SCHEMBL6289216

SCHEMBL6289216

CCCCC/C=C/c1ccccc1

nearest known ligand 0.62

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SIGMAR1 Q99720 2/20 0.49
TNNC1 P63316 1/20 0.48
EGFR P00533 1/20 0.46
HTR2A P28223 3/20 0.46
SOAT2 O75908 1/20 0.45
SOAT1 P35610 1/20 0.45
IDO1 P14902 1/20 0.44
PAM P19021 1/20 0.44
LMNA P02545 1/20 0.43
FAAH O00519 1/20 0.43
EPHX2 P34913 1/20 0.43
CYSLTR2 Q9NS75 2/20 0.43
CYSLTR1 Q9Y271 2/20 0.43

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
SCHEMBL714035 1.00 SIGMAR1 (0.49) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL455310 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL363637 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL29828 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL7796983 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL465270 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL6903530 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL9172117 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL6905623 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2
SCHEMBL2168403 0.98 TNNC1 (0.50) SIGMAR1TNNC1EGFRHTR2ASOAT2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108658718-B Preparation method of trans-stilbene compound 温州大学 2020-12-18 CN disclosed
CN-108658718-A A kind of preparation method of trans-stilbene compounds 温州大学 2018-10-16 CN disclosed
US-6900273-B1 Low-hygroscopicity low-birefringence resin compositions, molding material obtained therefrom, sheet or film, and optical part HITACHI CHEMICAL CO., LTD. (JP) 2005-05-31 US disclosed
US-6867323-B2 Cross-coupling reaction of organosilicon nucleophiles THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2005-03-15 US disclosed
US-20040220342-A1 Low-hygroscopicity low-birefringence resin compositions, molding material, sheet or film obtained therefrom, and optical part YAMASHITA YUKIHIKO (JP) 2004-11-04 US disclosed
US-20020183516-A1 Cross-coupling reaction of organosilicon nucleophiles UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN 2002-12-05 US disclosed
EP-1205517-A1 LOW-HYGROSCOPICITY LOW-BIREFRINGENCE RESIN COMPOSITIONS, MOLDING MATERIAL OBTAINED THEREFROM, SHEET OR FILM, AND OPTICAL PART HITACHI CHEMICAL COMPANY, LTD. (JP) 2002-05-15 EP disclosed
WO-2001094355-A1 CROSS-COUPLING REACTION OF ORGANOSILICON NUCLEOPHILES BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2001-12-13 WO disclosed
US-5659084-A LEUKOTRIENE ANTAGONIST SMITHKLINE BEECHAM CORPORATION (US) 1997-08-19 US disclosed
EP-0279474-B1 PROCESS FOR THE PREPARATION OF AN ESTER OF A 3-ARYL-SUBSTITUTED ACRYLIC ACID SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1991-09-11 EP disclosed
US-4855485-A Process for production of cinnamates SUN REFINING AND MARKETING COMPANY (US) 1989-08-08 US disclosed
US-4792623-A CURING AGENT, EXTENDER THE DOW CHEMICAL COMPANY (US) 1988-12-20 US disclosed
US-4789756-A REACTING ALKENYL AROMATIC WITH CARBON MONOXIDE AND ALCOHOL SHELL OIL COMPANY (US) 1988-12-06 US disclosed
EP-0279474-A1 Process for the preparation of an ester of a 3-aryl-substituted acrylic acid SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1988-08-24 EP disclosed
US-4737591-A Catalyst and process for production of cinnamates SUN REFINING AND MARKETING COMPANY (US) 1988-04-12 US disclosed
US-4620027-A OXIDATIVE CARBONYLATION OF STYRENE COMPOUNDS SUN REFINING AND MARKETING COMPANY (US) 1986-10-28 US disclosed
US-4578507-A Process for the production of cinnamic acid esters MITSUBISHI CHEMICAL INDUSTRIES LIMITED (JP) 1986-03-25 US disclosed
EP-0082258-B1 SUBSTITUTED M-PHENYLENEDIAMINES THE DOW CHEMICAL COMPANY (US) 1986-02-19 EP disclosed
EP-0152075-A2 Process for the production of cinnamic acid esters MITSUBISHI KASEI CORPORATION (JP) 1985-08-21 EP disclosed
EP-0082258-A1 Substituted m-phenylenediamines THE DOW CHEMICAL COMPANY (US) 1983-06-29 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 (1 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-20020183516-A1 Cross-coupling reaction of organosilicon nucleophiles TST, HPD, PCNA SIGMAR1 3222/4885TNNC1 4490/4885EGFR 2815/4885

“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.