JavaScript is disabled in your browser. Please enable JavaScript to view this website.
AB141290

Dynole® 2-24, Dynamin I and II inhibitor

Be the first to review this product! Submit a review

|

(1 Publication)

MW 371.6 Da, Purity >97%. Novel, potent dynamin I and II inhibitor (IC50 values are 0.56 and 5.4 μM respectively). Shows 4.4-fold selectivity for dynamin I. Highly potent inhibitor of clathrin mediated endocytosis (IC50 = 1.9 μM). Displays low cell toxicity.
1 Images
Chemical Structure - Dynole® 2-24, Dynamin I and II inhibitor (AB141290)
  • Chemical Structure

Lab

Chemical Structure - Dynole® 2-24, Dynamin I and II inhibitor (AB141290)

2D chemical structure image of ab141290, Dynole® 2-24, Dynamin I and II inhibitor

Key facts

CAS number

1416313-72-8

Purity

>97%

Form

Liquid

form

Molecular weight

371.6 Da

Molecular formula

C<sub>2</sub><sub>4</sub>H<sub>4</sub><sub>1</sub>N<sub>3</sub>

PubChem

71546959

Nature

Synthetic

Biochemical name

Dynole 2-24

Biological description

Novel, potent dynamin I and II inhibitor (IC50 values are 0.56 and 5.4 μM respectively). Shows 4.4-fold selectivity for dynamin I. Highly potent inhibitor of clathrin mediated endocytosis (IC50 = 1.9 μM). Displays low cell toxicity.

Canonical smiles

CCCCCCCCCCNCC1=CN(C2=CC=CC=C21)CCCN(C)C

InChi

InChI=1S/C24H41N3/c1-4-5-6-7-8-9-10-13-17-25-20-22-21-27(19-14-18-26(2)3)24-16-12-11-15-23(22)24/h11-12,15-16,21,25H,4-10,13-14,17-20H2,1-3H3

IUPAC Name

N-[[1-[3-(dimethylamino)propyl]indol-3-yl]methyl]decan-1-amine

Product details

Sold under exclusive licence from Children's Medical Research Institute and Newcastle Innovation Ltd. Dynole® is a trademark of Children's Medical Research Institute and Newcastle Innovation Ltd.

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions

Product protocols

Publications (1)

Recent publications for all applications. Explore the full list and refine your search

eLife 6: PubMed29271742

2017

Paxillin facilitates timely neurite initiation on soft-substrate environments by interacting with the endocytic machinery.

Applications

Unspecified application

Species

Unspecified reactive species

Ting-Ya Chang,Chen Chen,Min Lee,Ya-Chu Chang,Chi-Huan Lu,Shao-Tzu Lu,De-Yao Wang,Aijun Wang,Chin-Lin Guo,Pei-Lin Cheng
View all publications
websiteProtocolBooklet
en

Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

For licensing inquiries, please contact partnerships@abcam.com