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Also known as: 960404-48-2, Dapagliflozin propanediol monohydrate, Dapagliflozin propanediol hydrate, Farxiga, Dapagliflozin ((2s)-1,2-propanediol, hydrate), Bms-512148-05
Molecular Formula
C24H35ClO9
Molecular Weight
503.0  g/mol
InChI Key
GOADIQFWSVMMRJ-UPGAGZFNSA-N
FDA UNII
887K2391VH

Dapagliflozin Propanediol Monohydrate
Dapagliflozin Propanediol is the propanediol form of dapagliflozin, a selective sodium-glucose co-transporter subtype 2 (SGLT2) inhibitor with antihyperglycemic activity. Upon administration, dapagliflozin selectively targets and inhibits SGLT2, thereby preventing the reabsorption of glucose by the kidneys.
1 2D Structure

Dapagliflozin Propanediol Monohydrate

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
(2S,3R,4R,5S,6R)-2-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol;(2S)-propane-1,2-diol;hydrate
2.1.2 InChI
InChI=1S/C21H25ClO6.C3H8O2.H2O/c1-2-27-15-6-3-12(4-7-15)9-14-10-13(5-8-16(14)22)21-20(26)19(25)18(24)17(11-23)28-21;1-3(5)2-4;/h3-8,10,17-21,23-26H,2,9,11H2,1H3;3-5H,2H2,1H3;1H2/t17-,18-,19+,20-,21+;3-;/m10./s1
2.1.3 InChI Key
GOADIQFWSVMMRJ-UPGAGZFNSA-N
2.1.4 Canonical SMILES
CCOC1=CC=C(C=C1)CC2=C(C=CC(=C2)C3C(C(C(C(O3)CO)O)O)O)Cl.CC(CO)O.O
2.1.5 Isomeric SMILES
CCOC1=CC=C(C=C1)CC2=C(C=CC(=C2)[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)Cl.C[C@@H](CO)O.O
2.2 Other Identifiers
2.2.1 UNII
887K2391VH
2.3 Synonyms
2.3.1 MeSH Synonyms

1. (2s,3r,4r,5s,6r)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6- (hydroxymethyl)tetrahydro-2h-pyran-3,4,5-triol

2. 2-(3-(4-ethoxybenzyl)-4-chlorophenyl)-6-hydroxymethyltetrahydro-2h-pyran-3,4,5-triol

3. Bms 512148

4. Bms-512148

5. Bms512148

6. Dapagliflozin

7. Farxiga

8. Forxiga

2.3.2 Depositor-Supplied Synonyms

1. 960404-48-2

2. Dapagliflozin Propanediol Monohydrate

3. Dapagliflozin Propanediol Hydrate

4. Farxiga

5. Dapagliflozin ((2s)-1,2-propanediol, Hydrate)

6. Bms-512148-05

7. Dapagliflozin S-propylene Glycol Monohydrate

8. Dapagliflozin Propylene Glycolate Hydrate

9. Chebi:85079

10. Dapagliflozin Propanediol [usan]

11. Dapagliflozin Mixture With Propylene Glycol, Hydrate

12. 887k2391vh

13. (2s,3r,4r,5s,6r)-2-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol;(2s)-propane-1,2-diol;hydrate

14. Dapagliflozin [usan:inn]

15. Dapagliflozin Propylene Glycol Hydrate

16. (2s,3r,4r,5s,6r)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2h-pyran-3,4,5-triol Compound With (s)-propane-1,2-diol (1:1) Hydrate

17. D-glucitol, 1,5-anhydro-1-c-(4-chloro-3-((4-ethoxyphenyl)methyl)phenyl)-, (1s)-, Compd. With (2s)-1,2-propanediol, Hydrate (1:1:1)

18. Unii-887k2391vh

19. Dapagliflozin Propylene Glycolate Hydrate [jan]

20. Dapagliflozin (s)-propylene Glycol Hydrate

21. Chembl2103802

22. Dtxsid00914678

23. Ex-a2824

24. Dapagliflozin Propylene Glycol

25. Hy-10450a

26. Mfcd28167768

27. S5566

28. Akos027250601

29. Ccg-269711

30. Ac-29230

31. As-64915

32. Dapagliflozin (2s)-1,2-propanediol Hydrate

33. F20667

34. Bms-512148 (2s)-1,2-propanediol, Hydrate

35. Dapagliflozin (2s)-1,2-propanediol Monohydrate

36. Xigduo Component Dapagliflozin Propanediol

37. A900162

38. Dapagliflozin Propanediol Component Of Xigduo

39. Dapagliflozin Propanediol Monohydrate [who-dd]

40. Q27158320

41. Dapagliflozin Propanediol Monohydrate [ema Epar]

42. Dapagliflozin Compound With (2s)-1,2-propanediol Hydrate

43. Dapagliflozin Compound With (2s)-1,2-propanediol Hydrate [mi]

44. (2s)-propane-1,2-diol (2s,3r,4r,5s,6r)-2-{4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl}-6-(hydroxymethyl)oxane-3,4,5-triol Hydrate

45. (2s)-propane-1,2-diol--(1s)-1,5-anhydro-1-[4-chloro-3-(4-ethoxybenzyl)phenyl]-d-glucitol--water (1/1/1)

46. (2s,3r,4r,5s,6r)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro- 2h-pyran-3,4,5-triol, (2s)-propane-1,2-diol (1:1) Monohydrate

47. (2s,3r,4r,5s,6r)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2h-pyran-3,4,5-triol (s)-propane-1,2-diol Hydrate

48. (2s,3r,4r,5s,6r)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2h-pyran-3,4,5-triol, (2s)-propane-1,2-diol (1:1) Monohydrate

49. 1700615-13-9

2.4 Create Date
2008-09-29
3 Chemical and Physical Properties
Molecular Weight 503.0 g/mol
Molecular Formula C24H35ClO9
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count9
Rotatable Bond Count7
Exact Mass502.1969604 g/mol
Monoisotopic Mass502.1969604 g/mol
Topological Polar Surface Area141 Ų
Heavy Atom Count34
Formal Charge0
Complexity493
Isotope Atom Count0
Defined Atom Stereocenter Count6
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count3
4 Drug and Medication Information
4.1 Drug Indication

Forxiga is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise

- as monotherapy when metformin is considered inappropriate due to intolerance.

- in addition to other medicinal products for the treatment of type 2 diabetes.

For study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied.

Heart failure

- Forxiga is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction.

Chronic kidney disease

- Forxiga is indicated in adults for the treatment of chronic kidney disease.


Type 2 diabetes mellitus

Edistride is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise

- as monotherapy when metformin is considered inappropriate due to intolerance.

- in addition to other medicinal products for the treatment of type 2 diabetes.

For study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 and 5. 1.

Heart failure

Edistride is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction.

Chronic kidney disease

Edistride is indicated in adults for the treatment of chronic kidney disease.


5 Pharmacology and Biochemistry
5.1 MeSH Pharmacological Classification

Sodium-Glucose Transporter 2 Inhibitors

Compounds that inhibit SODIUM-GLUCOSE TRANSPORTER 2. They lower blood sugar by preventing the reabsorption of glucose by the kidney and are used in the treatment of TYPE 2 DIABETES MELLITUS. (See all compounds classified as Sodium-Glucose Transporter 2 Inhibitors.)


5.2 ATC Code

A10BK01


A10BK01


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10-Jan-2022
28-Jul-2025
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ABOUT THIS PAGE

Looking for 1700615-13-9 / Dapagliflozin Propanediol Monohydrate API manufacturers, exporters & distributors?

Dapagliflozin Propanediol Monohydrate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Dapagliflozin Propanediol Monohydrate 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 Dapagliflozin Propanediol Monohydrate manufacturer or Dapagliflozin Propanediol Monohydrate supplier for your needs.

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

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

API | Excipient name

Dapagliflozin Propanediol Monohydrate

Synonyms

960404-48-2, Dapagliflozin propanediol hydrate, Farxiga, Dapagliflozin ((2s)-1,2-propanediol, hydrate), Bms-512148-05, Dapagliflozin s-propylene glycol monohydrate

Cas Number

1700615-13-9

Unique Ingredient Identifier (UNII)

887K2391VH

About Dapagliflozin Propanediol Monohydrate

Dapagliflozin Propanediol is the propanediol form of dapagliflozin, a selective sodium-glucose co-transporter subtype 2 (SGLT2) inhibitor with antihyperglycemic activity. Upon administration, dapagliflozin selectively targets and inhibits SGLT2, thereby preventing the reabsorption of glucose by the kidneys.

Dapagliflozin Propanediol Monohydrate Manufacturers

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

Dapagliflozin Propanediol Monohydrate Suppliers

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

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

Dapagliflozin Propanediol Monohydrate USDMF

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

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

click here to find a list of Dapagliflozin Propanediol Monohydrate suppliers with USDMF on PharmaCompass.

Dapagliflozin Propanediol Monohydrate KDMF

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

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

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

click here to find a list of Dapagliflozin Propanediol Monohydrate suppliers with KDMF on PharmaCompass.

Dapagliflozin Propanediol Monohydrate WC

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

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

Dapagliflozin Propanediol Monohydrate 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 Dapagliflozin Propanediol Monohydrate as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Dapagliflozin Propanediol Monohydrate suppliers with NDC on PharmaCompass.

Dapagliflozin Propanediol Monohydrate GMP

Dapagliflozin Propanediol Monohydrate 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 Dapagliflozin Propanediol Monohydrate 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 Dapagliflozin Propanediol Monohydrate GMP manufacturer or Dapagliflozin Propanediol Monohydrate GMP API supplier for your needs.

Dapagliflozin Propanediol Monohydrate CoA

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

Dapagliflozin Propanediol Monohydrate CoA mostly includes findings from lab analyses of a specific batch. For each Dapagliflozin Propanediol Monohydrate 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.

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