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Also known as: 181183-52-8, Almotriptan maleate, Axert, Las 31416 d,l-malate acid, Almotriptan (malate), Almogran
Molecular Formula
C21H31N3O7S
Molecular Weight
469.6  g/mol
InChI Key
QHATUKWEVNMHRY-UHFFFAOYSA-N
FDA UNII
PJP312605E

Almotriptan Malate
Almotriptan Malate is the malate salt of almotriptan, a sulfonamide triptan with vasoconstrictor activity. Almotriptan selectively binds to and activates serotonin 5-HT 1B and 1D receptors in the central nervous system (CNS), thereby causing cerebral blood vessel constriction. This may lead to pain relief from vascular headaches. Almotriptan may also relieve vascular headaches by preventing the release of vasoactive neuropeptides from perivascular trigeminal axons in the dura mater during a migraine, by reducing extravasation of plasma proteins, and by decreasing the release of other mediators of inflammation from the trigeminal nerve.
1 2D Structure

Almotriptan Malate

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
N,N-dimethyl-2-[5-(pyrrolidin-1-ylsulfonylmethyl)-1H-indol-3-yl]ethanamine;2-hydroxybutanedioic acid
2.1.2 InChI
InChI=1S/C17H25N3O2S.C4H6O5/c1-19(2)10-7-15-12-18-17-6-5-14(11-16(15)17)13-23(21,22)20-8-3-4-9-20;5-2(4(8)9)1-3(6)7/h5-6,11-12,18H,3-4,7-10,13H2,1-2H3;2,5H,1H2,(H,6,7)(H,8,9)
2.1.3 InChI Key
QHATUKWEVNMHRY-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CN(C)CCC1=CNC2=C1C=C(C=C2)CS(=O)(=O)N3CCCC3.C(C(C(=O)O)O)C(=O)O
2.2 Other Identifiers
2.2.1 UNII
PJP312605E
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Almogran

2. Almotriptan

3. Axert

2.3.2 Depositor-Supplied Synonyms

1. 181183-52-8

2. Almotriptan Maleate

3. Axert

4. Las 31416 D,l-malate Acid

5. Almotriptan (malate)

6. Almogran

7. Pnu-180638e

8. Almotriptan Malate [usan]

9. Almotriptan D,l-hydrogenmalate

10. Chebi:53781

11. Las-31416 D,l-malate Acid

12. Pjp312605e

13. 181183-52-8(almotriptan Malate)

14. Las-31416-d,l-malate-acid

15. N,n-dimethyl-2-(5-((pyrrolidin-1-ylsulfonyl)methyl)-1h-indol-3-yl)ethan-1-amine 2-hydroxysuccinate

16. 1-(((3-(2-(dimethylamino)ethyl)indol-5-yl)methyl)sulfonyl)pyrrolidine Malate (1:1)

17. 1-(((3-(2-(dimethylamino)ethyl)-1h-indol-5-yl)methyl)sulfonyl)pyrrolidine, Hydroxybutanedioate (1:1)

18. N,n-dimethyl-2-[5-(pyrrolidin-1-ylsulfonylmethyl)-1h-indol-3-yl]ethanamine;2-hydroxybutanedioic Acid

19. Pnu 180638e

20. Unii-pjp312605e

21. Sr-05000001986

22. Axert (tn)

23. Almotriptan Malate (usp)

24. 1-[[[2-(dimethyl-amino)ethyl]-1h-indol-5-yl]methyl]sulfonyl]pyrrolidine Malate

25. Almotriptan Malate (axert)

26. 1-(((3-(2-(dimethylamino)ethyl)-1h-indol-5-yl)methyl)sulfonyl)pyrrolidine, Hydroxybutanedionate (1:1)

27. Mls006010048

28. Schembl221131

29. Almotriptan Maleate [mi]

30. Chembl1200521

31. Dtxsid1044225

32. Almotriptan Malate [vandf]

33. Almotriptan Malate(pnu180638)

34. Hms3651a12

35. Hms3884p05

36. Almotriptan Malate [mart.]

37. Almotriptan Malate [usp-rs]

38. Almotriptan Malate [who-dd]

39. Bcp05632

40. Hy-b0383

41. Mfcd08067740

42. Pnu180638

43. S2096

44. (zznon-labelled)almotriptan-d6 Malate

45. Akos015950790

46. Bcp9000276

47. Ccg-269445

48. Pnu 180638

49. Almotriptan Malate [orange Book]

50. Almotriptan Malate [ep Monograph]

51. Almotriptan Malate [usp Monograph]

52. As-12142

53. Butanedioic Acid, Hydroxy-, Compd. With 1-(((3-(2-(dimethylamino)ethyl)-1h-indol-5-yl)methyl)sulfonyl)pyrrolidine (1:1)

54. Smr004701216

55. Ft-0661519

56. Sw219418-1

57. D02825

58. F14758

59. J-011571

60. Sr-05000001986-2

61. Q27124206

62. 1-(((3-(2-(dimethylamino)ethyl)indol-5-yl)methyl)sulfonyl)pyrrolidine Malate

63. 3-[2-(dimethylamino)ethyl]-5-(pyrrolidin-1-ylsulfonylmethyl )-1h-indole Malate

64. 1-(((3-(2-(dimethylamino)ethyl)-1h-indol-5-yl)methyl)sulfonyl)pyrrolidine Hydroxybutanedioate

65. Butanedioic Acid, 2-hydroxy-, Compd. With N,n-dimethyl-5-[(1-pyrrolidinylsulfonyl)methyl]-1h-indole-3-ethanamine (1:1)

2.4 Create Date
2005-08-08
3 Chemical and Physical Properties
Molecular Weight 469.6 g/mol
Molecular Formula C21H31N3O7S
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count9
Rotatable Bond Count9
Exact Mass469.18827151 g/mol
Monoisotopic Mass469.18827151 g/mol
Topological Polar Surface Area160 Ų
Heavy Atom Count32
Formal Charge0
Complexity612
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
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 NameAlmotriptan malate
Drug LabelAXERT (almotriptan malate) Tablets contain almotriptan malate, a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist. Almotriptan malate is chemically designated as 1-[[[3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl]methyl]sulfonyl]pyrrolidi...
Active IngredientAlmotriptan malate
Dosage FormTablet
Routeoral
Strength6.25mg; 12.5mg
Market StatusTentative Approval
CompanyTeva Pharms

2 of 2  
Drug NameAlmotriptan malate
Drug LabelAXERT (almotriptan malate) Tablets contain almotriptan malate, a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist. Almotriptan malate is chemically designated as 1-[[[3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl]methyl]sulfonyl]pyrrolidi...
Active IngredientAlmotriptan malate
Dosage FormTablet
Routeoral
Strength6.25mg; 12.5mg
Market StatusTentative Approval
CompanyTeva Pharms

5 Pharmacology and Biochemistry
5.1 MeSH Pharmacological Classification

Serotonin Receptor Agonists

Endogenous compounds and drugs that bind to and activate SEROTONIN RECEPTORS. Many serotonin receptor agonists are used as ANTIDEPRESSANTS; ANXIOLYTICS; and in the treatment of MIGRAINE DISORDERS. (See all compounds classified as Serotonin Receptor Agonists.)


5.2 FDA Pharmacological Classification
5.2.1 Pharmacological Classes
Serotonin 1d Receptor Agonists [MoA]; Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]; Serotonin 1b Receptor Agonists [MoA]

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03-Jun-2021
28-Mar-2025
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DOSAGE - TABLET;ORAL - EQ 12.5MG BASE **Feder...DOSAGE - TABLET;ORAL - EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 21001

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DOSAGE - TABLET;ORAL - EQ 6.25MG BASE **Feder...DOSAGE - TABLET;ORAL - EQ 6.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 21001

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ABOUT THIS PAGE

Looking for 181183-52-8 / Almotriptan Malate API manufacturers, exporters & distributors?

Almotriptan Malate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Almotriptan Malate

Synonyms

181183-52-8, Almotriptan maleate, Axert, Las 31416 d,l-malate acid, Almotriptan (malate), Almogran

Cas Number

181183-52-8

Unique Ingredient Identifier (UNII)

PJP312605E

About Almotriptan Malate

Almotriptan Malate is the malate salt of almotriptan, a sulfonamide triptan with vasoconstrictor activity. Almotriptan selectively binds to and activates serotonin 5-HT 1B and 1D receptors in the central nervous system (CNS), thereby causing cerebral blood vessel constriction. This may lead to pain relief from vascular headaches. Almotriptan may also relieve vascular headaches by preventing the release of vasoactive neuropeptides from perivascular trigeminal axons in the dura mater during a migraine, by reducing extravasation of plasma proteins, and by decreasing the release of other mediators of inflammation from the trigeminal nerve.

Almogran Manufacturers

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

Almogran Suppliers

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

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

Almogran USDMF

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

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

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

Almogran CEP

A Almogran CEP of the European Pharmacopoeia monograph is often referred to as a Almogran Certificate of Suitability (COS). The purpose of a Almogran CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Almogran EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Almogran to their clients by showing that a Almogran CEP has been issued for it. The manufacturer submits a Almogran CEP (COS) as part of the market authorization procedure, and it takes on the role of a Almogran CEP holder for the record. Additionally, the data presented in the Almogran CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Almogran DMF.

A Almogran CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Almogran CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Almogran suppliers with CEP (COS) on PharmaCompass.

Almogran WC

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

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

Almogran 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 Almogran as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Almogran GMP

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

Almogran CoA

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

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

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