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EPROSARTAN

CAS No.
133040-01-4
Chemical Name:
EPROSARTAN
Synonyms
Teveten;Navixen;CS-1951;EPROSARTAN;SKB 108566;SKF-108566J;SKF-108566);Eprosartan-d4;prop-1-en-1-yl);13C6]-Eprosartan
CBNumber:
CB0135346
Molecular Formula:
C23H24N2O4S
Molecular Weight:
424.51
MDL Number:
MFCD00897872
MOL File:
133040-01-4.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

EPROSARTAN Properties

Melting point 250-253°C
storage temp. Sealed in dry,2-8°C
solubility Dichloromethane (Slightly), Methanol (Slightly)
form Solid
color Pale Yellow to Light Yellow
CAS DataBase Reference 133040-01-4
FDA UNII 2KH13Z0S0Y
ATC code C09CA02

Pharmacokinetic data

Protein binding 98%
Excreted unchanged in urine <2 (as metabolites)
Volume of distribution 13 Litres
Biological half-life 5-9 / Unchanged

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P305+P351+P338

EPROSARTAN price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC E590100 Eprosartan 133040-01-4 10mg $70 2021-12-16 Buy
Matrix Scientific 094012 Eprosartan 95+% 133040-01-4 1g $227 2021-12-16 Buy
American Custom Chemicals Corporation API0000548 EPROSARTAN 95.00% 133040-01-4 1G $284.55 2021-12-16 Buy
American Custom Chemicals Corporation RDL0006807 EPROSARTAN-D4 95.00% 133040-01-4 5MG $501.55 2021-12-16 Buy
Medical Isotopes, Inc. D33956 Eprosartan-d6 133040-01-4 1mg $600 2021-12-16 Buy
Product number Packaging Price Buy
E590100 10mg $70 Buy
094012 1g $227 Buy
API0000548 1G $284.55 Buy
RDL0006807 5MG $501.55 Buy
D33956 1mg $600 Buy

EPROSARTAN Chemical Properties,Uses,Production

Description

Teveten was launched in Germany for the treatment of hypertension. There are several ways in which it has been prepared, the shortest of which is four steps; beginning with displacement of 2-butyl-4-chloroimidazole-5-carboxaldehyde with methyl 4-(bromomethyl)benzoate. Teveten is an angiotensin Ⅱ antagonist selective for the AT, subtype receptor. It is a potent, highly selective, competitve antagonist with no agonist activity. Duration of action is similar to Enalapril (greater than 12 hr) but Teveten had a faster onset. While it is orally active, it rapidly dissociates from the receptor. This is contrary to its prolonged duration of action, which presumably results from slow removal from compartments within tissue, cells or matrix around the AT, receptor. It is not bound by BSA.

Chemical Properties

Light-Yellow Solid

Originator

SmithKline Beecham (UK)

Uses

Prototype of the imidazoleacrylic acid angiotensin II receptor antagonists. Antihypertensive

Uses

Eprosartan is a prototype of the imidazoleacrylic acid angiotensin II receptor antagonists. Eprosartan is an antihypertensive.

Uses

Eprosartan (E590100) impurity.

Definition

ChEBI: A member of the class of imidazoles and thiophenes that is an angiotensin II receptor antagonist used for the treatment of high blood pressure.

brand name

Teveten

Clinical Use

Angiotensin-II antagonist
Hypertension

Drug interactions

Potentially hazardous interactions with other drugs Anaesthetics: enhanced hypotensive effect.
Analgesics: antagonism of hypotensive effect and increased risk of renal impairment with NSAIDs; hyperkalaemia with ketorolac and other NSAIDs.
Antihypertensives: increased risk of hyperkalaemia hypotension and renal impairment with ACE inhibitors and aliskiren.
Ciclosporin: increased risk of hyperkalaemia and nephrotoxicity.
Diuretics: enhanced hypotensive effect; hyperkalaemia with potassium-sparing diuretics.
Epoetin: increased risk of hyperkalaemia; antagonism of hypotensive effect.
Lithium: reduced excretion, possibility of enhanced lithium toxicity.
Potassium salts: increased risk of hyperkalaemia.
Tacrolimus: increased risk of hyperkalaemia and nephrotoxicity.

Metabolism

Following oral and intravenous dosing with [14C] eprosartan in human subjects, eprosartan was the only drug-related compound found in the plasma and faeces. In the urine, approximately 20% of the radioactivity excreted was an acyl glucuronide of eprosartan with the remaining 80% being unchanged eprosartan
Eprosartan is eliminated by both biliary and renal excretion. Following intravenous [14C] eprosartan, about 61% of radioactivity is recovered in the faeces and about 37% in the urine. Following an oral dose of [14C] eprosartan, about 90% of radioactivity is recovered in the faeces and about 7% in the urine.

133040-03-6
143468-96-6
133040-01-4
Synthesis of EPROSARTAN from METHYL 4-[(2-BUTYL-5-FORMYL-1H-IMIDAZOL-1-YL)METHYL]BENZOATE and 2-Carbethoxy-3-(2-thienyl)propanoic acid
Global( 121)Suppliers
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View Lastest Price from EPROSARTAN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Eprosartan pictures 2021-10-20 Eprosartan
133040-01-4
US $15.00 / KG 1KG 99% 9000kg/per week Hebei Lingding Biotechnology Co., Ltd.
Eprosartan pictures 2020-05-10 Eprosartan
133040-01-4
US $0.00-0.00 / Kg 1KG 99.0% 500 MT Shaanxi Dideu Medichem Co. Ltd
  • Eprosartan pictures
  • Eprosartan
    133040-01-4
  • US $15.00 / KG
  • 99%
  • Hebei Lingding Biotechnology Co., Ltd.
  • Eprosartan pictures
  • Eprosartan
    133040-01-4
  • US $0.00-0.00 / Kg
  • 99.0%
  • Shaanxi Dideu Medichem Co. Ltd
4-[2-Butyl-5-(2-carboxy-3-thiophen-2-yl-propenyl)-imidazol-1-ylmethyl]-benzoic acid EPROSARTAN Eprosartan Mysylate (E)-3-[2-Butyl-1-[(4-carboxyphenyl)-methyl]imidazol-5-l]-2-(2-thienylmethyl)-2-propenoic Acid ((E)-3-[2-Butyl-1-[(4-carboxyphenyl)methyl]imidazol-5-yl]-2-(2-thienylmethyl)-2-propenoic Acid SKF-108566) SKF-108566J Teveten (E)- α-[[2-Butyl-1-[(4-carboxyphenyl)methyl]-1H-imidazol-5-y1]methylene]2-thiophenepropanoic acid (E)-3-[2-Butyl-1-(4-carboxybenzyl)-1H-imidazol-5-yl]-2-(2-thienylmethyl)acrylic acid 2-Thiophenepropanoic acid, α-[[2-butyl-1-[(4-carboxyphenyl)methyl]-1H-imidazol-5-yl]methylene]-, (αE)- Des[2-(2-thienylMethyl)] Eprosartan-2-carboxylic Acid (E)-2-Butyl-1-(p-carboxybenzyl)-α-2-thenyliMidazole-5-acrylic Acid (αE)-α-[[2-Butyl-1-[(4-carboxyphenyl)Methyl]-1H-iMidazol-5-yl]Methylene]-2-thiophenepropanoic Acid Navixen SKB 108566 2-[[2-Butyl-1-[[4-(carboxyphenyl)]Methyl]-1H-iMidazol-5-yl]Methylene]propanedioic Acid 4-[[2-Butyl-5-(2,2-dicarboxyvinyl)-1H-iMidazol-1yl)Methylbenzoic Acid Eprosartan-d4 (E)-4-((2-Butyl-5-(2-carboxy-3-(thiophen-2-yl)prop-1-en-1-yl)-1H-iMidazol-1-yl)Methyl)benzoic acid -1H-imidazol-1-yl) -4-((2-Butyl-5-(2-carboxy-3-(thiophen-2-yl) prop-1-en-1-yl) CS-1951 EPROSARTAN USP/EP/BP Eprosartan D6 HClQ: What is Eprosartan D6 HCl Q: What is the CAS Number of Eprosartan D6 HCl Q: What is the storage condition of Eprosartan D6 HCl Q: What are the applications of Eprosartan D6 HCl EprosartanQ: What is Eprosartan Q: What is the CAS Number of Eprosartan Q: What is the storage condition of Eprosartan Q: What are the applications of Eprosartan TIANFU-CHEM EPROSARTAN Eprosartan (SKF-108566J) 13C6]-Eprosartan Eprosartan (E)-3-[2-Butyl-1-[(4-carboxyphenyl)methyl]-imidazol-5-yl]-2-(2- thienyl methyl)-2-propenoic acid 133040-01-4 C23H24N2O4S Aromatics Heterocycles Impurities Intermediates Intermediates & Fine Chemicals Pharmaceuticals Sulfur & Selenium Compounds