SCHEMBL978653

SCHEMBL978653

O=S(=O)(O)F.O=S(=O)(O)F.O=S(=O)([O-])F.c1ccc([I+]c2ccccc2)cc1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
KDM4E B2RXH2 1/20 0.38
MAPT P10636 1/20 0.38
HPGD P15428 1/20 0.38
FAAH O00519 1/20 0.35
PRSS1 P07477 1/20 0.35
PRSS2 P07478 1/20 0.35
ELANE P08246 1/20 0.35
PRTN3 P24158 1/20 0.35
PRSS3 P35030 1/20 0.35
POLB P06746 1/20 0.35
CYP2D6 P10635 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
SNCA P37840 1/20 0.33
SRC P12931 1/20 0.32
HTR6 P50406 1/20 0.32
MMP2 P08253 2/20 0.32
CA2 P00918 4/20 0.31
CA12 O43570 2/20 0.31

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
SCHEMBL8972780 1.00 TSHR (0.39) TSHRSMN1; SMN2KDM4EMAPTHPGD
SCHEMBL11393462 0.93 FAAH (0.39) TSHRSMN1; SMN2KDM4EMAPTHPGD
Sulfuric Acid SCHEMBL1062108 0.89 TSHR (0.44) TSHRSMN1; SMN2KDM4EMAPTHPGD
Sulfuric Acid SCHEMBL1777697 0.84 HTR6 (0.39) TSHRSMN1; SMN2KDM4EMAPTHPGD
Sulfuric Acid SCHEMBL1780831 0.84 KDM4E (0.50) TSHRSMN1; SMN2KDM4EMAPTHPGD
SCHEMBL1628635 0.79 KEAP1 (0.39) HTR6MMP2CA2CA12CA9
SCHEMBL1718014 0.79 KEAP1 (0.44) TSHRSMN1; SMN2KDM4EMAPTHPGD
Anthraquinone SCHEMBL1405498 0.79 KMT2A (0.48) SMN1; SMN2KDM4EMAPTPOLBALDH1A1
Toliodium SCHEMBL8327648 0.79 TLR9 (0.42) SMN1; SMN2PRSS1PRSS2PRSS3POLB
Trifluoromethanesulfonic Acid SCHEMBL30407359 0.79 GPR3 (0.43) TSHRSMN1; SMN2KDM4EMAPTHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5981146-A CONTAINING A COMPOUND HAVING A SULFONIC ACID GROUP OR A CARBONIC ACID GROUP IS FORMED ON A CHEMICAL-AMPLIFICATION-TYPE RESIST FILM OF A SEMICONDUCTTOR SUBSTRATE, FOLLOWED BY PERFORMING EXPOSURE MITSUBISHI DENKI KABUSHIKI KAISHA (JP) 1999-11-09 US claimed
CN-118253469-A Laminate and method for producing same 株式会社东进世美肯 2024-06-28 CN disclosed
CN-112708046-B Ether super-early-strength polycarboxylate superplasticizer and preparation method thereof 科之杰新材料集团有限公司 2022-10-28 CN disclosed
US-7871751-B2 Resist composition MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2011-01-18 US disclosed
US-20080153031-A1 Resist composition MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2008-06-26 US disclosed
US-20040191672-A1 Resist composition MITSUBISHI GAS CHEMICAL CO., LTD. (JP) 2004-09-30 US disclosed
EP-1443362-A2 Resist composition MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2004-08-04 EP disclosed
US-5981146-A CONTAINING A COMPOUND HAVING A SULFONIC ACID GROUP OR A CARBONIC ACID GROUP IS FORMED ON A CHEMICAL-AMPLIFICATION-TYPE RESIST FILM OF A SEMICONDUCTTOR SUBSTRATE, FOLLOWED BY PERFORMING EXPOSURE MITSUBISHI DENKI KABUSHIKI KAISHA (JP) 1999-11-09 US disclosed
US-5565304-A ALKALI SOLUBLE BINDER RESIN FROM HYDROXYSTYRENEAND METHYLOLATED PHENOLIC COMPOUND OCG MICROELECTRONIC MATERIALS, INC. (US) 1996-10-15 US disclosed
US-5550004-A RESIN BINDER HAVING HYDROXYSTYRENE AND MONOMETHYLOLATED PHENOLIC COMPOUNDS OCG MICROELECTRONIC MATERIALS, INC. (US) 1996-08-27 US disclosed
EP-0727711-A2 Photoresist compositions containing supercritical fluid fractionated polymeric binder resins OCG MICROELECTRONIC MATERIALS, INC. (US) 1996-08-21 EP disclosed
EP-0697632-A2 Chemically amplified radiation-sensitive composition OCG MICROELECTRONIC MATERIALS, INC. (US) 1996-02-21 EP disclosed