SCHEMBL148389

SCHEMBL148389

N=Nc1ccc2ccccc2c1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR3E A5X5Y0 2/20 0.54
HTR3B O95264 2/20 0.54
HTR3A P46098 2/20 0.54
HTR3D Q70Z44 2/20 0.54
HTR3C Q8WXA8 2/20 0.54
MEN1 O00255 4/20 0.52
NPC1 O15118 4/20 0.52
RAB9A P51151 4/20 0.52
KMT2A Q03164 4/20 0.52
HSP90AA1 P07900 3/20 0.52
KDM4E B2RXH2 2/20 0.47
POLB P06746 1/20 0.47
SIGMAR1 Q99720 1/20 0.43
CYP2A6 P11509 6/20 0.42
CYP1A2 P05177 3/20 0.42
ALDH1A1 P00352 2/20 0.42
CYP3A4 P08684 1/20 0.42
HSD17B10 Q99714 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
CA1 P00915 1/20 0.42

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
SCHEMBL1354442 0.79 HTR3E (0.58) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL3283287 0.79 MEN1 (0.75) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL10017620 0.79 MEN1 (0.75) HTR3EHTR3BHTR3AHTR3DHTR3C
Tert-Butyl Formate SCHEMBL28678729 0.79 TDP1 (0.41) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL24713367 0.75 HTR3E (0.54) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL941460 0.75 HTR3E (0.54) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL1680572 0.75 HTR3E (0.54) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL13668023 0.75 HTR3E (0.54) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL148388 0.75 HTR3E (0.54) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL12475893 0.75 MEN1 (0.52) HTR3EHTR3BHTR3AHTR3DHTR3C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8344142-B2 perylenetetracarboxylic diimide core having side chains (groups or mesogens) attached to the core; to provide charge-transport materials having various volatilities, solubilities, crystallinity, and charge transport ability; organic light emitting diode; photovoltaic cells, light-emitting diodes GEORGIA TECH RESEARCH CORPORATION (US) 2013-01-01 US claimed
US-8039625-B2 Coronene charge-transport materials, methods of fabrication thereof, and methods of use thereof GEORGIA TECH RESEARCH CORPORATION (US) 2011-10-18 US claimed
US-20090044863-A1 CORONENE CHARGE-TRANSPORT MATERIALS, METHODS OF FABRICATION THEREOF, AND METHODS OF USE THEREOF NATIONAL SCIENCE FOUNDATION 2009-02-19 US claimed
US-20080223444-A1 Perylene Charge-Transport Materials, Methods of Fabrication Thereof, and Methods of Use Thereof GEORGIA TECH RESEARCH CORPORATION 2008-09-18 US claimed
WO-2006093965-A2 CORONENE CHARGE-TRANSPORT MATERIALS, METHODS OF FABRICATION THEREOF, AND METHODS OF USE THEREOF GEORGIA TECH RESEARCH CORPORATION (US) 2006-09-08 WO claimed
WO-2005124453-A2 PERYLENE CHARGE-TRANSPORT MATERIALS, METHODS OF FABRICATION THEREOF, AND METHODS OF USE THEREOF GEORGIA TECH RESEARCH CORPORATION (US) 2005-12-29 WO claimed
EP-1206456-B1 THERMOCHROMIC RYLENE DYES BASF AG (DE) 2004-11-17 EP claimed
US-4997919-A Azo direct dyes containing a non-reactive triazinyl moiety CIBA-GEIGY CORPORATION (US) 1991-03-05 US claimed
CN-113330096-B Use of substituted or unsubstituted polycyclic aromatic compounds for high resolution microscopy 马克斯·普朗克索赔科学公司 2024-05-31 CN disclosed
US-11958796-B2 Hydrophilic and particularly water soluble DBOV-derivatives MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2024-04-16 US disclosed
CN-112839922-B Hydrophilic and in particular water-soluble DBOV derivatives 马克斯·普朗克索赔科学公司 2024-04-02 CN disclosed
CN-111517964-B Method for splitting chiral compound 上海科技大学 2023-02-10 CN disclosed
CN-111423332-B Method for splitting chiral compound 上海科技大学 2023-02-10 CN disclosed
EP-3830217-B1 USE OF A SUBSTITUTED OR UNSUBSTITUTED POLYCYCLIC AROMATIC HYDROCARBON COMPOUND FOR HIGH-RESOLUTION MICROSCOPY MAX PLANCK GESELLSCHAFT (DE) 2022-07-20 EP disclosed
US-4594313-A Containing hetero rings FUJI PHOTO FILM CO., LTD. (JP) 1986-06-10 US disclosed
US-4590153-A CONTAINING MAGENTA COUPLER AND METAL COMPLEX FUJI PHOTO FILM CO., LTD. (JP) 1986-05-20 US disclosed
EP-0177765-A1 Silver halide color photographic material FUJI PHOTO FILM CO., LTD. (JP) 1986-04-16 EP disclosed
US-4579799-A AZULENIUM IODIDE SALTS, BINDERS, CHJARGE GENERATION AND TRANSPORT CANON KABUSHIKI KAISHA (JP) 1986-04-01 US disclosed
US-4565761-A Electrophotographic process utilizing an azulenium salt-containing photosensitive member CANON KABUSHIKI KAISHA (JP) 1986-01-21 US disclosed
US-4548886-A ELECTROGRAPHIC FILMS; OPTICAL RECORDING MEDIA CANON KABUSHIKI KAISHA (JP) 1985-10-22 US 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 (3 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-11958796-B2 Hydrophilic and particularly water soluble DBOV-derivatives NR1H4, HDGF, ABHD16A HTR3E 3018/4885HTR3B 2682/4885HTR3A 2398/4885
US-20080223444-A1 Perylene Charge-Transport Materials, Methods of Fabrication Thereof, and Methods of Use Thereof SLC43A1, SLC3A2, SLC16A3 HTR3E 969/4885HTR3B 2733/4885HTR3A 1301/4885
US-20090044863-A1 CORONENE CHARGE-TRANSPORT MATERIALS, METHODS OF FABRICATION THEREOF, AND METHODS OF USE THEREOF SLC18A3, CORO1C, SLC18A1 HTR3E 2085/4885HTR3B 2032/4885HTR3A 1937/4885

“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.