SCHEMBL749515

SCHEMBL749515

N=C(N)N/N=C1/CCc2ccc(NS(=O)(=O)c3ccc4ccccc4c3)cc21

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 4/20 0.73
PKM P14618 2/20 0.49
PKLR P30613 1/20 0.46
LMNA P02545 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.46
NLRP3 Q96P20 1/20 0.46
PRSS1 P07477 2/20 0.46
PRSS2 P07478 2/20 0.46
PRSS3 P35030 2/20 0.46
ST14 Q9Y5Y6 1/20 0.46
KMT2A Q03164 3/20 0.46
MEN1 O00255 2/20 0.46
ATM Q13315 1/20 0.46
ALDH1A1 P00352 2/20 0.45
GAA P10253 1/20 0.45
BRD4 O60885 1/20 0.45
AKR1C3 P42330 1/20 0.44
PGR P06401 1/20 0.44
PNMT P11086 1/20 0.43
F2 P00734 2/20 0.43

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
Hydrochloric Acid SCHEMBL732462 0.99 HTR6 (0.74) HTR6PKMPKLRLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL732461 0.99 HTR6 (0.74) HTR6PKMPKLRLMNASMN1; SMN2
SCHEMBL14290523 0.88 HTR6 (0.71) HTR6PKMPKLRLMNASMN1; SMN2
SCHEMBL732734 0.78 HTR6 (0.64) HTR6PKMPKLRLMNASMN1; SMN2
SCHEMBL14290577 0.77 HTR6 (0.63) HTR6PKMPKLRLMNASMN1; SMN2
SCHEMBL13442974 0.76 HTR6 (0.67) HTR6PKMPKLRLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL3614753 0.76 HTR6 (0.69) HTR6PKMPKLRLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL3614749 0.76 HTR6 (0.69) HTR6PKMPKLRLMNASMN1; SMN2
SCHEMBL13442963 0.71 HTR6 (0.77) HTR6
SCHEMBL730225 0.71 HTR6 (0.77) HTR6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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
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-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-20080027073-A1 Substituted indanyl sulfonamide compounds, their preparation and use as medicaments LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2008-01-31 US 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

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-20080027073-A1 Substituted indanyl sulfonamide compounds, their preparation and use as medicaments HTR6, HTR5A, GPR6 HTR6 1/4885PKM 2059/4885PKLR 2027/4885
US-20100069378-A1 SUBSTITUTED INDANYL SULFONAMIDE COMPOUNDS, THEIR PREPARATION AND USE AS MEDICAMENTS HTR6, HTR5A, GPR6 HTR6 1/4885PKM 1949/4885PKLR 1901/4885

“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.