Toluene

Toluene

SCHEMBL11063478

C=CCO.Cc1ccccc1

nearest known ligand 0.55

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 5/20 0.55
▸ LMNA P02545 1/20 0.55
▸ ALOX12 P18054 1/20 0.55
▸ ACHE P22303 1/20 0.55
▸ MEN1 O00255 1/20 0.39
▸ NPC1 O15118 1/20 0.39
▸ RAB9A P51151 1/20 0.39
▸ KMT2A Q03164 1/20 0.39
▸ CES2 O00748 1/20 0.38
▸ CES1 P23141 1/20 0.38
▸ TP53 P04637 1/20 0.38
▸ TDP1 Q9NUW8 1/20 0.38
▸ ATM Q13315 1/20 0.38
▸ C5AR1 P21730 1/20 0.37
▸ ALDH1A1 P00352 2/20 0.36
▸ CYP2C19 P33261 1/20 0.36
▸ MAPT P10636 1/20 0.36
▸ MMP9 P14780 1/20 0.36
▸ HPGD P15428 1/20 0.36
▸ CNR2 P34972 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.

Compoundsimilaritytop predictedshared targets
P-Xylene SCHEMBL27502894 0.87 TSHR (0.53) TSHRLMNAACHEMEN1KMT2A
Toluene SCHEMBL28686825 0.83 LMNA (0.52) TSHRLMNAALOX12ACHEMEN1
O-Xylene SCHEMBL27502895 0.82 ACHE (0.53) TSHRACHEMEN1KMT2ATP53
Toluene SCHEMBL9479181 0.82 ACHE (0.58) TSHRLMNAALOX12ACHEMEN1
Toluene SCHEMBL27472683 0.81 ACHE (0.65) TSHRLMNAALOX12ACHEMEN1
Toluene SCHEMBL28319329 0.80 ACHE (0.55) TSHRLMNAALOX12ACHEMEN1
Toluene SCHEMBL28830923 0.80 TSHR (0.55) TSHRLMNAALOX12ACHETP53
Toluene SCHEMBL27540769 0.80 ACHE (0.55) TSHRLMNAALOX12ACHEMEN1
Toluene SCHEMBL1221331 0.79 LMNA (0.61) TSHRLMNAALOX12ACHEMEN1
Biphenyl SCHEMBL3258858 0.79 ALDH1A1 (0.50) TSHRLMNAALOX12KMT2AALDH1A1

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114149312-A Preparation method of 4-hydroxybutanal 万华化学集团股份有限公司 2022-03-08 — — CN claimed
CN-114149312-A Preparation method of 4-hydroxybutanal 万华化学集团股份有限公司 2022-03-08 — — CN disclosed
CN-107597192-B Catalyst for hydroformylation reaction and hydroformylation reaction method 万华化学集团股份有限公司 2020-06-02 — — CN disclosed
CN-107597192-A A kind of catalyst and hydroformylation reaction method for hydroformylation reaction 万华化学集团股份有限公司 2018-01-19 — — CN disclosed
CN-104837872-B The purposes of the polymer composition that ethylene vinyl ester copolymers and (methyl) alkyl acrylate are constituted, its preparation method and its pour-point depressant as crude oil, mineral oil or mineral oil product 巴斯夫欧洲公司 2017-08-08 — — CN disclosed
CN-104768909-A Process control with raman spectroscopy LYONDELL CHEMICAL TECH LP 2015-07-08 — — CN disclosed
CN-103601620-A Preparation method of 9,10-di(4-hydroxy alkoxy alcohol-phenyl)-phenanthrene aromatic diol UNIV SHENYANG TECHNOLOGY 2014-02-26 — — CN disclosed
CN-1196664-C hydroformylation of allyl alcohol ARCO CHEM TECH (US) 2005-04-13 — — CN disclosed
CN-1394197-A hydroformylation of allyl alcohol ARCO CHEM TECH (US) 2003-01-29 — — CN disclosed
US-4426491-A UNSATURATED ANHYDRIDE, POLYOL, POLYAMINE OR AMINOALCOL, UNSATURATED COMPOUND UNION CARBIDE CORPORATION (US) 1984-01-17 — — US disclosed
EP-0042614-A1 Curable physical mixtures and composites therefrom UNION CARBIDE CORPORATION (US) 1981-12-30 — — EP disclosed
US-4105697-A Process for the preparation of α, β-ethylenic aldehydes RHONE-POULENC INDUSTRIES (FR) 1978-08-08 — — US disclosed
US-4046816-A NOBLE METAL DEHYDROGENATION CATALYST HOECHST AKTIENGESELLSCHAFT (DT) 1977-09-06 — — US disclosed
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