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Chemistry

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Also known as: 330784-47-9, Stendra, Spedra, Ta 1790, Ta-1790, (s)-4-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)pyrrolidin-1-yl)-n-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide
Molecular Formula
C23H26ClN7O3
Molecular Weight
483.9  g/mol
InChI Key
WEAJZXNPAWBCOA-INIZCTEOSA-N
FDA UNII
DR5S136IVO

Avanafil
Avanafil is an orally available phosphodiesterase type 5 (PDE5) inhibitor with vasodilatory activity. Avanafil selectively inhibits PDE5, thus inhibiting the degradation of cyclic guanosine monophosphate (cGMP) found in the smooth muscle of the corpus cavernosa of the penis. The inhibition of cGMP degradation results in prolonged muscle relaxation, vasodilation, and blood engorgement of the corpus cavernosa, thereby prolonging penile erection.
Avanafil is a Phosphodiesterase 5 Inhibitor. The mechanism of action of avanafil is as a Phosphodiesterase 5 Inhibitor.
1 2D Structure

Avanafil

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
4-[(3-chloro-4-methoxyphenyl)methylamino]-2-[(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide
2.1.2 InChI
InChI=1S/C23H26ClN7O3/c1-34-19-6-5-15(10-18(19)24)11-27-21-17(22(33)28-13-20-25-7-3-8-26-20)12-29-23(30-21)31-9-2-4-16(31)14-32/h3,5-8,10,12,16,32H,2,4,9,11,13-14H2,1H3,(H,28,33)(H,27,29,30)/t16-/m0/s1
2.1.3 InChI Key
WEAJZXNPAWBCOA-INIZCTEOSA-N
2.1.4 Canonical SMILES
COC1=C(C=C(C=C1)CNC2=NC(=NC=C2C(=O)NCC3=NC=CC=N3)N4CCCC4CO)Cl
2.1.5 Isomeric SMILES
COC1=C(C=C(C=C1)CNC2=NC(=NC=C2C(=O)NCC3=NC=CC=N3)N4CCC[C@H]4CO)Cl
2.2 Other Identifiers
2.2.1 UNII
DR5S136IVO
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 4-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)-1-pyrrolidinyl)-n-(2-pyrimidinylmethyl)-5-pyrimidinecarboxamide

2. Stendra

2.3.2 Depositor-Supplied Synonyms

1. 330784-47-9

2. Stendra

3. Spedra

4. Ta 1790

5. Ta-1790

6. (s)-4-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)pyrrolidin-1-yl)-n-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

7. Chebi:66876

8. Dr5s136ivo

9. (s)-2-(2-hydroxymethyl-1-pyrrolidinyl)-4-(3-chloro-4-methoxybenzylamino)-5-[(2-pyrimidinylmethyl)carbamoyl]pyrimidine

10. (s)-4-(3-chloro-4-methoxybenzylamino)-2-(2-hydroxymethylpyrrolidin-1-yl)-n-pyrimidin-2-ylmethyl-5-pyrimidinecarboxamide

11. (s)-4-[(3-chloro-4-methoxybenzyl)amino]-2-[2-(hydroxymethyl)-1-pyrrolidinyl]-n-(2pyrimidinylmethyl)-5-pyrimidinecarboxamide

12. 4-[(3-chloro-4-methoxybenzyl)amino]-2-[(2s)-2-(hydroxymethyl)pyrrolidin-1-yl]-n-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

13. 4-[(3-chloro-4-methoxyphenyl)methylamino]-2-[(2s)-2-(hydroxymethyl)pyrrolidin-1-yl]-n-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

14. 4-((3-chloro-4-methoxybenzyl)amino)-2-((2s)-2-(hydroxymethyl)pyrrolidin-1-yl)-n-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

15. 5-pyrimidinecarboxamide, 4-(((3-chloro-4-methoxyphenyl)methyl)amino)-2-((2s)-2-(hydroxymethyl)-1-pyrrolidinyl)-n-(2-pyrimidinylmethyl)-

16. Stendra (tn)

17. Avanafil [usan:inn]

18. Unii-dr5s136ivo

19. Zepeed

20. Ine-5-carboxamide

21. Spedra (tn)

22. Avanafil [usan]

23. Avanafil (usan/inn)

24. Avanafil [inn]

25. Avanafil [mi]

26. Avanafil [vandf]

27. Avanafil [mart.]

28. Avanafil [who-dd]

29. Avanafil 100 Microg/ml In Acetonitrile:dimethylsulfoxide

30. Schembl118799

31. Avanafil [orange Book]

32. Gtpl7448

33. Chembl1963681

34. Amy1794

35. Dtxsid50186727

36. 4-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)-1-pyrrolidinyl)-n-(2-pyrimidinylmethyl)-5-pyrimidinecarboxamide

37. Bdbm50036629

38. Cs1566

39. Mfcd11977961

40. S4019

41. Ta1790

42. Zinc11677857

43. Akos024462448

44. Ccg-229896

45. Db06237

46. Vi-0162

47. Ncgc00386241-01

48. As-20106

49. Hy-18252

50. Sw219217-1

51. D03217

52. Ab01565827_02

53. J-019006

54. Q2873270

55. Brd-k65781196-001-01-4

56. (s)-2-(2-hydroxymethyl-1-pyrrolidinyl)-4-(3-chloro-4-methoxybenzylamino)-5-[n-(2-pyrimidylmethyl)carbamoyl]-pyrimidine

57. (s)-4-[(3-chlor-4-methoxybenzyl)amino]-2-[2-(hydroxymethyl)-1- Pyrrolidinyl]-n-(2-pyrimidinylmethyl)-5-pyrimidinecarboxamid

58. 4-[(3-chloranyl-4-methoxy-phenyl)methylamino]-2-[(2s)-2-(hydroxymethyl)pyrrolidin-1-yl]-n-(pyrimidin-2-ylmethyl)pyrimid

59. 4-[(3-chloranyl-4-methoxy-phenyl)methylamino]-2-[(2s)-2-(hydroxymethyl)pyrrolidin-1-yl]-n-(pyrimidin-2-ylmethyl)pyrimid Ine-5-carboxamide

60. Avanafil; (s)-4-chloro-6-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)pyrrolidin-1-yl)-n-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

61. E6l

2.4 Create Date
2006-10-25
3 Chemical and Physical Properties
Molecular Weight 483.9 g/mol
Molecular Formula C23H26ClN7O3
XLogP32.6
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count9
Rotatable Bond Count9
Exact Mass483.1785654 g/mol
Monoisotopic Mass483.1785654 g/mol
Topological Polar Surface Area125 Ų
Heavy Atom Count34
Formal Charge0
Complexity642
Isotope Atom Count0
Defined Atom Stereocenter Count1
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 NameStendra
PubMed HealthAvanafil (By mouth)
Drug ClassesErectile Dysfunction Agent
Drug LabelSTENDRA (avanafil) is a selective inhibitor of cGMP-specific PDE5.Avanafil is designated chemically as (S)-4-[(3-Chloro-4-methoxybenzyl)amino]-2-[2-(hydroxymethyl)-1-pyrrolidinyl]-N-(2-pyrimidinylmethyl)-5-pyrimidinecarboxamide and has the following...
Active IngredientAvanafil
Dosage FormTablet
RouteOral
Strength200mg; 100mg; 50mg
Market StatusPrescription
CompanyVivus

2 of 2  
Drug NameStendra
PubMed HealthAvanafil (By mouth)
Drug ClassesErectile Dysfunction Agent
Drug LabelSTENDRA (avanafil) is a selective inhibitor of cGMP-specific PDE5.Avanafil is designated chemically as (S)-4-[(3-Chloro-4-methoxybenzyl)amino]-2-[2-(hydroxymethyl)-1-pyrrolidinyl]-N-(2-pyrimidinylmethyl)-5-pyrimidinecarboxamide and has the following...
Active IngredientAvanafil
Dosage FormTablet
RouteOral
Strength200mg; 100mg; 50mg
Market StatusPrescription
CompanyVivus

4.2 Drug Indication

Avanafil is indicated for the treatment of erectile dysfunction.


FDA Label


Treatment of erectile dysfunction in adult men.

In order for Spedra to be effective, sexual stimulation is required.


5 Pharmacology and Biochemistry
5.1 Pharmacology

Avanafil is a strong competitive inhibitor of phosphodiesterase 5 (PDE5) with a demonstrated _in vitro_ IC50 of 5.2 nM. Its inhibitory effects on PDE5 are 100-fold more potent than on PDE6 and >1000-fold more potent than on other PDE enzymes, meaning it is less likely to cause visual disturbances and cardiovascular adverse effects when compared with less selective PDE5 inhibitors such as [sildenafil] and [vardenafil]. It has a relatively quick onset of action allowing for administration as early as 15 minutes prior to sexual activity. PDE5 inhibitors like avanafil can cause significant drug interactions when administered alongside certain antihypertensive agents (e.g. alpha blockers, substantial amounts of alcohol). PDE5 inhibitors have also been associated with the development of non-arteritic anterior ischemic optic neuropathy (NAION), a rare condition that typically presents as sudden loss of vision in one or both eyes and appears to be more common in patients with a "crowded" optic disc. Patients presenting with any degree of vision loss should immediately discontinue use of all PDE5 inhibitors and seek medical attention. In some jurisdictions, a history of NAION or other degenerative retinal disorders is considered a contraindication to avanafil therapy.


5.2 FDA Pharmacological Classification
5.2.1 Active Moiety
AVANAFIL
5.2.2 FDA UNII
DR5S136IVO
5.2.3 Pharmacological Classes
Phosphodiesterase 5 Inhibitors [MoA]; Phosphodiesterase 5 Inhibitor [EPC]
5.3 ATC Code

G04BE10


G04BE10

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


G - Genito urinary system and sex hormones

G04 - Urologicals

G04B - Urologicals

G04BE - Drugs used in erectile dysfunction

G04BE10 - Avanafil


5.4 Absorption, Distribution and Excretion

Absorption

Avanafil is rapidly absorbed following oral administration (Tmax of 30-45 minutes) and appears to have low to moderate oral bioavailability, though formal studies have not been conducted. Administration with a meal results in a mean delay in Tmax of 1.12 to 1.25 hours, a 39% mean reduction in Cmax, and a negligible effect on AUC.


Route of Elimination

Following oral administration, avanafil is extensively metabolized. Approximately 62% of a given dose is excreted as metabolites in the feces and approximately 21% as metabolites in the urine.


Volume of Distribution

The apparent volume of distribution of avanafil is 47 to 83 L.


5.5 Metabolism/Metabolites

Avanafil is extensively metabolized, primarily by CYP3A4 and to a lesser extent by CYP2C9. There are two major metabolites formed, M4 and M16, which exist in the plasma at concentrations 23% and 29% that of the parent compound, respectively. The M16 metabolite lacks pharmacologic effect, but the M4 metabolite has an inhibitory potency for PDE5 18% that of avanafil and accounts for approximately 4% of the observed pharmacologic activity of avanafil.


5.6 Biological Half-Life

Studies have demonstrated variability in the terminal elimination half-life of avanafil, with estimates ranging between 5 - 17 hours.


5.7 Mechanism of Action

Avanafil inhibits the cGMP-specific phosphodiesterase type 5 (PDE5) which is responsible for the degradation of cGMP in the corpus cavernosum located around the penis. Sexual arousal results in the local release of nitric oxide, which in turn stimulates the enzyme guanylate cyclase to produce cGMP. Elevated levels of cGMP result in local smooth muscle relaxation and increased blood flow to the penis (i.e. an erection). As PDE5 inhibitors like avanafil require the endogenous release of nitric oxide in order to exert their pharmacologic effect, they have no effect on the user in the absence of sexual stimulation/arousal.


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06-Jan-2021
22-Nov-2024
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DRUG PRODUCT COMPOSITIONS

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DOSAGE - TABLET;ORAL - 100MG

USFDA APPLICATION NUMBER - 202276

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DOSAGE - TABLET;ORAL - 200MG

USFDA APPLICATION NUMBER - 202276

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DOSAGE - TABLET;ORAL - 50MG

USFDA APPLICATION NUMBER - 202276

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ABOUT THIS PAGE

Looking for 330784-47-9 / Avanafil API manufacturers, exporters & distributors?

Avanafil manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Avanafil 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 Avanafil manufacturer or Avanafil supplier for your needs.

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

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

API | Excipient name

Avanafil

Synonyms

330784-47-9, Stendra, Spedra, Ta 1790, Ta-1790, (s)-4-((3-chloro-4-methoxybenzyl)amino)-2-(2-(hydroxymethyl)pyrrolidin-1-yl)-n-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide

Cas Number

330784-47-9

Unique Ingredient Identifier (UNII)

DR5S136IVO

About Avanafil

Avanafil is an orally available phosphodiesterase type 5 (PDE5) inhibitor with vasodilatory activity. Avanafil selectively inhibits PDE5, thus inhibiting the degradation of cyclic guanosine monophosphate (cGMP) found in the smooth muscle of the corpus cavernosa of the penis. The inhibition of cGMP degradation results in prolonged muscle relaxation, vasodilation, and blood engorgement of the corpus cavernosa, thereby prolonging penile erection.

Avanafil Manufacturers

A Avanafil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Avanafil, including repackagers and relabelers. The FDA regulates Avanafil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Avanafil 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 Avanafil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Avanafil Suppliers

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

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

Avanafil USDMF

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

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

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

Avanafil KDMF

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

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

After submitting a Avanafil 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 Avanafil API can apply through the Korea Drug Master File (KDMF).

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

Avanafil WC

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

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

Avanafil 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 Avanafil as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Avanafil 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 Avanafil 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 Avanafil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Avanafil NDC to their finished compounded human drug products, they may choose to do so.

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

Avanafil GMP

Avanafil 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 Avanafil 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 Avanafil GMP manufacturer or Avanafil GMP API supplier for your needs.

Avanafil CoA

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

Avanafil CoA mostly includes findings from lab analyses of a specific batch. For each Avanafil 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.

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