Details
Stereochemistry | ACHIRAL |
Molecular Formula | H2MoS4 |
Molecular Weight | 226.22 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
S[Mo](S)(=S)=S
InChI
InChIKey=IEGNLZVDENYZEJ-UHFFFAOYSA-L
InChI=1S/Mo.2H2S.2S/h;2*1H2;;/q+2;;;;/p-2
Molecular Formula | H2MoS4 |
Molecular Weight | 226.22 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Tiomolibdic acid salt, Bis-choline tetrathiomolybdate (ATN-224, WTX-101), is under investigation as a therapy against different cancers and Wilson’s disease (WD). ATN-224 is a second-generation analog of ammonium tetrathiomolybdate. ATN-224 is a novel copper chelator. ATN-224 inhibits CuZn superoxide dismutase 1 (SOD1) leading to antiangiogenic and antitumor effects. Strategically tailoring combination regimens that include ATN-224 and target ROS may be a viable approach to advance the treatment of melanoma. ATN-224 is in phase III clinical trial for the treatment of Hepatolenticular degeneration. WTX-101 is in phase II clinical trials for the treatment of Wilson's disease. Once daily WTX-101 treatment over 24 weeks improved neurologic disease, hepatic status and copper control in newly diagnosed WD patients. WTX-101 appears well tolerated. Drug-induced, paradoxical, neurological deterioration was not observed. This compound has received orphan drug designation in both the United States and the European Union. WTX-101 was originally discovered by University of Michigan and now is being developed by Wilson Therapeutics by acquisition.
Approval Year
PubMed
Title | Date | PubMed |
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Redox-related antimelanoma activity of ATN-224. | 2009 Dec |
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Copper chelator ATN-224 inhibits endothelial function by multiple mechanisms. | 2009 May |
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Development of a new bimodal imaging methodology: a combination of fluorescence microscopy and high-resolution secondary ion mass spectrometry. | 2010 Oct |
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Copper chelation enhances antitumor efficacy and systemic delivery of oncolytic HSV. | 2012 Sep 15 |
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The copper chelator ATN-224 induces peroxynitrite-dependent cell death in hematological malignancies. | 2013 Jul |
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A non-comparative randomized phase II study of 2 doses of ATN-224, a copper/zinc superoxide dismutase inhibitor, in patients with biochemically recurrent hormone-naïve prostate cancer. | 2013 Jul |
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Targeting SOD1 reduces experimental non–small-cell lung cancer. | 2014 Jan |
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The copper chelator ATN-224 induces caspase-independent cell death in diffuse large B cell lymphoma. | 2014 Jul |
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Targeting antioxidants for cancer therapy. | 2014 Nov 1 |
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ATN-224 enhances antitumor efficacy of oncolytic herpes virus against both local and metastatic head and neck squamous cell carcinoma. | 2015 |
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Change in PSA velocity is a predictor of overall survival in men with biochemically-recurrent prostate cancer treated with nonhormonal agents: combined analysis of four phase-2 trials. | 2015 Mar |
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Down-regulation of superoxide dismutase 1 by PMA is involved in cell fate determination and mediated via protein kinase D2 in myeloid leukemia cells. | 2015 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:43:36 GMT 2023
by
admin
on
Sat Dec 16 16:43:36 GMT 2023
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Record UNII |
206J6X63BE
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Record Status |
Validated (UNII)
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Record Version |
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