⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL5180442 | 0.87 | — | — | |
| SCHEMBL15080934 | 0.81 | TDP1 (0.32) | — | |
| SCHEMBL3806335 | 0.77 | TDP1 (0.41) | — | |
| SCHEMBL23653782 | 0.74 | — | — | |
| SCHEMBL8998478 | 0.73 | — | — | |
| SCHEMBL10349774 | 0.72 | — | — | |
| SCHEMBL8765339 | 0.72 | — | — | |
| SCHEMBL3491755 | 0.72 | TDP1 (0.38) | — | |
| SCHEMBL8076843 | 0.72 | — | — | |
| SCHEMBL8768371 | 0.72 | — | — |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 18 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20240329480-A1 | Dynamic Glass Element Using Reversible Metal Electrodeposition Electrolytes with Tunable PH with High Opacity and Excellent Resting Stability and Electrolytes Useful Therefore | The Board of Regents of the Nevada System of Higher Education on Behalf of the Univ of Nevada (US) | 2024-10-03 | — | — | US | disclosed |
| WO-2022221094-A1 | DYNAMIC GLASS ELEMENT USING REVERSIBLE METAL ELECTRODEPOSITION ELECTROLYTES WITH TUNABLE PH WITH HIGH OPACITY AND EXCELLENT RESTING STABILITY AND ELECTROLYTES USEFUL THEREFORE | THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION, ON BEHALF OF THE UNIVERSITY OF NEVADA, RENO (US) | 2022-10-20 | — | — | WO | disclosed |
| US-20180305400-A1 | STABILIZED COMPOUNDS HAVING SECONDARY STRUCTURE MOTIFS | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2018-10-25 | — | — | US | disclosed |
| US-9951099-B2 | Stabilized compounds having secondary structure motifs | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2018-04-24 | — | — | US | disclosed |
| US-20170088581-A1 | STABILIZED COMPOUNDS HAVING SECONDARY STRUCTURE MOTIFS | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2017-03-30 | — | — | US | disclosed |
| US-9505801-B2 | Stabilized compounds having secondary structure motifs | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2016-11-29 | — | — | US | disclosed |
| US-8895699-B2 | Stabilized compounds having secondary structure motifs | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2014-11-25 | — | — | US | disclosed |
| US-20140162339-A1 | Stabilized Compounds Having Secondary Structure Motifs | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2014-06-12 | — | — | US | disclosed |
| US-20130211046-A1 | Stabilized Compounds Having Secondary Structure Motifs | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2013-08-15 | — | — | US | disclosed |
| US-8324428-B2 | Stabilized compounds having secondary structure motifs | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2012-12-04 | — | — | US | disclosed |
| US-20110028753-A1 | Stabilized Compounds Having Secondary Structure Motifs | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2011-02-03 | — | — | US | disclosed |
| US-7786072-B2 | synthesizing a peptide from a selected number of natural or non-natural amino acids; stabilized p53 donor helical peptides | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2010-08-31 | — | — | US | disclosed |
| CN-100549155-C | Remove the composition that residue is used in the semiconductor production | EKC TECHNOLOGY INC (US) | 2009-10-14 | — | — | CN | disclosed |
| CN-100341992-C | Composition and method for removing residues from semiconductor manufacturing | EKC TECHNOLOGY INC (US) | 2007-10-10 | — | — | CN | disclosed |
| US-7192713-B1 | synthesizing a peptide from a selected number of natural or non-natural amino acids; stabilized p53 donor helical peptides | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2007-03-20 | — | — | US | disclosed |
| CN-1721516-A | Semiconductor process residue removal composition | EKC TECHNOLOGY INC (US) | 2006-01-18 | — | — | CN | disclosed |
| US-20060008848-A1 | synthesizing a peptide from a selected number of natural or non-natural amino acids; stabilized p53 donor helical peptides | NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT | 2006-01-12 | — | — | US | disclosed |
| CN-1465687-A | Composition and method for removing residues from semiconductor manufacturing | EKC������˾ | 2004-01-07 | — | — | CN | disclosed |