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Details

Stereochemistry ACHIRAL
Molecular Formula C30H31FN2O
Molecular Weight 454.5783
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SIRAMESINE

SMILES

FC1=CC=C(C=C1)N2C=C(CCCCN3CCC4(CC3)OCC5=C4C=CC=C5)C6=C2C=CC=C6

InChI

InChIKey=XWAONOGAGZNUSF-UHFFFAOYSA-N
InChI=1S/C30H31FN2O/c31-25-12-14-26(15-13-25)33-21-23(27-9-2-4-11-29(27)33)7-5-6-18-32-19-16-30(17-20-32)28-10-3-1-8-24(28)22-34-30/h1-4,8-15,21H,5-7,16-20,22H2

HIDE SMILES / InChI

Molecular Formula C30H31FN2O
Molecular Weight 454.5783
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

Siramesine is a sigma2 opioid agonist under development by H Lundbeck as a potential treatment for anxiety. In March 1998, the compound was licensed to Forest Laboratories under a strategic alliance. In August 2000, siramesine entered phase II trials. Siramesine has been shown to trigger cell death of cancer cells and to exhibit a potent anticancer activity in vivo. Siramesine triggers cell death through destabilisation of mitochondria, but not lysosomes. Siramesine is a lysosomotropic detergent that induces cytoprotective autophagosome accumulation. Siramesine involves lysosomal leakage and oxidative stress.

CNS Activity

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
0.12 nM [IC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown
Primary
Unknown
Primary
Unknown

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
Mice: daily treatment with 0.0018 umol/kg (1 ug/kg) for 1, 2, 3 and 4 weeks
Route of Administration: Other
In Vitro Use Guide
Siramesine can induce rapid cell death in a number of cancer cell lines at concentrations above 20 uM.
Substance Class Chemical
Record UNII
3IX8CWR24V
Record Status Validated (UNII)
Record Version