Predicted protein targets (top 14)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | IDO1 | P14902 | 2/20 | 0.52 |
| ▸ | RXRA | P19793 | 2/20 | 0.51 |
| ▸ | RXRB | P28702 | 2/20 | 0.51 |
| ▸ | RXRG | P48443 | 2/20 | 0.51 |
| ▸ | CES2 | O00748 | 1/20 | 0.46 |
| ▸ | PRKCA | P17252 | 1/20 | 0.45 |
| ▸ | PRKCD | Q05655 | 1/20 | 0.45 |
| ▸ | ACHE | P22303 | 1/20 | 0.42 |
| ▸ | MTOR | P42345 | 1/20 | 0.41 |
| ▸ | DAO | P14920 | 2/20 | 0.40 |
| ▸ | TACR1 | P25103 | 4/20 | 0.40 |
| ▸ | MLYCD | O95822 | 1/20 | 0.40 |
| ▸ | ACP3 | P15309 | 1/20 | 0.38 |
| ▸ | KIF11 | P52732 | 1/20 | 0.38 |
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 | |
|---|---|---|---|---|
| SCHEMBL12871778 | 0.89 | RXRA (0.45) | IDO1RXRARXRBRXRGCES2 | |
| SCHEMBL3279035 | 0.86 | RXRA (0.46) | IDO1RXRARXRBRXRGCES2 | |
| SCHEMBL29876769 | 0.86 | RXRA (0.46) | IDO1RXRARXRBRXRGCES2 | |
| SCHEMBL21474429 | 0.86 | ACHE (0.58) | IDO1RXRARXRBRXRGCES2 | |
| SCHEMBL16951240 | 0.84 | RXRA (0.45) | IDO1RXRARXRBRXRGCES2 | |
| SCHEMBL799344 | 0.84 | RXRA (0.45) | IDO1RXRARXRBRXRGPRKCA | |
| SCHEMBL2773850 | 0.84 | RXRA (0.45) | IDO1RXRARXRBRXRGCES2 | |
| SCHEMBL630541 | 0.84 | RXRA (0.45) | IDO1RXRARXRBRXRGPRKCA | |
| SCHEMBL129085 | 0.84 | RXRA (0.45) | IDO1RXRARXRBRXRGCES2 | |
| SCHEMBL130263 | 0.84 | RXRA (0.45) | IDO1RXRARXRBRXRGCES2 |
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 557 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113999342-B | Migratable polymer-based functional modifier and preparation method and application thereof | 厦门大学 | 2022-08-12 | — | — | CN | claimed |
| CN-113999342-A | Migratable polymer-based functional modifier and preparation method and application thereof | 厦门大学 | 2022-02-01 | — | — | CN | claimed |
| CN-113214045-A | Preparation process of high-purity 3, 5-bis (trifluoromethyl) benzyl alcohol | 宁夏忠同生物科技有限公司 | 2021-08-06 | — | — | CN | claimed |
| US-9616459-B1 | Polymeric coatings for fortification of visible, infrared, and laser optical devices | LOCKHEED MARTIN CORPORATION (US) | 2017-04-11 | — | — | US | claimed |
| US-8952083-B2 | Fluorocopolymer composition and its production process | ASAHI GLASS COMPANY, LIMITED (JP) | 2015-02-10 | — | — | US | claimed |
| EP-1993991-B1 | PROCESS FOR THE PREPARATION OF 3,5-BIS (TRIFLUOROMETHYL)-N-METHYLBENZYLAMINE | MITENI SPA (IT) | 2010-09-22 | — | — | EP | claimed |
| EP-1993991-A2 | PROCESS FOR THE PREPARATION OF 3,5-BIS (TRIFLUOROMETHYL)-N-METHYLBENZYLAMINE | MITENI S.p.A. (IT) | 2008-11-26 | — | — | EP | claimed |
| EP-1115693-B9 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL $i(TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO CO (US) | 2007-12-19 | — | — | EP | claimed |
| WO-2007107818-A2 | PROCESS FOR THE PREPARATION OF 3,5-BIS (TRIFLUOROMETHYL)-N-METHYLBENZYLAMINE | MITENI S.P.A. (IT) | 2007-09-27 | — | — | WO | claimed |
| EP-1673329-B1 | PROCESS FOR THE PREPARATION 3,5-BIS(TRIFLUOROMETHYL)BENZYLALCOHOL | MITENI SPA (IT) | 2007-09-12 | — | — | EP | claimed |
| EP-1115695-A1 | (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(N+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | claimed |
| EP-1115693-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL $i(TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | claimed |
| EP-1115694-A1 | SUBSTITUTED N-ALIPHATIC-N-AROMATIC (TERTIARY)-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | claimed |
| WO-2000018724-A1 | (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(n+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | claimed |
| WO-2000018723-A1 | SUBSTITUTED N-ALIPHATIC-N-AROMATIC TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | claimed |
| WO-2000018721-A1 | SUBSTITUTED POLYCYCLIC ARYL AND HETEROARYL TERTIARY-HETEROALKYLAMINES USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | claimed |
| US-5922117-A | Ink compositions containing alcohols | XEROX CORPORATION (US) | 1999-07-13 | — | — | US | claimed |
| US-5897940-A | Ink jet transparencies | XEROX CORPORATION (US) | 1999-04-27 | — | — | US | claimed |
| US-5663265-A | FREE RADICAL COPOLYMERIZATION FOR COATINGS | HOECHST AKTIENGESELLSCHAFT (DE) | 1997-09-02 | — | — | US | claimed |
| US-5596057-A | INTERPOLYMER FROM STERICALLY HINDERED UNSATURATED ESTERS | HOECHST AKTIENGESELLSCHAFT (DE) | 1997-01-21 | — | — | US | claimed |