ZANAPEZIL

Details

Stereochemistry	ACHIRAL
Molecular Formula	C25H32N2O
Molecular Weight	376.5344
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

O=C(CCC1CCN(CC2=CC=CC=C2)CC1)C3=CC4=C(CCCCN4)C=C3

InChI

InChIKey=PMBLXLOXUGVTGB-UHFFFAOYSA-N

InChI=1S/C25H32N2O/c28-25(23-11-10-22-8-4-5-15-26-24(22)18-23)12-9-20-13-16-27(17-14-20)19-21-6-2-1-3-7-21/h1-3,6-7,10-11,18,20,26H,4-5,8-9,12-17,19H2

HIDE SMILES / InChI

Molecular Formula	C25H32N2O
Molecular Weight	376.5344
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8057278 | https://www.ncbi.nlm.nih.gov/pubmed/8667190

Zanapezil (TAK-147) is a selective reversible acetylcholine (ACh) esterase inhibitor that was designed as a drug for Alzheimer's disease (AD) treatment. The development of the drug was discontinued due to a lack of a dose-dependent effect in the trials.

CNS Activity

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Acetylcholinesterase 207 Target ID: CHEMBL220 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8667190 \| https://www.ncbi.nlm.nih.gov/pubmed/11763163	Inhibitor 8297		51.2 nM [IC50]

Conditions

Condition	Modality	Targets	Highest Phase	Product
Alzheimer’s disease 272 Sources: https://www.ncbi.nlm.nih.gov/pubmed/14535624	Primary		Phase III 656	Unknown Approved Use Unknown

PubMed

Title	Date	PubMed
Effect of 3-[1-(phenylmethyl)-4-piperidinyl]-1-(2,3,4,5-tetrahydro-1H-1-benzazepin-8-yl)-1-propanone fumarate, a novel acetylcholinesterase inhibitor, on spatial cognitive impairment induced by chronic cerebral hypoperfusion in rats.	2002 Oct 4	12359317
Comparison of the effect of TAK-147 (zanapezil) and E-2020 (donepezil) on extracellular acetylcholine level and blood flow in the ventral hippocampus of freely moving rats.	2004 Jun 25	15158174
Effect of oral administration of zanapezil (TAK-147) for 21 days on acetylcholine and monoamines levels in the ventral hippocampus of freely moving rats.	2005 Aug	15951830

Patents

Sample Use Guides

In Vivo Use Guide

Daily oral administration of TAK-147 (1 mg/kg) for 40 days increased phosphocreatine and ATP levels in brains of aged Fischer rats.

Route of Administration: Oral

In Vitro Use Guide

The inhibitory potency of TAK-147 towards AChE activity (IC50) was found to be 51.2 nM in vitro. AChE activities were measured using the radioisotopic method on male Wistar rats' cerebral cortices.

Substance Class	Chemical Created by `admin` on `Sat Dec 16 16:04:42 UTC 2023` Edited by `admin` on `Sat Dec 16 16:04:42 UTC 2023`
Record UNII	0A0800O89N
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

ZANAPEZIL

Official Name

English

zanapezil [INN]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C47792