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
SMILES
FC1=CC=C(C=C1)N2C=C(CCCCN3CCC4(CC3)OCC5=CC=CC=C45)C6=CC=CC=C26
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
| Molecular Formula | C30H31FN2O |
| Molecular Weight | 454.5783 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionCurator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/7783131 | https://www.ncbi.nlm.nih.gov/pubmed/24091661
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/7783131 | https://www.ncbi.nlm.nih.gov/pubmed/24091661
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26051466 | https://www.ncbi.nlm.nih.gov/pubmed/9400007
Curator's Comment: Siramesine easily penetrated the blood-brain barrier
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0033024 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23058984 |
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Target ID: CHEMBL613288 |
0.12 nM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9400007
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24091661
Siramesine can induce rapid cell death in a number of cancer cell lines at concentrations above 20 uM.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:19:41 GMT 2025
by
admin
on
Wed Apr 02 09:19:41 GMT 2025
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| Record UNII |
3IX8CWR24V
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English |
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NCI_THESAURUS |
C28197
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CHEMBL61479
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7831
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300000036980
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3IX8CWR24V
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9829526
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DB06555
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147817-50-3
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DTXSID90163810
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SIRAMESINE
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C73302
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TARGET -> AGONIST |
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |
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