SCHEMBL3376008

SCHEMBL3376008

CS(=O)(=O)O.Cc1oc(-c2ccccc2)nc1CCO

nearest known ligand 0.59

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. 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
KDM4E B2RXH2 1/20 0.59
PPARG P37231 12/20 0.54
PPARA Q07869 8/20 0.54
NPC1 O15118 1/20 0.54
RAB9A P51151 1/20 0.54
HRH3 Q9Y5N1 1/20 0.53
LMNA P02545 1/20 0.53
HPGD P15428 1/20 0.52
SLC9A1 P19634 1/20 0.52
PPARD Q03181 1/20 0.51
FFAR1 O14842 1/20 0.48
MAPT P10636 1/20 0.47

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
SCHEMBL979145 0.91 KDM4E (0.65) KDM4EPPARGPPARANPC1RAB9A
SCHEMBL4888378 0.88 RAB9A (0.62) KDM4EPPARGPPARANPC1RAB9A
SCHEMBL2980690 0.88 KDM4E (0.58) KDM4EPPARGPPARANPC1RAB9A
SCHEMBL28975550 0.87 KDM4E (0.52) KDM4EPPARGPPARANPC1RAB9A
SCHEMBL5022312 0.82 KDM4E (0.61) KDM4EPPARGPPARANPC1RAB9A
SCHEMBL3590990 0.82 NPC1 (0.47) KDM4EPPARGPPARANPC1RAB9A
SCHEMBL821405 0.82 PPARG (0.59) KDM4EPPARGPPARAHRH3HPGD
SCHEMBL3530493 0.82 RAB9A (0.53) KDM4EPPARGPPARANPC1RAB9A
SCHEMBL7157388 0.82 KDM4E (0.47) KDM4EPPARGPPARANPC1RAB9A
SCHEMBL5204314 0.82 KDM4E (0.54) KDM4EPPARGPPARANPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1231482-C Process for preparing thiazolidinedione derivatives and intermediates HOFFMANN LA ROCHE (CH) 2005-12-14 CN claimed
CN-1422267-A Processes for the preparation of thiazolidinedione derivatives and intermediates HOFFMANN LA ROCHE (CH) 2003-06-04 CN claimed
EP-1401433-B1 AZOLE ACID DERIVATIVES, ALONE OR IN COMBINATION, FOR TREATING DIABETES AND DYSLIPIDEMIAS; AND FOR TREATING MALIGNANT DISEASES BRISTOL MYERS SQUIBB CO (US) 2010-11-10 EP disclosed
US-7579479-B2 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method BRISTOL-MYERS SQUIBB COMPANY (US) 2009-08-25 US disclosed
EP-1218361-B1 OXA- AND THIAZOLE DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS BRISTOL MYERS SQUIBB CO (US) 2009-01-07 EP disclosed
US-7452907-B2 Conformationally constrained analogs useful as antidiabetic and antiobesity agents and method BRISTOL-MYERS SQUIBB COMPANY (US) 2008-11-18 US disclosed
EP-1939188-A1 Oxa-and thiazole derivatives useful as antidiabetic and antiobesity agents Bristol-Myers Squibb Company (US) 2008-07-02 EP disclosed
US-7241780-B2 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method BRISTOLS-MYERS SQUIBB COMPANY (US) 2007-07-10 US disclosed
US-20070015797-A1 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method CHENG PETER T 2007-01-18 US disclosed
US-7105556-B2 Conformationally constrained analogs useful as antidiabetic and antiobesity agents and method BRISTOL-MYERS SQUIBB COMPANY (US) 2006-09-12 US disclosed
US-20060189598-A1 Conformationally constrained analogs useful as antidiabetic and antiobesity agents and method CHENG PETER T 2006-08-24 US disclosed
WO-2003040114-A1 SUBSTITUTED ACID DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD BRISTOL-MYERS SQUIBB COMPANY (US) 2003-05-15 WO disclosed
US-20030092697-A1 Conformationally constrained analogs useful as antidiabetic and antiobesity agents and method BRISTOL-MYERS SQUIBB COMPANY 2003-05-15 US disclosed
US-20030087935-A1 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method CHENG PETER T (US) 2003-05-08 US disclosed
US-20030069275-A1 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method CHENG PETER T (US) 2003-04-10 US disclosed
CN-1402712-A Novel heterocyclic compounds and salts thereof and medicinal use of same KYOTO PHARMA IND (JP) 2003-03-12 CN disclosed
WO-2002096357-A2 CONFORMATIONALLY CONSTRAINED ANALOGS USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD BRISTOL-MYERS SQUIBB COMPANY (US) 2002-12-05 WO disclosed
EP-1218361-A1 OXA- AND THIAZOLE DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS BRISTOL-MYERS SQUIBB COMPANY (US) 2002-07-03 EP disclosed
US-6414002-B1 ANTILIPEMIC AGENTS; ANTICANCER, ANTITUMOR AGENTS BRISTOL-MYERS SQUIBB COMPANY 2002-07-02 US disclosed
WO-2001021602-A1 OXA- AND THIAZOLE DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS BRISTOL-MYERS SQUIBB COMPANY (US) 2001-03-29 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 (5 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-20030092697-A1 Conformationally constrained analogs useful as antidiabetic and antiobesity agents and method GPR119, LIPC, GLP1R KDM4E 1789/4885PPARG 155/4885PPARA 169/4885
US-20030069275-A1 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method GPR119, LIPC, PNLIP KDM4E 2366/4885PPARG 69/4885PPARA 48/4885
US-20030087935-A1 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method GPR119, LIPC, PNLIP KDM4E 2366/4885PPARG 69/4885PPARA 48/4885
US-20060189598-A1 Conformationally constrained analogs useful as antidiabetic and antiobesity agents and method GPR119, LIPC, GLP1R KDM4E 1071/4885PPARG 170/4885PPARA 80/4885
US-20070015797-A1 Substituted acid derivatives useful as antidiabetic and antiobesity agents and method GPR119, LIPC, ACACA KDM4E 2164/4885PPARG 65/4885PPARA 24/4885

“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.