Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | FFAR1 | O14842 | 20/20 | 0.72 |
| ▸ | FFAR4 | Q5NUL3 | 5/20 | 0.72 |
| ▸ | CHRM2 | P08172 | 1/20 | 0.57 |
| ▸ | S1PR1 | P21453 | 1/20 | 0.57 |
| ▸ | FPR1 | P21462 | 1/20 | 0.57 |
| ▸ | FPR3 | P25089 | 1/20 | 0.57 |
| ▸ | GPR183 | P32249 | 1/20 | 0.57 |
| ▸ | APLNR | P35414 | 1/20 | 0.57 |
| ▸ | GPR65 | Q8IYL9 | 1/20 | 0.57 |
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 | |
|---|---|---|---|---|
| SCHEMBL1551253 | 0.84 | FFAR1 (1.00) | FFAR1FFAR4CHRM2S1PR1FPR1 | |
| SCHEMBL297973 | 0.83 | KEAP1 (0.64) | FFAR1FFAR4 | |
| SCHEMBL18165302 | 0.82 | FFAR1 (0.77) | FFAR1FFAR4CHRM2S1PR1FPR1 | |
| SCHEMBL240565 | 0.82 | FFAR1 (0.70) | FFAR1FFAR4 | |
| SCHEMBL12087474 | 0.81 | FFAR1 (1.00) | FFAR1FFAR4CHRM2S1PR1FPR1 | |
| SCHEMBL1510186 | 0.80 | FFAR1 (0.69) | FFAR1FFAR4 | |
| SCHEMBL1550238 | 0.79 | FFAR1 (1.00) | FFAR1FFAR4 | |
| SCHEMBL1337387 | 0.78 | FFAR1 (0.69) | FFAR1FFAR4 | |
| SCHEMBL22540433 | 0.78 | FFAR1 (0.70) | FFAR1FFAR4CHRM2S1PR1FPR1 | |
| SCHEMBL1550173 | 0.77 | FFAR1 (1.00) | FFAR1FFAR4CHRM2S1PR1FPR1 |
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 11 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-6603070-B2 | Convergent method for the synthesis of light harvesting rods. The rods are oligomers of the formula A1(Ab+1)b, wherein b is at least 1, A1 through Ab+1 are covalently coupled rod segments, and each rod segment A1 through A1+b comprises a | NORTH CAROLINA STATE UNIVERSITY | 2003-08-05 | — | — | US | disclosed |
| US-6596935-B2 | Chromophores absorb light and exhibit intrinsic molecular level rectification in the flow of excited-state energy and ground-state holes | NORTH CAROLINA STATE UNIVERSITY | 2003-07-22 | — | — | US | disclosed |
| US-20030111108-A1 | Convergent synthesis of multiporphyrin light-harvesting rods | UNITED STATES DEPARTMENT OF ENERGY | 2003-06-19 | — | — | US | disclosed |
| EP-1319255-A1 | LIGHT HARVESTING ARRAYS | NORTH CAROLINA STATE UNIVERSITY (US) | 2003-06-18 | — | — | EP | disclosed |
| EP-1303884-A1 | SOLAR CELLS INCORPORATING LIGHT HARVESTING ARRAYS | NORTH CAROLINA STATE UNIVERSITY (US) | 2003-04-23 | — | — | EP | disclosed |
| WO-2003019621-A2 | CONVERGENT SYNTHESIS OF MULTIPORPHYRIN LIGHT-HARVESTING RODS | NORTH CAROLINA STATE UNIVERSITY (US) | 2003-03-06 | — | — | WO | disclosed |
| US-20020185173-A1 | Solar cells incorporating light harvesting arrays | NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR | 2002-12-12 | — | — | US | disclosed |
| US-6420648-B1 | SOLAR CELLS | NORTH CAROLINA STATE UNIVERSITY | 2002-07-16 | — | — | US | disclosed |
| US-6407330-B1 | A CIRCUIT ELECTRICALLY COUPLED TO SAID SOLAR CELL; LIGHT HARVESTING RODS OF NON-DISCOTIC BACKBONE POLYMER CONTAINING CHROMOPHORE GROUPS | NORTH CAROLINA STATE UNIVERSITY | 2002-06-18 | — | — | US | disclosed |
| WO-2002009196-A1 | LIGHT HARVESTING ARRAYS | NORTH CAROLINA STATE UNIVERSITY (US) | 2002-01-31 | — | — | WO | disclosed |
| WO-2002009197-A1 | SOLAR CELLS INCORPORATING LIGHT HARVESTING ARRAYS | NORTH CAROLINA STATE UNIVERSITY (US) | 2002-01-31 | — | — | WO | disclosed |