SCHEMBL8259798

SCHEMBL8259798

CCCc1cc(Oc2ccccc2)ccc1C

nearest known ligand 0.49

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 6/20 0.49
PPARG P37231 6/20 0.42
TSHR P16473 1/20 0.41
TDP1 Q9NUW8 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
NPC1 O15118 1/20 0.40
HPGD P15428 1/20 0.40
CRHBP P24387 1/20 0.40
RAB9A P51151 1/20 0.40
CRHR2 Q13324 1/20 0.40
PPARD Q03181 1/20 0.39
TRPM8 Q7Z2W7 1/20 0.39
MAOB P27338 1/20 0.39
PPARA Q07869 2/20 0.39

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
SCHEMBL28382945 0.91 TAAR1 (0.44) LTA4HPPARGL3MBTL1HPGDPPARD
SCHEMBL13679030 0.88 TAAR1 (0.47) PPARGTDP1L3MBTL1PPARDPPARA
SCHEMBL15186253 0.86 LTA4H (0.50) LTA4HTSHRNPC1HPGDCRHBP
SCHEMBL8259799 0.85 PPARG (0.46) PPARGPPARDPPARA
SCHEMBL14431591 0.82 PPARG (0.38) LTA4HPPARGL3MBTL1RAB9APPARD
SCHEMBL14431706 0.82 SLC6A4 (0.47) NPC1RAB9AMAOB
SCHEMBL2412893 0.81 LTA4H (0.47) LTA4HPPARGPPARD
SCHEMBL8262759 0.81 PPARG (0.41) LTA4HPPARGL3MBTL1RAB9APPARD
SCHEMBL20439168 0.81 LTA4H (0.53) LTA4HTSHRTDP1L3MBTL1NPC1
SCHEMBL10357434 0.80 TAAR1 (0.37) LTA4HPPARGTSHRPPARDPPARA

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
US-20110251171-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE BACH ANDREW THOMAS 2011-10-13 US disclosed
US-20100152255-A1 Organic Compounds DAMON ROBERT EDSON 2010-06-17 US disclosed
US-7700637-B2 Organic compounds NOVARTIS AG (CH) 2010-04-20 US disclosed
US-7652061-B2 N-acyl nitrogen heterocycles as ligands of peroxisome proliferator-activated receptors NOVARTIS A.G. (CH) 2010-01-26 US disclosed
EP-1638963-B1 N-ACYL NITROGEN HETEROCYCLES AS LIGANDS OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS NOVARTIS AG (CH) 2009-09-09 EP disclosed
US-7538135-B2 Benzenesulfonylamino compounds and pharmaceutical compositions containing these compounds NOVARTIS AG (CH) 2009-05-26 US disclosed
US-20090118160-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE BACH ANDREW THOMAS 2009-05-07 US disclosed
US-20080221336-A1 Pparalpha/Gamma Agonists and Processes of Preparing GARRETT CHRISTINE E 2008-09-11 US disclosed
US-20080131475-A1 Methods of Use of Dual Ppar Agonist Compounds and Drug Delivery Devices Containing Such Compounds COHEN DAVID SAUL 2008-06-05 US disclosed
US-20070299047-A1 Combination of Organic Compounds MAHER WILLIAM 2007-12-27 US disclosed
EP-1448523-B1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE NOVARTIS AG (CH) 2007-08-22 EP disclosed
US-20070135502-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE BACH ANDREW T 2007-06-14 US disclosed
US-7183304-B2 such as (R)-1-{4-[4-(4-Phenoxy-2-propyl-phenoxy)-butoxy]-benzenesulfonyl}-azetidine-2-carboxylic acid, used as peroxisome proliferator-activated receptor agonists; hypoglycemic agents NOVARTIS AG (CH) 2007-02-27 US disclosed
US-20070043020-A1 Benzenesulfonylamino compounds and pharmaceutical compositions containing these compounds NOVARTIS AG (CH) 2007-02-22 US disclosed
US-20070004704-A1 Such as 6-Methyl-2-[4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonylamino]-benzoic acid which binds Peroxisome Proliferator-Activated Receptors; conditions in which impaired glucose tolerance, hyperglycemia and insulin resistance are implicated, such as type-1 and type-2 diabetes, and Syndrome X NOVARTIS AG (CH) 2007-01-04 US disclosed
WO-2006084757-A2 COMBINATION OF CA/MG SALT OF VALSARTAN WITH AN ANTIDIABETIC AGENT NOVARTIS AG (CH) 2006-08-17 WO disclosed
WO-2006029349-A1 COMBINATION OF ORGANIC COMPOUNDS NOVARTIS AG (CH) 2006-03-16 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 (9 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-20090118160-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE PPARG, PPARA, PPARD LTA4H 1212/4885PPARG 1/4885TSHR 972/4885
US-20100152255-A1 Organic Compounds PPARG, FABP2, PPARA LTA4H 1319/4885PPARG 1/4885TSHR 1631/4885
US-20110251171-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE PPARG, PPARA, PPARD LTA4H 1212/4885PPARG 1/4885TSHR 972/4885
US-20070135502-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE PPARG, PPARA, PPARD LTA4H 1212/4885PPARG 1/4885TSHR 972/4885
US-20070043020-A1 Benzenesulfonylamino compounds and pharmaceutical compositions containing these compounds PPARG, PPARA, PPARD LTA4H 2155/4885PPARG 1/4885TSHR 1281/4885
US-20070299047-A1 Combination of Organic Compounds GLP1R, PPARG, GCGR LTA4H 1798/4885PPARG 2/4885TSHR 389/4885
US-20080221336-A1 Pparalpha/Gamma Agonists and Processes of Preparing PPARA, PPARG, PPARD LTA4H 1822/4885PPARG 2/4885TSHR 407/4885
US-20070004704-A1 Such as 6-Methyl-2-[4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonylamino]-benzoic acid which binds Peroxisome Proliferator-Activated Receptors; conditions in which impaired glucose tolerance, hyperglycemia and insulin resistance are implicated, such as type-1 and type-2 diabetes, and Syndrome X PPARG, GPR119, PPARA LTA4H 2450/4885PPARG 1/4885TSHR 1998/4885
US-20080131475-A1 Methods of Use of Dual Ppar Agonist Compounds and Drug Delivery Devices Containing Such Compounds PPARA, PPARD, PPARG LTA4H 1844/4885PPARG 3/4885TSHR 483/4885

“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.