Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C10H15NO |
Molecular Weight | 165.2322 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C#CCO[C@H]1CN2CCC1CC2
InChI
InChIKey=XVFJONKUSLSKSW-JTQLQIEISA-N
InChI=1S/C10H15NO/c1-2-7-12-10-8-11-5-3-9(10)4-6-11/h1,9-10H,3-8H2/t10-/m0/s1
Molecular Formula | C10H15NO |
Molecular Weight | 165.2322 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Talsaclidine (WAL-2014) is a selective full agonist of M1 muscarinic receptor, having partial agonist activity on the M2 and M3 subtypes (with no in vivo consequences). The general receptor profile of talsaclidine demonstrates a nearly specific interaction with muscarinic receptors, having only weak binding affinity for alpha1- and nicotinic receptors. The drug is being tested in phase III of clinical trials for the treatment of Alzheimer's disease.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL216 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11392631 |
18.0 nM [EC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2.7 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10188789 |
0.5 mg single, oral dose: 0.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
TALSACLIDINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
730 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10188789 |
160 mg single, oral dose: 160 mg route of administration: Oral experiment type: SINGLE co-administered: |
TALSACLIDINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
12 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10188789 |
0.5 mg single, oral dose: 0.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
TALSACLIDINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
4500 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10188789 |
160 mg single, oral dose: 160 mg route of administration: Oral experiment type: SINGLE co-administered: |
TALSACLIDINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
99% EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/11037112 |
TALSACLIDINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
PubMed
Title | Date | PubMed |
---|---|---|
M1 muscarinic agonists can modulate some of the hallmarks in Alzheimer's disease: implications in future therapy. | 2003 |
|
Beta-secretase BACE1 is differentially controlled through muscarinic acetylcholine receptor signaling. | 2004 Jul 15 |
|
Zinc uptake is mediated by M1 muscarinic acetylcholine receptors in differentiated SK-SH-SY5Y cells. | 2006 Feb |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT02248116
Talsaclidine is administered orally at a dose of 24 mg, three times a day.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9272924
Isolated tracheal muscle from guinea-pigs was incubated with 1-3000 uM of talsaclidine to test the muscarinic receptor agonism.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:52:03 GMT 2023
by
admin
on
Fri Dec 15 18:52:03 GMT 2023
|
Record UNII |
1O8VSL798T
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C47796
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
1O8VSL798T
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
C96885
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
100000083228
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
SUB10814MIG
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
7270
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
DB12287
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
CHEMBL2111051
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
Talsaclidine
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
147025-53-4
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
71792
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY | |||
|
DTXSID20163565
Created by
admin on Fri Dec 15 18:52:03 GMT 2023 , Edited by admin on Fri Dec 15 18:52:03 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
TARGET -> AGONIST |
|
||
|
SALT/SOLVATE -> PARENT |
|
||
|
TARGET->PARTIAL AGONIST |
|
||
|
TARGET->PARTIAL AGONIST |
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |
|