SCHEMBL949716

SCHEMBL949716

CC(=O)c1cn(S(=O)(=O)c2ccccc2)c2ccccc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 1/20 1.00
▸ SMN1; SMN2 Q16637 1/20 1.00
▸ PLK1 P53350 1/20 0.72
▸ MEN1 O00255 1/20 0.72
▸ KMT2A Q03164 1/20 0.72
▸ AKR1C3 P42330 1/20 0.66
▸ AKR1C1 Q04828 1/20 0.66
▸ TNF P01375 3/20 0.62
▸ HTR6 P50406 9/20 0.58
▸ TNFSF11 O14788 2/20 0.58
▸ ALOX5 P09917 2/20 0.55
▸ PTGS2 P35354 1/20 0.55

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
SCHEMBL30393652 1.00 LMNA (1.00) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL949348 0.90 LMNA (0.82) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL948989 0.88 AKR1C3 (0.83) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL946881 0.86 LMNA (0.76) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL31202601 0.86 LMNA (0.76) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL946441 0.86 LMNA (0.76) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL8998784 0.85 LMNA (0.74) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL4926276 0.85 LMNA (0.74) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL15577151 0.85 LMNA (0.73) LMNASMN1; SMN2PLK1MEN1KMT2A
SCHEMBL8999130 0.84 PLK1 (1.00) LMNASMN1; SMN2PLK1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105198787-A N-benzenesulfonyl-3-acetyl indole acyl hydrazone compound, preparation method and application UNIV HENAN SCIENCE & TECH 2015-12-30 — — CN disclosed
CN-105198869-A Oxazoline derivative and preparation method and application of oxazoline derivative and prepartion method in preparing antibacterial agent of plant pathogenic fungi UNIV HENAN SCIENCE & TECH 2015-12-30 — — CN disclosed
CN-105198787-A N-benzenesulfonyl-3-acetyl indole acyl hydrazone compound, preparation method and application UNIV HENAN SCIENCE & TECH 2015-12-30 — — CN disclosed
CN-105061287-A N-substituted benzenesulfonyl-3-propionyl indole derivative, preparation method and application UNIV HENAN SCIENCE & TECH 2015-11-18 — — CN disclosed
CN-105052936-A Application for N-benzenesulfonyl-3-(2-yl-ethanoyl)-6-methylindole derivatives UNIV HENAN SCIENCE & TECH 2015-11-18 — — CN disclosed
CN-102321009-A Arylhydrazone derivate, preparation method thereof and application in preparing anti-HIV-1 medicines UNIV NORTHWEST A&F 2012-01-18 — — CN disclosed
US-7875605-B2 1-Benzenesulfonyl-3-(4-methylpiperazin-1-ylmethyl)-5-nitro-1 H-indole; 1-[[5-Bromo-1-(2-Bromo-4-methoxybenzenesulfonyl)-indo1-3-yl]methyl][1,4]diazepane; useful for treating psychotic and neurodegenerative disorders e.g. schizophrenia, Alzheimer's disease, Parkinson's disease and Huntington's chorea SUVEN LIFE SCIENCES LIMITED (IN) 2011-01-25 — — US disclosed
EP-1581492-B1 N-ARYLSULFONYL-3-SUBSTITUTED INDOLES HAVING SEROTONIN RECEPTOR AFFINITY, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITION CONTAINING THEM SUVEN LIFE SCIENCES LTD (IN) 2008-07-16 — — EP disclosed
CN-1317276-C Indolylpiperidine compound and preparation process and use thereof SHANGHAI PHARMACEUTICAL INST C (CN) 2007-05-23 — — CN disclosed
US-20060223890-A1 N-arylsulfonyl-3-substituted indoles having serotonin receptor affinity, process for their preparation and pharmaceutical composition containing them SUVEN LIFE SCIENCES LIMITED (IN) 2006-10-05 — — US disclosed
EP-1581492-A1 N-ARYLSULFONYL-3-SUBSTITUTED INDOLES HAVING SEROTONIN RECEPTOR AFFINITY, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITION CONTAINING THEM Suven Life Sciences Limited (IN) 2005-10-05 — — EP disclosed
US-6906095-B2 Indolylalkylidenehydrazine-carboximidamide derivatives as 5-hydroxytryptamine-6 ligands WYETH (US) 2005-06-14 — — US disclosed
WO-2004048330-A1 N-ARYLSULFONYL-3-SUBSTITUTED INDOLES HAVING SEROTONIN RECEPTOR AFFINITY, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITION CONTAINING THEM SUVEN LIFE SCIENCES LIMITED (IN) 2004-06-10 — — WO disclosed
US-20040002527-A1 Indolylalkylidenehydrazine-carboximidamide derivatives as 5-hydroxytryptamine-6 ligands WYETH 2004-01-01 — — US disclosed
CN-1345724-A Indolylpiperidine compound and preparation process and use thereof SHANGHAI PHARMACEUTICAL INST C (CN) 2002-04-24 — — CN disclosed
US-5210193-A Bactericide AMERICAN CYANAMID COMPANY (US) 1993-05-11 — — US disclosed
US-4940710-A 7-(substituted)piperazinyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids AMERICAN CYANAMID COMPANY (US) 1990-07-10 — — 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-20040002527-A1 Indolylalkylidenehydrazine-carboximidamide derivatives as 5-hydroxytryptamine-6 ligands HTR6, HTR5A, HTR2A LMNA 4212/4885SMN1; SMN2 3120/4885PLK1 2857/4885
US-20060223890-A1 N-arylsulfonyl-3-substituted indoles having serotonin receptor affinity, process for their preparation and pharmaceutical composition containing them HTR3A, HTR3C, HTR2C LMNA 2304/4885SMN1; SMN2 2056/4885PLK1 1465/4885

“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.

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