SCHEMBL5420063

SCHEMBL5420063

O=c1c2cccc3c2-c2c1cccc2c3=O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 4/20 0.46
▸ HPGD P15428 3/20 0.46
▸ MAOA P21397 3/20 0.46
▸ KDM4E B2RXH2 2/20 0.46
▸ GLA P06280 2/20 0.46
▸ SMN1; SMN2 Q16637 2/20 0.46
▸ LMNA P02545 2/20 0.46
▸ HTT P42858 2/20 0.46
▸ MAPT P10636 2/20 0.46
▸ CYP3A4 P08684 2/20 0.46
▸ HSD17B10 Q99714 2/20 0.46
▸ GAA P10253 1/20 0.46
▸ ATM Q13315 1/20 0.46
▸ PGAM1 P18669 1/20 0.46
▸ CASP1 P29466 1/20 0.46
▸ CASP7 P55210 1/20 0.46
▸ POLB P06746 3/20 0.37
▸ TDP1 Q9NUW8 2/20 0.37
▸ CA1 P00915 1/20 0.36
▸ CA2 P00918 1/20 0.36

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
SCHEMBL31675099 1.00 ALDH1A1 (0.46) ALDH1A1HPGDMAOAKDM4EGLA
SCHEMBL1445657 0.93 MAOA (0.39) ALDH1A1HPGDMAOAKDM4EGLA
SCHEMBL29365936 0.93 MAOA (0.39) ALDH1A1HPGDMAOAKDM4EGLA
SCHEMBL23463116 0.91 ALDH1A1 (0.46) ALDH1A1HPGDMAOAKDM4EGLA
SCHEMBL30409594 0.80 KDM4E (0.33) ALDH1A1HPGDMAOAKDM4EGLA
SCHEMBL4311602 0.77 — —
SCHEMBL25060702 0.76 ALDH1A1 (0.35) ALDH1A1HPGDMAOAKDM4EGLA
SCHEMBL28973342 0.76 KDM4E (0.30) ALDH1A1HPGDMAOAKDM4EGLA
SCHEMBL12319595 0.76 RAB9A (0.39) ALDH1A1HPGDKDM4ESMN1; SMN2MAPT
Ammonia Solution, Strong SCHEMBL11616909 0.74 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4137482-B1 THERMALLY ACTIVATED DELAYED FLUORESCENCE MATERIAL, PREPARATION METHOD THEREFOR AND ORGANIC ELECTROLUMINESCENT DEVICE WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECH CO LTD (CN) 2025-08-20 — — EP claimed
US-12168746-B2 Thermally activated delayed fluorescent material, preparing method thereof, and organic electroluminescent device WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECHNOLOGY CO., LTD. (CN) 2024-12-17 — — US claimed
US-20230137446-A1 THERMALLY ACTIVATED DELAYED FLUORESCENT MATERIAL, PREPARING METHOD THEREOF, AND ORGANIC ELECTROLUMINESCENT DEVICE WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECHNOLOGY CO., LTD. (CN) 2023-05-04 — — US claimed
EP-4137482-A1 THERMALLY ACTIVATED DELAYED FLUORESCENCE MATERIAL, PREPARATION METHOD THEREFOR AND ORGANIC ELECTROLUMINESCENT DEVICE Wuhan China Star Optoelectronics Semiconductor Display Technology Co., Ltd. (CN) 2023-02-22 — — EP claimed
EP-4137482-B1 THERMALLY ACTIVATED DELAYED FLUORESCENCE MATERIAL, PREPARATION METHOD THEREFOR AND ORGANIC ELECTROLUMINESCENT DEVICE WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECH CO LTD (CN) 2025-08-20 — — EP disclosed
US-12168746-B2 Thermally activated delayed fluorescent material, preparing method thereof, and organic electroluminescent device WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECHNOLOGY CO., LTD. (CN) 2024-12-17 — — US disclosed
US-20230137446-A1 THERMALLY ACTIVATED DELAYED FLUORESCENT MATERIAL, PREPARING METHOD THEREOF, AND ORGANIC ELECTROLUMINESCENT DEVICE WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECHNOLOGY CO., LTD. (CN) 2023-05-04 — — US disclosed
US-20230137446-A1 THERMALLY ACTIVATED DELAYED FLUORESCENT MATERIAL, PREPARING METHOD THEREOF, AND ORGANIC ELECTROLUMINESCENT DEVICE WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECHNOLOGY CO., LTD. (CN) 2023-05-04 — — US disclosed
US-20230137446-A1 THERMALLY ACTIVATED DELAYED FLUORESCENT MATERIAL, PREPARING METHOD THEREOF, AND ORGANIC ELECTROLUMINESCENT DEVICE WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECHNOLOGY CO., LTD. (CN) 2023-05-04 — — US disclosed
US-20230137446-A1 THERMALLY ACTIVATED DELAYED FLUORESCENT MATERIAL, PREPARING METHOD THEREOF, AND ORGANIC ELECTROLUMINESCENT DEVICE WUHAN CHINA STAR OPTOELECTRONICS SEMICONDUCTOR DISPLAY TECHNOLOGY CO., LTD. (CN) 2023-05-04 — — US disclosed
EP-4137482-A1 THERMALLY ACTIVATED DELAYED FLUORESCENCE MATERIAL, PREPARATION METHOD THEREFOR AND ORGANIC ELECTROLUMINESCENT DEVICE Wuhan China Star Optoelectronics Semiconductor Display Technology Co., Ltd. (CN) 2023-02-22 — — EP disclosed
EP-4137482-A1 THERMALLY ACTIVATED DELAYED FLUORESCENCE MATERIAL, PREPARATION METHOD THEREFOR AND ORGANIC ELECTROLUMINESCENT DEVICE Wuhan China Star Optoelectronics Semiconductor Display Technology Co., Ltd. (CN) 2023-02-22 — — EP disclosed
US-6835296-B2 Electrochemical polymerization; polyfluorenone; light emitting diodes IM&T RESEARCH, INC. 2004-12-28 — — US disclosed
US-20040206633-A1 oxidation of aromatic hydrocarbons into cyclopentanone compound; oxidation of fluorene into polyfluorenone IM&T RESEARCH, INC. 2004-10-21 — — US disclosed
US-20040210033-A1 Electrochemistry polymerization; blend of aromatic resin and cyclopentanone ; oxidation to polyfluorenes IM&T RESEARCH, INC. 2004-10-21 — — US disclosed
US-6767446-B2 ELECTROLYTIC POLYMERIZATION OF AROMATIC HYDROCARBONS SUCH AS FLUORENE IN THE PRESENCE OF AN ESTER; OXIDIZING RESULTING POLYMER TO PRODUCE A CYCLOPENTANONE-CONTAINING POLYMER SUCH AS POLY(9-FLUORENONE); LIGHT EMITTING DIODES IM&T RESEARCH, INC. 2004-07-27 — — US disclosed
US-20030081432-A1 Electrolytic polymerization of aromatic hydrocarbons such as fluorene in the presence of an ester; oxidizing resulting polymer to produce a cyclopentanone-containing polymer such as poly(9-fluorenone); light emitting diodes IM&T RESEARCH, INC. 2003-05-01 — — US disclosed
US-20030066757-A1 Method for preparing polymers containing cyclopentanone structures IM&T RESEARCH, INC. 2003-04-10 — — US disclosed
US-20030044680-A1 Polymers contain units having at least one cyclopentanone structure condensed with at least two aromatic rings. e.g., units of 9-fluorenone, cyclopenta(def)fluorene-4,8-dione, and benzo(b)fluoren-11-one. IM&T RESEARCH, INC. 2003-03-06 — — US disclosed
US-20030044680-A1 Polymers contain units having at least one cyclopentanone structure condensed with at least two aromatic rings. e.g., units of 9-fluorenone, cyclopenta(def)fluorene-4,8-dione, and benzo(b)fluoren-11-one. IM&T RESEARCH, INC. 2003-03-06 — — 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 (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-12168746-B2 Thermally activated delayed fluorescent material, preparing method thereof, and organic electroluminescent device CD69, ETFA, RPS19 ALDH1A1 225/4885HPGD 1972/4885MAOA 1105/4885
US-20230137446-A1 THERMALLY ACTIVATED DELAYED FLUORESCENT MATERIAL, PREPARING METHOD THEREOF, AND ORGANIC ELECTROLUMINESCENT DEVICE DNTT, CD69, DUT ALDH1A1 350/4885HPGD 2157/4885MAOA 1510/4885

“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.

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