SCHEMBL148472

SCHEMBL148472

CCCCCCCCCNC=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 6/20 1.00
ADH1B P00325 4/20 1.00
ADH1A P07327 4/20 1.00
ADH7 P40394 4/20 1.00
ADH1C P00326 3/20 1.00
ADH4 P08319 2/20 1.00
TSHR P16473 3/20 0.55
ALDH1A1 P00352 1/20 0.55
FAAH O00519 2/20 0.48
TRPV1 Q8NER1 1/20 0.48
S1PR2 O95136 2/20 0.45
S1PR4 O95977 2/20 0.45
S1PR1 P21453 2/20 0.45
S1PR3 Q99500 2/20 0.45
ZDHHC20 Q5W0Z9 1/20 0.45
ZDHHC2 Q9UIJ5 1/20 0.45

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
SCHEMBL303653 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C
SCHEMBL145544 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C
SCHEMBL9660807 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C
SCHEMBL9661679 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C
SCHEMBL302735 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C
SCHEMBL9661848 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C
SCHEMBL58363 1.00
SCHEMBL9658779 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C
SCHEMBL4879688 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C
SCHEMBL305123 1.00 EPHX1 (1.00) EPHX1ADH1BADH1AADH7ADH1C

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 484 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
CN-112280567-B Composition comprising compound functioning as dichromatic pigment 住友化学株式会社 2024-06-25 CN disclosed
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
CN-113376963-B Coloring composition and compound 住友化学株式会社 2024-05-28 CN disclosed
CN-113376962-B Coloring composition and compound 住友化学株式会社 2024-05-28 CN disclosed
CN-113376965-B Coloring composition and compound 住友化学株式会社 2024-05-28 CN disclosed
CN-113376964-B Coloring composition and compound 住友化学株式会社 2024-04-26 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
EP-0023770-A1 Cationic pyridone azo dyestuffs, certain novel coupling components from which they are derived and processes for the manufacture of the dyestuffs and the coupling components IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1981-02-11 EP disclosed
EP-0023017-A1 Process for the preparation of symmetrical thioindigo compounds or mixtures of symmetrical and asymmetrical thioindigo compounds as well as bis-(phenylthio)maleic acid derivatives and thionaphthenones per se CIBA-GEIGY AG (CH) 1981-01-28 EP disclosed
EP-0023016-A1 Process for the preparation of asymmetrical thioindigo compounds as well as thionaphthenones as such CIBA-GEIGY AG (CH) 1981-01-28 EP disclosed
US-4167509-A PYRIDINIUM-SUBSTITUTED; YELLOW SHADES ON ACRYLONITRILE POLYMERS IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1979-09-11 US disclosed
US-4124579-A FOR POLYMERIC MATERIALS IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1978-11-07 US disclosed
US-4089865-A Certain thiazole compounds SYNTEX (U.S.A.) INC. (US) 1978-05-16 US disclosed
US-4001421-A THIAZOLE CARDIOVASCULAR AGENTS SYNTEX (U.S.A.) INC. (US) 1977-01-04 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 EPHX1 398/4885ADH1B 170/4885ADH1A 86/4885
US-20080223444-A1 Perylene Charge-Transport Materials, Methods of Fabrication Thereof, and Methods of Use Thereof SLC43A1, SLC3A2, SLC16A3 EPHX1 2731/4885ADH1B 1391/4885ADH1A 1792/4885
US-20090044863-A1 CORONENE CHARGE-TRANSPORT MATERIALS, METHODS OF FABRICATION THEREOF, AND METHODS OF USE THEREOF SLC18A3, CORO1C, SLC18A1 EPHX1 3018/4885ADH1B 1551/4885ADH1A 2347/4885

“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.