SCHEMBL4060271

SCHEMBL4060271

COc1ccccc1C(=O)c1ccccc1O

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.62
ALOX15 P16050 3/20 0.62
AR P10275 2/20 0.62
CYP3A4 P08684 2/20 0.62
HPGD P15428 2/20 0.62
CYP1A2 P05177 1/20 0.62
PGR P06401 1/20 0.62
ADORA3 P0DMS8 1/20 0.62
CHRM1 P11229 1/20 0.62
TBXA2R P21731 1/20 0.62
SLC6A2 P23975 1/20 0.62
CYP2C19 P33261 1/20 0.62
ADRA1A P35348 1/20 0.62
HIF1A Q16665 1/20 0.62
HTT P42858 3/20 0.59
KMT2A Q03164 3/20 0.59
ALDH1A1 P00352 2/20 0.59
L3MBTL1 Q9Y468 1/20 0.59
TSHR P16473 2/20 0.57
TP53 P04637 2/20 0.57

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
SCHEMBL29658169 0.90 CTSD (0.62) LMNAALOX15CHRM1HTTCA1
SCHEMBL322168 0.90 CTSD (0.62) LMNAALOX15CHRM1HTTCA1
SCHEMBL27789892 0.88 CTSD (0.60) LMNAALOX15HTTCA1CA2
SCHEMBL489859 0.87 ALOX15 (0.60) LMNAALOX15ARCYP3A4HPGD
SCHEMBL28608000 0.87 ALOX15 (0.60) LMNAALOX15ARCYP3A4HPGD
SCHEMBL29120698 0.86 LMNA (0.55) LMNAALOX15ARCYP3A4HPGD
SCHEMBL30320256 0.84 LMNA (0.62) LMNAALOX15ARCYP3A4HPGD
SCHEMBL5709859 0.84 LMNA (0.62) LMNAALOX15ARCYP3A4HPGD
SCHEMBL7061561 0.84 LMNA (0.53) LMNAALOX15ARCYP3A4HPGD
SCHEMBL7330142 0.84 LMNA (0.61) LMNAALOX15ARCYP3A4HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1994005276-A1 CYTOTOXIC COMPOUNDS MORGAN LEE R (US) 1994-03-17 WO claimed
US-20090186987-A1 Processing Conditions Of Polyethylene Articles In Course Of Their Manufacture By Melt Processing CLARIANT FINANCE (BVI) LIMITED (VG) 2009-07-23 US disclosed
US-20090186987-A1 Processing Conditions Of Polyethylene Articles In Course Of Their Manufacture By Melt Processing CLARIANT FINANCE (BVI) LIMITED (VG) 2009-07-23 US disclosed
US-20090186987-A1 Processing Conditions Of Polyethylene Articles In Course Of Their Manufacture By Melt Processing CLARIANT FINANCE (BVI) LIMITED (VG) 2009-07-23 US disclosed
EP-2046883-A1 IMPROVED PROCESSING CONDITIONS OF POLYETHYLENE ARTICLES IN COURSE OF THEIR MANUFACTURE BY MELT PROCESSING Clariant International Ltd. (CH) 2009-04-15 EP disclosed
WO-2008012319-A1 IMPROVED PROCESSING CONDITIONS OF POLYETHYLENE ARTICLES IN COURSE OF THEIR MANUFACTURE BY MELT PROCESSING CLARIANT INTERNATIONAL LTD (CH) 2008-01-31 WO disclosed
WO-2008012319-A1 IMPROVED PROCESSING CONDITIONS OF POLYETHYLENE ARTICLES IN COURSE OF THEIR MANUFACTURE BY MELT PROCESSING CLARIANT INTERNATIONAL LTD (CH) 2008-01-31 WO disclosed
US-6670512-B2 Molecular templates for metal complexation STRYKER JEFFREY MARK (CA) 2003-12-30 US disclosed
US-6613797-B2 New xanthone derivatives useful for treating protozoan diseases INTERLAB, INC. 2003-09-02 US disclosed
US-20020183540-A1 Substituted tetraarylethylene compounds THE GOVERNORS OF THE UNIVERSITY OF ALBERTA 2002-12-05 US disclosed
EP-0888052-A4 XANTHONE ANALOGS FOR THE TREATMENT OF INFECTIOUS DISEASES INTERLAB CORP (US) 2002-05-22 EP disclosed
US-20020055644-A1 Xanthone analogs for treating infectious diseases and complexation of heme and porphyrins INTERLAB, INC. 2002-05-09 US disclosed
WO-2001041773-A1 XANTHONE ANALOGS FOR TREATING INFECTIOUS DISEASES AND COMPLEXATION OF HEME AND PORPHYRINS INTERLAB, INC. (US) 2001-06-14 WO disclosed
US-5977077-A PARASITICIDES; ANTIPROTOZOA AGENT INTERLAB CORPORATION (US) 1999-11-02 US disclosed
EP-0888052-A1 XANTHONE ANALOGS FOR THE TREATMENT OF INFECTIOUS DISEASES INTERLAB CORPORATION (US) 1999-01-07 EP disclosed
WO-1997034482-A1 XANTHONE ANALOGS FOR THE TREATMENT OF INFECTIOUS DISEASES INTERLAB CORP. (US) 1997-09-25 WO disclosed
US-4710584-A Derivatives of 3-benzylidene camphor, process for their preparation and their use as protective agents against UV rays and as medicaments L'OREAL (FR) 1987-12-01 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-20020183540-A1 Substituted tetraarylethylene compounds ABL1, ETV6, ALK LMNA 3557/4885ALOX15 3539/4885AR 240/4885
US-20020055644-A1 Xanthone analogs for treating infectious diseases and complexation of heme and porphyrins XPA, XDH, HMOX1 LMNA 45/4885ALOX15 353/4885AR 4724/4885

“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.