⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL15292931 | 0.60 | — | — | |
| SCHEMBL49646 | 0.59 | — | — | |
| SCHEMBL49720 | 0.59 | — | — | |
| SCHEMBL4802647 | 0.59 | — | — | |
| Water SCHEMBL23525631 | 0.56 | — | — | |
| SCHEMBL189693 | 0.56 | — | — | |
| Fluoride SCHEMBL1057439 | 0.56 | — | — | |
| Hydrochloric Acid SCHEMBL4467690 | 0.56 | — | — | |
| SCHEMBL6700452 | 0.56 | — | — | |
| SCHEMBL1794632 | 0.56 | — | — |
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 119 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119462691-A | Quinoline acridine-5, 9-diketone MR-TADF red light luminescent material and preparation method and application thereof | 常州大学 | 2025-02-18 | — | — | CN | claimed |
| CN-114621115-B | Method for synthesizing oxime compounds under photocatalysis condition | 河南大学 | 2023-05-23 | — | — | CN | claimed |
| CN-114621115-A | Method for synthesizing oxime compound under photocatalysis condition | 河南大学 | 2022-06-14 | — | — | CN | claimed |
| EP-0822835-A1 | HYBRID MAGNETIC RESONANCE CONTRAST AGENTS | IMARX PHARMACEUTICAL CORP. (US) | 1998-02-11 | — | — | EP | claimed |
| WO-1996032967-A1 | HYBRID MAGNETIC RESONANCE CONTRAST AGENTS | IMARX PHARMACEUTICAL CORPORATION (US) | 1996-10-24 | — | — | WO | claimed |
| CN-115974809-B | Method for preparing benzo [ d ] isothiazolin-3 (2H) -ketone through oxygen transfer reaction | 北京探微精细化工科技有限公司 | 2023-06-27 | — | — | CN | disclosed |
| EP-3706742-B1 | PRMT5 INHIBITORS | MERCK SHARP & DOHME LLC (US) | 2023-03-15 | — | — | EP | disclosed |
| CN-108884050-B | Tetrahydroisoquinoline derivatives | UCB生物制药私人有限公司 | 2022-07-05 | — | — | CN | disclosed |
| CN-114621115-A | Method for synthesizing oxime compound under photocatalysis condition | 河南大学 | 2022-06-14 | — | — | CN | disclosed |
| CN-113754696-A | Phosphaphenanthrene derivative, preparation and flame-retardant application | 华中师范大学 | 2021-12-07 | — | — | CN | disclosed |
| CN-108430965-B | Method for producing (meth) acrylic acid | 三菱化学株式会社 | 2021-03-16 | — | — | CN | disclosed |
| US-10947234-B2 | PRMT5 inhibitors | MERCK SHARP & DOHME CORP. (US) | 2021-03-16 | — | — | US | disclosed |
| EP-0810196-A1 | Method for inhibiting polymerization of (meth) acrylic acid or esters thereof | MITSUBISHI CHEMICAL CORPORATION (JP) | 1997-12-03 | — | — | EP | disclosed |
| WO-1997027582-A1 | MAGNETIC RECORDING MEDIUM | EMTEC MAGNETICS GMBH (DE) | 1997-07-31 | — | — | WO | disclosed |
| WO-1997027232-A1 | POLYMERS SUITABLE AS DISPERSING RESINS | BASF AKTIENGESELLSCHAFT (DE) | 1997-07-31 | — | — | WO | disclosed |
| WO-1996032967-A1 | HYBRID MAGNETIC RESONANCE CONTRAST AGENTS | IMARX PHARMACEUTICAL CORPORATION (US) | 1996-10-24 | — | — | WO | disclosed |
| EP-0496796-B1 | METHOD AND COMPOSITIONS FOR INHIBITION OF DISORDERS ASSOCIATED WITH OXIDATIVE DAMAGE | OKLAHOMA MED RES FOUND (US) | 1994-08-31 | — | — | EP | disclosed |
| EP-0135280-B1 | NEW POLYMERIZATION PROCESS AND POLYMERS PRODUCED THEREBY | COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) | 1993-05-12 | — | — | EP | disclosed |
| EP-0496796-A1 | METHOD AND COMPOSITIONS FOR INHIBITION OF DISORDERS ASSOCIATED WITH OXIDATIVE DAMAGE. | OKLAHOMA MED RES FOUND (US) | 1992-08-05 | — | — | EP | disclosed |
| WO-1991005552-A1 | METHOD AND COMPOSITIONS FOR INHIBITION OF DISORDERS ASSOCIATED WITH OXIDATIVE DAMAGE | OKLAHOMA MEDICAL RESEARCH FOUNDATION (US) | 1991-05-02 | — | — | WO | disclosed |