SCHEMBL819788

SCHEMBL819788

O=S(=O)(O)C(Br)c1ccccc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SRC P12931 3/20 0.54
ALDH1A1 P00352 2/20 0.52
CES2 O00748 2/20 0.48
CES1 P23141 2/20 0.48
TSHR P16473 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
LMNA P02545 3/20 0.41
KDM4E B2RXH2 1/20 0.41
GMNN O75496 1/20 0.41
POLB P06746 1/20 0.41
MAPT P10636 1/20 0.41
HPGD P15428 1/20 0.41
PMP22 Q01453 1/20 0.41
KMT2A Q03164 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
CYP2D6 P10635 1/20 0.41
CYP2C19 P33261 1/20 0.41
MAPK1 P28482 1/20 0.39
ACP1 P24666 1/20 0.38

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
SCHEMBL28007758 0.80 CES2 (0.46) SRCALDH1A1CES2CES1TSHR
SCHEMBL27390102 0.78 SRC (0.56) SRCALDH1A1CES2CES1TSHR
SCHEMBL11755998 0.77 SRC (0.34) SRCALDH1A1
SCHEMBL7616312 0.76 CES2 (0.43) SRCALDH1A1CES2CES1TRPA1
SCHEMBL935224 0.76 CES2 (0.43) SRCALDH1A1CES2CES1LMNA
SCHEMBL7790529 0.76 SRC (0.43) SRCALDH1A1CES2CES1TSHR
SCHEMBL153281 0.75 SRC (0.58) SRCALDH1A1CES2CES1TSHR
SCHEMBL496890 0.75 SRC (0.58) SRCALDH1A1CES2CES1TSHR
SCHEMBL9197961 0.74 HTR6 (0.44) SRCALDH1A1CES2CES1TSHR
SCHEMBL9244633 0.73 SRC (0.56) SRCALDH1A1CES2CES1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110903480-A Preparation method of controllable molecular weight polysulfone 万华化学集团股份有限公司 2020-03-24 CN claimed
US-5279899-A Metal coated polyamide having a sulfonate containing compound at interface MONSANTO COMPANY (US) 1994-01-18 US claimed
WO-1993019239-A1 SULFONATED POLYAMIDES MONSANTO COMPANY (US) 1993-09-30 WO claimed
CN-118515685-A Synthesis of halichondrin 哈佛大学的校长及成员们 2024-08-20 CN disclosed
US-9570773-B2 Fluorine-based polymer electrolyte membrane ASAHI KASEI E-MATERIALS CORPORATION (JP) 2017-02-14 US disclosed
EP-2128919-B1 POLYELECTROLYTE COMPOSITION, POLYELECTROLYTE MEMBRANE, MEMBRANE ELECTRODE ASSEMBLY, AND SOLID POLYMER ELECTROLYTE FUEL CELL ASAHI KASEI E MATERIALS CORP (JP) 2016-05-11 EP disclosed
EP-2613390-B1 FLUORINE-CONTAINING POLYMER ELECTROLYTE MEMBRANE ASAHI KASEI E MATERIALS CORP (JP) 2016-01-13 EP disclosed
EP-2405517-B1 FLUORINE-CONTAINING POLYMER ELECTROLYTE MEMBRANE ASAHI KASEI E MATERIALS CORP (JP) 2014-08-13 EP disclosed
US-8795927-B2 Highly durable electrode catalyst layer ASAHI KASEI KABUSHIKI KAISHA (JP) 2014-08-05 US disclosed
EP-2722921-A1 Fluoropolymer electrolyte membrane Asahi Kasei E-materials Corporation (JP) 2014-04-23 EP disclosed
US-20130244135-A1 FLUORINE-BASED POLYMER ELECTROLYTE MEMBRANE ASAHI KASEI E-MATERIALS CORPORATION (JP) 2013-09-19 US disclosed
EP-2128919-A1 POLYELECTROLYTE COMPOSITION, POLYELECTROLYTE MEMBRANE, MEMBRANE ELECTRODE ASSEMBLY, AND SOLID POLYMER ELECTROLYTE FUEL CELL Asahi Kasei E-materials Corporation (JP) 2009-12-02 EP disclosed
CN-101506185-A Tetrahydrofuro [3, 2-B] pyrrol-3-one intermediates ARMURA THERAPEUTICS LTD (GB) 2009-08-12 CN disclosed
US-20080096078-A1 Highly Durable Electrode Catalyst Layer ASAHI KASEI KABUSHIKI KAISHA (JP) 2008-04-24 US disclosed
EP-1788654-A1 SOLID POLYMER ELECTROLYTE MEMBRANE AND METHOD FOR PRODUCING SAME Asahi Kasei Chemicals Corporation (JP) 2007-05-23 EP disclosed
US-20060199062-A1 Solid polymer electrolyte membrane and production method of the same ASAHI KASEI CHEMICALS CORPORATION (JP) 2006-09-07 US disclosed
EP-1363897-A2 ANTAGONISTS OF MCP-1 FUNCTION AND METHODS OF USE THEREOF TELIK, INC. (US) 2003-11-26 EP disclosed
WO-2002070509-A2 ANTAGONISTS OF MCP-1 FUNCTION AND METHODS OF USE THEREOF TELIK, INC. (US) 2002-09-12 WO disclosed
US-5206427-A Process for the preparation of aromatic (di)chlorosulphonic acids and (di)bromosulphonic acids BAYER AKTIENGESELLSCHAFT (DE) 1993-04-27 US disclosed
US-4009085-A ELECTRODEPOSITION OF CHROMIUM OXIDE M & T CHEMICALS INC. (US) 1977-02-22 US disclosed