Skip to Content
Merck
CN

A256

9-Amino-1,2,3,4-tetrahydroacridine bis 1,7-heptylene dihydrochloride

>97%, solid

Synonym(s):

heptylene-bis(THA) dihydrochloride, heptylene-bis(tacrine) dihydrochloride

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C33H40N4 · 2HCl
CAS Number:
224445-12-9
Molecular Weight:
565.62
UNSPSC Code:
12352202
PubChem Substance ID:
24890669
MDL number:
MFCD08062163

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

1S/C33H40N4.2ClH/c1(2-12-22-34-32-24-14-4-8-18-28(24)36-29-19-9-5-15-25(29)32)3-13-23-35-33-26-16-6-10-20-30(26)37-31-21-11-7-17-27(31)33;;/h4,6,8,10,14,16,18,20H,1-3,5,7,9,11-13,15,17,19,21-23H2,(H,34,36)(H,35,37);2*1H

SMILES string

Cl.Cl.C(CCCNc1c2CCCCc2nc3ccccc13)CCCNc4c5CCCCc5nc6ccccc46

InChI key

RHKXINFBJWDTSK-UHFFFAOYSA-N

assay

>97%

form

solid

color

white

solubility

H2O: >10 mg/mL

storage temp.

2-8°C

Looking for similar products? Visit Product Comparison Guide

Legal Information

Sold under exclusive license from Mayo Foundation for Medical Education and Research.

Disclaimer

Extremely hygroscopic; store desiccated

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis of alkylene linked bis-THA and linked benzyl-THA as highly potent and selective inhibitors and molecular probes of acetylcholinesterase.
Pang, et al.
Journal of the Chemical Society. Perkin Transactions 1, 171-171 (1997)
Y P Pang et al.
The Journal of biological chemistry, 271(39), 23646-23649 (1996-09-27)
We report highly potent, selective, and low cost bifunctional acetylcholinesterase (AChE) inhibitors developed by our two-step prototype optimization strategy utilizing computer modeling of ligand docking with target proteins: 1) identify low affinity sites normally missed by x-ray crystallography; and 2)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service