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Also known as: 635702-64-6, Pazopanib hcl, Votrient, Pazopanib (hydrochloride), Armala, Unii-33y9anm545
Molecular Formula
C21H24ClN7O2S
Molecular Weight
474.0  g/mol
InChI Key
MQHIQUBXFFAOMK-UHFFFAOYSA-N
FDA UNII
33Y9ANM545

Pazopanib Hydrochloride
Pazopanib Hydrochloride is the hydrochloride salt of a small molecule inhibitor of multiple protein tyrosine kinases with potential antineoplastic activity. Pazopanib selectively inhibits vascular endothelial growth factor receptors (VEGFR)-1, -2 and -3, c-kit and platelet derived growth factor receptor (PDGF-R), which may result in inhibition of angiogenesis in tumors in which these receptors are upregulated.
1 2D Structure

Pazopanib Hydrochloride

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
5-[[4-[(2,3-dimethylindazol-6-yl)-methylamino]pyrimidin-2-yl]amino]-2-methylbenzenesulfonamide;hydrochloride
2.1.2 InChI
InChI=1S/C21H23N7O2S.ClH/c1-13-5-6-15(11-19(13)31(22,29)30)24-21-23-10-9-20(25-21)27(3)16-7-8-17-14(2)28(4)26-18(17)12-16;/h5-12H,1-4H3,(H2,22,29,30)(H,23,24,25);1H
2.1.3 InChI Key
MQHIQUBXFFAOMK-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CC1=C(C=C(C=C1)NC2=NC=CC(=N2)N(C)C3=CC4=NN(C(=C4C=C3)C)C)S(=O)(=O)N.Cl
2.2 Other Identifiers
2.2.1 UNII
33Y9ANM545
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Gw 780604

2. Gw 786034b

3. Gw-780604

4. Gw-786034b

5. Gw780604

6. Gw786034b

7. Pazopanib

8. Votrient

2.3.2 Depositor-Supplied Synonyms

1. 635702-64-6

2. Pazopanib Hcl

3. Votrient

4. Pazopanib (hydrochloride)

5. Armala

6. Unii-33y9anm545

7. Pazopanib Monohydrochloride

8. Pazopanib Hcl (gw786034 Hcl)

9. Gw786034b

10. Gw-786034b

11. Pazopanib (as Hydrochloride)

12. Gw786034 (hydrochloride)

13. 5-[[4-[(2,3-dimethylindazol-6-yl)-methylamino]pyrimidin-2-yl]amino]-2-methylbenzenesulfonamide;hydrochloride

14. Chebi:71217

15. 33y9anm545

16. S1035

17. 5-((4-((2,3-dimethyl-2h-indazol-6-yl)(methyl)amino)pyrimidin-2-yl)amino)-2-methylbenzenesulfonamide Hydrochloride

18. 5-((4-((2,3-dimethyl-2h-indazol-6-yl)methylamino)pyrimidin-2-yl)amino)-2-methylbenzenesulfonamide Monohydrochloride

19. 5-({4-[(2,3-dimethyl-2h-indazol-6-yl)(methyl)amino]pyrimidin-2-yl}amino)-2-methylbenzene-1-sulfonamide Hydrochloride

20. 5-{4-[(2,3-dimethyl-2h-indazol-6-yl)-methyl-amino]-pyrimidin-2-ylamino}-2-methyl-benzenesulfonamide Hydrochloride

21. Benzenesulfonamide, 5-((4-((2,3-dimethyl-2h-indazol-6-yl)methylamino)-2-pyrimidinyl)amino)-2-methyl-, Monohydrochloride

22. Patorma

23. Gw786034 Hcl

24. Votrient Hcl

25. Votrient (tn)

26. 5-({4-[(2,3-dimethyl-2h-indazol-6-yl)(methyl)amino]pyrimidin-2-yl}amino)-2-methylbenzenesulfonamide Hydrochloride

27. Pazopanib Hydrochloride [usan:jan]

28. Mls004774147

29. Schembl159487

30. Pazopanib Hydrochloride- Bio-x

31. Pazopanib Hydrochloride [usan]

32. Chembl1201733

33. Dtxsid70212956

34. Ex-a956

35. Pazopanib Hcl (gw786034 )

36. Bcp02203

37. Pazopanib Hydrochloride (jan/usan)

38. Pazopanib Hydrochloride [mi]

39. Mfcd12546138

40. Nsc737754

41. Pazopanib Hydrochloride [jan]

42. Akos015958593

43. Bcp9001052

44. Ccg-269485

45. Cs-0126

46. Gsk-786034

47. Ks-1458

48. Nsc-737754

49. Pazopanib Hydrochloride [mart.]

50. Pb31655

51. Sb10367

52. Pazopanib Hydrochloride [who-dd]

53. Ac-24726

54. Bp166746

55. Hy-12009

56. Smr003500790

57. Am20090655

58. Ft-0687642

59. P2243

60. Pazopanib Hydrochloride [orange Book]

61. Sw218082-2

62. Ec-000.2347

63. D05380

64. A834417

65. Q27888072

66. 5-({4-[(2,3-dimethyl-2h-indazol-6-yl)(methyl)amino]-2-pyrimidinyl}amino)-2-methylbenzenesulfonamide Hydrochloride

67. 5-(4-((2,3-dimethyl-2h-indazol-6-yl)(methyl)amino)pyrimidin-2-ylamino)-2-methylbenzenesulfonamide Hydrochloride

68. 5-(4-((2,3-dimethyl-2h-indazol-6-yl)(methyl)amino)pyrimidin-2-ylamino)-2-methylbenzenesulfonamide Hydrochloride;5-[[4-[(2,3-dimethylindazol-6-yl)-methyl-amino]pyrimidin-2-yl]amino]-2-methyl-benzenesulfonamide Hydrochloride

69. 5-[[4-[(2,3-dimethylindazol-6-yl)-methylamino]pyrimidin-2-yl]amino]-2-methylbenzenesulfonamide Hydrochloride

70. Benzenesulfonamide, 5-[[4-[(2,3-dimethyl-2h-indazol-6-yl)methylamino]-2-pyrimidinyl]amino]-2-methyl-, Hydrochloride (1:1)

2.4 Create Date
2006-10-26
3 Chemical and Physical Properties
Molecular Weight 474.0 g/mol
Molecular Formula C21H24ClN7O2S
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count8
Rotatable Bond Count5
Exact Mass473.1400719 g/mol
Monoisotopic Mass473.1400719 g/mol
Topological Polar Surface Area127 Ų
Heavy Atom Count32
Formal Charge0
Complexity717
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Drug Information
1 of 2  
Drug NameVotrient
PubMed HealthPazopanib (By mouth)
Drug ClassesAntineoplastic Agent, Immunological Agent
Active IngredientPazopanib hydrochloride
Dosage FormTablet
RouteOral
Strengtheq 200mg base; eq 400mg base
Market StatusPrescription
CompanyGlaxosmithkline

2 of 2  
Drug NameVotrient
PubMed HealthPazopanib (By mouth)
Drug ClassesAntineoplastic Agent, Immunological Agent
Active IngredientPazopanib hydrochloride
Dosage FormTablet
RouteOral
Strengtheq 200mg base; eq 400mg base
Market StatusPrescription
CompanyGlaxosmithkline

4.2 Drug Indication

* Renal-cell carcinoma (RCC):

Votrient is indicated in adults for the first-line treatment of advanced renal-cell carcinoma (RCC) and for patients who have received prior cytokine therapy for advanced disease.

* Soft-tissue sarcoma (STS):

Votrient is indicated for the treatment of adult patients with selective subtypes of advanced soft-tissue sarcoma (STS) who have received prior chemotherapy for metastatic disease or who have progressed within 12 months after (neo)adjuvant therapy.

Efficacy and safety have only been established in certain STS histological tumour subtypes.


5 Pharmacology and Biochemistry
5.1 FDA Pharmacological Classification
5.1.1 Pharmacological Classes
Cytochrome P450 2D6 Inhibitors [MoA]; Cytochrome P450 3A4 Inhibitors [MoA]; Kinase Inhibitor [EPC]; Protein Kinase Inhibitors [MoA]; Cytochrome P450 2C8 Inhibitors [MoA]
5.2 ATC Code

L01XE11


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11-Jan-2021
17-Dec-2024
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ABOUT THIS PAGE

Pazopanib Hydrochloride Manufacturers

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

Pazopanib Hydrochloride Suppliers

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

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

Pazopanib Hydrochloride USDMF

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

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

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

Pazopanib Hydrochloride KDMF

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

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

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

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

Pazopanib Hydrochloride WC

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

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

Pazopanib Hydrochloride 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 Pazopanib Hydrochloride as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Pazopanib Hydrochloride GMP

Pazopanib Hydrochloride 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 Pazopanib Hydrochloride 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 Pazopanib Hydrochloride GMP manufacturer or Pazopanib Hydrochloride GMP API supplier for your needs.

Pazopanib Hydrochloride CoA

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

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

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