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Details

Stereochemistry ACHIRAL
Molecular Formula C22H24ClN3OS2
Molecular Weight 446.028
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SPICLOMAZINE

SMILES

ClC1=CC=C2SC3=CC=CC=C3N(CCCN4CCC5(CC4)NC(=O)CS5)C2=C1

InChI

InChIKey=CFOYBMUYCBSDAL-UHFFFAOYSA-N
InChI=1S/C22H24ClN3OS2/c23-16-6-7-20-18(14-16)26(17-4-1-2-5-19(17)29-20)11-3-10-25-12-8-22(9-13-25)24-21(27)15-28-22/h1-2,4-7,14H,3,8-13,15H2,(H,24,27)

HIDE SMILES / InChI

Molecular Formula C22H24ClN3OS2
Molecular Weight 446.028
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

Spiclomazine induces apoptosis associated with the suppression of migration and invasion in pancreatic carcinoma cells

CNS Activity

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Diceplon
Primary
Unknown

PubMed

Sample Use Guides

In Vivo Use Guide
oral administration of 5-10 mg
Route of Administration: Oral
In Vitro Use Guide
Treatment with Clospirazine hydrochloride (spiclomazine) for 24 and 48 h resulted in a time and dose-dependent growth reduction of CFPAC-1 and MIA PaCa-2 cell lines examined by MTT assay. This small molecule inhibited the cell growth to approximately 61.1+/-5.3%, 76.4+/-3.2% and 90.4+/-0.5% of control in CFPAC-1 cells, and 79.3+/-1.0%, 84.5+/-1.5% and 93.6+/-0.2% of control in MIA PaCa-2 cells at the concentrations of 30, 40, and 50 mg/mL for 48 h, respectively.
Substance Class Chemical
Record UNII
G2V8248111
Record Status Validated (UNII)
Record Version