SCHEMBL650467

SCHEMBL650467

N#Cc1ccc2c(c1)C[C@H](NS(=O)(=O)c1ccccc1)CN2Cc1cccnc1

nearest known ligand 0.71

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
FNTA P49354 17/20 0.71
FNTB P49356 17/20 0.71
THRB P10828 1/20 0.46
CACNA1G O43497 1/20 0.44
CACNA1H O95180 1/20 0.44
CACNA1I Q9P0X4 1/20 0.44

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
SCHEMBL650468 1.00 FNTA (0.71) FNTAFNTBTHRBCACNA1GCACNA1H
SCHEMBL648851 0.91 FNTA (0.71) FNTAFNTBTHRB
SCHEMBL648852 0.91 FNTA (0.71) FNTAFNTBTHRB
SCHEMBL653554 0.91 FNTA (0.71) FNTAFNTBTHRB
SCHEMBL651288 0.90 FNTA (0.71) FNTAFNTBTHRB
SCHEMBL651287 0.90 FNTA (0.71) FNTAFNTBTHRB
SCHEMBL651451 0.85 FNTA (0.67) FNTAFNTBTHRB
SCHEMBL651452 0.85 FNTA (0.67) FNTAFNTBTHRB
SCHEMBL651191 0.85 FNTA (0.67) FNTAFNTBTHRB
SCHEMBL650165 0.85 FNTA (0.67) FNTAFNTBTHRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7884113-B2 Tetrahydroquinoline derivatives as cannabinoid receptor modulators BRISTOL-MYERS SQUIBB COMPANY (US) 2011-02-08 US claimed
US-20080194625-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS BRISTOL-MYERS SQUIBB COMPANY 2008-08-14 US claimed
US-20050014786-A1 Tetrahydroquinoline derivatives as cannabinoid receptor modulators BRISTOL-MYERS SQUIBB COMPANY 2005-01-20 US claimed
US-6590022-B1 Emulsion polymerization, drying WACKER-CHEMIE GMBH (DE) 2003-07-08 US claimed
EP-1036101-B1 METHOD FOR PRODUCING PROTECTIVE COLLOID-STABILISED VINYL AROMATIC-1.3-DIENE-COPOLYMERS WACKER CHEMIE GMBH (DE) 2001-08-16 EP claimed
EP-1023331-B1 METHOD FOR PRODUCING POLYMERS STABILISED WITH PROTECTIVE COLLOIDS WACKER CHEMIE GMBH (DE) 2001-06-13 EP claimed
US-20180282440-A1 PROCESS FOR PREPARING VINYL ACETATE-ETHYLENE COPOLYMERS BY EMULSION POLYMERIZATION WACKER CHEMIE AG (DE) 2018-10-04 US disclosed
US-8722788-B2 Transparent TPU (thermoplastic polyurethanes)/PMMA (polymethyl (meth) acrylate) blends with improved low-temperature impact resistance EVONIK ROEHM GMBH (DE) 2014-05-13 US disclosed
US-8420709-B2 Coating composition, (meth)acrylic polymer and monomer mixture for producing the (meth)acrylic polymer EVONIK RÖHM GMBH (DE) 2013-04-16 US disclosed
US-8119808-B2 Tetrahydroquinoline derivatives as cannabinoid receptor modulators BRISTOL-MYERS SQUIBB COMPANY (US) 2012-02-21 US disclosed
US-8119734-B2 Process for preparing aqueous dispersions EVONIK ROEHM GMBH (DE) 2012-02-21 US disclosed
US-20110318595-A1 COATING COMPOSITION, (METH)ACRYLIC POLYMER AND MONOMER MIXTURE FOR PRODUCING THE (METH)ACRYLIC POLYMER EVONIK ROEHM GMBH (DE) 2011-12-29 US disclosed
US-20110218291-A1 PROCESS FOR PREPARING AQUEOUS DISPERSIONS EVONIK ROEHM GMBH (DE) 2011-09-08 US disclosed
US-20080194625-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS BRISTOL-MYERS SQUIBB COMPANY 2008-08-14 US disclosed
US-20080132627-A1 Impact-Resistant Poly(Meth)Acrylate Moulding Masses With High Thermal Stability ROEHM GMBH (DE) 2008-06-05 US disclosed
US-20060052515-A1 Process for producing aqueou dispersions ROEHM GMBH & CO. KG (DE) 2006-03-09 US disclosed
US-20050014786-A1 Tetrahydroquinoline derivatives as cannabinoid receptor modulators BRISTOL-MYERS SQUIBB COMPANY 2005-01-20 US disclosed
US-6590022-B1 Emulsion polymerization, drying WACKER-CHEMIE GMBH (DE) 2003-07-08 US disclosed
US-6090868-A ONE OR MORE ORGANIC POLYMER POWDERS WHICH ARE REDISPERSIBLE IN WATER AND ONE OR MORE ORGANOSILICON POWDERS WHICH ARE REDISPERSIBLE IN WATER ARE ADDED TO THE DRY COATING OR BINDER COMPOSITION. WACKER-CHEMIE GMBH (DE) 2000-07-18 US disclosed
US-5753733-A Redispersible, silicon-modified dispersion powder composition, process for its preparation and its use WACKER-CHEMIE GMBH (DE) 1998-05-19 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-20050014786-A1 Tetrahydroquinoline derivatives as cannabinoid receptor modulators CNR2, CNR1, OPRL1 FNTA 1368/4885FNTB 2071/4885THRB 809/4885
US-20080194625-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS CNR2, CNR1, OPRL1 FNTA 1368/4885FNTB 2071/4885THRB 809/4885

“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.