⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL31352918 | 1.00 | — | — | |
| SCHEMBL28844936 | 1.00 | — | — | |
| SCHEMBL29793519 | 1.00 | — | — | |
| SCHEMBL157229 | 1.00 | — | — | |
| SCHEMBL16553398 | 1.00 | — | — | |
| SCHEMBL29886140 | 1.00 | — | — | |
| Fluoride SCHEMBL11154391 | 0.71 | — | — | |
| SCHEMBL10685135 | 0.71 | — | — | |
| Hydrochloric Acid SCHEMBL7075086 | 0.71 | — | — | |
| SCHEMBL8641934 | 0.71 | — | — |
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 16 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1285082-B1 | METHOD COMPRISING THE INDIRECT ELECTROCHEMICAL REGENERATION OF NAD(P)H | BASF AG (DE) | 2006-12-27 | — | — | EP | claimed |
| JP-1289805-A | — | — | None | — | — | JP | disclosed |
| JP-1289806-A | — | — | None | — | — | JP | disclosed |
| US-20250110071-A1 | USING HYPERPOLARISED 15N DERIVED SYNTHONS TO CREATE HYPERPHARMACEUTICALS THROUGH SABRE | UNIVERSITY OF YORK (GB) | 2025-04-03 | — | — | US | disclosed |
| WO-2023144521-A1 | USING HYPERPOLARISED 15N DERIVED SYNTHONS TO CREATE HYPERPHARMACEUTICALS THROUGH SABRE | UNIVERSITY OF YORK (GB) | 2023-08-03 | — | — | WO | disclosed |
| EP-2062906-A1 | Coordination complex system comprising tautomeric ligands | Universiteit van Amsterdam (NL) | 2009-05-27 | — | — | EP | disclosed |
| US-6863781-B2 | Process for photocatalysis and two-electron mixed-valence complexes | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2005-03-08 | — | — | US | disclosed |
| US-20030201161-A1 | Process for photocatalysis and two-electron mixed-valence complexes | NATIONAL SCIENCE FOUNDATION | 2003-10-30 | — | — | US | disclosed |
| WO-2003076073-A1 | PROCESS FOR THE PHOTOCATALYTIC PRODUCTION OF HYDROGEN FROM PROTIC SOLUTIONS USING TWO-ELECTRON MIXED-VALANCE BINUCLEAR COMPLEXES AND SUCH COMPLEXES | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2003-09-18 | — | — | WO | disclosed |
| JP-H01289805-A | HYDROGENATION OF OLEFINICALLY UNSATURATED POLYMER | ASAHI CHEM IND CO LTD | 1989-11-21 | — | — | JP | disclosed |
| JP-H01289806-A | SELECTIVE HYDROGENATION OF OLEFINICALLY UNSATURATED POLYMER CONTAINING FUNCTIONAL GROUP | ASAHI CHEM IND CO LTD | 1989-11-21 | — | — | JP | disclosed |
| US-4746760-A | HALOGENATION BY COMPLEXING | CHEVRON RESEARCH COMPANY (US) | 1988-05-24 | — | — | US | disclosed |
| US-4511745-A | HALOGENATION, PENTAMETHYLCYCLOPENTADIENYL TRIMETHYLPHOSPHINE RHODIUM DIHYDRIDE | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE UNITED STATES DEPARTMENT OF ENERGY (US) | 1985-04-16 | — | — | US | disclosed |
| US-4444898-A | Heterocatalyst system | UNIVERSITY PATENTS, INC. (US) | 1984-04-24 | — | — | US | disclosed |
| EP-0098289-A1 | HETEROCATALYST SYSTEM | UNIVERSITY PATENTS, INC. (US) | 1984-01-18 | — | — | EP | disclosed |
| WO-1983002404-A1 | HETEROCATALYST SYSTEM | UNIVERSITY PATENTS INC (US) | 1983-07-21 | — | — | WO | disclosed |