SCHEMBL1194547

SCHEMBL1194547

CCOc1cc(C(CS(C)(=O)=O)N2C(=O)c3ccccc3C2=O)ccc1OC

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
PDE4B Q07343 19/20 1.00
PDE4C Q08493 18/20 1.00
PDE4A P27815 15/20 1.00
PDE4D Q08499 15/20 1.00
HTR2B P41595 1/20 0.70
TNF P01375 1/20 0.63

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
SCHEMBL9977547 1.00 PDE4B (1.00) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL29603817 1.00 PDE4B (1.00) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL9977589 0.91 PDE4B (1.00) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL1194004 0.91 PDE4B (1.00) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL537805 0.90 PDE4B (1.00) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL537071 0.90 PDE4B (1.00) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL29372989 0.90 PDE4B (1.00) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL1566155 0.89 PDE4B (0.81) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL1193944 0.89 PDE4B (0.81) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL28453492 0.89 PDE4B (0.80) PDE4BPDE4CPDE4APDE4DHTR2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2305248-B1 Substituted phenethylsulfones and method of reducing tnf-alpha levels CELGENE CORP (US) 2013-05-08 EP claimed
EP-2305248-A1 Substituted phenethylsulfones and method of reducing tnf-alpha levels CELGENE CORPORATION (US) 2011-04-06 EP claimed
EP-1752148-A2 Substituted phenethylsulfones for the treatment of inflammatory, infectious, immunological or malignant disease CELGENE CORPORATION (US) 2007-02-14 EP claimed
EP-1126839-B1 SUBSTITUTED PHENETHYLSULFONES AND METHOD OF REDUCING TNF-ALPHA AND PDE-IV LEVELS CELGENE CORP (US) 2007-01-03 EP claimed
US-6020358-A REDUCING TUMOR NECROSIS FACTOR CONCENTRATION CELGENE CORPORATION (US) 2000-02-01 US claimed
EP-2305248-B1 Substituted phenethylsulfones and method of reducing tnf-alpha levels CELGENE CORP (US) 2013-05-08 EP disclosed
US-8263637-B2 Methods for treatment of multiple myeloma using cyclopropane carboxylic acid {2-[(is)-1-(3-ethoxy-4-methoxy-phenyl)-2-methanesulfonyl-ethyl]-3-oxo-2,3-dihydro-1 h-isoindol-4-yl}-amide CELGENE CORPORATION (US) 2012-09-11 US disclosed
US-20120165292-A2 METHODS FOR TREATMENT OF MULTIPLE MYELOMA USING CYCLOPROPANE CARBOXYLIC ACID {2-(Is)-(3-eTHOXY-4METHOXY-PHENYL)-2-METHANESULFONYL-ETHYL}-3-OXO-2.3-DIHYDRO-1H-ISOINDOL-4-YL}-AMIDE CELGENE CORPORATION (US) 2012-06-28 US disclosed
WO-2012083153-A1 OLIGOMER-CONTAINING APREMILAST MOIETY COMPOUNDS NEKTAR THERAPEUTICS (US) 2012-06-21 WO disclosed
EP-2305248-A1 Substituted phenethylsulfones and method of reducing tnf-alpha levels CELGENE CORPORATION (US) 2011-04-06 EP disclosed
US-20110038832-A1 METHOD FOR TREATMENT OF MACULAR DEGENERATION USING (+)-2-[1-(3-ETHOXY-4-METHOXYPHENYL)-2-METHYLSULFONYLETHYL]-4-ACETYLAMINOISOINDOLINE-1,3-DIONE CELGENE CORPORATION 2011-02-17 US disclosed
EP-2258363-A1 Compositions for treatment of cancers CELGENE CORPORATION (US) 2010-12-08 EP disclosed
WO-2003086373-A1 METHODS FOR IDENTIFICATION OF MODULATORS OF ANGIOGENESIS, COMPOUNDS DISCOVERED THEREBY, AND METHODS OF TREATMENT USING THE COMPOUNDS CELGENE CORPORATION (US) 2003-10-23 WO disclosed
EP-1242082-A1 METHODS AND COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF ATHEROSCLEROSIS, RESTENOSIS AND RELATED DISORDERS CELGENE CORPORATION (US) 2002-09-25 EP disclosed
US-20020054899-A1 Methods and compositions for the prevention and treatment of atherosclerosis, restenosis and related disorders CELGENE CORP. 2002-05-09 US disclosed
EP-1126839-A1 SUBSTITUTED PHENETHYLSULFONES AND METHOD OF REDUCING TNF ALPHA LEVELS CELGENE CORPORATION (US) 2001-08-29 EP disclosed
WO-2001043743-A1 METHODS AND COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF ATHEROSCLEROSIS, RESTENOSIS AND RELATED DISORDERS CELGENE CORP. (US) 2001-06-21 WO disclosed
WO-2000025777-A1 SUBSTITUTED PHENETHYLSULFONES AND METHOD OF REDUCING TNFαLEVELS CELGENE CORPORATION (US) 2000-05-11 WO disclosed
US-6020358-A REDUCING TUMOR NECROSIS FACTOR CONCENTRATION CELGENE CORPORATION (US) 2000-02-01 US disclosed
US-6011050-A Substituted phenethylsulfones and method of reducing TNFα levels CELGENE CORPORATION (US) 2000-01-04 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-20120165292-A2 METHODS FOR TREATMENT OF MULTIPLE MYELOMA USING CYCLOPROPANE CARBOXYLIC ACID {2-(Is)-(3-eTHOXY-4METHOXY-PHENYL)-2-METHANESULFONYL-ETHYL}-3-OXO-2.3-DIHYDRO-1H-ISOINDOL-4-YL}-AMIDE IL2, HDGF, VEGFA PDE4B 1724/4885PDE4C 1641/4885PDE4A 1843/4885
US-20110038832-A1 METHOD FOR TREATMENT OF MACULAR DEGENERATION USING (+)-2-[1-(3-ETHOXY-4-METHOXYPHENYL)-2-METHYLSULFONYLETHYL]-4-ACETYLAMINOISOINDOLINE-1,3-DIONE ALDH1A2, MTNR1A, MTNR1B PDE4B 438/4885PDE4C 452/4885PDE4A 243/4885

“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.