Rosiglitazone

Rosiglitazone

SCHEMBL504723

CN(CCOc1ccc(CC2SC(=O)NC2=O)cc1)c1ccccn1.CN(CCOc1ccc(CC2SC(=O)NC2=O)cc1)c1ccccn1.O=C(O)/C=C\C(=O)O.O=C(O)/C=C\C(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PPARG

The experimentally established mechanism targets of Rosiglitazone. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
PPARG known ✓ P37231 12/20 1.00
RARG P13631 1/20 1.00
RXRA P19793 1/20 1.00
PPARA Q07869 2/20 0.56
KMT2A Q03164 1/20 0.52
FFAR1 O14842 6/20 0.51
KDM4E B2RXH2 2/20 0.51
ALDH1A1 P00352 2/20 0.51
MAPT P10636 2/20 0.51
PKM P14618 2/20 0.51
HTT P42858 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.48

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
Rosiglitazone SCHEMBL5734118 1.00 PPARG (1.00) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL122053 1.00 PPARG (1.00) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL29376790 1.00 PPARG (1.00) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL466397 1.00 PPARG (1.00) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL19469505 1.00 PPARG (1.00) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL29757195 1.00 PPARG (1.00) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL5556077 1.00 PPARG (1.00) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL19023 1.00 PPARG (1.00) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL5735765 0.99 PPARG (0.98) PPARGRARGRXRAPPARAKMT2A
Rosiglitazone SCHEMBL2118157 0.99 PPARG (0.98) PPARGRARGRXRAPPARAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2120924-B1 AN ANTI-DIABETIC EXTRACT OF HONEYBUSH ZADEC APS (DK) 2016-03-09 EP disclosed
US-9273021-B2 Dibenzofuran derivatives as inhibitors of fructose 1,6-bisphosphatase and methods of use thereof TRUSTEES OF BOSTON COLLEGE (US) 2016-03-01 US disclosed
US-20120251643-A1 ANTI-DIABETIC EXTRACT OF HONEYBUSH ZADEC APS (DK) 2012-10-04 US disclosed
US-20120028892-A1 INHIBITORS OF FRUCTOSE 1,6-BISPHOSPHATASE AND METHODS OF USE THEREOF TRUSTEES OF BOSTON COLLEGE (US) 2012-02-02 US disclosed
US-20110045108-A1 ANTI-DIABETIC EXTRACT OF HONEYBUSH ZADEC APS (DK) 2011-02-24 US disclosed
US-20100291034-A1 COMBINATIONS OF HCV PROTEASE INHIBITOR(S) AND CYP3A4 INHIBITOR(S), AND METHODS OF TREATMENT RELATED THERETO SCHERING CORPORATION (US) 2010-11-18 US disclosed
WO-2010091185-A2 INHIBITORS OF FRUCTOSE 1,6-BISPHOSPHATASE AND METHODS OF USE THEREOF TRUSTEES OF BOSTON COLLEGE (US) 2010-08-12 WO disclosed
EP-2120924-A2 AN ANTI-DIABETIC EXTRACT OF HONEYBUSH Zadec APS (DK) 2009-11-25 EP disclosed
US-7612058-B2 Methods for inhibiting sterol absorption SCHERING CORPORATION (US) 2009-11-03 US disclosed
EP-1799263-A4 REDUCING ER STRESS IN THE TREATMENT OF OBESITY AND DIABETES HARVARD COLLEGE (US) 2009-07-29 EP disclosed
WO-2002096415-A2 USE OF AZETIDINONE SUBSTITUTED DERIVATIVES IN THE TREATMENT OF ALZHEIMER'S DISEASE SCHERING CORPORATION (US) 2002-12-05 WO disclosed
US-20020169134-A1 Use of substituted azetidinone compounds for the treatment of sitosterolemia SCHERING CORPORATION 2002-11-14 US disclosed
US-20020151536-A1 Combinations of peroxisome proliferator-activated receptor (PPAR) activator(s) and sterol absorption inhibitor(s) and treatments for vascular indications SCHERING CORPORATION 2002-10-17 US disclosed
US-20020147184-A1 Combinations of sterol absorption inhibitor(s) with blood modifier(s) for treating vascular conditions SCHERING CORPORATION 2002-10-10 US disclosed
WO-2002058732-A2 COMBINATIONS OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR) ACTIVATOR(S) AND STEROL ABSORPTION INHIBITOR(S) AND TREATMENTS FOR VASCULAR INDICATIONS SCHERING CORPORATION (US) 2002-08-01 WO disclosed
WO-2002058685-A2 COMBINATIONS OF NICOTINIC ACID AND DERIVATIVES THEREOF AND STEROL ABSORPTION INHIBITOR(S) AND TREATMENTS FOR VASCULAR INDICATIONS SCHERING CORPORATION (US) 2002-08-01 WO disclosed
WO-2002058731-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH CARDIOVASCULAR AGENT(S) FOR THE TREATMENT OF VASCULAR CONDITIONS SCHERING CORPORATION (US) 2002-08-01 WO disclosed
WO-2002058734-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH BLOOD MODIFIER(S) FOR TREATING VASCULAR CONDITIONS SCHERING CORPORATION (US) 2002-08-01 WO disclosed
WO-2002058733-A2 COMBINATIONS OF BILE ACID SEQUESTRANT(S) AND STEROL ABSORPTION INHIBITOR(S) AND TREATMENTS FOR VASCULAR INDICATIONS SCHERING CORPORATION (US) 2002-08-01 WO disclosed
WO-2002058696-A2 THE USE OF SUBSTITUTED AZETIDINONE COMPOUNDS FOR THE TREATMENT OF SITOSTEROLEMIA SCHERING CORPORATION (US) 2002-08-01 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 (7 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-20020151536-A1 Combinations of peroxisome proliferator-activated receptor (PPAR) activator(s) and sterol absorption inhibitor(s) and treatments for vascular indications PPARG, PPARA, PPARD PPARG 1/4885RARG 117/4885RXRA 37/4885
US-20110045108-A1 ANTI-DIABETIC EXTRACT OF HONEYBUSH IAPP, DPP4, DPP3 PPARG 1228/4885RARG 3879/4885RXRA 4253/4885
US-20120251643-A1 ANTI-DIABETIC EXTRACT OF HONEYBUSH IAPP, DPP4, DPP3 PPARG 1228/4885RARG 3879/4885RXRA 4253/4885
US-20100291034-A1 COMBINATIONS OF HCV PROTEASE INHIBITOR(S) AND CYP3A4 INHIBITOR(S), AND METHODS OF TREATMENT RELATED THERETO CYP3A43, CYP3A4, CYP3A7 PPARG 1660/4885RARG 2228/4885RXRA 1846/4885
US-20120028892-A1 INHIBITORS OF FRUCTOSE 1,6-BISPHOSPHATASE AND METHODS OF USE THEREOF FBP1, SLC5A1, ALDOA PPARG 2273/4885RARG 4803/4885RXRA 4555/4885
US-20020147184-A1 Combinations of sterol absorption inhibitor(s) with blood modifier(s) for treating vascular conditions APOB, FABP2, CYP46A1 PPARG 769/4885RARG 917/4885RXRA 643/4885
US-20020169134-A1 Use of substituted azetidinone compounds for the treatment of sitosterolemia CYP46A1, CYP27A1, CYP51A1 PPARG 1488/4885RARG 2581/4885RXRA 2008/4885

“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.