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4-Ethyl-3-(3-methoxypropoxyl)benzoic acid, also known as Eptifibatide, is a synthetic peptide that functions as an antagonist of platelet aggregation. It is characterized by its ability to inhibit the formation of blood clots, making it a crucial antiplatelet medication in the management of cardiovascular conditions.

895240-77-4

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895240-77-4 Usage

Uses

Used in Cardiovascular Applications:
4-Ethyl-3-(3-methoxypropoxyl)benzoic acid is used as an antiplatelet agent for preventing the formation of blood clots in patients who have undergone cardiovascular procedures such as angioplasty. It achieves this by blocking the glycoprotein IIb/IIIa receptor on platelet surfaces, thereby reducing the risk of complications like heart attacks and strokes.
Used in Hospital Settings:
4-Ethyl-3-(3-methoxypropoxyl)benzoic acid is used as an intravenous medication in hospital settings under the supervision of healthcare professionals. This ensures that patients receive the appropriate dosage and monitoring for potential side effects such as bleeding, bruising, and dizziness, which are crucial for maintaining patient safety and therapeutic outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 895240-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,2,4 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 895240-77:
(8*8)+(7*9)+(6*5)+(5*2)+(4*4)+(3*0)+(2*7)+(1*7)=204
204 % 10 = 4
So 895240-77-4 is a valid CAS Registry Number.

895240-77-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-3-(3-methoxypropoxy)benzoic acid

1.2 Other means of identification

Product number -
Other names 4-ethyl-3-(3-methoxypropoxyl)benzoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:895240-77-4 SDS

895240-77-4Downstream Products

895240-77-4Relevant academic research and scientific papers

The P1 N-isopropyl motif bearing hydroxyethylene dipeptide isostere analogues of aliskiren are in vitro potent inhibitors of the human aspartyl protease renin

Yamaguchi, Yasuchika,Menear, Keith,Cohen, Nissim-Claude,Mah, Robert,Cumin, Frédéric,Schnell, Christian,Wood, Jeanette M.,Maibaum, Jürgen

scheme or table, p. 4863 - 4867 (2010/05/18)

Novel nonpeptide small molecule renin inhibitors bearing an N-isopropyl P1 motif were designed based on initial lead structures 1 and aliskiren (2). (P3-P1)-Benzamide derivatives such as 9a and 34, as well as the corresponding P1 basic tertiary amine derivatives 10 and 35 were found to display low nanomolar inhibition against human renin in vitro.

3, 4-SUBSTITUTED PYRROLIDINE DERIVATIVES FOR THE TREATMENT OF HYPERTENSION

-

Page/Page column 165, (2010/11/24)

The invention relates to the use of (3,4-di-, 3,3,4-tri, 3,4,4-tri- or 3,3,4,4-tetra-)substituted pyrrolidine compounds for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; compounds that are part of a subclass of these substituted pyrrolidine compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (= disorder) that depends on activity of renin; new compounds that are part of a subclass of these substituted pyrrolidine compounds; pharmaceutical formulations comprising said substituted pyrrolidine compounds, and/or a method of treatment comprising administering said substituted pyrrolidine compounds, a method for the manufacture especially of said new substituted pyrrolidine compounds, as well as novel intermediates, starting materials and/or partial steps for their synthesis. The substituted pyrrolidine compounds are of the formula (I), wherein R1, R2, R3, R4, R5 and T are defined as in the specification.

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