SCHEMBL1635965

SCHEMBL1635965

NS(=O)(=O)C(C=Cc1ccccc1)c1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP1A2 P05177 1/20 0.49
▸ LMNA P02545 4/20 0.41
▸ ALDH1A1 P00352 2/20 0.41
▸ GAA P10253 1/20 0.41
▸ MAPT P10636 1/20 0.41
▸ PTGES2 Q9H7Z7 1/20 0.37
▸ PPARG P37231 1/20 0.37
▸ NFE2L2 Q16236 1/20 0.37
▸ MAOB P27338 2/20 0.37
▸ CYP19A1 P11511 1/20 0.36
▸ MAOA P21397 1/20 0.36
▸ TRPA1 O75762 1/20 0.36
▸ ALOX5 P09917 1/20 0.36
▸ MAPK1 P28482 1/20 0.36
▸ PRMT1 Q99873 1/20 0.36
▸ AHR P35869 1/20 0.36
▸ CYP2C19 P33261 1/20 0.36
▸ TDP1 Q9NUW8 1/20 0.36
▸ STS P08842 1/20 0.36
▸ HDAC3 O15379 1/20 0.35

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
SCHEMBL7107955 0.85 CYP1A2 (0.52) CYP1A2LMNAALDH1A1GAAMAPT
SCHEMBL7107957 0.85 CYP1A2 (0.52) CYP1A2LMNAALDH1A1GAAMAPT
SCHEMBL5076198 0.81 CYP1A2 (0.49) CYP1A2LMNAALDH1A1GAAMAPT
SCHEMBL16628452 0.76 CA1 (0.39) ALDH1A1CYP2C19
SCHEMBL7166967 0.75 CA1 (0.38) LMNAALDH1A1MAPTCYP2C19TDP1
SCHEMBL28184213 0.74 CYP3A4 (0.47) CYP1A2LMNAALDH1A1GAAMAPT
SCHEMBL5074691 0.74 NFE2L2 (0.50) CYP1A2LMNAALDH1A1GAAMAPT
SCHEMBL2418539 0.74 CYP19A1 (0.50) CYP1A2LMNAALDH1A1GAAMAPT
SCHEMBL29091807 0.71 CYP1A2 (0.52) CYP1A2LMNAALDH1A1GAAMAPT
SCHEMBL27999893 0.70 CYP1A2 (0.41) CYP1A2LMNAALDH1A1GAAPPARG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3138832-A1 SUBSTITUTED PHENOXY- AND PHENYLTHIO- DERIVATIVES FOR TREATING PROLIFERATIVE DISORDERS Temple University - Of The Commonwealth System of Higher Education (US) 2017-03-08 — — EP disclosed
EP-1740530-B1 SUBSTITUTED PHENOXY- AND PHENYLTHIO-DERIVATIVES FOR TREATING PROLIFERATIVE DISORDERS UNIV TEMPLE (US) 2016-09-28 — — EP disclosed
US-7932242-B2 Anticancer agents; radiation and chemical resistance TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2011-04-26 — — US disclosed
US-20080058290-A1 Substituted Phenoxy-and Phenylthio-Derivatives for Treating Proliferative Disorders TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2008-03-06 — — US disclosed
EP-1740530-A4 SUBSTITUTED PHENOXY- AND PHENYLTHIO- DERIVATIVES FOR TREATING PROLIFERATIVE DISORDERS UNIV TEMPLE (US) 2008-02-27 — — EP disclosed
EP-1740530-A2 SUBSTITUTED PHENOXY- AND PHENYLTHIO- DERIVATIVES FOR TREATING PROLIFERATIVE DISORDERS Temple University of the Commonwealth System of Higher Education (US) 2007-01-10 — — EP disclosed
WO-2005089269-A2 SUBSTITUTED PHENOXY- AND PHENYLTHIO- DERIVATIVES FOR TREATING PROLIFERATIVE DISORDERS TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2005-09-29 — — 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 (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-20080058290-A1 Substituted Phenoxy-and Phenylthio-Derivatives for Treating Proliferative Disorders PCNA, MKI67, TP53 CYP1A2 1234/4885LMNA 2048/4885ALDH1A1 564/4885

“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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