SCHEMBL633906

SCHEMBL633906

CCCCCCCNS(=O)(=O)c1ccccc1

nearest known ligand 0.82

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 9/20 0.82
LMNA P02545 2/20 0.82
PKM P14618 2/20 0.82
KDM4E B2RXH2 1/20 0.82
SMN1; SMN2 Q16637 1/20 0.82
TSHR P16473 1/20 0.71
EPHX2 P34913 1/20 0.68
TBXA2R P21731 1/20 0.66
MAPK1 P28482 2/20 0.63
RECQL P46063 1/20 0.62
CA12 O43570 1/20 0.59
CA9 Q16790 1/20 0.59
HTT P42858 1/20 0.57
MEN1 O00255 1/20 0.56
KMT2A Q03164 1/20 0.56

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
SCHEMBL5020960 1.00 ALDH1A1 (0.82) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
SCHEMBL578633 1.00 ALDH1A1 (0.82) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
SCHEMBL578832 1.00 ALDH1A1 (0.82) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
SCHEMBL578728 1.00 ALDH1A1 (0.82) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
SCHEMBL579136 1.00 ALDH1A1 (0.82) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
SCHEMBL1279062 1.00 ALDH1A1 (0.82) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
SCHEMBL366844 0.98 ALDH1A1 (0.79) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
Bicarbonate SCHEMBL9492528 0.95 ALDH1A1 (0.74) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
Trimethylammonium SCHEMBL27862582 0.95 ALDH1A1 (0.74) ALDH1A1LMNAPKMKDM4ESMN1; SMN2
Bicarbonate SCHEMBL9491178 0.95 ALDH1A1 (0.74) ALDH1A1LMNAPKMKDM4ESMN1; SMN2

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
US-4339372-A Process of preparing stabilized polychloroprene latex DISTUGIL (FR) 1982-07-13 US claimed
CN-115974732-A Method for preparing alkyl sulfonyl fluoride 中国石油大学(华东) 2023-04-18 CN disclosed
EP-2302000-B1 CURABLE COMPOSITION AND CATALYST COMPOSITION KANEKA CORP (JP) 2016-11-16 EP disclosed
US-9051501-B2 Curable composition and catalyst composition KANEKA CORPORATION (JP) 2015-06-09 US disclosed
EP-2100923-B1 CURABLE COMPOSITION KANEKA CORP (JP) 2013-03-13 EP disclosed
EP-2088173-B1 CURABLE COMPOSITION AND CATALYST COMPOSITION KANEKA CORP (JP) 2012-02-22 EP disclosed
US-8008386-B2 Curable composition KANEKA CORPORATION (JP) 2011-08-30 US disclosed
EP-2302000-A1 Curable composition and catalyst composition KANEKA CORPORATION (JP) 2011-03-30 EP disclosed
US-20100063215-A1 CURABLE COMPOSITION KANEKA CORPORATION (JP) 2010-03-11 US disclosed
US-20100041810-A1 CURABLE COMPOSITION AND CATALYST COMPOSITION KANEKA CORPORATION (JP) 2010-02-18 US disclosed
EP-2100923-A1 CURABLE COMPOSITION Kaneka Corporation (JP) 2009-09-16 EP disclosed
EP-2088173-A1 CURABLE COMPOSITION AND CATALYST COMPOSITION Kaneka Corporation (JP) 2009-08-12 EP disclosed
WO-1999041756-A1 INTRINSICALLY CONDUCTIVE POLYMER BLENDS HAVING A LOW PERCOLATION THRESHOLD ZIPPERLING KESSLER & CO. (GMBH & CO.) (DE) 1999-08-19 WO disclosed
US-5908898-A ELECTRICALLY INSULATIVE THERMOPLASTIC MATRIX POLYMER DISPERSED THROUGH AN INTRINSICALLY CONDUCTIVE POLYMER SALT THAT IS INCOMPATIBLE WITH THE MATRIX POLYMER, A THERMOPLASTIC CONDUCTIVE PHASE POLYMER THAT IS PARTIALLY COMPATIBLE WITH MONSANTO COMPANY (US) 1999-06-01 US disclosed
WO-1999019391-A1 INTRINSICALLY CONDUCTIVE POLYMER/PLASTICIZER BLENDS WITH ENHANCED CONDUCTIVITY ZIPPERLING KESSLER & CO. (GMBH & CO.) (DE) 1999-04-22 WO disclosed
US-5871671-A Intrinsically conductive polymer/plasticizer blends with enhanced conductivity MONSANTO COMPANY (US) 1999-02-16 US disclosed
US-4339372-A Process of preparing stabilized polychloroprene latex DISTUGIL (FR) 1982-07-13 US disclosed