Predicted protein targets (top 6)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | FFAR2 | O15552 | 17/20 | 0.65 |
| ▸ | AKR1C3 | P42330 | 1/20 | 0.50 |
| ▸ | AKR1C2 | P52895 | 1/20 | 0.50 |
| ▸ | MEN1 | O00255 | 2/20 | 0.48 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.48 |
| ▸ | LMNA | P02545 | 1/20 | 0.48 |
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 | |
|---|---|---|---|---|
| SCHEMBL1677207 | 1.00 | FFAR2 (0.65) | FFAR2AKR1C3AKR1C2MEN1KMT2A | |
| SCHEMBL1405698 | 1.00 | FFAR2 (0.65) | FFAR2AKR1C3AKR1C2MEN1KMT2A | |
| SCHEMBL27563008 | 0.98 | FFAR2 (0.62) | FFAR2AKR1C3AKR1C2MEN1KMT2A | |
| Hydrochloric Acid SCHEMBL9862940 | 0.98 | FFAR2 (0.62) | FFAR2AKR1C3AKR1C2MEN1KMT2A | |
| Hydrochloric Acid SCHEMBL9862939 | 0.98 | FFAR2 (0.62) | FFAR2AKR1C3AKR1C2MEN1KMT2A | |
| Ammonia Solution, Strong SCHEMBL10607681 | 0.98 | FFAR2 (0.62) | FFAR2AKR1C3AKR1C2MEN1KMT2A | |
| Benzil SCHEMBL27273806 | 0.88 | CES2 (0.59) | FFAR2LMNA | |
| SCHEMBL7525386 | 0.86 | FFAR2 (0.53) | FFAR2MEN1KMT2ALMNA | |
| Hydrochloric Acid SCHEMBL10916853 | 0.85 | AKR1C3 (0.51) | FFAR2AKR1C3AKR1C2 | |
| SCHEMBL9871299 | 0.84 | FFAR2 (0.61) | FFAR2MEN1KMT2ALMNA |
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 1156 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118771956-A | Carboxylic acid decarboxylation coupling conversion method using sulfur hexafluoride as oxidizing reagent | 国网安徽省电力有限公司电力科学研究院 | 2024-10-15 | — | — | CN | claimed |
| CN-116947627-A | Acylation reaction method of 2- (4-chlorophenyl) -3-methylbutyryl chloride | 安徽海顺化工有限公司 | 2023-10-27 | — | — | CN | claimed |
| CN-115232014-A | Preparation method of novel splitting agent | 贵州中赛科博化工有限公司 | 2022-10-25 | — | — | CN | claimed |
| CN-112341330-A | Acidification reaction process and device for preparing 2-4- (chlorphenyl) -3-methylbutyryl chloride | 安徽海顺化工有限公司 | 2021-02-09 | — | — | CN | claimed |
| CN-110612119-A | Phospholipid ether (PLE) CAR T cell tumor targeting (CTCT) agents | 西雅图儿童医院（DBA西雅图儿童研究所） | 2019-12-24 | — | — | CN | claimed |
| US-20180072598-A1 | METHOD FOR PRODUCING MICROBIOLOGIC AGENT, AND MICROBIOLOGIC AGENT | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2018-03-15 | — | — | US | claimed |
| EP-2325385-B1 | COMPOSITION FOR THE IMPREGNATION OF FIBERS, FABRICS AND NETTINGS IMPARTING A PROTECTIVE ACTIVITY AGAINST PESTS | BASF SE (DE) | 2017-10-04 | — | — | EP | claimed |
| EP-2545129-B1 | POSITIVELY CHARGED INK COMPOSITION | HEWLETT PACKARD INDIGO BV (NL) | 2016-11-16 | — | — | EP | claimed |
| US-8927635-B2 | Positively charged ink composition | HEWLETT-PACKARD INDIGO B.V. (NL) | 2015-01-06 | — | — | US | claimed |
| EP-2545129-A1 | POSITIVELY CHARGED INK COMPOSITION | Hewlett-Packard Indigo B.V. (NL) | 2013-01-16 | — | — | EP | claimed |
| US-4293504-A | Process for preparing optically active α-cyano-3-(4-halogenophenoxy)-benzyl 2-(4-chlorophenyl)isovalerate | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1981-10-06 | — | — | US | claimed |
| US-4283415-A | ACYLOXY-CYANOALKYL SUBSTITUTED DIPHENYL ETHER AND POLYVINYL ALCOHOL OR GUM ARABIC | SUMITOMO CHEMICAL COMPANY LIMITED (JP) | 1981-08-11 | — | — | US | claimed |
| EP-0006284-B1 | RACEMIZING OF OPTICALLY ACTIVE ALPHA-SUBSTITUTED-ALPHA-PHENYLACETIC ACIDS | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1981-04-08 | — | — | EP | claimed |
| EP-0026650-A2 | Insecticidal synergistic mixtures of 0,0-diethyl 0-(3,5,6-trichloro-2-pyridinyl)phosphorothioate and 4-chloro-alpha-(1-methylethyl)benzene-acetic acid:cyano(6-phenoxy-2-pyridinyl)methyl ester and method of killing and controlling insects | THE DOW CHEMICAL COMPANY (US) | 1981-04-08 | — | — | EP | claimed |
| US-4245116-A | REACTING WITH AN ALKALI METAL OR ALKALINE EARTH METAL HYDROXIDE OR CARBONATE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1981-01-13 | — | — | US | claimed |
| US-4238406-A | Method for preparing a mixture of stereoisomers of α-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)isovalerate | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1980-12-09 | — | — | US | claimed |
| US-4237313-A | HEATING TO 150C | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1980-12-02 | — | — | US | claimed |
| EP-0006284-A1 | Racemizing of optically active alpha-substituted-alpha-phenylacetic acids | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1980-01-09 | — | — | EP | claimed |
| EP-0002289-A1 | Process for converting a stereoisomeric ester into its diastereoisomer; crystalline (-)-S-alpha-cyano-3-phenoxybenzyl (+)-S-alpha-isopropyl-4-chlorophenylacetate | SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) | 1979-06-13 | — | — | EP | claimed |
| EP-0001944-A2 | Esters of alpha-halogenated alcohols, method of preparation and application to the synthesis of esters of alpha-cyano substituted alcohols | ROUSSEL-UCLAF (FR) | 1979-05-16 | — | — | EP | claimed |