

40. Etravirine [jan]

41. Etravirine [usan]

42. Etravirine [vandf]

43. Etravirine [mart.]

44. Etravirine [who-dd]

45. Schembl52691

46. Etravirine [ema Epar]

47. Etravirine [orange Book]

48. Dtxsid30181412

49. Hms3651p20

50. Zinc602632

51. Bcp03562

52. Ex-a4282

53. Bdbm50103642

54. S3080

55. 4-({6-amino-5-bromo-2-[(4-

56. Akos015896355

57. Ac-8503

58. Bcp9000006

59. Ccg-269074

60. Cs-0435

61. Db06414

62. He-0088

63. Pb32778

64. 4-[[4-amino-5-bromo-6-(4-cyano-2,6-dimethylphenyloxy)-2-pyrimidinyl]amino]benzonitrile

65. 4-[6-amino-5-bromo-2-(4-cyanoanilino)pyrimidin-4-yl]oxy-3,5-dimethyl-benzonitrile

66. Ncgc00345885-02

67. Ncgc00345885-04

68. Ba164437

69. Hy-90005

70. Bcp0726000193

71. Db-067700

72. Am20080899

73. Cyanophenyl)amino]pyrimidin-4-yl}oxy)-3,5-

74. Ft-0658058

75. Ft-0668442

76. Ft-0668443

77. Sw219570-1

78. A26965

79. D04112

80. Ab01566873_01

81. A818671

82. Q414762

83. Sr-01000944895

84. J-513179

85. Sr-01000944895-1

86. 4-(6-amino-5-bromo-2-(4-cyanophenylamino)pyrimidin-4-ylamino)-3,5-dimethylbenzonitrile

87. 4-[[4-amino 5-bromo-6-(4-cyano-2,6-dimethylphenyloxy)-2-pyrimidinyl]amino]benzonitrile

88. 4-[[4-amino-5-bromo-6-(4-cyano-2,6-dimethylphenyloxy)-2-pyrimidinyl]-amino]benzonitrile

89. 4-[[6-amino-5-bromo-2-(4-cyanoanilino)-4-pyrimidinyl]oxy]-3,5-dimethylbenzonitrile

90. 4-[6-amino-5-bromo-2-(4-cyano-phenylamino)-pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile

91. 4-((6-amino-5-bromo-2-((4-cyanophenyl) Amino) Pyrimidin-4-yl) Oxy)-3, 5-dimethylbenzonitrile

92. 4-[[6-amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3, 5 Cdimethylbenzonitrile

93. 4-[[6-amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethyl -benzonitrile

94. 4-[6-azanyl-5-bromanyl-2-[(4-cyanophenyl)amino]pyrimidin-4-yl]oxy-3,5-dimethyl-benzenecarbonitrile

2.4 Create Date
2005-06-24
3 Chemical and Physical Properties
Molecular Weight 435.3 g/mol
Molecular Formula C20H15BrN6O
XLogP34.5
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count4
Exact Mass434.04907 g/mol
Monoisotopic Mass434.04907 g/mol
Topological Polar Surface Area121 Ų
Heavy Atom Count28
Formal Charge0
Complexity609
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Drug and Medication Information
4.1 Drug Information
1 of 2  
Drug NameIntelence
PubMed HealthEtravirine (By mouth)
Drug ClassesAntiretroviral Agent
Drug LabelINTELENCE (etravirine) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) of human immunodeficiency virus type 1 (HIV-1).The chemical name for etravirine is 4-[[6-amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethylbenzon...
Active IngredientEtravirine
Dosage FormTablet
RouteOral
Strength200mg; 25mg; 100mg
Market StatusPrescription
CompanyJanssen R And D

2 of 2  
Drug NameIntelence
PubMed HealthEtravirine (By mouth)
Drug ClassesAntiretroviral Agent
Drug LabelINTELENCE (etravirine) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) of human immunodeficiency virus type 1 (HIV-1).The chemical name for etravirine is 4-[[6-amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethylbenzon...
Active IngredientEtravirine
Dosage FormTablet
RouteOral
Strength200mg; 25mg; 100mg
Market StatusPrescription
CompanyJanssen R And D

4.2 Drug Indication

Indicated as an adjunct therapy in the treatment of adult HIV-1 infections resistant to therapy with other NNRTIs and antiretroviral agents.


FDA Label


Intelence, in combination with a boosted protease inhibitor and other antiretroviral medicinal products, is indicated for the treatment of human-immunodeficiency-virus-type-1 (HIV-1) infection in antiretroviral-treatment-experienced adult patients and in antiretroviral-treatment-experienced paediatric patients from six years of age.

This indication is based on week-48 analyses from two phase-III trials in highly pretreated patients where Intelence was investigated in combination with an optimised background regimen (OBR) which included darunavir/ritonavir. The indication in paediatric patients is based on 48-week analyses of a single-arm, phase-II trial in antiretroviral-treatment-experienced paediatric patients.


5 Pharmacology and Biochemistry
5.1 Pharmacology

Clinical trials have shown no prolongation of QT intervals on electrocardiograms after 8 days of dosing.


5.2 MeSH Pharmacological Classification

Reverse Transcriptase Inhibitors

Inhibitors of reverse transcriptase (RNA-DIRECTED DNA POLYMERASE), an enzyme that synthesizes DNA on an RNA template. (See all compounds classified as Reverse Transcriptase Inhibitors.)


5.3 FDA Pharmacological Classification
5.3.1 Active Moiety
ETRAVIRINE
5.3.2 FDA UNII
0C50HW4FO1
5.3.3 Pharmacological Classes
Cytochrome P450 2C9 Inhibitors [MoA]; Cytochrome P450 3A Inducers [MoA]; Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]; Non-Nucleoside Analog [EXT]; Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]; Cytochrome P450 2C19 Inhibitors [MoA]; Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
5.4 ATC Code

J05AG04


J05AG04

S76 | LUXPHARMA | Pharmaceuticals Marketed in Luxembourg | Pharmaceuticals marketed in Luxembourg, as published by d'Gesondheetskeess (CNS, la caisse nationale de sante, www.cns.lu), mapped by name to structures using CompTox by R. Singh et al. (in prep.). List downloaded from https://cns.public.lu/en/legislations/textes-coordonnes/liste-med-comm.html. Dataset DOI:10.5281/zenodo.4587355


J - Antiinfectives for systemic use

J05 - Antivirals for systemic use

J05A - Direct acting antivirals

J05AG - Non-nucleoside reverse transcriptase inhibitors

J05AG04 - Etravirine


5.5 Absorption, Distribution and Excretion

Absorption

Maximum oral absorption is achieved in 2.5-4 hours. Absorption is unaffected by the concomitant use of oral ranitidine or omeprazole, which decrease gastric acidity. Administration under fasting conditions resulted in a near 50% decrease in systemic exposure (AUC) when compared to administration after a meal.


Route of Elimination

After a 800mg dose of radio-labelled etraverine, 93.7% was found to undergo fecal elimination, with 81.2% - 86.4% eliminated unchanged. 1.2% of the dose was renally eliminated, changed. Etravirine is dialyzable (hemodialysis).


Volume of Distribution

Distribution of etravirine into compartments other than plasma has not been evaluated in humans.


Clearance

Renal clearance of etravirine is negligible (<1.2%), thus no dose adjustments are required in patients with renal impairment. Clearance is shown to be reduced in patients with Hepatitis B and/or co-infection, however, the safety profile of etravirine does not call for dosage adjustments.


5.6 Metabolism/Metabolites

Metabolized (in vitro) by the liver CYP450 enzymes: CYP3A4, CYP2C9, CYP2C19. The major metabolites formed by a methyl hydroxylation of the dimethylbenzonitrile moiety retained less than 90% of etravirine's activity.


5.7 Biological Half-Life

Half life of 9.05-41 hours.


5.8 Mechanism of Action

Etravirine exerts its effects via direct inhibition of the reverse transcriptase enzyme of human immunodeficiency virus type 1 (HIV-1). It directly binds reverse transcriptase and consequently blocks DNA-dependent and RNA-dependent polymerase activity. Etravirine does not inhibit human DNA polymerase alpha, beta or gamma.


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18-May-2022
25-Apr-2025
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DOSAGE - TABLET;ORAL - 100MG

USFDA APPLICATION NUMBER - 22187

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DOSAGE - TABLET;ORAL - 200MG

USFDA APPLICATION NUMBER - 22187

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DOSAGE - TABLET;ORAL - 25MG

USFDA APPLICATION NUMBER - 22187

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ABOUT THIS PAGE

Looking for 269055-15-4 / Etravirine API manufacturers, exporters & distributors?

Etravirine manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Etravirine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Etravirine manufacturer or Etravirine supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etravirine manufacturer or Etravirine supplier.

PharmaCompass also assists you with knowing the Etravirine API Price utilized in the formulation of products. Etravirine API Price is not always fixed or binding as the Etravirine Price is obtained through a variety of data sources. The Etravirine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Etravirine

Synonyms

269055-15-4, Intelence, Tmc-125, Tmc125, Etravirine (tmc125), Tmc 125

Cas Number

269055-15-4

Unique Ingredient Identifier (UNII)

0C50HW4FO1

About Etravirine

Etravirine is a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor. Etravirine is designed to be active against HIV isolates with mutations that confer resistance to the two most commonly prescribed first-generation NNRTIs. It can bind the enzyme reverse transcriptase (RT) in multiple conformations, both for native and mutant RT, thereby blocking the enzymatic activity of RT.

3m8p Manufacturers

A 3m8p manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3m8p, including repackagers and relabelers. The FDA regulates 3m8p manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3m8p API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of 3m8p manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

3m8p Suppliers

A 3m8p supplier is an individual or a company that provides 3m8p active pharmaceutical ingredient (API) or 3m8p finished formulations upon request. The 3m8p suppliers may include 3m8p API manufacturers, exporters, distributors and traders.

click here to find a list of 3m8p suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

3m8p USDMF

A 3m8p DMF (Drug Master File) is a document detailing the whole manufacturing process of 3m8p active pharmaceutical ingredient (API) in detail. Different forms of 3m8p DMFs exist exist since differing nations have different regulations, such as 3m8p USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 3m8p DMF submitted to regulatory agencies in the US is known as a USDMF. 3m8p USDMF includes data on 3m8p's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 3m8p USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 3m8p suppliers with USDMF on PharmaCompass.

3m8p KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a 3m8p Drug Master File in Korea (3m8p KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 3m8p. The MFDS reviews the 3m8p KDMF as part of the drug registration process and uses the information provided in the 3m8p KDMF to evaluate the safety and efficacy of the drug.

After submitting a 3m8p KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their 3m8p API can apply through the Korea Drug Master File (KDMF).

click here to find a list of 3m8p suppliers with KDMF on PharmaCompass.

3m8p WC

A 3m8p written confirmation (3m8p WC) is an official document issued by a regulatory agency to a 3m8p manufacturer, verifying that the manufacturing facility of a 3m8p active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 3m8p APIs or 3m8p finished pharmaceutical products to another nation, regulatory agencies frequently require a 3m8p WC (written confirmation) as part of the regulatory process.

click here to find a list of 3m8p suppliers with Written Confirmation (WC) on PharmaCompass.

3m8p NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing 3m8p as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 3m8p API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture 3m8p as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain 3m8p and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 3m8p NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 3m8p suppliers with NDC on PharmaCompass.

3m8p GMP

3m8p Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of 3m8p GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right 3m8p GMP manufacturer or 3m8p GMP API supplier for your needs.

3m8p CoA

A 3m8p CoA (Certificate of Analysis) is a formal document that attests to 3m8p's compliance with 3m8p specifications and serves as a tool for batch-level quality control.

3m8p CoA mostly includes findings from lab analyses of a specific batch. For each 3m8p CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

3m8p may be tested according to a variety of international standards, such as European Pharmacopoeia (3m8p EP), 3m8p JP (Japanese Pharmacopeia) and the US Pharmacopoeia (3m8p USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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