SCHEMBL3249787

SCHEMBL3249787

CC(=O)c1ccc(Cl)c(NS(C)(=O)=O)c1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.53
SMN1; SMN2 Q16637 4/20 0.53
KDM4E B2RXH2 4/20 0.49
HSD17B10 Q99714 1/20 0.49
HPGD P15428 2/20 0.48
MAPT P10636 3/20 0.45
LMNA P02545 2/20 0.45
HTT P42858 2/20 0.45
SCN9A Q15858 1/20 0.44
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
FLT1 P17948 1/20 0.43
FLT4 P35916 1/20 0.43
KDR P35968 1/20 0.43
TSHR P16473 1/20 0.41
FABP4 P15090 1/20 0.41
NEU3 Q9UQ49 1/20 0.41
HDAC8 Q9BY41 1/20 0.41
CPT2 P23786 1/20 0.41
CPT1A P50416 1/20 0.41

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
SCHEMBL3526841 0.87 ALDH1A1 (0.60) ALDH1A1SMN1; SMN2KDM4EHSD17B10MAPT
SCHEMBL9624571 0.87 SMN1; SMN2 (0.53) ALDH1A1SMN1; SMN2KDM4EHSD17B10HPGD
SCHEMBL7532986 0.84 ADRB3 (0.48) ALDH1A1SMN1; SMN2KDM4EHSD17B10HPGD
SCHEMBL10543746 0.84 PYGL (0.53) ALDH1A1SMN1; SMN2KDM4EHSD17B10HPGD
SCHEMBL14389382 0.84 KDM4E (0.70) ALDH1A1SMN1; SMN2KDM4EHSD17B10HPGD
SCHEMBL13719670 0.83 KDM4E (0.46) ALDH1A1SMN1; SMN2KDM4EHSD17B10HPGD
SCHEMBL14038485 0.83 ALDH1A1 (0.47) ALDH1A1SMN1; SMN2KDM4EHSD17B10HPGD
SCHEMBL7109004 0.83 HTT (0.56) ALDH1A1SMN1; SMN2KDM4EHPGDMAPT
SCHEMBL1120778 0.81 ADRB3 (0.46) ALDH1A1SMN1; SMN2KDM4EHSD17B10HPGD
SCHEMBL966589 0.81 ADRB3 (0.58) ALDH1A1SMN1; SMN2KDM4EHSD17B10HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10072000-B2 Method of treating insomnia with halogenated pyrazolo[1,5-a]pyrimidines FERRER INTERNACIONAL, S.A. (ES) 2018-09-11 US disclosed
US-20160368912-A9 HALOGENATED PYRAZOLO[1,5-A]PYRIMIDINES, PROCESSES, USES, COMPOSITIONS AND INTERMEDIATES FERRER INTERNACTIONAL, S.A. (ES) 2016-12-22 US disclosed
US-20130331401-A1 Halogenated Pyrazolo[1,5-A]Pyrimidines, Processes, Uses, Compositions and Intermediates FERRER INTERNACTIONAL, S.A. (ES) 2013-12-12 US disclosed
US-20130331610-A1 Halogenated Pyrazolo[1,5-A]Pyrimidines, Processes, Uses, Compositions and Intermediates FERRER INTERNACIONAL, S.A. (ES) 2013-12-12 US disclosed
US-8530482-B2 Halogenated pyrazolo[1,5-A]pyrimidines, processes, uses, compositions and intermediates FERRER INTERNACIONAL, S.A. (ES) 2013-09-10 US disclosed
EP-1899343-B1 HALOGENATED PYRAZOLO [1,5-A]PYRIMIDINES, PROCESSES, USES AS GABA-A RECEPTORS LIGAND, COMPOSITIONS AND INTERMEDIATES FERRER INT (ES) 2010-05-12 EP disclosed
US-20090111848-A1 Halogenated Pyrazolo[1,5-A]Pyrimidines, Processes, Uses, Compositions and Intermediates FERRER INTERNACIONAL, S.A. (ES) 2009-04-30 US disclosed
EP-1899343-A1 HALOGENATED PYRAZOLO [1,5-A]PYRIMIDINES, PROCESSES, USES AS GABA-A RECEPTORS LIGAND, COMPOSITIONS AND INTERMEDIATES Ferrer Internacional, S.A. (ES) 2008-03-19 EP disclosed
WO-2006136530-A1 HALOGENATED PYRAZOLO [1,5-A]PYRIMIDINES, PROCESSES, USES AS GABA-A RECEPTORS LIGAND, COMPOSITIONS AND INTERMEDIATES FERRER INTERNACIONAL, S.A. (ES) 2006-12-28 WO disclosed
EP-1736475-A1 Halogenated pyrazolo[1,5-a]pyrimidines, processes, uses, compositions and intermediates FERRER INTERNACIONAL, S.A. (ES) 2006-12-27 EP disclosed
EP-1254885-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE SECONDARY ALCOHOLS HAVING NITROGENOUS OR OXYGENIC FUNCTIONAL GROUPS Asahi Kasei Kabushiki Kaisha (JP) 2002-11-06 EP disclosed
EP-1209150-A1 PROCESSES FOR THE PREPARATION OF TRICYCLIC AMINO ALCOHOL DERIVATIVES Asahi Kasei Kabushiki Kaisha (JP) 2002-05-29 EP disclosed
EP-1195371-A1 PROCESS FOR THE PREPARATION OF TRICYCLIC AMINO ALCOHOL DERIVATIVES Asahi Kasei Kabushiki Kaisha (JP) 2002-04-10 EP disclosed
US-20020028835-A1 Cyclic amine phenyl beta-3 adrenergic receptor agonists WYETH 2002-03-07 US disclosed
WO-2002006232-A1 CYCLIC AMINE PHENYL BETA-3 ADRENERGIC RECEPTOR AGONISTS WYETH (US) 2002-01-24 WO disclosed
EP-1174425-A1 NOVEL METHOD FOR MANUFACTURING TRICYCLIC AMINO ALCOHOL DERIVATIVES Asahi Kasei Kabushiki Kaisha (JP) 2002-01-23 EP disclosed
US-6187809-B1 BETA-3 ADRENALINE RECEPTOR AGONIST DRUGS FOR THE TREATMENT OF DIABETES, OBESITY, AND HYPERLIPEMIA; 2-(N-(2-(DIBENZOFURAN-3-YLOXY)ETHYL)AMINO)-1-PHENYLETHANOL, FOR EXAMPLE ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 2001-02-13 US disclosed
US-6172099-B1 CARBAZOLE, DIBENZOFURAN, OR DIBENZOTHIOPHENE DERIVATIVES; DIETETICS, ANTIDIABETIC AGENTS; ANTILIPEMICS ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 2001-01-09 US disclosed
US-6037362-A CARBAZOLE DERIVATIVES; DEPROTECTING, AMINATION; ANTILIPEMIC AND ANTIDIABETIC AGENTS; B-ADRENALINE RECEPTOR AGONISTS; DIETETICS ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 2000-03-14 US disclosed
EP-0882707-A1 NOVEL TRICYCLIC COMPOUNDS AND DRUG COMPOSITIONS CONTAINING THE SAME Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1998-12-09 EP 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 (6 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-20130331401-A1 Halogenated Pyrazolo[1,5-A]Pyrimidines, Processes, Uses, Compositions and Intermediates GABRA5, GABRA1, RYR1 ALDH1A1 684/4885SMN1; SMN2 1345/4885KDM4E 1328/4885
US-10072000-B2 Method of treating insomnia with halogenated pyrazolo[1,5-a]pyrimidines GABRA5, GABRA1, GABBR1 ALDH1A1 502/4885SMN1; SMN2 1267/4885KDM4E 1019/4885
US-20130331610-A1 Halogenated Pyrazolo[1,5-A]Pyrimidines, Processes, Uses, Compositions and Intermediates GABRA5, GABRA1, RYR1 ALDH1A1 684/4885SMN1; SMN2 1345/4885KDM4E 1328/4885
US-20160368912-A9 HALOGENATED PYRAZOLO[1,5-A]PYRIMIDINES, PROCESSES, USES, COMPOSITIONS AND INTERMEDIATES GABRA5, GABRA1, RYR1 ALDH1A1 684/4885SMN1; SMN2 1345/4885KDM4E 1328/4885
US-20090111848-A1 Halogenated Pyrazolo[1,5-A]Pyrimidines, Processes, Uses, Compositions and Intermediates GABRA5, GABRA1, RYR1 ALDH1A1 684/4885SMN1; SMN2 1345/4885KDM4E 1328/4885
US-20020028835-A1 Cyclic amine phenyl beta-3 adrenergic receptor agonists ADRB1, ADRB3, ADRB2 ALDH1A1 1091/4885SMN1; SMN2 3999/4885KDM4E 4266/4885

“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.