SCHEMBL5049280

SCHEMBL5049280

C=C(c1ccc(Br)cc1)c1ccc(Br)cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.55
HTT P42858 1/20 0.55
GFER P55789 1/20 0.55
HSD17B10 Q99714 1/20 0.55
GPR55 Q9Y2T6 1/20 0.55
CES2 O00748 1/20 0.52
CES1 P23141 1/20 0.52
CYP2A6 P11509 1/20 0.50
CA1 P00915 3/20 0.48
CA2 P00918 3/20 0.48
ALOX15 P16050 2/20 0.45
GSK3B P49841 2/20 0.44
OGG1 O15527 1/20 0.42
LMNA P02545 1/20 0.41
HDAC3 O15379 1/20 0.41
HDAC4 P56524 1/20 0.41
HDAC1 Q13547 1/20 0.41
HDAC7 Q8WUI4 1/20 0.41
HDAC2 Q92769 1/20 0.41
HDAC10 Q969S8 1/20 0.41

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
SCHEMBL6343638 1.00 MAPT (0.55) MAPTHTTGFERHSD17B10GPR55
SCHEMBL2287032 0.89 MEN1 (0.54) MAPTHTTGFERHSD17B10GPR55
SCHEMBL7685490 0.89 MAPT (0.75) MAPTHTTGFERHSD17B10GPR55
SCHEMBL10076323 0.87 MAPT (0.44) MAPTHTTGFERHSD17B10GPR55
SCHEMBL6339597 0.82 MAPT (0.66) MAPTCES2CES1CA1CA2
Dimethylamine SCHEMBL6342856 0.82 MEN1 (0.52) MAPTHTTGFERHSD17B10GPR55
SCHEMBL6342854 0.82 MEN1 (0.68) MAPTHTTGFERHSD17B10GPR55
SCHEMBL21679933 0.81 CES2 (0.52) MAPTCES2CES1CYP2A6CA1
SCHEMBL14596409 0.79 CES2 (0.50) MAPTCES2CES1CYP2A6CA1
SCHEMBL17547225 0.79 CES2 (0.50) CES2CES1CYP2A6CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109336894-A One kind having AIE effect rigidity Conjugate macrocycle compound and its preparation and application 东华大学 2019-02-15 CN claimed
US-12127473-B2 Di-, tri- and tetraphenylindane derivates and their use in organic electronics DOTTIKON ES HOLDING AG (CH) 2024-10-22 US disclosed
CN-117551023-A Preparation method and application of N-thio-phenyl phthalimide compound 太原理工大学 2024-02-13 CN disclosed
CN-117447370-A Preparation method of aggregation-induced emission material tetraaryl divinyl sulfide 山西蓬勃健康科技有限公司 2024-01-26 CN disclosed
US-20220006020-A1 DI-, TRI- AND TETRAPHENYLINDANE DERIVATES AND THEIR USE IN ORGANIC ELECTRONICS DOTTIKON ES HOLDING AG (CH) 2022-01-06 US disclosed
EP-3877357-A1 DI-, TRI- AND TETRAPHENYLINDANE DERIVATIVES AND THEIR USE IN ORGANIC ELECTRONICS DOTTIKON ES HOLDING AG (CH) 2021-09-15 EP disclosed
CN-113365976-A Diphenylindane, triphenylindane and tetraphenylindan derivatives and their use in organic devices 多蒂肯独家合成控股公司 2021-09-07 CN disclosed
CN-109265311-B Phenyl fluorene derivative and preparation method and application thereof 上海兆维科技发展有限公司 2021-06-04 CN disclosed
EP-3650438-A1 DI-, TRI- AND TETRAPHENYLINDANE DERIVATIVES AND THEIR USE IN ORGANIC ELECTRONICS DOTTIKON ES HOLDING AG (CH) 2020-05-13 EP disclosed
CN-109336894-A One kind having AIE effect rigidity Conjugate macrocycle compound and its preparation and application 东华大学 2019-02-15 CN disclosed
CN-105272962-A Synthetic method of 1,3-dithiane structure-containing polysubstituted olefin derivatives UNIV LANZHOU 2016-01-27 CN disclosed
US-7902744-B2 Heteroionic junction light emitting electrochemical cell THE STATE OF OREGON ACTING BY AND THROUGH THE STATE BOARD OF HIGHER EDUCATION ON BEHALF OF THE UNIVERSITY OF OREGON (US) 2011-03-08 US disclosed
US-20080191616-A1 Polymer light-emitting devices based on interfaces enables by internally compensated doped conjugated ionomers OREGON, UNIVERSITY OF 2008-08-14 US disclosed
US-20080157662-A1 Heteroionic junction light emitting electrochemical cell OREGON, UNIVERSITY OF 2008-07-03 US disclosed
US-5631264-A NEUROLOGICAL DISORDERS SANOFI WINTHROP, INC. (US) 1997-05-20 US disclosed
US-5604224-A NEURODEGENERATIVE DISORDERS STERLING WINTHROP INC. (US) 1997-02-18 US disclosed
US-5569655-A Substituted heterocyclylisoquinolinium salts and compositions and method of use thereof STERLING WINTHROP INC. (US) 1996-10-29 US disclosed
US-5554620-A Substituted 6,11-ethano-6,11-dihydrobenzo[b] quinolizinium salts and compositions and methods of use thereof STERLING WINTHROP INC. (US) 1996-09-10 US disclosed
EP-0656359-A1 Substituted 6,11-ethano-6,11-dihydrobenzo[b]quinolizinium salts and compositionsand methods of use thereof STERLING WINTHROP INC. (US) 1995-06-07 EP disclosed
EP-0647641-A1 Substituted heterocyclylisoquinolinium salts and compositions and methods of usethereof STERLING WINTHROP INC. (US) 1995-04-12 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 (2 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-20220006020-A1 DI-, TRI- AND TETRAPHENYLINDANE DERIVATES AND THEIR USE IN ORGANIC ELECTRONICS NR0B2, KCNJ2, TRRAP MAPT 2927/4885HTT 1767/4885GFER 2895/4885
US-12127473-B2 Di-, tri- and tetraphenylindane derivates and their use in organic electronics NR0B2, KCNJ2, TRRAP MAPT 2927/4885HTT 1767/4885GFER 2895/4885

“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.