Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 1/20 | 0.38 |
| ▸ | THRB | P10828 | 1/20 | 0.38 |
| ▸ | CA1 | P00915 | 1/20 | 0.32 |
| ▸ | CA2 | P00918 | 1/20 | 0.32 |
| ▸ | MMP1 | P03956 | 1/20 | 0.32 |
| ▸ | MMP2 | P08253 | 1/20 | 0.32 |
| ▸ | MMP9 | P14780 | 1/20 | 0.32 |
| ▸ | MMP8 | P22894 | 1/20 | 0.32 |
| ▸ | MMP13 | P45452 | 1/20 | 0.32 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 | |
|---|---|---|---|---|
| SCHEMBL7073599 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL1986351 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL1983621 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL500248 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL6236854 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL847419 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL395116 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL6233841 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL916204 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 | |
| SCHEMBL395716 | 1.00 | LMNA (0.38) | LMNATHRBCA1CA2MMP1 |
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 50 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20200041393-A1 | METHOD OF CONCENTRATING ANALYTES, AND SYSTEM FOR CONCENTRATING AND DETECTING ANALYTES | COMMISSARIAT À L'ÉNERGIE ATOMIQUE ET AUX ÉNERGIES ALTERNATIVES (CEA) (FR) | 2020-02-06 | — | — | US | claimed |
| US-20030194378-A1 | Novel aerosol formulation containing a polar fluorinated molecule | ASTRAZENECA AB (SE) | 2003-10-16 | — | — | US | claimed |
| EP-1303258-A1 | NOVEL AEROSOL FORMULATION CONTAINING A POLAR FLUORINATED MOLECULE | AstraZeneca AB (SE) | 2003-04-23 | — | — | EP | claimed |
| WO-2002003958-A1 | NOVEL AEROSOL FORMULATION CONTAINING A POLAR FLUORINATED MOLECULE | ASTRAZENECA AB (SE) | 2002-01-17 | — | — | WO | claimed |
| US-11402307-B2 | Method for concentrating analytes | COMMISSARIAT À L'ÉNERGIE ATOMIQUE ET AUX ÉNERGIES ALTERNATIVES (CEA) (FR) | 2022-08-02 | — | — | US | disclosed |
| US-20200041393-A1 | METHOD OF CONCENTRATING ANALYTES, AND SYSTEM FOR CONCENTRATING AND DETECTING ANALYTES | COMMISSARIAT À L'ÉNERGIE ATOMIQUE ET AUX ÉNERGIES ALTERNATIVES (CEA) (FR) | 2020-02-06 | — | — | US | disclosed |
| US-10384937-B2 | Method of generating hydrogen from the reaction of stabilized aluminum nanoparticles with water and method of forming stabilized aluminum nanoparticles | UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE AIR FORCE (US) | 2019-08-20 | — | — | US | disclosed |
| US-9492989-B2 | Composition and method for manufacture of a fibrous polyurethane composite product | HAUPT ROBERT A (US) | 2016-11-15 | — | — | US | disclosed |
| EP-2099408-B1 | FLUOROPOLYMER-BASED EMULSIONS FOR THE INTRAVENOUS DELIVERY OF FLUORINATED VOLATILE ANESTHETICS | WISCONSIN ALUMNI RES FOUND (US) | 2016-10-05 | — | — | EP | disclosed |
| US-20150266730-A1 | METHOD OF GENERATING HYDROGEN FROM THE REACTION OF STABILIZED ALUMINUM NANOPARTICLES WITH WATER AND METHOD OF FORMING STABILIZED ALUMINUM NANOPARTICLES | UNIVERSITY OF DAYTON | 2015-09-24 | — | — | US | disclosed |
| US-9011572-B1 | Method of generating hydrogen from the reaction of stabilized aluminum nanoparticles with water and method of forming stabilized aluminum nanoparticles | UNIVERSITY OF DAYTON (US) | 2015-04-21 | — | — | US | disclosed |
| US-9000048-B2 | Fluoropolymer-based emulsions for the intravenous delivery of fluorinated volatile anesthetics | WISCONSIN ALUMNI RESEARCH FOUNDATION (US) | 2015-04-07 | — | — | US | disclosed |
| EP-1036790-A1 | Perfluoro group-containing compounds and hardened polymer of the same | Kyoeisha Chemical Co., Ltd. (JP) | 2000-09-20 | — | — | EP | disclosed |
| US-6084057-A | POLYAMIC ACID WHERE THE AMINE COMPONENT IS A POLARIZABLE DIAMINE HAVING A FLUOROCARBON MOIETY AND POLAR GROUP COMPRISING A PI ELECTRON SYSTEM CONTAINING AT LEAST ONE HETEROATOM; POLYIMIDE THEREFROM | ELSICON, INC. (US) | 2000-07-04 | — | — | US | disclosed |
| US-6043337-A | FIR LIQUID CRYSTAL DISPLAY ELEMENTS | ELSICON, INC. (US) | 2000-03-28 | — | — | US | disclosed |
| US-5929201-A | A POLYAMIC ACID IS THE REACTION PRODUCT OF A FLUORINATED MONOAMINE, A DIAMINE AND ATLEAST ONE TETERACARBOXYLIC DIANHYDRIDE | ELSICON, INC. (US) | 1999-07-27 | — | — | US | disclosed |
| WO-1998053361-A2 | POLARIZABLE AMINES AND POLYIMIDES FOR OPTICAL ALIGNMENT OF LIQUID CRYSTALS | ALLIANT TECHSYSTEMS INC. (US) | 1998-11-26 | — | — | WO | disclosed |
| WO-1998052990-A1 | FLUORINATED AMINE PRODUCTS | ALLIANT TECHSYSTEMS INC. (US) | 1998-11-26 | — | — | WO | disclosed |
| EP-0837085-A1 | POLYCARBONATE-BASE POLYMER, PRODUCTION PROCESS, RESIN COATING FLUID PREPARED THEREFROM, AND ELECTROPHOTOGRAPHIC PHOTORECEPTOR PREPARED THEREFROM | IDEMITSU KOSAN COMPANY LIMITED (JP) | 1998-04-22 | — | — | EP | disclosed |
| US-5512207-A | Azaaromatic compounds, process for their preparation, and their use in liquid-crystalline mixtures | HOECHST AKTIENGESELLSCHAFT (DE) | 1996-04-30 | — | — | US | disclosed |