Predicted protein targets (top 8)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | DPP4 | P27487 | 2/20 | 0.48 |
| ▸ | PNMT | P11086 | 3/20 | 0.46 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.44 |
| ▸ | TAAR1 | Q96RJ0 | 6/20 | 0.43 |
| ▸ | HTR2A | P28223 | 1/20 | 0.40 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.38 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.38 |
| ▸ | LOXL2 | Q9Y4K0 | 1/20 | 0.36 |
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 | |
|---|---|---|---|---|
| SCHEMBL31203 | 0.87 | TDP1 (0.55) | DPP4TDP1TAAR1HTR2A | |
| SCHEMBL29534868 | 0.87 | TDP1 (0.55) | DPP4TDP1TAAR1HTR2A | |
| SCHEMBL5629736 | 0.86 | DPP4 (0.45) | DPP4PNMTTDP1TAAR1HTR2A | |
| SCHEMBL6875195 | 0.85 | TAAR1 (0.60) | TDP1TAAR1HTR2ASMN1; SMN2LOXL2 | |
| SCHEMBL28807672 | 0.82 | DPP4 (0.35) | DPP4PNMTTDP1TAAR1 | |
| SCHEMBL15247 | 0.81 | PNMT (0.63) | DPP4PNMTTAAR1KDM4ESMN1; SMN2 | |
| SCHEMBL29405036 | 0.81 | PNMT (0.63) | DPP4PNMTTAAR1KDM4ESMN1; SMN2 | |
| Propanol SCHEMBL29016029 | 0.80 | DPP4 (0.48) | DPP4PNMTTAAR1KDM4ESMN1; SMN2 | |
| SCHEMBL2553273 | 0.79 | DPP4 (0.52) | DPP4PNMTTAAR1KDM4ESMN1; SMN2 | |
| SCHEMBL3051426 | 0.79 | TAAR1 (0.61) | DPP4PNMTTAAR1HTR2ASMN1; SMN2 |
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 84 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-10125226-B2 | Scale-up process of bifunctionalized triblock copolymers with secondary and tertiary amines, with application in dewatering and desalting of heavy crude oils | INSTITUTO MEXICANO DEL PETROLEO (MX) | 2018-11-13 | — | — | US | claimed |
| CN-106459831-A | Improvements in or relating to organic compounds | 奇华顿股份有限公司 | 2017-02-22 | — | — | CN | claimed |
| CN-105308162-A | Compounds for a controlled release of active molecules | FIRMENICH & CIE | 2016-02-03 | — | — | CN | claimed |
| CN-103641769-B | The preparation method of isoindoline hydrochloride | ASTATECH (CHENGDU) PHARM. CO., LTD. (CN) | 2015-11-04 | — | — | CN | claimed |
| US-20140364566-A1 | SCALE-UP PROCESS OF BIFUNCTIONALIZED TRIBLOCK COPOLYMERS WITH SECONDARY AND TERTIARY AMINES, WITH APPLICATION IN DEWATERING AND DESALTING OF HEAVY CRUDE OILS | INSTITUTO MEXICANO DEL PETROLEO (MX) | 2014-12-11 | — | — | US | claimed |
| CN-103641769-A | Preparation method of isoindoline hydrochloride | ASTATECH CHENGDU PHARMACEUTICAL CO LTD | 2014-03-19 | — | — | CN | claimed |
| CN-101193950-A | Fragrance alcohol-releasing polysiloxane | DEGUSSA (DE) | 2008-06-04 | — | — | CN | claimed |
| CN-100390261-C | Compositions comprising photo-labile perfume delivery systems | PROCTER & GAMBLE (US) | 2008-05-28 | — | — | CN | claimed |
| CN-1553948-A | Compositions comprising photo-labile perfume delivery systems | — | 2004-12-08 | — | — | CN | claimed |
| CN-1254552-A | Ceratin-fibre composition for oxidation dying and method for dying with solid composition | OREAL (FR) | 2000-05-31 | — | — | CN | claimed |
| US-20230278959-A1 | Synthesis of Optically Active Indoline Derivatives Via Ruthenium(II)-Catalyzed Enantioselective C-H Functionalization | MISSISSIPPI STATE UNIVERSITY | 2023-09-07 | — | — | US | disclosed |
| EP-3941424-A1 | HAIR COLORANT COMPOSITIONS | Wella International Operations Switzerland Sàrl (CH) | 2022-01-26 | — | — | EP | disclosed |
| US-10604509-B2 | Nrf2 regulators | GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED (GB) | 2020-03-31 | — | — | US | disclosed |
| CN-109310636-A | The production method of dosage form | OMYA国际股份公司 | 2019-02-05 | — | — | CN | disclosed |
| CN-109310637-A | The production method of dosage form | OMYA国际股份公司 | 2019-02-05 | — | — | CN | disclosed |
| CN-1233284-A | Fragrance delivery system for liquid detergent compositions | PROCTER & GAMBLE (US) | 1999-10-27 | — | — | CN | disclosed |
| CN-1210858-A | Optically active bisoxazoline compounds, process for their preparation and their use | SUMITOMO CHEMICAL CO (JP) | 1999-03-17 | — | — | CN | disclosed |
| CN-1202163-A | Benzothiazolone derivatives | ASTRA PHARMA PROD (GB) | 1998-12-16 | — | — | CN | disclosed |
| EP-0087676-B1 | PROCESS FOR THE PREPARATION OF O-ACYLAMINOMETHYLBENZYL HALOGENIDES | BASF Aktiengesellschaft (DE) | 1987-12-16 | — | — | EP | disclosed |
| EP-0087676-A1 | Process for the preparation of o-acylaminomethylbenzyl halogenides | BASF Aktiengesellschaft (DE) | 1983-09-07 | — | — | EP | 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-20230278959-A1 | Synthesis of Optically Active Indoline Derivatives Via Ruthenium(II)-Catalyzed Enantioselective C-H Functionalization | INMT, IDO2, WEE2 | DPP4 4110/4885PNMT 277/4885TDP1 2890/4885 |
| US-10604509-B2 | Nrf2 regulators | NFE2L2, KEAP1, NQO1 | DPP4 3682/4885PNMT 1835/4885TDP1 4202/4885 |
“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.