Sugi Predict

Sugi Predict / Compounds / SCHEMBL719260

SCHEMBL719260

SCHEMBL719260

CCOP(OCC)OC(c1ccccc1)c1ccccc1

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HTT P42858 2/20 0.40
▸ SCN1A P35498 3/20 0.39
▸ SCN2A Q99250 3/20 0.39
▸ SCN3A Q9NY46 3/20 0.39
▸ LMNA P02545 3/20 0.39
▸ CYP1A2 P05177 1/20 0.39
▸ CHRM2 P08172 1/20 0.39
▸ CHRM4 P08173 1/20 0.39
▸ CHRM5 P08912 1/20 0.39
▸ ADRA2A P08913 1/20 0.39
▸ CYP2D6 P10635 1/20 0.39
▸ CHRM1 P11229 1/20 0.39
▸ TSHR P16473 1/20 0.39
▸ ADRA2B P18089 1/20 0.39
▸ CHRM3 P20309 1/20 0.39
▸ SLC6A2 P23975 1/20 0.39
▸ HRH2 P25021 1/20 0.39
▸ HTR2A P28223 1/20 0.39
▸ HTR2C P28335 1/20 0.39
▸ SLC6A4 P31645 1/20 0.39

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
SCHEMBL5953984 0.82 LTB4R (0.39) LMNAADRA2AADRA2BPOLBMEN1
SCHEMBL719844 0.82 MLKL (0.33) LMNASMN1; SMN2KDM4EMEN1KMT2A
SCHEMBL27639201 0.81 LMNA (0.35) LMNAHTR2AHRH1MAPK1POLB
SCHEMBL8633097 0.80 AOC3 (0.39) L3MBTL1
SCHEMBL3889250 0.80 IDO1 (0.41) HTTSCN1ASCN2ASCN3ALMNA
SCHEMBL28369454 0.77 IDO1 (0.40) HTTSCN1ASCN2ASCN3ALMNA
SCHEMBL385592 0.72 LTA4H (0.43) LMNATSHRL3MBTL1LTA4H
SCHEMBL443626 0.72 LTA4H (0.43) LMNATSHRL3MBTL1LTA4H
Bromide SCHEMBL2510983 0.72 TAAR1 (0.36) LMNASLC6A2SLC6A4SLC6A3POLB
SCHEMBL3992907 0.72 SCN1A (0.55) HTTSCN1ASCN2ASCN3ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108003390-B A kind of compound organo-tin het stabilizer of environment-friendly type and preparation method thereof 广州市联诺化工科技有限公司 2019-07-05 — — CN claimed
CN-106380729-B Novel PVC heat stabilizer 邵卫东 2019-01-29 — — CN claimed
CN-108003390-A A kind of compound organo-tin het stabilizer of environment-friendly type and preparation method thereof 广州市联诺化工科技有限公司 2018-05-08 — — CN claimed
CN-106380729-A Novel PVC heat stablizer 邵卫东 2017-02-08 — — CN claimed
JP-11158165-A — — None — — JP disclosed
CN-119108899-A Application of triarylamine compound as laser gain medium in laser device 北京润泽云溪科技有限公司 2024-12-10 — — CN disclosed
CN-106380729-B Novel PVC heat stabilizer 邵卫东 2019-01-29 — — CN disclosed
CN-106380729-A Novel PVC heat stablizer 邵卫东 2017-02-08 — — CN disclosed
EP-2460796-A1 INDOLE DERIVATIVE Hodogaya Chemical Co., Ltd. (JP) 2012-06-06 — — EP disclosed
US-20120052427-A1 INDOLE DERIVATIVES HODOGAYA CHEMICAL CO., LTD. (JP) 2012-03-01 — — US disclosed
US-20060147823-A1 Electrophotographic photoreceptor and charge-transporting material for electrophotographic photoreceptor TAKASAGO INTERNATIONAL CORPORATION (JP) 2006-07-06 — — US disclosed
WO-2004074943-A1 ELECTROPHOTOGRAPHIC PHOTORECEPTOR AND CHARGE-TRANSPORTING MATERIAL FOR ELECTROPHOTOGRAPHIC PHOTORECEPTOR TAKASAGO INTERNATIONAL CORPORATION (JP) 2004-09-02 — — WO disclosed
JP-H11158165-A PHENOTHIAZINE DERIVATIVE, PHENOXAZINE DERIVATIVE, CHARGE TRANSPORT MATERIAL AND ELECTROPHOTOGRAPHIC PHOTORECEPTOR USING THE SAME TAKASAGO INTERNATL CORP 1999-06-15 — — JP disclosed
US-5910610-A Triphenylamine derivative, charge-transporting material comprising the same, and electrophotographic photoreceptor TAKASAGO INTERNATIONAL CORPORATION (JP) 1999-06-08 — — US disclosed
EP-0650956-B1 Triphenylamine derivatives, and charge-transporting materials and electrophotographic photoreceptors containing such derivatives TAKASAGO PERFUMERY CO LTD (JP) 1998-07-15 — — EP disclosed
US-5736284-A HIGH SOLUBILITY IN POLYMER BINDER TAKASAGO INTERNATIONAL CORPORATION (JP) 1998-04-07 — — US disclosed
EP-0812820-A1 TRIPHENYLAMINE DERIVATIVES, AND CHARGE TRANSPORT MATERIAL AND ELECTROPHOTOGRAPHIC PHOTORECEPTOR PREPARED THEREFROM Takasago International Corporation (JP) 1997-12-17 — — EP disclosed
US-5573878-A HIGH CHARGING POTENTIALS, HIGH CARRIER MOBILITY TAKASAGO INTERNATIONAL CORPORATION (JP) 1996-11-12 — — US disclosed
US-5567560-A Triphenylamine derivative charge-transporting material containing electrophotographic photoreceptor TAKASAGO INTERNATIONAL CORPORATION (JP) 1996-10-22 — — US disclosed
EP-0650956-A1 Triphenylamine derivatives, and charge-transporting materials and electrophotographic photoreceptors containing such derivatives Takasago International Corporation (JP) 1995-05-03 — — EP 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-20120052427-A1 INDOLE DERIVATIVES SLC43A1, SLC19A1, SLC7A5 HTT 1996/4885SCN1A 1061/4885SCN2A 1022/4885

“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.