SCHEMBL732734

SCHEMBL732734

O=C1CCc2ccc(NS(=O)(=O)c3ccc4ccccc4c3)cc21

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 4/20 0.64
PKM P14618 2/20 0.62
SMN1; SMN2 Q16637 3/20 0.57
LMNA P02545 2/20 0.57
PKLR P30613 1/20 0.56
ATM Q13315 1/20 0.56
KMT2A Q03164 5/20 0.55
NLRP3 Q96P20 1/20 0.55
PGR P06401 1/20 0.53
BRD4 O60885 2/20 0.53
MEN1 O00255 4/20 0.52
ALDH1A1 P00352 3/20 0.51
MAPT P10636 2/20 0.51
GAA P10253 1/20 0.51
HTT P42858 1/20 0.51
PNMT P11086 1/20 0.51
AKR1C3 P42330 1/20 0.50
HTR1A P08908 1/20 0.50
HTR2A P28223 1/20 0.50
HTR2C P28335 1/20 0.50

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
SCHEMBL14290577 0.86 HTR6 (0.63) HTR6PKMSMN1; SMN2LMNAPKLR
SCHEMBL9178059 0.80 ALDH1A1 (0.64) PKMSMN1; SMN2LMNAATMBRD4
SCHEMBL2906268 0.78 PKM (0.55) HTR6PKMSMN1; SMN2LMNAPKLR
SCHEMBL749515 0.78 HTR6 (0.73) HTR6PKMSMN1; SMN2LMNAPKLR
Hydrochloric Acid SCHEMBL732461 0.77 HTR6 (0.74) HTR6PKMSMN1; SMN2LMNAPKLR
Hydrochloric Acid SCHEMBL732462 0.77 HTR6 (0.74) HTR6PKMSMN1; SMN2LMNAPKLR
SCHEMBL30326699 0.77 DRD2 (0.58) HTR6SMN1; SMN2LMNABRD4ALDH1A1
SCHEMBL28383011 0.77 DRD2 (0.58) HTR6SMN1; SMN2LMNABRD4ALDH1A1
SCHEMBL2581047 0.77 PKM (1.00) PKMPKLRALDH1A1
SCHEMBL28379967 0.77 HSD17B2 (0.56) PKMSMN1; SMN2LMNAPKLRKMT2A

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2202222-A2 Indene derivatives, their preparation and use as medicaments LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2010-06-30 EP claimed
US-20090163547-A1 INDENE DERIVATIVES, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2009-06-25 US claimed
CN-101356149-A Indene derivatives, their preparation and use as medicaments ESTEVE LABOR DR (ES) 2009-01-28 CN claimed
US-8217041-B2 Indene derivatives, their preparation and use as medicaments Laboratories del Sr. Esteve, S.A. (ES) 2012-07-10 US disclosed
US-8217041-B2 Indene derivatives, their preparation and use as medicaments Laboratories del Sr. Esteve, S.A. (ES) 2012-07-10 US disclosed
US-8217041-B2 Indene derivatives, their preparation and use as medicaments Laboratories del Sr. Esteve, S.A. (ES) 2012-07-10 US disclosed
US-8138210-B2 Substituted indanyl sulfonamide compounds, their preparation and use as medicaments LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2012-03-20 US disclosed
EP-2202222-A2 Indene derivatives, their preparation and use as medicaments LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2010-06-30 EP disclosed
US-20100069378-A1 SUBSTITUTED INDANYL SULFONAMIDE COMPOUNDS, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2010-03-18 US disclosed
US-20090163547-A1 INDENE DERIVATIVES, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2009-06-25 US disclosed
US-20090163547-A1 INDENE DERIVATIVES, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2009-06-25 US disclosed
US-20090163547-A1 INDENE DERIVATIVES, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2009-06-25 US disclosed
CN-101356149-A Indene derivatives, their preparation and use as medicaments ESTEVE LABOR DR (ES) 2009-01-28 CN disclosed
EP-1884515-A1 Substituted indanyl sulfonamide compounds, their preparation and use as medicaments Laboratorios del Dr. Esteve S.A. (ES) 2008-02-06 EP disclosed
US-20080027073-A1 Substituted indanyl sulfonamide compounds, their preparation and use as medicaments LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2008-01-31 US disclosed
WO-2007054257-A2 INDENE DERIVATIVES, THEIR PREPARATION AND USE AS MEDICAMENTS LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2007-05-18 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 (3 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-20080027073-A1 Substituted indanyl sulfonamide compounds, their preparation and use as medicaments HTR6, HTR5A, GPR6 HTR6 1/4885PKM 2059/4885SMN1; SMN2 3328/4885
US-20100069378-A1 SUBSTITUTED INDANYL SULFONAMIDE COMPOUNDS, THEIR PREPARATION AND USE AS MEDICAMENTS HTR6, HTR5A, GPR6 HTR6 1/4885PKM 1949/4885SMN1; SMN2 3411/4885
US-20090163547-A1 INDENE DERIVATIVES, THEIR PREPARATION AND USE AS MEDICAMENTS HTR6, HTR5A, HTR1A HTR6 1/4885PKM 1938/4885SMN1; SMN2 4168/4885

“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.