Welcome to LookChem.com Sign In|Join Free
  • or
ALPHA-CONOTOXIN GI, a peptide derived from the venom of the Conus geographus cone snail, is an antagonist of nicotinic acetylcholine receptors, specifically targeting the α9α10 subtype in auditory hair cells. Its unique properties make it a valuable tool for studying the auditory system and developing new medications for hearing-related conditions. Furthermore, its ability to inhibit the release of pro-inflammatory compounds from immune cells positions it as a potential therapeutic agent for chronic pain and inflammatory disorders, garnering ongoing research and interest in neuroscience and pharmacology.

76862-65-2

Post Buying Request

76862-65-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

76862-65-2 Usage

Uses

Used in Neuroscience Research:
ALPHA-CONOTOXIN GI is used as a research tool for studying the role of nicotinic acetylcholine receptors in the auditory system, particularly the α9α10 subtype found in auditory hair cells.
Used in Pharmaceutical Development:
ALPHA-CONOTOXIN GI is used as a potential therapeutic agent for developing new medications targeting conditions affecting the auditory system, leveraging its antagonistic properties against specific nicotinic acetylcholine receptors.
Used in Pain Management:
ALPHA-CONOTOXIN GI is used as a potential therapeutic agent for chronic pain management, due to its ability to inhibit the release of pro-inflammatory compounds from immune cells, thereby reducing inflammation and pain.
Used in Inflammatory Disorder Treatment:
In the field of inflammatory disorders, ALPHA-CONOTOXIN GI is used as a potential therapeutic agent for treating conditions characterized by excessive inflammation, again capitalizing on its capacity to modulate immune cell activity and reduce the release of pro-inflammatory mediators.

Check Digit Verification of cas no

The CAS Registry Mumber 76862-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,6 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76862-65:
(7*7)+(6*6)+(5*8)+(4*6)+(3*2)+(2*6)+(1*5)=172
172 % 10 = 2
So 76862-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C55H80N20O18S4/c1-25-44(83)72-36-21-95-97-22-37(73-45(84)29(56)9-10-42(80)81)52(91)74-38(51(90)69-33(16-40(57)78)54(93)75-12-4-8-39(75)53(92)65-25)23-96-94-20-35(43(58)82)71-50(89)34(19-76)70-48(87)31(14-26-5-2-6-28(77)13-26)67-49(88)32(15-27-17-61-24-64-27)68-47(86)30(7-3-11-62-55(59)60)66-41(79)18-63-46(36)85/h2,5-6,13,17,24-25,29-39,76-77H,3-4,7-12,14-16,18-23,56H2,1H3,(H2,57,78)(H2,58,82)(H,61,64)(H,63,85)(H,65,92)(H,66,79)(H,67,88)(H,68,86)(H,69,90)(H,70,87)(H,71,89)(H,72,83)(H,73,84)(H,74,91)(H,80,81)(H4,59,60,62)/t25-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-/m0/s1

76862-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name α-CONOTOXIN GI

1.2 Other means of identification

Product number -
Other names GLU-CYS-CYS-ASN-PRO-ALA-CYS-GLY-ARG-HIS-TYR-SER-CYS-NH2

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:76862-65-2 SDS

76862-65-2Downstream Products

76862-65-2Relevant academic research and scientific papers

High-throughput production of two disulphide-bridge toxins

Upert, Grégory,Mourier, Gilles,Pastor, Alexandra,Verdenaud, Marion,Alili, Doria,Servent, Denis,Gilles, Nicolas

supporting information, p. 8408 - 8411 (2014/07/22)

A quick and efficient production method compatible with high-throughput screening was developed using 36 toxins belonging to four different families of two disulphide-bridge toxins. Final toxins were characterized using HPLC co-elution, CD and pharmacological studies. This journal is the Partner Organisations 2014.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 76862-65-2