SCHEMBL4729843

SCHEMBL4729843

C=CCSc1ccccc1OC(C)=O

nearest known ligand 0.68

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
▸ PTGS2 P35354 20/20 0.68

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
SCHEMBL11667339 0.84 PTGS2 (0.48) PTGS2
SCHEMBL80588 0.84 PTGS2 (0.48) PTGS2
SCHEMBL942835 0.79 PTGS2 (0.64) PTGS2
SCHEMBL27044926 0.79 PTGS2 (0.69) PTGS2
SCHEMBL10647305 0.78 MTNR1A (0.50) PTGS2
SCHEMBL14273054 0.78 PTGS2 (0.79) PTGS2
SCHEMBL8854000 0.78 L3MBTL1 (0.40) PTGS2
SCHEMBL14273053 0.78 PTGS2 (0.68) PTGS2
SCHEMBL13659627 0.77 PTGS2 (1.00) PTGS2
SCHEMBL6535129 0.76 PTGS2 (1.00) PTGS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210196731-A1 COMPOSITIONS AND METHODS FOR TREATING OCULAR INFLAMMATION AND OCULAR SCARRING ARMSTRONG JAMES JACOB BRUVALL (CA) 2021-07-01 — — US disclosed
EP-3801624-A1 COMPOSITIONS AND METHODS FOR TREATING OCULAR INFLAMMATION AND OCULAR SCARRING Armstrong, James Jacob Bruvall (CA) 2021-04-14 — — EP disclosed
WO-2019227207-A1 COMPOSITIONS AND METHODS FOR TREATING OCULAR INFLAMMATION AND OCULAR SCARRING ARMSTRONG JAMES JACOB BRUVALL (CA) 2019-12-05 — — WO disclosed
WO-2014015341-A2 COMPOSITIONS AND METHODS FOR SUBSTRATE-SELECTIVE INHIBITION OF ENDOCANNABINOID OXYGENATION VANDERBILT UNIVERSITY (US) 2014-01-23 — — WO disclosed
EP-1476149-B1 SUBSTITUTED HYDRAZONES AS INHIBITORS OF CYCLOOXYGENASE-2 UNIV TEMPLE (US) 2008-08-06 — — EP disclosed
US-RE39681-E1 1-(4-sulfamyaryl)-3-substituted-5-aryl-2-pyrazolines and inhibitors of cyclooxygenase-2 TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2007-06-05 — — US disclosed
EP-1191931-B1 1-(4-SULFAMYLPHENYL)-3-TRIFLUOROMETHYL-5-ARYL-2-PYRAZOLINES AS INHIBITORS OF CYCLOOXYGENASE-2 UNIV TEMPLE (US) 2007-05-09 — — EP disclosed
US-20070066651-A1 Pyrazoline derivatives useful for the treatment of cancer LABORATORIOS DEL DR. ESTEVE S.A. (ES) 2007-03-22 — — US disclosed
US-7122571-B2 Substituted hydrazones as inhibitors of cyclooxygenase-2 TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2006-10-17 — — US disclosed
EP-1476149-A4 SUBSTITUTED HYDRAZONES AS INHIBITORS OF CYCLOOXYGENASE-2 UNIV TEMPLE (US) 2005-09-14 — — EP disclosed
US-6656968-B1 Selectively inhibit the cyclooxygenase activity of COX-2 over COX-1; addition polymers of compound TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION 2003-12-02 — — US disclosed
US-20030187035-A1 Substituted hydrazones as inhibitors of cyclooxygenase-2 TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION 2003-10-02 — — US disclosed
WO-2003049698-A2 SUBSTITUTED HYDRAZONES AS INHIBITORS OF CYCLOOXYGENASE-2 TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2003-06-19 — — WO disclosed
EP-1191931-A4 1-(4-SULFAMYLARYL)-3-SUBSTITUTED-5-ARYL-2-PYRAZOLINES AS INHIBITORS OF CYCLOOXYGENASE-2 UNIV TEMPLE (US) 2002-11-27 — — EP disclosed
US-6376519-B1 ANTIINFLAMMATORY AGENTS, ANTICANCER AGENTS TEMPLE UNIVERSITY-OF THE COMMONWEALTH OF HIGHER EDUCATION 2002-04-23 — — US disclosed
EP-1191931-A1 1-(4-SULFAMYLARYL)-3-SUBSTITUTED-5-ARYL-2-PYRAZOLINES AS INHIBITORS OF CYCLOOXYGENASE-2 Temple University of the Commonwealth System of Higher Education (US) 2002-04-03 — — EP disclosed
EP-1191929-A2 (Z)-STYRYL ACETOXYPHENYL SULFIDES AS CYCLOOXYGENASE INHIBITORS Temple University of the Commonwealth System of Higher Education (US) 2002-04-03 — — EP disclosed
WO-2000077169-A2 (Z)-STYRYL ACETOXYPHENYL SULFIDES AS CYCLOOXYGENASE INHIBITORS TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2000-12-21 — — WO disclosed
WO-2000076503-A1 1-(4-SULFAMYLARYL)-3-SUBSTITUTED-5-ARYL-2-PYRAZOLINES AS INHIBITORS OF CYCLOOXYGENASE-2 TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2000-12-21 — — WO disclosed
WO-2000076983-A1 1-(4-ARYLSULFONYL)-3-SUBSTITUTED-5-ARYL-2-PYRAZOLINES AS INHIBITORS OF CYCLOOXYGENASE-2 TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2000-12-21 — — WO 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-20030187035-A1 Substituted hydrazones as inhibitors of cyclooxygenase-2 PTGS1, PTGS2, PTGES2 PTGS2 2/4885
US-20070066651-A1 Pyrazoline derivatives useful for the treatment of cancer PTGIS, PTGS1, PTGIR PTGS2 4/4885

“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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