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122752-16-3

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122752-16-3 Usage

Biological Activity

[d-ala2]-deltorphin ii (dadelt ii) is a natural agonist of δ opioid receptor with ki or ic50 value of 0.41 nm [1, 2].opioid receptors are most abundant in the central nervous system, but are also localized in many peripheral tissues in mammalian organisms. there are three types of opioid receptors that are well-defined; the μ, δ and κ receptors [2].[d-pen2, d-pen5]enkephalin (dpdpe) is a second highly selective agonist of δ [3]. treatment with dpdpe at 1 m for as short as 3 min significantly diminished the inhibition of the opioid receptor in ng108-15 cells to cyclic amp production. that means neuronal delta opioid receptor underwent acute desensitization. this desensitization was temporally parallel to the phosphorylation of delta opioid receptor 3 min. after agonist stimulation [4].i.c.v. administration of dadelt ii from 0.38-12.78 nm resulted in a dose- and time-related antinociception. 10 min after the administration of dadelt ii, the maximal antinociceptive response was seen. until 60 min after the administration of dadelt ii, effects were detected. these antinociceptive effects of i.c.v. dadelt ii were antagonized by the selective δ antagonist, ici 174,864 [3]. after supraspinal and spinal administration in rats intracerebroventricularly, dadelt ii at 0.2, 1, 10 μg/rat in a dose-related fashion inhibited diarrhea and colonic bead expulsion but did not show any effect on the rate of small intestine transit. spinal administration of dadelt ii at the same dose produced similar results. naltrindole is a selective antagonist of the δ opioid receptor. subcutaneous pretreatment with naltrindole at 1 and 10 mg/kg antagonized effects of dadelt ii partially and completely, respectively [1].

Biochem/physiol Actions

Selective δ2 opioid receptor agonist

references

[1]. broccardo m, improta g. antidiarrheal and colonic antipropulsive effects of spinal and supraspinal administration of the natural δ opioid receptor agonist,[d-ala2] deltorphin ii, in the rat. european journal of pharmacology, 1992, 218(1): 69-73.[2]. janecka a, fichna j, janecki t. opioid receptors and their ligands. current topics in medicinal chemistry, 2004, 4(1): 1-17.[3]. jiang q, mosberg hi, porreca f. antinociceptive effects of [d-ala2] deltorphin ii, a highly selective δ agonist in vivo. life sciences, 1990, 47(11): pl43-pl47.[4]. cai y, zhang y, wu y, et al. δ opioid receptor in neuronal cells undergoes acute and homologous desensitization. biochemical and biophysical research communications, 1996, 219(2): 342-347.

Check Digit Verification of cas no

The CAS Registry Mumber 122752-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,7,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 122752-16:
(8*1)+(7*2)+(6*2)+(5*7)+(4*5)+(3*2)+(2*1)+(1*6)=103
103 % 10 = 3
So 122752-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C38H54N8O10/c1-20(2)31(37(55)41-19-29(40)48)46-38(56)32(21(3)4)45-35(53)27(15-16-30(49)50)43-36(54)28(18-23-9-7-6-8-10-23)44-33(51)22(5)42-34(52)26(39)17-24-11-13-25(47)14-12-24/h6-14,20-22,26-28,31-32,47H,15-19,39H2,1-5H3,(H2,40,48)(H,41,55)(H,42,52)(H,43,54)(H,44,51)(H,45,53)(H,46,56)(H,49,50)/t22-,26+,27+,28+,31+,32?/m1/s1

122752-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [D-Ala2]-Deltorphin II

1.2 Other means of identification

Product number -
Other names Tyr-D-Ala-Phe-Glu-Val-Val-Gly amide

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:122752-16-3 SDS

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