(E)-1,2-Di-P-Tolylethene

(E)-1,2-Di-P-Tolylethene

SCHEMBL1305580

Cc1ccc(/C=C/c2ccc(C)cc2)cc1

nearest known ligand 0.74

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NFE2L2 Q16236 6/20 0.74
▸ RELA Q04206 1/20 0.67
▸ PTGS1 P23219 2/20 0.61
▸ PTGS2 P35354 2/20 0.61
▸ ALOX5 P09917 1/20 0.61
▸ CA1 P00915 1/20 0.59
▸ CYP2A6 P11509 1/20 0.58
▸ ACHE P22303 1/20 0.57
▸ TDP1 Q9NUW8 1/20 0.57
▸ NPC1 O15118 2/20 0.55
▸ RAB9A P51151 2/20 0.55
▸ SMN1; SMN2 Q16637 2/20 0.55
▸ FBP1 P09467 1/20 0.54
▸ TUBB4A P04350 1/20 0.54
▸ TUBB P07437 1/20 0.54
▸ TUBA3C P0DPH7 1/20 0.54
▸ TUBA1B P68363 1/20 0.54
▸ TUBA4A P68366 1/20 0.54
▸ TUBB4B P68371 1/20 0.54
▸ TUBB3 Q13509 1/20 0.54

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
SCHEMBL318785 1.00 NFE2L2 (0.74) NFE2L2RELAPTGS1PTGS2ALOX5
SCHEMBL318786 1.00 NFE2L2 (0.74) NFE2L2RELAPTGS1PTGS2ALOX5
(E)-1,2-Di-P-Tolylethene SCHEMBL1305582 1.00 NFE2L2 (0.74) NFE2L2RELAPTGS1PTGS2ALOX5
(E)-1,2-Di-P-Tolylethene SCHEMBL1793692 1.00 NFE2L2 (0.74) NFE2L2RELAPTGS1PTGS2ALOX5
SCHEMBL700269 0.88 NFE2L2 (0.61) NFE2L2RELAPTGS1PTGS2ALOX5
SCHEMBL4585859 0.88 NFE2L2 (0.61) NFE2L2RELAPTGS1PTGS2ALOX5
SCHEMBL4585865 0.88 NFE2L2 (0.61) NFE2L2RELAPTGS1PTGS2ALOX5
SCHEMBL7164327 0.88 NFE2L2 (0.61) NFE2L2RELAPTGS1PTGS2ALOX5
SCHEMBL1239547 0.88 NFE2L2 (0.61) NFE2L2RELAPTGS1PTGS2ALOX5
SCHEMBL4585867 0.88 NFE2L2 (0.61) NFE2L2RELAPTGS1PTGS2ALOX5

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 80 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2013260-B1 PROCESS FOR THE PREPARATION OF POLYESTERS CONTAINING 1,4-CYCLOHEXANEDIMETHANOL EASTMAN CHEM CO (US) 2016-04-06 — — EP claimed
US-4620055-A Preparation of styrene and stilbene compounds EASTMAN KODAK COMPANY (US) 1986-10-28 — — US claimed
US-12312373-B2 Cyclopropane skeleton monophosphine ligands, palladium complexes thereof, preparation methods and application NANKAI UNIVERSITY (CN) 2025-05-27 — — US disclosed
WO-2025063197-A1 CRYSTAL, METHOD FOR PRODUCING CRYSTAL, AND METHOD FOR INDUCING SELF-ORGANIZATION OF SILANOL COMPOUND 国立研究開発法人産業技術総合研究所 2025-03-27 — — WO disclosed
EP-4471039-A1 CYCLOPROPANE SKELETON MONOPHOSPHINE LIGAND AND PALLADIUM COMPLEX THEREOF AS WELL AS PREPARATION METHOD AND USE THEREOF Nankai University (CN) 2024-12-04 — — EP disclosed
CN-114174312-B Air-stable Ni (0) -olefin complexes and their use as catalysts or precatalysts 科勒研究有限公司 2024-11-22 — — CN disclosed
US-20240376136-A1 CYCLOPROPANE SKELETON MONOPHOSPHINE LIGANDS, PALLADIUM COMPLEXES THEREOF, PREPARATION METHODS AND APPLICATION EXTRAORDINARY SYNERGY TECHNOLOGY (TIANJIN) CO., LTD (CN) 2024-11-14 — — US disclosed
CN-116693543-B Calixarene-derived supermolecule macrocyclic host compound, preparation method and application thereof 上海大学 2024-10-29 — — CN disclosed
US-12084538-B2 Method for producing polymer LG CHEM, LTD. (KR) 2024-09-10 — — US disclosed
CN-116535439-B Cyclopropane skeleton monophosphine ligand and palladium complex thereof, and preparation method and application thereof 南开大学 2024-05-28 — — CN disclosed
US-11798810-B2 Resist underlayer film-forming composition containing amide solvent NISSAN CHEMICAL CORPORATION (JP) 2023-10-24 — — US disclosed
EP-0265373-B1 PROCESS FOR CURING POLYISOCYANATE COATINGS CIBA-GEIGY AG (CH) 1991-03-13 — — EP disclosed
US-4861806-A PHOTOPOLYMERIZATION, LATENCY CIBA-GEIGY CORPORATION (US) 1989-08-29 — — US disclosed
US-4620055-A Preparation of styrene and stilbene compounds EASTMAN KODAK COMPANY (US) 1986-10-28 — — US disclosed
US-4533505-A REACTION OF ETHYLENE IWITH ACID HALIDES IN THE PRESENCE OF A BASE AND A PALLADIUM CATALYST CIBA-GEIGY CORPORATION (US) 1985-08-06 — — US disclosed
EP-0062005-B1 PROCESS FOR THE MANUFACTURE OF STYRENE AND/OR STILBENE DERIVATIVES CIBA-GEIGY AG (CH) 1985-06-26 — — EP disclosed
EP-0062005-A1 Process for the manufacture of styrene and/or stilbene derivatives CIBA-GEIGY AG (CH) 1982-10-06 — — EP disclosed
US-4158099-A FROM SCHIFF BASES AND BIPHENYL COMPOUND CIBA-GEIGY AG (CH) 1979-06-12 — — US disclosed
US-3991049-A Aromatic compounds containing ethylene double bonds, processes for their manufacture and use CIBA-GEIGY AG (CH) 1976-11-09 — — US disclosed
US-3946081-A OXIDATION CATALYSTS, GROUP V, VI, OR VII OXIDES BAYER AKTIENGESELLSCHAFT (DT) 1976-03-23 — — 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-12312373-B2 Cyclopropane skeleton monophosphine ligands, palladium complexes thereof, preparation methods and application DDT, CPNE4, PIN1 NFE2L2 1865/4885RELA 4057/4885PTGS1 2267/4885
US-20240376136-A1 CYCLOPROPANE SKELETON MONOPHOSPHINE LIGANDS, PALLADIUM COMPLEXES THEREOF, PREPARATION METHODS AND APPLICATION DDT, CPNE4, PIN1 NFE2L2 1865/4885RELA 4057/4885PTGS1 2267/4885

“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.

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