SCHEMBL3669684

SCHEMBL3669684

CC(=O)Nc1ccc([S+](c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NAPRT Q6XQN6 1/20 0.69
▸ HSD17B10 Q99714 1/20 0.69
▸ MAPT P10636 4/20 0.66
▸ RAB9A P51151 3/20 0.66
▸ KMT2A Q03164 3/20 0.66
▸ NPC1 O15118 2/20 0.66
▸ POLB P06746 2/20 0.66
▸ TAAR1 Q96RJ0 1/20 0.66
▸ ALDH1A1 P00352 5/20 0.61
▸ L3MBTL1 Q9Y468 2/20 0.61
▸ GAA P10253 1/20 0.61
▸ SMN1; SMN2 Q16637 5/20 0.59
▸ CACNA1B Q00975 1/20 0.59
▸ APBA1 Q02410 1/20 0.59
▸ HTT P42858 2/20 0.57
▸ MEN1 O00255 2/20 0.55
▸ TDP1 Q9NUW8 1/20 0.55
▸ CA12 O43570 1/20 0.55
▸ BRD4 O60885 1/20 0.55
▸ NR1I2 O75469 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
SCHEMBL1061931 0.93 NAPRT (0.60) NAPRTHSD17B10MAPTRAB9AKMT2A
Perchlorate SCHEMBL8463115 0.93 NAPRT (0.60) NAPRTHSD17B10MAPTRAB9AKMT2A
SCHEMBL31501975 0.93 NAPRT (0.60) NAPRTHSD17B10MAPTRAB9AKMT2A
SCHEMBL10922931 0.87 NAPRT (0.62) NAPRTHSD17B10MAPTRAB9AKMT2A
Acetanilide SCHEMBL1332076 0.83 NAPRT (1.00) NAPRTHSD17B10MAPTRAB9AKMT2A
Acetanilide SCHEMBL24681 0.83 NAPRT (1.00) NAPRTHSD17B10MAPTRAB9AKMT2A
SCHEMBL19669626 0.83 NAPRT (1.00) NAPRTHSD17B10MAPTRAB9AKMT2A
Acetanilide SCHEMBL16922180 0.83 NAPRT (1.00) NAPRTHSD17B10MAPTRAB9AKMT2A
Acetanilide SCHEMBL3359084 0.83 NAPRT (1.00) NAPRTHSD17B10MAPTRAB9AKMT2A
SCHEMBL6689000 0.82 ALDH1A1 (0.55) NAPRTHSD17B10MAPTRAB9AKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7297724-B2 Photoiniators having triarylsulfonium and arylsulfinate ions 3M INNOVATIVE PROPERTIES COMPANY (US) 2007-11-20 — — US claimed
EP-1684698-A1 PHOTOINITIATORS HAVING TRIARYLSULFONIUM AND ARYLSULFINATE IONS 3M Innovative Properties Company (US) 2006-08-02 — — EP claimed
US-20060111463-A1 PHOTOINIATORS HAVING TRIARYLSULFONIUM AND ARYLSULFINATE IONS 3M INNOVATIVE PROPERTIES COMPANY 2006-05-25 — — US claimed
US-7026367-B2 Photoiniators having triarylsulfonium and arylsulfinate ions 3M INNOVATIVE PROPERTIES COMPANY (US) 2006-04-11 — — US claimed
WO-2005034885-A1 PHOTOINITIATORS HAVING TRIARYLSULFONIUM AND ARYLSULFINATE IONS 3M INNOVATIVE PROPERTIES COMPANY (US) 2005-04-21 — — WO claimed
US-20050070621-A1 Photoiniators having triarylsulfonium and arylsulfinate ions 3M INNOVATIVE PROPERTIES COMPANY 2005-03-31 — — US claimed
CN-117777895-A Curable pressure sensitive adhesives with improved adhesive properties 德莎欧洲股份公司 2024-03-29 — — CN disclosed
CN-114380929-B Functionalized (co) polymers for adhesive systems 德莎欧洲股份公司 2024-02-06 — — CN disclosed
WO-2024012932-A1 UNCROSSLINKED POLYEPOXIDE AND ADHESIVE COMPOUND COMPRISING SAID POLYEPOXIDE TESA SE (DE) 2024-01-18 — — WO disclosed
CN-116829671-A Adhesive substances based on polyvinyl aromatic-polydiene-block copolymers with increased thermal shear strength 德莎欧洲股份公司 2023-09-29 — — CN disclosed
CN-116731649-A Curable adhesives with improved die-cuttability and improved impact properties 德莎欧洲股份公司 2023-09-12 — — CN disclosed
CN-111978898-B Method for producing pressure-sensitive adhesive reactive adhesive tape 德莎欧洲股份公司 2022-09-09 — — CN disclosed
CN-114380929-A Functionalized (co) polymers for adhesive systems 德莎欧洲股份公司 2022-04-22 — — CN disclosed
US-7026367-B2 Photoiniators having triarylsulfonium and arylsulfinate ions 3M INNOVATIVE PROPERTIES COMPANY (US) 2006-04-11 — — US disclosed
WO-2005034885-A1 PHOTOINITIATORS HAVING TRIARYLSULFONIUM AND ARYLSULFINATE IONS 3M INNOVATIVE PROPERTIES COMPANY (US) 2005-04-21 — — WO disclosed
US-20050070621-A1 Photoiniators having triarylsulfonium and arylsulfinate ions 3M INNOVATIVE PROPERTIES COMPANY 2005-03-31 — — US disclosed
EP-0931103-B1 MONOMERS, OLIGOMERS AND POLYMERS WITH TERMINAL OXIRANE GROUPS, METHOD OF PREPARATION AND POLYMERISATION UNDER RADIATION EXPOSURE UCB SA (BE) 2004-06-09 — — EP disclosed
US-6417243-B1 POLYESTERURETHANE BLOCKS UCB, S.A. (BE) 2002-07-09 — — US disclosed
EP-0931103-A1 MONOMERS, OLIGOMERS AND POLYMERS WITH TERMINAL OXIRANE GROUPS, METHOD OF PREPARATION AND POLYMERISATION UNDER RADIATION EXPOSURE UCB, S.A. (BE) 1999-07-28 — — EP disclosed
WO-1998014497-A1 MONOMERS, OLIGOMERS AND POLYMERS WITH TERMINAL OXIRANE GROUPS, METHOD OF PREPARATION AND POLYMERISATION UNDER RADIATION EXPOSURE UCB, S.A. (BE) 1998-04-09 — — WO disclosed
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