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1EXCIPIENTS BY APPLICATIONS

Chemistry

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Also known as: Guanabenz, 5051-62-7, Hydrazinecarboximidamide, 2-[(2,6-dichlorophenyl)methylene]-, (e)-, Dsstox_cid_25666, Dsstox_rid_81042, Dsstox_gsid_45666
Molecular Formula
C8H8Cl2N4
Molecular Weight
231.08  g/mol
InChI Key
WDZVGELJXXEGPV-UHFFFAOYSA-N

Icodextrin
An alpha-2 selective adrenergic agonist used as an antihypertensive agent.
1 2D Structure

Icodextrin

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
2-[(2,6-dichlorophenyl)methylideneamino]guanidine
2.1.2 InChI
InChI=1S/C8H8Cl2N4/c9-6-2-1-3-7(10)5(6)4-13-14-8(11)12/h1-4H,(H4,11,12,14)
2.1.3 InChI Key
WDZVGELJXXEGPV-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1=CC(=C(C(=C1)Cl)C=NN=C(N)N)Cl
2.2 Synonyms
2.2.1 MeSH Synonyms

1. 2,6 Dichlorobenzylideneaminoguanidine

2. 2,6-dichlorobenzylideneaminoguanidine

3. Acetate Wyeth-ayerst, Guanabenz

4. Acetate, Guanabenz

5. Br 750

6. Br-750

7. Br750

8. Guanabenz

9. Guanabenz Acetate

10. Guanabenz Acetate Wyeth-ayerst

11. Guanabenz Monoacetate

12. Monoacetate, Guanabenz

13. Wy 8678

14. Wy-8678

15. Wy8678

16. Wyeth Ayerst Of Guanabenz Acetate

17. Wyeth-ayerst Of Guanabenz Acetate

18. Wytensin

2.2.2 Depositor-Supplied Synonyms

1. Guanabenz

2. 5051-62-7

3. Hydrazinecarboximidamide, 2-[(2,6-dichlorophenyl)methylene]-, (e)-

4. Dsstox_cid_25666

5. Dsstox_rid_81042

6. Dsstox_gsid_45666

7. Cas-5051-62-7

8. Ncgc00024846-03

9. Spectrum_000843

10. Prestwick0_000096

11. Prestwick1_000096

12. Spectrum2_001114

13. Spectrum3_000445

14. Spectrum4_000567

15. Kbiogr_000974

16. Kbioss_001323

17. Divk1c_000010

18. Spbio_001248

19. Spbio_001991

20. Chembl1313657

21. Dtxsid6045666

22. Kbio1_000010

23. Kbio2_001323

24. Kbio2_003891

25. Kbio2_006459

26. Kbio3_001310

27. Ninds_000010

28. Hms2233d12

29. Hms3370a17

30. Bcp30851

31. Tox21_110932

32. Akos017264577

33. Tox21_110932_1

34. Zinc242701441

35. Db00629

36. 2,6-dichlorobenzaldehyde Guanylhydrazone

37. Mrf-0000008

38. Ncgc00024846-08

39. Db-051784

40. Ft-0635524

41. Guanabenzum;wy-8678; Wy 8678; Wy8678

42. N-(2,6-dichlorobenzylidene)-n'-amidino Hydrazine

43. Sr-01000721838

44. Sr-01000721838-5

45. Q27164730

2.3 Create Date
2005-03-25
3 Chemical and Physical Properties
Molecular Weight 231.08 g/mol
Molecular Formula C8H8Cl2N4
XLogP31.7
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass230.0126017 g/mol
Monoisotopic Mass230.0126017 g/mol
Topological Polar Surface Area76.8 Ų
Heavy Atom Count14
Formal Charge0
Complexity228
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count1
Covalently Bonded Unit Count1
4 Drug and Medication Information
4.1 Drug Indication

For management of High blood pressure


FDA Label


5 Pharmacology and Biochemistry
5.1 Pharmacology

Guanabenz, a centrally acting α-2 adrenergic agonist, is indicated for treatment of hypertension.


5.2 MeSH Pharmacological Classification

Adrenergic alpha-2 Receptor Agonists

Compounds that bind to and activate ADRENERGIC ALPHA-2 RECEPTORS. (See all compounds classified as Adrenergic alpha-2 Receptor Agonists.)


Antihypertensive Agents

Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. (See all compounds classified as Antihypertensive Agents.)


5.3 Absorption, Distribution and Excretion

Absorption

Approximately 75% absorbed from gastrointestinal tract


5.4 Metabolism/Metabolites

Hepatic


5.5 Biological Half-Life

6 hours.


5.6 Mechanism of Action

Guanabenz's antihypertensive effect is thought to be due to central alpha-adrenergic stimulation, which results in a decreased sympathetic outflow to the heart, kidneys, and peripheral vasculature in addition to a decreased systolic and diastolic blood pressure and a slight slowing of pulse rate. Chronic administration of guanabenz also causes a decrease in peripheral vascular resistance.


API SUPPLIERS

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01

Baxter Healthcare Corporation

U.S.A

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Antibody Engineering
Not Confirmed
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Baxter Healthcare Corporation

U.S.A

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Antibody Engineering
Not Confirmed
USDMF arrow-down Click Us! arrow-down
CEP/COS JDMF EU-WC NDC arrow-down KDMF VMF Others AUDIT
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02

FandaChem

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Antibody Engineering
Not Confirmed
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FandaChem

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Antibody Engineering
Not Confirmed
USDMF CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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03

HAINAN YEW PHARMACEUTICAL CO LTD

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Antibody Engineering
Not Confirmed
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HAINAN YEW PHARMACEUTICAL CO LTD

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Antibody Engineering
Not Confirmed
USDMF CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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Shenzhen Haorui

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Antibody Engineering
Not Confirmed
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KDMF

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Roquette

France
Antibody Engineering
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Roquette

France
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Not Confirmed

Icodextrin

Registrant Name : Rocket Korea Ltd.

Registration Date : 2024-08-28

Registration Number : 20240828-211-J-1682

Manufacturer Name : ROQUETTE FRERES

Manufacturer Address : 1 Rue de la Haute Loge, 62136 LESTREM, France

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