Sugi Predict

Sugi Predict / Compounds / SCHEMBL2150002

SCHEMBL2150002

SCHEMBL2150002

O=C(O)c1c(F)c(F)c(F)c(F)c1F.[Zn]

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CES2 O00748 1/20 0.42
▸ CES1 P23141 1/20 0.42
▸ MEN1 O00255 7/20 0.41
▸ KMT2A Q03164 7/20 0.41
▸ SMN1; SMN2 Q16637 2/20 0.41
▸ CRHBP P24387 1/20 0.41
▸ CRHR2 Q13324 1/20 0.41
▸ GAA P10253 1/20 0.39
▸ HTT P42858 2/20 0.39
▸ PKM P14618 1/20 0.38
▸ CYP1A2 P05177 1/20 0.36
▸ MAPK1 P28482 2/20 0.36
▸ LMNA P02545 1/20 0.36
▸ TP53 P04637 1/20 0.36
▸ TSHR P16473 2/20 0.35
▸ KDM4E B2RXH2 1/20 0.34
▸ ASPH Q12797 1/20 0.34
▸ KDM8 Q8N371 1/20 0.34
▸ CA12 O43570 1/20 0.33
▸ CA1 P00915 1/20 0.33

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
SCHEMBL203915 0.97 CES2 (0.43) CES2CES1MEN1KMT2ASMN1; SMN2
SCHEMBL1118381 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; SMN2
SCHEMBL7776700 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; SMN2
Ammonia Solution, Strong SCHEMBL11055563 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; SMN2
SCHEMBL16756190 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; SMN2
Hydrochloric Acid SCHEMBL11033629 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; SMN2
Ammonia Solution, Strong SCHEMBL20291864 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; SMN2
SCHEMBL336420 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; SMN2
SCHEMBL28389339 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; SMN2
SCHEMBL27824169 0.93 CES2 (0.42) CES2CES1MEN1KMT2ASMN1; 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 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114725536-B Water-based zinc-manganese battery electrolyte and application thereof 中南大学 2024-05-28 — — CN claimed
CN-114725536-A Aqueous zinc-manganese battery electrolyte and application thereof 中南大学 2022-07-08 — — CN claimed
CN-119751185-A Preparation method of polyfluoro biaryl compound 台州学院 2025-04-04 — — CN disclosed
CN-114725536-B Water-based zinc-manganese battery electrolyte and application thereof 中南大学 2024-05-28 — — CN disclosed
CN-117550975-A Preparation method of polyfluoroaryl or heteroaryl derivative 福建润华化工有限公司 2024-02-13 — — CN disclosed
CN-111763225-B Preparation method of anhydrous tris (pentafluorophenyl) borane 卫星化学股份有限公司 2023-02-10 — — CN disclosed
CN-114725536-A Aqueous zinc-manganese battery electrolyte and application thereof 中南大学 2022-07-08 — — CN disclosed
CN-111763225-A Preparation method of anhydrous tris (pentafluorophenyl) borane 浙江卫星石化股份有限公司 2020-10-13 — — CN disclosed
US-10581001-B2 Organic electronic component having a charge carrier generation layer and the use of a zinc complex as a P-type dopant in charge carrier generation layers OSRAM OLED GMBH (DE) 2020-03-03 — — US disclosed
US-10256422-B2 Organic electronic component, use of a zinc complex as a p-dopant for organic electronic matrix materials OSRAM OLED GMBH (DE) 2019-04-09 — — US disclosed
CN-106796986-B The application of organic electronic assembly, zinc complex as the p dopant for organic electronic basis material 欧司朗OLED股份有限公司 2019-04-05 — — CN disclosed
US-7202317-B2 Polymerization of i-butene in hydrocarbon media using bis(borane) co-initiators THE UNIVERSITY OF AKRON (US) 2007-04-10 — — US disclosed
US-7196149-B2 Polymerization of i-butane in hydrocarbon media using bis(borane) co-initiators THE UNIVERSITY OF AKRON (US) 2007-03-27 — — US disclosed
EP-1620476-A4 POLYMERIZATION OF I-BUTENE IN HYDROCARBON MEDIA USING BIS(BORANE)CO-INITIATORS UNIV AKRON (US) 2007-03-07 — — EP disclosed
EP-1620476-A2 POLYMERIZATION OF I-BUTENE IN HYDROCARBON MEDIA USING BIS(BORANE)CO-INITIATORS The University of Akron (US) 2006-02-01 — — EP disclosed
US-20060004159-A1 Polymerization of i-butene in hydrocarbon media using bis(borane) co-initiators UNIVERSITY OF AKRON, THE 2006-01-05 — — US disclosed
US-20050027086-A1 Polymerization of i-butene in hydrocarbon media using bis(borane) co-initiators UNIVERSITY OF AKRON, THE 2005-02-03 — — US disclosed
WO-2004094481-A2 POLYMERIZATION OF I-BUTENE IN HYDROCARBON MEDIA USING BIS(BORANE)CO-INITIATORS THE UNIVERSITY OF AKRON (US) 2004-11-04 — — WO disclosed
US-5744646-A Preparation of tris (pentafluorophenyl) borane THE DOW CHEMICAL COMPANY (US) 1998-04-28 — — US disclosed
WO-1997039003-A1 PREPARATION OF TRIS(PENTAFLUOROPHENYL)BORANE THE DOW CHEMICAL COMPANY (US) 1997-10-23 — — 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-10581001-B2 Organic electronic component having a charge carrier generation layer and the use of a zinc complex as a P-type dopant in charge carrier generation layers SCO2, NCOA4, NR4A2 CES2 1089/4885CES1 2555/4885MEN1 4301/4885

“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.