SCHEMBL1414871

SCHEMBL1414871

NS(=O)(=O)NCCc1ccccc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 7/20 0.67
CA2 P00918 7/20 0.67
CA12 O43570 6/20 0.67
CA9 Q16790 4/20 0.67
CA14 Q9ULX7 3/20 0.64
CA7 P43166 1/20 0.64
HSD17B10 Q99714 1/20 0.64
CA5A P35218 2/20 0.61
PRMT1 Q99873 2/20 0.59
ALDH1A1 P00352 3/20 0.58
LMNA P02545 2/20 0.58
CYP3A4 P08684 2/20 0.58
KDM4E B2RXH2 1/20 0.58
GAA P10253 1/20 0.58
MAPT P10636 1/20 0.58
BLM P54132 1/20 0.58
GFER P55789 1/20 0.58
PMP22 Q01453 1/20 0.58
CA4 P22748 2/20 0.58
TAAR1 Q96RJ0 1/20 0.54

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
SCHEMBL30958759 0.88 POLB (0.68) CA1CA2CA12CA9CA14
SCHEMBL31398260 0.80 CA1 (0.68) CA1CA2CA12CA9CA14
SCHEMBL3367299 0.79 PRMT1 (0.54) CA12CA9CA14CA7HSD17B10
SCHEMBL15672851 0.79 MEN1 (0.58) HSD17B10PRMT1ALDH1A1LMNACYP3A4
SCHEMBL4520702 0.79 POLB (0.79) CA12CA9CA14CA7HSD17B10
SCHEMBL4601440 0.79 CA1 (0.59) CA1CA2HSD17B10PRMT1ALDH1A1
SCHEMBL1168754 0.79 ALDH1A1 (0.63) CA12CA9CA14CA7HSD17B10
SCHEMBL21034352 0.79 TAAR1 (0.59) CA12CA9CA14CA7HSD17B10
SCHEMBL49549 0.78 CA2 (1.00) CA1CA2CA12CA9CA14
SCHEMBL412302 0.78 ALDH1A1 (0.79) CA1CA2HSD17B10PRMT1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0034432-B1 SULFAMOYL-SUBSTITUTED PHENETHYLAMINE DERIVATIVES, THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS, CONTAINING THEM YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1984-04-25 EP claimed
EP-2661436-B1 NOVEL SULFAMIDE PIPERAZINE DERIVATIVES AS PROTEIN TYROSINE KINASE INHIBITORS AND PHARMACEUTICAL USE THEREOF LEO PHARMA AS (DK) 2016-04-13 EP disclosed
EP-2661436-B1 NOVEL SULFAMIDE PIPERAZINE DERIVATIVES AS PROTEIN TYROSINE KINASE INHIBITORS AND PHARMACEUTICAL USE THEREOF LEO PHARMA AS (DK) 2016-04-13 EP disclosed
US-9233964-B2 Sulfamide piperazine derivatives as protein tyrosine kinase inhibitors and pharmaceutical use therof LEO PHARMA A/S (DK) 2016-01-12 US disclosed
US-9233964-B2 Sulfamide piperazine derivatives as protein tyrosine kinase inhibitors and pharmaceutical use therof LEO PHARMA A/S (DK) 2016-01-12 US disclosed
US-9233964-B2 Sulfamide piperazine derivatives as protein tyrosine kinase inhibitors and pharmaceutical use therof LEO PHARMA A/S (DK) 2016-01-12 US disclosed
US-20130345194-A1 SUBSTITUTED CYCLOPENTYL-AZINES AS CASR-ACTIVE COMPOUNDS LEO PHARMA A/S (DK) 2013-12-26 US disclosed
EP-2661436-A1 NOVEL SULFAMIDE PIPERAZINE DERIVATIVES AS PROTEIN TYROSINE KINASE INHIBITORS AND PHARMACEUTICAL USE THEREOF Leo Pharma A/S (DK) 2013-11-13 EP disclosed
CN-103298817-A Novel sulfamide piperazine derivatives as protein tyrosine kinase inhibitors and pharmaceutical use thereof LEO PHARMA AS 2013-09-11 CN disclosed
US-8299021-B2 Macrocyclic inhibitors of hepatitis C virus replication INTERMUNE, INC. (US) 2012-10-30 US disclosed
CN-1816523-A N-(2-phenylethyl)sulfamide derivatives as integrin alpha4 antagonists ALMIRALL PRODESFARMA SA (ES) 2006-08-09 CN disclosed
EP-1622867-A1 N-(2-PHENYLETHYL)SULFAMIDE DERIVATIVES AS INTEGRIN ALPHA4 ANTAGONISTS Almirall Prodesfarma, S.A. (ES) 2006-02-08 EP disclosed
WO-2005075415-A1 A METHOD OF PREPARATION OF (R)-(-)-5(2-AMINOPROPYL)-2-METHOXYBENZENESULFONAMIDE ZENTIVA, A.S. (CZ) 2005-08-18 WO disclosed
WO-2005063701-A1 SYNTHESIS OF OPTICALLY PURE (R)-5-(2-AMINOPROPYL)-2-METHOXYBENZENESULPHONAMIDE LEK PHARMACEUTICALS D.D. (CH) 2005-07-14 WO disclosed
WO-2004099126-A1 N-(2-PHENYLETHYL)SULFAMIDE DERIVATIVES AS INTEGRIN α4 ANTAGONISTS ALMIRALL PRODESFARMA SA (ES) 2004-11-18 WO disclosed
WO-2003035608-A1 A METHOD OF THE PREPARATION OF (R)-(-)-5`2-`2-(2-ETHOXYPHENOXY) ETHYLAMINO! PROPYL!-2-METHOXYBENZENESULPHONAMIDE (TAMSULOSIN) LECIVA, A.S. (CZ) 2003-05-01 WO disclosed
EP-0805812-B1 BICYCLIC SUBSTITUTED HEXAHYDROBENZ(E)ISOINDOLE ALPHA-1- ADRENERGIC ANTAGONISTS ABBOTT LAB (US) 2001-06-13 EP disclosed
EP-0749302-A4 HYDROXAMIC ACID AND CARBOXYLIC ACID DERIVATIVES, PROCESS FOR THEIR PREPARATION AND USE THEREOF SANOFI WINTHROP INC (US) 1999-08-25 EP disclosed
EP-0749302-A1 HYDROXAMIC ACID AND CARBOXYLIC ACID DERIVATIVES, PROCESS FOR THEIR PREPARATION AND USE THEREOF SANOFI WINTHROP, INC. (US) 1996-12-27 EP disclosed
WO-1995022966-A1 HYDROXAMIC ACID AND CARBOXYLIC ACID DERIVATIVES, PROCESS FOR THEIR PREPARATION AND USE THEREOF SANOFI WINTHROP, INC. (US) 1995-08-31 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 (1 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-20130345194-A1 SUBSTITUTED CYCLOPENTYL-AZINES AS CASR-ACTIVE COMPOUNDS JAK1, CNKSR1, TSHR CA1 506/4885CA2 1068/4885CA12 1620/4885

“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.