SCHEMBL4847439

SCHEMBL4847439

COc1ccc(C(CC(=O)NO)N2C(=O)c3cccc(C)c3C2=O)cc1OC1CCCC1

nearest known ligand 0.70

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
PDE4A P27815 13/20 0.70
PDE4B Q07343 13/20 0.70
PDE4C Q08493 13/20 0.70
PDE4D Q08499 13/20 0.70
TNF P01375 9/20 0.60

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
SCHEMBL6099727 0.95 PDE4A (0.70) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL6098195 0.92 PDE4A (0.68) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL825522 0.91 PDE4A (0.82) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL4925142 0.91 PDE4A (0.67) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL3127722 0.91 PDE4A (0.83) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL3131798 0.90 PDE4A (0.66) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL4848579 0.90 PDE4A (0.69) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL4855594 0.90 PDE4A (0.64) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL3131810 0.89 PDE4A (0.64) PDE4APDE4BPDE4CPDE4DTNF
SCHEMBL537107 0.87 PDE4A (0.74) PDE4APDE4BPDE4CPDE4DTNF

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7091356-B2 Substituted alkanohydroxamic acids and method of reducing TNFα levels CELGENE CORPORATION 2006-08-15 US claimed
US-20040006096-A1 Substituted alkanohydroxamic acids and method of reducing TNFalpha levels CELGENE CORPORATION 2004-01-08 US claimed
US-6656964-B2 Reducing levels of tumor necrosis factor alpha; inhibition of undesireable levels of matrix metalloproteinases CELGENE CORPORATION 2003-12-02 US claimed
EP-1035848-B1 SUBSTITUTED ALKANOHYDROXAMIC ACIDS AND METHOD OF REDUCING TNF-ALPHA LEVELS CELGENE CORP (US) 2003-04-23 EP claimed
US-20010049371-A1 Method of inhibiting phosphodiesterases with substituted alkanohydroxamic acids CALGENE CORPORATION 2001-12-06 US claimed
EP-1035848-A4 SUBSTITUTED ALKANOHYDROXAMIC ACIDS AND METHOD OF REDUCING TNF-ALPHA LEVELS CELGENE CORP (US) 2001-05-23 EP claimed
US-6214857-B1 REDUCES TUMOR NECROSIS FACTOR LEVELS CELGENE CORPORATION 2001-04-10 US claimed
EP-1035848-A1 SUBSTITUTED ALKANOHYDROXAMIC ACIDS AND METHOD OF REDUCING TNF-ALPHA LEVELS CELGENE CORPORATION (US) 2000-09-20 EP claimed
WO-1999006041-A1 SUBSTITUTED ALKANOHYDROXAMIC ACIDS AND METHOD OF REDUCING TNFα LEVELS CELGENE CORPORATION (US) 1999-02-11 WO claimed
US-20080280967-A1 Substituted acylhydroxamic acids and method of reducing TNFalpha levels CELGENE CORPORATION 2008-11-13 US disclosed
US-7345062-B2 Substituted acylhydroxamic acids and method of reducing TNFαlevels CELGENE CORPORATION (US) 2008-03-18 US disclosed
US-7091356-B2 Substituted alkanohydroxamic acids and method of reducing TNFα levels CELGENE CORPORATION 2006-08-15 US disclosed
US-20040167174-A1 Substituted acylhydroxamic acids and method of reducing TNFalpha levels CELGENE 2004-08-26 US disclosed
US-6699899-B1 ISOINDOLE DERIVATIVES; ANTIINFLAMMATORY, ANTIPYRETIC, AND ANTICOAGULANT AGENTS CELGENE CORPORATION 2004-03-02 US disclosed
US-20040006096-A1 Substituted alkanohydroxamic acids and method of reducing TNFalpha levels CELGENE CORPORATION 2004-01-08 US disclosed
EP-1246620-A4 SUBSTITUTED ACYLHYDROXAMIC ACIDS AND METHOD OF REDUCING TNF-G(A) LEVELS CELGENE CORP (US) 2003-06-18 EP disclosed
EP-1246620-A1 SUBSTITUTED ACYLHYDROXAMIC ACIDS AND METHOD OF REDUCING TNF-G(A) LEVELS CELGENE CORPORATION (US) 2002-10-09 EP disclosed
WO-2001045702-A1 SUBSTITUTED ACYLHYDROXAMIC ACIDS AND METHOD OF REDUCING TNFα LEVELS CELGENE CORPORATION (US) 2001-06-28 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 (4 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-20080280967-A1 Substituted acylhydroxamic acids and method of reducing TNFalpha levels APEH, TNF, ACOX3 PDE4A 30/4885PDE4B 70/4885PDE4C 53/4885
US-20040167174-A1 Substituted acylhydroxamic acids and method of reducing TNFalpha levels TNF, APEH, ACOX3 PDE4A 14/4885PDE4B 42/4885PDE4C 30/4885
US-20040006096-A1 Substituted alkanohydroxamic acids and method of reducing TNFalpha levels TNF, TNFRSF1A, LTA PDE4A 10/4885PDE4B 54/4885PDE4C 37/4885
US-20010049371-A1 Method of inhibiting phosphodiesterases with substituted alkanohydroxamic acids PDE3A, PDE2A, PDE3B PDE4A 6/4885PDE4B 15/4885PDE4C 14/4885

“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.