Predicted protein targets (top 10)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CNR1 | P21554 | 3/20 | 0.50 |
| ▸ | TACR1 | P25103 | 1/20 | 0.46 |
| ▸ | PTGS1 | P23219 | 3/20 | 0.45 |
| ▸ | PTGS2 | P35354 | 3/20 | 0.45 |
| ▸ | MGLL | Q99685 | 3/20 | 0.45 |
| ▸ | FAAH | O00519 | 2/20 | 0.45 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.40 |
| ▸ | CYP19A1 | P11511 | 4/20 | 0.38 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.37 |
| ▸ | RAB9A | P51151 | 1/20 | 0.37 |
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 | |
|---|---|---|---|---|
| SCHEMBL5584090 | 1.00 | CNR1 (0.50) | CNR1TACR1PTGS1PTGS2MGLL | |
| SCHEMBL5584007 | 1.00 | CNR1 (0.50) | CNR1TACR1PTGS1PTGS2MGLL | |
| SCHEMBL39409 | 1.00 | CNR1 (0.50) | CNR1TACR1PTGS1PTGS2MGLL | |
| SCHEMBL11353453 | 0.95 | CNR1 (0.43) | CNR1TACR1PTGS1PTGS2MGLL | |
| SCHEMBL11153550 | 0.94 | CNR1 (0.48) | CNR1TACR1MGLLFAAHALDH1A1 | |
| SCHEMBL6017344 | 0.89 | TACR1 (0.47) | CNR1TACR1PTGS1PTGS2MGLL | |
| SCHEMBL5605674 | 0.88 | TACR1 (0.46) | CNR1TACR1PTGS1PTGS2MGLL | |
| SCHEMBL6030261 | 0.88 | CNR1 (0.50) | CNR1TACR1PTGS1PTGS2MGLL | |
| SCHEMBL11765260 | 0.87 | CNR1 (0.42) | CNR1TACR1ALDH1A1SMN1; SMN2RAB9A | |
| SCHEMBL11091144 | 0.87 | CNR1 (0.49) | CNR1TACR1PTGS1PTGS2MGLL |
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 47 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20190055414-A1 | N-HALAMINES COMPOUNDS AS MULTIFUNCTIONAL ADDITIVES | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM | 2019-02-21 | — | — | US | claimed |
| EP-1999166-B2 | MODIFIED WAXES, A PROCESS FOR THEIR PREPARATION, AND THEIR USE | CLARIANT INT LTD (CH) | 2016-09-21 | — | — | EP | claimed |
| US-20150166796-A1 | N-Halamines Compounds as Multifunctional Additives | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM | 2015-06-18 | — | — | US | claimed |
| US-8765848-B2 | Modified waxes, a process for their preparation, and their use | CLARIANT FINANCE (BVI) LIMITED (VG) | 2014-07-01 | — | — | US | claimed |
| US-20100286319-A1 | Modified Waxes, a Process for Their Preparation, and Their Use | CLARIANT FINANCE (BVI) LIMITED (VG) | 2010-11-11 | — | — | US | claimed |
| EP-1999166-B1 | MODIFIED WAXES, A PROCESS FOR THEIR PREPARATION, AND THEIR USE | CLARIANT FINANCE BVI LTD (VG) | 2010-05-19 | — | — | EP | claimed |
| EP-1999166-A1 | MODIFIED WAXES, A PROCESS FOR THEIR PREPARATION, AND THEIR USE | Clariant International Ltd. (CH) | 2008-12-10 | — | — | EP | claimed |
| WO-2007104689-A1 | MODIFIED WAXES, A PROCESS FOR THEIR PREPARATION, AND THEIR USE | CLARIANT INTERNATIONAL LTD (CH) | 2007-09-20 | — | — | WO | claimed |
| US-20070062884-A1 | N-halamines compounds as multifunctional additives | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 2007-03-22 | — | — | US | claimed |
| EP-4532595-A1 | POLYCARBONATE COMPOSITION CONTAINING COMBINATION OF HYDROXYPHENYL TRIAZINES AND UV ABSORBERS | BASF SE (DE) | 2025-04-09 | — | — | EP | disclosed |
| WO-2023227472-A1 | POLYCARBONATE COMPOSITION CONTAINING COMBINATION OF HYDROXYPHENYL TRIAZINES AND UV ABSORBERS | BASF SE (DE) | 2023-11-30 | — | — | WO | disclosed |
| WO-2023203869-A1 | PHOTOREACTIVE ORGANOPOLYSILOXANE, METHOD FOR PRODUCING SAME, AND PHOTOCURABLE COMPOSITION | 信越化学工業株式会社 | 2023-10-26 | — | — | WO | disclosed |
| EP-3775020-A1 | USE OF AN ULTRAVIOLET RADIATION ABSORBING COMPOSITION AS A LIGHT STABILIZER FOR A SHAPED ARTIFICIAL POLYMER ARTICLE | BASF SE (DE) | 2021-02-17 | — | — | EP | disclosed |
| US-10689526-B2 | N-halamines compounds as multifunctional additives | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 2020-06-23 | — | — | US | disclosed |
| US-5550234-A | STABILIZERS WITH VERY LOW VOLATILITY AT ELEVATED TEMPERATURES | HOECHST AKTIENGESELLSCHAFT (DE) | 1996-08-27 | — | — | US | disclosed |
| EP-0718357-A2 | Flame-resistant moulding composition having improved light stability | HOECHST AKTIENGESELLSCHAFT (DE) | 1996-06-26 | — | — | EP | disclosed |
| EP-0705836-A1 | Polyalkylpiperidine compounds | HOECHST AKTIENGESELLSCHAFT (DE) | 1996-04-10 | — | — | EP | disclosed |
| EP-0690060-A1 | Two crystal modifications of a diketopyrrolopyrrole | HOECHST AKTIENGESELLSCHAFT (DE) | 1996-01-03 | — | — | EP | disclosed |
| EP-0685465-A1 | Butine- or hexadiine linked hindered amines as stabilizer | CIBA-GEIGY AG (CH) | 1995-12-06 | — | — | EP | disclosed |
| US-4371644-A | Piperidine derivatives and their use as polymer stabilizers | SANKYO COMPANY LTD. (JP) | 1983-02-01 | — | — | 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 (2 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-20150166796-A1 | N-Halamines Compounds as Multifunctional Additives | NIT2, AAAS, NACA | CNR1 4484/4885TACR1 3925/4885PTGS1 3492/4885 |
| US-10689526-B2 | N-halamines compounds as multifunctional additives | NIT2, AAAS, NACA | CNR1 4484/4885TACR1 3925/4885PTGS1 3492/4885 |
“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.