ChemicalBook >> CAS DataBase List >>spinorphin

spinorphin

CAS No.
137201-62-8
Chemical Name:
spinorphin
Synonyms
LVVYPWT;spinorphin;Spinorphin 137201-62-8;inhibit,Inhibitor,Spinorphin;L-Threonine, L-leucyl-L-valyl-L-valyl-L-tyrosyl-L-prolyl-L-tryptophyl-
CBNumber:
CB11350574
Molecular Formula:
C45H64N8O10
Molecular Weight:
877.04
MDL Number:
MOL File:
137201-62-8.mol
Last updated:2023-05-18 11:30:58

spinorphin Properties

storage temp. Desiccate at -20°C
solubility Soluble to 1 mg/ml in H2O
form solid
color White
Water Solubility Soluble to 1 mg/ml in water
Stability Hygroscopic

spinorphin price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 29914 Spinorphin 137201-62-8 500μg $68 2024-03-01 Buy
Cayman Chemical 29914 Spinorphin 137201-62-8 1mg $121 2024-03-01 Buy
Cayman Chemical 29914 Spinorphin 137201-62-8 5mg $335 2024-03-01 Buy
Cayman Chemical 29914 Spinorphin 137201-62-8 10mg $535 2024-03-01 Buy
Tocris 2931 Spinorphin 137201-62-8 1 $115 2021-12-16 Buy
Product number Packaging Price Buy
29914 500μg $68 Buy
29914 1mg $121 Buy
29914 5mg $335 Buy
29914 10mg $535 Buy
2931 1 $115 Buy

spinorphin Chemical Properties,Uses,Production

Uses

Spinorphin is a novel neuropeptide, which exhibits complete inhibition of agonist-induced nociception.It is peptide analogs with branched amino acid probes and their therapeutic use.

Definition

ChEBI: Spinorphin is an oligopeptide.

Biological Activity

spinorphin is an endogenous inhibitor of enkephalin-degrading enzymes (aminopeptidase, dipeptidyl aminopeptidase iii, angiotensin-converting enzyme and enkephalinase) [1]. also, it is a potent antagonist of human p2x3 receptor and the n-formylpeptide receptor subtype fpr with ic50 value of 8.3 pm for p2x3 receptor[2][3].enkephalin degrading enzymes are a series of enzymes that hydrolyze enkephalins, which play an important role in management of blood pressure, pain, hypertension and cardiovascular diseases.in human embryonic kidney (hek) 293 cells transfected with mouse fpr, spinorphin induced a typical rise in the intracellular ca2+ concentration with ec50 of 128 μm. also, in normal mouse neutrophils, spinorphin induced calcium flux in a dose-dependent way. while the neutrophils from mice deficient in the fmlf receptor subtype fpr didn’t response [3].in mice, intrathecal administration of spinorphin inhibited the allodynia induced by intrathecal nociceptin in a dose-dependent way. furthermore, spinorphin enhanced the inhibitory effect of enkephalin on allodynia induced by nociceptin [4].

References

[1]. nishimura k, hazato t. isolation and identification of an endogenous inhibitor of enkephalin-degrading enzymes from bovine spinal cord. biochem biophys res commun, 1993, 194(2): 713-719.
[2]. jung ky, moon hd, lee ge, et al. structure-activity relationship studies of spinorphin as a potent and selective human p2x(3) receptor antagonist. j med chem, 2007, 50(18): 4543-4547.
[3]. liang ts, gao jl, fatemi o, et al. the endogenous opioid spinorphin blocks fmet-leu-phe-induced neutrophil chemotaxis by acting as a specific antagonist at the n-formylpeptide receptor subtype fpr. j immunol, 2001, 167(11): 6609-6614.
[4]. honda m, okutsu h, matsuura t, et al. spinorphin, an endogenous inhibitor of enkephalin-degrading enzymes, potentiates leu-enkephalin-induced anti-allodynic and antinociceptive effects in mice. jpn j pharmacol, 2001, 87(4): 261-267.

spinorphin Preparation Products And Raw materials

Raw materials

Preparation Products

spinorphin Suppliers

Global( 60)Suppliers
Supplier Tel Email Country ProdList Advantage
Shenzhen Nexconn Pharmatechs Ltd
+86-755-89396905 +86-15013857715 admin@nexconn.com China 10248 58
Career Henan Chemica Co
+86-0371-86658258 15093356674; laboratory@coreychem.com China 30255 58
BOC Sciences
+16314854226 inquiry@bocsci.com United States 19743 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
Hebei Miaoyin Technology Co.,Ltd
+86-17367732028 +86-17367732028 kathy@hbyinsheng.com China 3582 58
Nanjing TGpeptide
+86-13347807150 +86-13347807150 support@tgpeptide.com China 3279 58
Zhejiang Hangyu API Co., Ltd
+8617531972939 anna@api-made.com China 2944 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Sichuan Jisheng Biopharmaceutical
+86-0833-2598903 +8619981963231 jane@jsjpharm.cn China 175 58
spinorphin Spinorphin 137201-62-8 L-Threonine, L-leucyl-L-valyl-L-valyl-L-tyrosyl-L-prolyl-L-tryptophyl- LVVYPWT inhibit,Inhibitor,Spinorphin 137201-62-8 Purinergics P2 receptor