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Argipressin

  • CasNo: 113-79-1
  • Purity:
  • Appearance: White powder

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1.What is the Argipressine ?

ADH (vasopressin) is released primarily in response to increases in plasma osmolarity or decreases in blood volume. It produces its antidiuretic activity in the kidney, causing the cortical and medullary parts of the collecting duct to become more permeable to water, thereby increasing water reabsorption, reducing serum osmolarity, and increasing its volume. It produces this effect by binding to a subset of vasopressin receptors called V2 that have relatively high affinity for the hormone. ADH also has actions at sites other than the kidney. V2 receptors also mediate an increase in circulating levels of two proteins involved in blood coagulation: factor VIII and von Willebrand’s factor.At higher concentrations, ADH interacts with V1 receptors to cause a general constriction of most blood vessels. It also interacts with V3 (or V1b) receptors to increase ACTH release, although the major control of ACTH release occurs through corticotropin-releasing hormone.

[Arg8]-Vasopressin solution was used as an antigen for preparing preadsorbed antisera for immunocytochemistry. The product was used in L6 cell culture of the C5 subclone for differentiation studies.

Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH<sub>2</sub>
34223-44-4

Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2

Captopril disulfide
64806-05-9

Captopril disulfide

Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH<sub>2</sub>
113-79-1,5591-81-1,66513-06-2,66513-07-3,76023-59-1,89576-32-9

Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2

captopril
62571-86-2

captopril

Conditions
Conditions Yield
In water; at 25 ℃; for 5h; Equilibrium constant; pH 7.0;
C<sub>55</sub>H<sub>80</sub>N<sub>16</sub>O<sub>15</sub>S<sub>3</sub>

C55H80N16O15S3

C<sub>55</sub>H<sub>80</sub>N<sub>16</sub>O<sub>15</sub>S<sub>3</sub>

C55H80N16O15S3

Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH<sub>2</sub>
113-79-1,5591-81-1,66513-06-2,66513-07-3,76023-59-1,89576-32-9

Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2

captopril
62571-86-2

captopril

Conditions
Conditions Yield
In water; at 25 ℃; for 5h; Rate constant; Equilibrium constant; pH 7.0;

2.What is the CAS number for Argipressine ?

The CAS number of Argipressine is 113-79-1.

More information of Argipressine 113-79-1 are:

CAS Number

113-79-1

Density

1.59 g/cm3

Flash Point

113℃

HS CODE

2937190000

PSA

512.03000

LogP

1.16100

Pka

9.90±0.15(Predicted)

3.What are another words for Argipressine ?

Synonyms for Argipressine 113-79-1:3-(Phenylalanine)-8-arginineoxytocin;8-L-Arginine-vasopressin;AVP;Arg8-vasopressin;Arginine antidiuretic hormone;Arginine-8-vasopressin;Arginine-vasopressin;1,2-Dithia-5,8,11,14,17-pentaazacycloeicosane-10-propionamide,19-amino-13-benzyl-7-(carbamoylmethyl)-4-[2-[[1-[(carbamoylmethyl)carbamoyl]-4-guanidinobutyl]carbamoyl]-1-pyrrolidinylcarbonyl]-16-p-hydroxybenzyl-6,9,12,15,18-pentaoxo-(6CI);

4.What is the molecular formula of Argipressine?

The chemical formula of  Argipressine is C46H65N15O12S2 which containing 46 Carbon atoms,65 Hydrogen atoms,15 Nitrogen atoms,12 Oxygen atoms and 2 Sulfur atoms,and the molecular weight of  Argipressine is 1084.25.

5.What is Argipressine (113-79-1) used for?

Argipressine, also known as [Arg8]-Vasopressin, is the predominant form of mammalian vasopressin, an antidiuretic hormone. It is a nonapeptide containing an arginine at residue 8 and two disulfide-linked cysteines at residues 1 and 6. Argipressine is available under the brand name Pitressin (Parke-Davis).

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

Relevant articles related to Argipressine:

Article

Source

Discovery of a highly selective and efficient reagent for formation of intramolecular disulfide bonds in peptides

Shi, Tiesheng,Rabenstein, Dallas L.

, p. 6809 - 6815 (2007/10/03)

Trans-Dichlorotetracyanoplatinate(IV) as a Reagent for the Rapid and Quantitative Formation of Intramolecular Disulfide Bonds in Peptides

Shi, Tiesheng,Rabenstein, Dallas L.

, p. 4590 - 4595 (2007/10/03)

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