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129979-57-3

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129979-57-3 Usage

Description

Argipressin Acetate is a peptide hormone that exhibits vasoconstrictive and antidiuretic properties. It binds to the vascular arginine vasopressin receptor, V1, with Kd values of 1.31 and 1.44 nM in A7r5 rat aortic smooth muscle cells and neonatal rat cardiomyocytes, respectively. Argipressin Acetate also stimulates the intracellular release of calcium in A7r5 cells (EC50 = 5 nM). In rat models, it has been shown to induce hypertension and tachycardia when injected into the lateral septal nuclei at a dose of 100-400 ng and increase heart rate and mean arterial pressure (MAP) when injected into the medial amygdaloid body at a dose of 150-600 ng.

Uses

Used in Pharmaceutical Industry:
Argipressin Acetate is used as a vasoconstrictor and antidiuretic agent for the treatment of conditions such as diabetes insipidus, nocturnal enuresis, and heart failure. Its ability to bind to the vascular arginine vasopressin receptor, V1, and stimulate the intracellular release of calcium makes it a valuable drug for managing these conditions.
Used in Cardiovascular Research:
Argipressin Acetate is used as a research tool in cardiovascular studies to investigate the effects of vasoconstriction and antidiuresis on heart rate, mean arterial pressure, and other related parameters. Its ability to induce hypertension and tachycardia in rat models makes it a useful compound for understanding the underlying mechanisms of these physiological responses.
Used in Smooth Muscle Cell Research:
Argipressin Acetate is used as a research tool in smooth muscle cell studies to explore the binding affinity and signaling pathways of the vascular arginine vasopressin receptor, V1. Its interaction with A7r5 rat aortic smooth muscle cells and neonatal rat cardiomyocytes provides valuable insights into the role of this receptor in smooth muscle cell function and its potential as a therapeutic target.

Check Digit Verification of cas no

The CAS Registry Mumber 129979-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,9,7 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129979-57:
(8*1)+(7*2)+(6*9)+(5*9)+(4*7)+(3*9)+(2*5)+(1*7)=193
193 % 10 = 3
So 129979-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C46H65N15O12S2.C2H4O2/c47-27-22-74-75-23-33(45(73)61-17-5-9-34(61)44(72)56-28(8-4-16-53-46(51)52)39(67)54-21-37(50)65)60-43(71)32(20-36(49)64)59-40(68)29(14-15-35(48)63)55-41(69)31(18-24-6-2-1-3-7-24)58-42(70)30(57-38(27)66)19-25-10-12-26(62)13-11-25;1-2(3)4/h1-3,6-7,10-13,27-34,62H,4-5,8-9,14-23,47H2,(H2,48,63)(H2,49,64)(H2,50,65)(H,54,67)(H,55,69)(H,56,72)(H,57,66)(H,58,70)(H,59,68)(H,60,71)(H4,51,52,53);1H3,(H,3,4)/t27-,28-,29-,30-,31-,32-,33-,34-;/m0./s1

129979-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name <8-arginine>vasopressin

1.2 Other means of identification

Product number -
Other names [ARG8]VASOPRESSIN TFA

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:129979-57-3 SDS

129979-57-3Downstream Products

129979-57-3Relevant articles and documents

NEW SYTHESIS OF VASOPRESSIN AND ITS DE-9-GLYCINE ANALOGS

Panseuvich, O. S.,Chipens, G. I.,Korps, A. O.,Pavar, A. P.

, p. 370 - 375 (2007/10/02)

A unified scheme is proposed for the synthesis of vasopressin (I), de-9-glycinevasopressin (II), and de-9-glycinamidevasopressin (III) which has been developed on the basis of the tetrapeptide Glm-Asn-Cys(Bzl)-Pro and other homologous fragments of neurohypophyseal hormones as common initial and intermediate compounds.The free dithiols obtained by the reduction of protected derivatives of (I)-(III) by sodium in liquid ammonia have been oxidized to the corresponding cyclic disulfides (I)-(III) with the aid of 1 M H2O2 at 0-5 deg C and pH (8.5.The vasopressor activities of (I)-(III) a re, respectively 470 +/- 20, 1.7, and 0.5 IU/mg (rat, in vivo).

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