⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL454510 | 0.93 | — | — | |
| SCHEMBL9615755 | 0.79 | KDM1A (0.30) | — | |
| SCHEMBL16544487 | 0.79 | KDM1A (0.30) | — | |
| SCHEMBL9806307 | 0.77 | — | — | |
| SCHEMBL728353 | 0.77 | — | — | |
| SCHEMBL11722482 | 0.77 | — | — | |
| SCHEMBL9282674 | 0.77 | ADRA2A (0.34) | — | |
| SCHEMBL24432934 | 0.76 | ALDH1A1 (0.35) | — | |
| SCHEMBL11724746 | 0.76 | ALDH1A1 (0.35) | — | |
| SCHEMBL10877314 | 0.76 | ALDH1A1 (0.35) | — |
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 154 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2023153435-A1 | PREPREG, CARBON FIBER-REINFORCED PLASTIC, AND METHOD FOR MANUFACTURING PREPREG | 三菱ケミカル株式会社 | 2023-08-17 | — | — | WO | disclosed |
| CN-111587185-B | Binding printing plate | 株式会社小村技术 | 2022-03-11 | — | — | CN | disclosed |
| CN-111587185-A | Binding printing plate | 株式会社小村技术 | 2020-08-25 | — | — | CN | disclosed |
| WO-2019188271-A1 | CONNECTED PRINTING PLATE | 株式会社コムラテック | 2019-10-03 | — | — | WO | disclosed |
| EP-1699897-B1 | CURABLE SILOXANE COMPOSITION WITH MODIFIED SURFACE PROPERTIES | MOMENTIVE PERFORMANCE MAT INC (DE) | 2015-10-28 | — | — | EP | disclosed |
| US-7846550-B2 | reactive alkenyl-containing siloxane polymer whose content of silanetriol or Si/OH/4 units does not exceed 10 mol-%, optional siloxane crosslinking agent, catalyst, polysiloxane pressure sensitive adhesive that is noreactive with first components, and solvent, auxillary additives; adhesive tape, labels | MOMENTIVE PERFORMANCE MATERIALS GMBH (DE) | 2010-12-07 | — | — | US | disclosed |
| US-7700658-B2 | (R)-chiral halogenated substituted fused heterocyclic amino compounds useful for inhibiting cholesterol ester transfer protein activity | PFIZER INC. (US) | 2010-04-20 | — | — | US | disclosed |
| US-20090156685-A1 | (R)-CHIRAL HALOGENATED SUBSTITUTED FUSED HETEROCYCLIC AMINO COMPOUNDS USEFUL FOR INHIBITING CHOLESTEROL ESTER TRANSFER PROTEIN ACTIVITY | PFIZER INC | 2009-06-18 | — | — | US | disclosed |
| EP-1115693-B9 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL $i(TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO CO (US) | 2007-12-19 | — | — | EP | disclosed |
| US-20070275255-A1 | reactive alkenyl-containing siloxane polymer whose content of silanetriol or Si/OH/4 units does not exceed 10 mol-%, optional siloxane crosslinking agent, catalyst, polysiloxane pressure sensitive adhesive that is noreactive with first components, and solvent, auxillary additives; adhesive tape, labels | GE BAYER SILICONES GMBH & CO., KG (DE) | 2007-11-29 | — | — | US | disclosed |
| EP-1115695-A1 | (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(N+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | disclosed |
| EP-1115693-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL $i(TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | disclosed |
| WO-2000069832-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL PYRYMIDINONES USEFUL AS ANTICOAGULANTS | PHARMACIA CORPORATION (US) | 2000-11-23 | — | — | WO | disclosed |
| WO-2000069833-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL URACILS AS ANTICOAGULATIVE AGENTS | PHARMACIA CORPORATION (US) | 2000-11-23 | — | — | WO | disclosed |
| WO-2000069826-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL PYRIDONES USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE | PHARMACIA CORPORATION (US) | 2000-11-23 | — | — | WO | disclosed |
| WO-2000069834-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL PYRAZINONES USEFUL FOR SELECTIVE INHIBITION OF THE COAGULATION CASCADE | PHARMACIA CORPORATION (US) | 2000-11-23 | — | — | WO | disclosed |
| WO-2000063195-A1 | NOVEL HETEROCYCLIC AMINO CARBONYL DERIVATIVES USEFUL AS NITRIC OXIDE SYNTHASE INHIBITORS | G.D. SEARLE & CO. (US) | 2000-10-26 | — | — | WO | disclosed |
| WO-2000018723-A1 | SUBSTITUTED N-ALIPHATIC-N-AROMATIC TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | disclosed |
| WO-2000018724-A1 | (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(n+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | disclosed |
| WO-2000018721-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | disclosed |