Predicted protein targets (top 6)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | UGT2B7 | P16662 | 1/20 | 0.34 |
| ▸ | EPHX1 | P07099 | 1/20 | 0.33 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.32 |
| ▸ | CA1 | P00915 | 1/20 | 0.30 |
| ▸ | CA2 | P00918 | 1/20 | 0.30 |
| ▸ | CA4 | P22748 | 1/20 | 0.30 |
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 | |
|---|---|---|---|---|
| SCHEMBL4608224 | 1.00 | UGT2B7 (0.34) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL814238 | 1.00 | UGT2B7 (0.34) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL21441575 | 1.00 | UGT2B7 (0.34) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL4606059 | 1.00 | UGT2B7 (0.34) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL4605915 | 1.00 | UGT2B7 (0.34) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL28166839 | 0.85 | UGT2B7 (0.35) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL4152571 | 0.83 | UGT2B7 (0.45) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL4147353 | 0.83 | UGT2B7 (0.45) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL7169835 | 0.83 | UGT2B7 (0.45) | UGT2B7EPHX1CYP1A2CA1CA2 | |
| SCHEMBL4152574 | 0.83 | UGT2B7 (0.45) | UGT2B7EPHX1CYP1A2CA1CA2 |
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 20 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1347035-B1 | Isomer composition containing optically active ethyl trans-2,2,6-trimethylcyclohexylcarboxylate and fragrance composition containing the isomer composition | TAKASAGO PERFUMERY CO LTD (JP) | 2008-07-23 | — | — | EP | claimed |
| US-20030207789-A1 | Isomer composition containing optically active ethyl trans-2,2,6-trimethylcyclohexylcarboxylate and fragrance composition containing the isomer composition | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2003-11-06 | — | — | US | claimed |
| EP-1347035-A2 | Isomer composition containing optically active ethyl trans-2,2,6-trimethylcyclohexylcarboxylate and fragrance composition containing the isomer composition | Takasago International Corporation (JP) | 2003-09-24 | — | — | EP | claimed |
| CN-103917093-B | Opsin binding ligands, compositions, and methods of use | 比卡姆药品公司 | 2017-08-11 | — | — | CN | disclosed |
| CN-106431988-A | Opsin-binding ligands, compositions and methods of use | 比卡姆药品公司 | 2017-02-22 | — | — | CN | disclosed |
| EP-1347035-B1 | Isomer composition containing optically active ethyl trans-2,2,6-trimethylcyclohexylcarboxylate and fragrance composition containing the isomer composition | TAKASAGO PERFUMERY CO LTD (JP) | 2008-07-23 | — | — | EP | disclosed |
| EP-1347036-B1 | Isomer composition excellent in chemical resistance containing optically active trans-1(2,2,6-trimethylcyclohexyl)-2-buten-1-one and fragrance composition containing the isomer composition | TAKASAGO PERFUMERY CO LTD (JP) | 2008-06-25 | — | — | EP | disclosed |
| US-6930083-B2 | Isomer composition excellent in chemical resistance containing optically active trans-1-(2,2,6-trimethylcyclohexyl)-2-buten-1-one and fragrance compositions containing the isomer composition | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2005-08-16 | — | — | US | disclosed |
| EP-1162191-B1 | (1S,6R)- And/or (1R,6S)-2,2,6-trimethylcyclohexyl methyl ketone, process for producing the same, and perfume composition containing the same | TAKASAGO PERFUMERY CO LTD (JP) | 2005-06-29 | — | — | EP | disclosed |
| EP-1468978-A1 | Process for producing (1S,6R)-2,2,6-trimethylcyclohexyl methyl ketone and/or (1R,6S)-2,2,6-trimethylcyclohexyl methyl ketone | Takasago International Corporation (JP) | 2004-10-20 | — | — | EP | disclosed |
| US-6770618-B2 | ORGANOLEPTIC; PLANT EXTRACTS; MIXTURES | TAKASAGO INTERNATIONAL CORP. (JP) | 2004-08-03 | — | — | US | disclosed |
| US-20030207790-A1 | Isomer composition excellent in chemical resistance containing optically active trans-1-(2,2,6-trimethylcyclohexyl)-2-buten-1-one and fragrance compositions containing the isomer composition | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2003-11-06 | — | — | US | disclosed |
| US-20030207789-A1 | Isomer composition containing optically active ethyl trans-2,2,6-trimethylcyclohexylcarboxylate and fragrance composition containing the isomer composition | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2003-11-06 | — | — | US | disclosed |
| EP-1347036-A2 | Isomer composition excellent in chemical resistance containing optically active trans-1(2,2,6-trimethylcyclohexyl)-2-buten-1-one and fragrance composition containing the isomer composition | Takasago International Corporation (JP) | 2003-09-24 | — | — | EP | disclosed |
| EP-1347035-A2 | Isomer composition containing optically active ethyl trans-2,2,6-trimethylcyclohexylcarboxylate and fragrance composition containing the isomer composition | Takasago International Corporation (JP) | 2003-09-24 | — | — | EP | disclosed |
| US-20020042356-A1 | (1S,6R)-2,2,6-Trimethylcyclohexyl methyl ketone and/or (1R,6S)-2,2,6-trimethylcyclohexyl methyl ketone, process for producing the same, and perfume composition containing the same | TAKASAGO INTERNATIONAL CORP. (JP) | 2002-04-11 | — | — | US | disclosed |
| EP-1162191-A2 | (1S,6R)- And/or (1R,6S)-2,2,6-trimethylcyclohexyl methyl ketone, process for producing the same, and perfume composition containing the same | Takasago International Corporation (JP) | 2001-12-12 | — | — | EP | disclosed |
| US-4136066-A | PERFUME | P.F.W. BEHEER B.V. (NL) | 1979-01-23 | — | — | US | disclosed |
| US-4109022-A | ORGANOLEPTIC; FRUIT-LIKE | P.F.W. BEHEER B.V. (NL) | 1978-08-22 | — | — | US | disclosed |
| US-3956392-A | PERFUME, FLAVORS | P.F.W. BEHEER B.V. (NL) | 1976-05-11 | — | — | US | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20020042356-A1 | (1S,6R)-2,2,6-Trimethylcyclohexyl methyl ketone and/or (1R,6S)-2,2,6-trimethylcyclohexyl methyl ketone, process for producing the same, and perfume composition containing the same | MINK1, TEKT1, TMT1A | UGT2B7 3014/4885EPHX1 197/4885CYP1A2 447/4885 |
| US-20030207790-A1 | Isomer composition excellent in chemical resistance containing optically active trans-1-(2,2,6-trimethylcyclohexyl)-2-buten-1-one and fragrance compositions containing the isomer composition | TAS1R1, TAS1R2, TAS2R1 | UGT2B7 1691/4885EPHX1 1568/4885CYP1A2 282/4885 |
| US-20030207789-A1 | Isomer composition containing optically active ethyl trans-2,2,6-trimethylcyclohexylcarboxylate and fragrance composition containing the isomer composition | ETV1, ELP1, TAS1R2 | UGT2B7 3510/4885EPHX1 1058/4885CYP1A2 851/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.