SCHEMBL5012113

SCHEMBL5012113

CCCCCCn1c2ccccc2c2cc(N)ccc21

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.68
MEN1 O00255 1/20 0.68
ALDH1A1 P00352 1/20 0.68
MAPT P10636 1/20 0.68
HPGD P15428 1/20 0.68
MAPK1 P28482 1/20 0.68
HTT P42858 1/20 0.68
HBB P68871 1/20 0.68
KMT2A Q03164 1/20 0.68
HSD17B10 Q99714 1/20 0.68
TDP1 Q9NUW8 1/20 0.68
CNR2 P34972 10/20 0.59
SIGMAR1 Q99720 1/20 0.58
NPC1 O15118 1/20 0.53
PSEN1 P49768 6/20 0.53
PSEN2 P49810 6/20 0.53
APH1B Q8WW43 6/20 0.53
NCSTN Q92542 6/20 0.53
APH1A Q96BI3 6/20 0.53
PSENEN Q9NZ42 6/20 0.53

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
SCHEMBL9397292 1.00 KDM4E (0.68) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL8124194 1.00 KDM4E (0.68) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL1149765 0.98 KDM4E (0.69) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL11340644 0.96 KDM4E (0.76) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL31739343 0.94 ALDH1A1 (0.71) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL10945941 0.94 ALDH1A1 (0.71) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL30884614 0.92 KDM4E (0.54) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL29208327 0.92 KDM4E (0.54) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL11757062 0.88 KDM4E (0.76) KDM4EMEN1ALDH1A1MAPTHPGD
SCHEMBL551644 0.86 PSEN1 (0.62) CNR2PSEN1PSEN2APH1BNCSTN

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112251497-A Nucleic acid liquid phase hybridization capture detection method based on magnetic separation and enzyme catalysis 段江波 2021-01-22 CN claimed
WO-2023195319-A1 POSITIVE PHOTOSENSITIVE PIGMENT COMPOSITION, CURED FILM CONTAINING CURED PRODUCT THEREOF, AND ORGANIC EL DISPLAY DEVICE 東レ株式会社 2023-10-12 WO disclosed
CN-110167911-B Hole-transporting organic molecules containing enamine groups for optoelectronic and photoelectrochemical devices 考纳斯科技大学 2022-07-05 CN disclosed
US-11329229-B2 Hole transporting organic molecules containing enamine groups for optoelectronic and photoelectrochemical devices KAUNO TECHNOLOGIES UNIVERSITETAS (LT) 2022-05-10 US disclosed
CN-112251497-A Nucleic acid liquid phase hybridization capture detection method based on magnetic separation and enzyme catalysis 段江波 2021-01-22 CN disclosed
CN-110167911-A Hole transport organic molecules for the group containing enamine of photoelectron and photoelectrochemicalcell cell 考纳斯科技大学 2019-08-23 CN disclosed
EP-3515884-A2 HOLE TRANSPORTING ORGANIC MOLECULES CONTAINING ENAMINE GROUPS FOR OPTOELECTRONIC AND PHOTOELECTROCHEMICAL DEVICES Kauno Technologijos Universitetas (LT) 2019-07-31 EP disclosed
US-20190229272-A1 HOLE TRANSPORTING ORGANIC MOLECULES CONTAINING ENAMINE GROUPS FOR OPTOELECTRONIC AND PHOTOELECTROCHEMICAL DEVICES Kauno technologijos universitetas (LT) 2019-07-25 US disclosed
WO-2018051278-A2 HOLE TRANSPORTING ORGANIC MOLECULES CONTAINING ENAMINE GROUPS FOR OPTOELECTRONIC AND PHOTOELECTROCHEMICAL DEVICES Kauno technologijos universitetas (LT) 2018-03-22 WO disclosed
EP-0887817-B1 Photoelectric material using organic photosensitising dyes and manufacturing method thereof SHARP KK (JP) 2008-05-28 EP disclosed
CN-1152942-C Molecular twisty type electroluminescence material containing current carrier transmission functional group and its application 华东理工大学 2004-06-09 CN disclosed
CN-1272523-A Molecular twisty type electroluminescence material containing current carrier transmission functional group and its application UNIV HUADONG SCIENCE & ENG (CN) 2000-11-08 CN disclosed
US-6043428-A SEMICONDUCTOR ATTACHED TO A PHOTOSENSITIZING DYE SUCH AS PHTHALOCYANINE, DIOXAZINE, OR INDIGO WHICH HAS INTERLOCKING GROUP AND HYDROPHOBIC GROUP(S), BY DIPPING IN HYDROPHOBIC OR APROTIC SOLVENT; DURABLE, EFFICIENT PHOTOELECTRIC MATERIAL SHARP KABUSHIKI KAISHA (JP) 2000-03-28 US disclosed
EP-0887817-A2 Photoelectric material using organic photosensitising dyes and manufacturing method thereof SHARP KABUSHIKI KAISHA (JP) 1998-12-30 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-20190229272-A1 HOLE TRANSPORTING ORGANIC MOLECULES CONTAINING ENAMINE GROUPS FOR OPTOELECTRONIC AND PHOTOELECTROCHEMICAL DEVICES OCIAD1, OCIAD2, SLCO4C1 KDM4E 4217/4885MEN1 1830/4885ALDH1A1 594/4885
US-11329229-B2 Hole transporting organic molecules containing enamine groups for optoelectronic and photoelectrochemical devices OCIAD1, OCIAD2, SLCO4C1 KDM4E 4217/4885MEN1 1830/4885ALDH1A1 594/4885

“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.