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SML0148

Imidapril hydrochloride

≥98% (HPLC)

Sinónimos:

(4S)-3-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1-methyl-2-oxo-4-imidazolidinecarboxylic acid hydrochloride, Novaloc, TA 6366, Tanapril

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Talla/SKUDisponibilidadPrecio
10 mg
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125,00 €
50 mg
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487,00 €
413,95 €

Acerca de este artículo

Fórmula empírica (notación de Hill):
C20H27N3O6 · HCl
Número CAS:
Peso molecular:
441.91
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥98% (HPLC)
Form:
powder

125,00 €


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Quality Segment

assay

≥98% (HPLC)

form

powder

optical activity

[α]/D -50 to -70° in ethanol (c=0.5)

color

white to tan

solubility

H2O: ≥5 mg/mL

originator

Trinity Pharma Solutions

storage temp.

−20°C

SMILES string

Cl.CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N2[C@@H](CN(C)C2=O)C(O)=O

InChI

1S/C20H27N3O6.ClH/c1-4-29-19(27)15(11-10-14-8-6-5-7-9-14)21-13(2)17(24)23-16(18(25)26)12-22(3)20(23)28;/h5-9,13,15-16,21H,4,10-12H2,1-3H3,(H,25,26);1H/t13-,15-,16-;/m0./s1

InChI key

LSLQGMMMRMDXHN-GEUPQXMHSA-N

General description

Imidapril comprises large acyl moiety and is hydrolyzed by carboxylesterase (CES) 1.

Application

Imidapril hydrochloride may be used to test its effect on pharyngeal and laryngeal muscle to treat impaired swallowing.
Imidapril hydrochloride was used as a standard in bioequivalence test by LC/MS method.

Biochem/physiol Actions

Angiotensin Converting Enzyme (ACE) inhibitor
Imidapril is a potent angiotensin converting enzyme inhibitor and anti-hypertensive.
Imidapril hydrochloride is a long-acting inhibitor of angiotensin converting enzyme used in the treatment of hypertension, congestive heart failure and diabetic nephropathy. It restores decreased airway sensation and bladder sensation in patients with multiple sclerosis.

Features and Benefits

This compound is featured on the Angiotensin Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Trinity Pharma Solutions. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

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Este artículo
B0935R0404T4827
description

≥98% (HPLC)

description

≥98% (HPLC), solid

description

≥98% (HPLC)

description

≥98% (HPLC), white, powder

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

form

powder

form

solid

form

powder

form

powder

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

−20°C

storage temp.

-

storage temp.

2-8°C

storage temp.

-

solubility

H2O: ≥5 mg/mL

solubility

H2O: >5 mg/mL

solubility

DMSO: ~18 mg/mL

solubility

DMSO: ≥20 mg/mL

originator

Trinity Pharma Solutions

originator

Novartis

originator

Sanofi Aventis

originator

Abbott


Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Preguntas

  1. Can this be used as CRM or standard for testing products for release?

    1 respuesta
    1. This product is not classified as a Certified Reference Material (CRM) or a pharmaceutical secondary standard for product release testing, as these designations are not part of its specifications.

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