⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL1565011 | 0.70 | — | — | |
| SCHEMBL20716 | 0.70 | — | — | |
| SCHEMBL10939947 | 0.67 | — | — | |
| SCHEMBL943593 | 0.67 | — | — | |
| Ammonia Solution, Strong SCHEMBL29186443 | 0.67 | — | — | |
| SCHEMBL10516740 | 0.67 | — | — | |
| SCHEMBL1140456 | 0.67 | — | — | |
| SCHEMBL859191 | 0.64 | — | — | |
| Ethylene SCHEMBL5850 | 0.64 | — | — | |
| SCHEMBL700310 | 0.64 | — | — |
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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-8501854-B2 | Templated metal oxide particles and methods of making | 3M INNOVATIVE PROPERTIES COMPANY (US) | 2013-08-06 | — | — | US | disclosed |
| EP-1877468-B1 | TEMPLATED SEMICONDUCTOR PARTICLES AND METHODS OF MAKING | 3M INNOVATIVE PROPERTIES CO (US) | 2012-01-18 | — | — | EP | disclosed |
| US-20110207868-A1 | TEMPLATED METAL OXIDE PARTICLES AND METHODS OF MAKING | 3M INNOVATIVE PROPERTIES COMPANY | 2011-08-25 | — | — | US | disclosed |
| EP-2344514-A2 | SYNTHETIC METHODS AND DERIVATIVES OF TRIPHOSPHATE OLIGONUCLEOTIDES | Alnylam Pharmaceuticals Inc. (US) | 2011-07-20 | — | — | EP | disclosed |
| US-7956001-B2 | Templated metal oxide particles and methods of making | 3M INNOVATIVE PROPERTIES COMPANY (US) | 2011-06-07 | — | — | US | disclosed |
| US-20100234213-A1 | TEMPLATED METAL OXIDE PARTICLES AND METHODS OF MAKING | 3M INNOVATIVE PROPERTIES COMPANY | 2010-09-16 | — | — | US | disclosed |
| WO-2010028079-A2 | SYNTHETIC METHODS AND DERIVATIVES OF TRIPHOSPHATE OLIGONUCLEOTIDES | ALNYLAM PHARMACEUTICALS, INC (US) | 2010-03-11 | — | — | WO | disclosed |
| US-7588701-B2 | Cored dendrimer comprising crosslinked dendrons surrounding a central interior region that is free of organic material, a semiconductor particle within cored dendrimer, having a size that is no greater than an outer dimension of cored dendrimer and that is greater than central interior region | 3M INNOVATIVE PROPERTIES COMPANY (US) | 2009-09-15 | — | — | US | disclosed |
| EP-2066584-A2 | TEMPLATED METAL OXIDE PARTICLES AND METHODS OF MAKING | 3M Innovative Properties Company (US) | 2009-06-10 | — | — | EP | disclosed |
| US-20080265221-A1 | TEMPLATED SEMICONDUCTOR PARTICLES AND METHODS OF MAKING | 3M INNOVATIVE PROPERTIES COMPANY | 2008-10-30 | — | — | US | disclosed |
| WO-2006105029-A2 | TEMPLATED METAL PARTICLES WITHIN A CROSSLINKED, CORED DENDRIMER AND METHODS OF MAKING | 3M INNOVATIVE PROPERTIES COMPANY (US) | 2006-10-05 | — | — | WO | disclosed |
| US-20060219159-A1 | Templated semiconductor particles and methods of making | 3M INNOVATIVE PROPERTIES COMPANY | 2006-10-05 | — | — | US | disclosed |
| EP-0642507-B1 | TRANSITION STATE ANALOGUES OF COCAINE, THEIR USE FOR PRODUCING CATALYTIC ANTIBODIES AGAINST COCAINE AND USE OF THE SAME IN DIAGNOSIS AND THERAPY | UNIV COLUMBIA (US) | 2004-02-04 | — | — | EP | disclosed |
| US-6566084-B1 | Detecting hydrolysis of cocaine compound; obtain cocaine mixture, incubate with antibody, monitor generation of benzoic zacid | THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK | 2003-05-20 | — | — | US | disclosed |
| US-6184013-B1 | ANTIBODY FOR REDUCING CONCENTRATION OF DRUG IN PATIENT | THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK | 2001-02-06 | — | — | US | disclosed |
| US-5990285-A | ANTIBODY CAPABLE OF BINDING A TRANSITION STATE ANALOG FOR THE HYDROLYSIS OF COCAINE BENZOYL ESTER GROUP; TREATMENT OF DRUG ABUSE, DRUG DEPENDENCE, OVERDOSES | THE TRUSTEES OF COLUMBIA UNIVERSITY (US) | 1999-11-23 | — | — | US | disclosed |
| US-5977314-A | ANTIBODY CAPABLE OF CATALYZING THE HYDROLYSIS OF COCAINE AT BENZOYL ESTER GROUP AND AGAINST SPECIFIC STRUCTURAL COMPOUNDS LISTED; FOR DECREASING CONCENTRATION OF COCAINE IN A SUBJECT | THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) | 1999-11-02 | — | — | US | disclosed |
| EP-0642507-A4 | CATALYTIC ANTIBODIES AGAINST COCAINE AND METHODS OF USING AND PRODUCING SAME. | — | 1995-03-29 | — | — | EP | disclosed |
| EP-0642507-A1 | CATALYTIC ANTIBODIES AGAINST COCAINE AND METHODS OF USING AND PRODUCING SAME | The Trustees of Columbia University in the City of New York (US) | 1995-03-15 | — | — | EP | disclosed |
| WO-1993020076-A1 | CATALYTIC ANTIBODIES AGAINST COCAINE AND METHODS OF USING AND PRODUCING SAME | THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) | 1993-10-14 | — | — | WO | disclosed |