SCHEMBL132989

SCHEMBL132989

O=P(c1ccccc1)(c1ccccc1)c1ccc2ccccc2c1-c1c(P(=O)(c2ccccc2)c2ccccc2)ccc2ccccc12

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
WDR5 P61964 1/20 0.44
ALDH1A1 P00352 4/20 0.41
HSD17B10 Q99714 2/20 0.41
CYP2A6 P11509 1/20 0.41
TSHR P16473 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
DNMT1 P26358 1/20 0.39
HPRT1 P00492 1/20 0.38
NPSR1 Q6W5P4 2/20 0.38
MAPT P10636 1/20 0.37
CES1 P23141 1/20 0.37
POLB P06746 1/20 0.37
HTT P42858 1/20 0.37
KDM4E B2RXH2 1/20 0.37
LMNA P02545 1/20 0.37
MAPK1 P28482 1/20 0.37
PAX8 Q06710 1/20 0.36
GPR84 Q9NQS5 1/20 0.36
CA2 P00918 1/20 0.35
CA4 P22748 1/20 0.35

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
SCHEMBL29382484 1.00 WDR5 (0.44) WDR5ALDH1A1HSD17B10CYP2A6TSHR
SCHEMBL4401115 0.90 MAPT (0.43) WDR5ALDH1A1TSHRNPSR1MAPT
SCHEMBL4403131 0.90 MAPT (0.43) WDR5ALDH1A1TSHRNPSR1MAPT
SCHEMBL12336891 0.90 MAPT (0.43) WDR5ALDH1A1TSHRNPSR1MAPT
SCHEMBL19884356 0.90 WDR5 (0.38) WDR5ALDH1A1HSD17B10CYP2A6TSHR
SCHEMBL6053369 0.90 WDR5 (0.38) WDR5ALDH1A1HSD17B10CYP2A6TSHR
SCHEMBL11991070 0.90 WDR5 (0.38) WDR5ALDH1A1HSD17B10CYP2A6TSHR
SCHEMBL7025867 0.90 KMT2A (0.42) WDR5ALDH1A1HSD17B10NPSR1MAPT
SCHEMBL18867021 0.89 DNMT1 (0.39) WDR5ALDH1A1HSD17B10CYP2A6TSHR
SCHEMBL6242989 0.88 DNMT1 (0.41) WDR5ALDH1A1HSD17B10CYP2A6TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11355721-B2 Organic light emitting device comprising polar matrix, metal dopant and silver cathode NOVALED GMBH (DE) 2022-06-07 US claimed
EP-3109915-B1 ORGANIC LIGHT EMITTING DEVICE COMPRISING POLAR MATRIX AND METAL DOPANT NOVALED GMBH (DE) 2021-07-21 EP claimed
EP-3109919-B1 N-DOPED SEMICONDUCTING MATERIAL COMPRISING POLAR MATRIX AND METAL DOPANT NOVALED GMBH (DE) 2021-06-23 EP claimed
US-10749115-B2 N-doped semiconducting material comprising polar matrix and metal dopant NOVALED GMBH (DE) 2020-08-18 US claimed
US-20190036032-A1 N-Doped Semiconducting Material Comprising Polar Matrix and Metal Dopant NOVALED GMBH (DE) 2019-01-31 US claimed
US-20180190922-A1 Organic Light Emitting Device Comprising Polar Matrix, Metal Dopant and Silver Cathode NOVALED GMBH (DE) 2018-07-05 US claimed
US-20180182960-A1 Organic Light Emitting Device Comprising Polar Matrix and Metal Dopant NOVALED GMBH (DE) 2018-06-28 US claimed
EP-3109919-A1 N-DOPED SEMICONDUCTING MATERIAL COMPRISING POLAR MATRIX AND METAL DOPANT Novaled GmbH (DE) 2016-12-28 EP claimed
EP-3109916-A1 ORGANIC LIGHT EMITTING DEVICE COMPRISING POLAR MATRIX, METAL DOPANT AND SILVER CATHODE Novaled GmbH (DE) 2016-12-28 EP claimed
EP-3109915-A1 ORGANIC LIGHT EMITTING DEVICE COMPRISING POLAR MATRIX AND METAL DOPANT Novaled GmbH (DE) 2016-12-28 EP claimed
US-12416629-B2 Hollow polymer fiber optic system for single analyte and multiplexed analyte detection REVVITY HEALTH SCIENCES, INC. (US) 2025-09-16 US disclosed
US-20250074925-A1 RARE EARTH COMPLEX SAGAMI CHEMICAL RESEARCH INSTITUTE (JP) 2025-03-06 US disclosed
EP-4365180-A1 RARE EARTH COMPLEX Tosoh Corporation (JP) 2024-05-08 EP disclosed
EP-3374538-B1 PROCESS FOR MAKING A METAL CONTAINING LAYER NOVALED GMBH (DE) 2024-02-21 EP disclosed
EP-3380827-B1 HOLLOW POLYMER FIBER OPTIC SYSTEM FOR SINGLE ANALYTE AND MULTIPLEXED ANALYTE DETECTION REVVITY HEALTH SCIENCES INC (US) 2023-11-29 EP disclosed
US-20020091273-A1 Method for the regioselective preparation of substituted benzo[g]quinoline3-carbonitriles and benzo[g]quinazolines AMERICAN HOME PRODUCTS CORPORATION 2002-07-11 US disclosed
WO-2002053528-A1 METHOD FOR THE REGIOSELECTIVE PREPARATION OF SUBSTITUTED BENZO[G]QUINOLINE-3-CARBONITRILES AND BENZO[G]QUINAZOLINES WYETH (US) 2002-07-11 WO disclosed
US-6288268-B1 REACTION OF OLEFIN WITH ALCOHOL, OXYGEN AND CARBON MONOXIDE IN THE PRESENCE OF CATALYST FOR BISALKOXYCARBONYLATION WITH NOBLE MEYAL AND PHOSPHINE CHALCOGENIDE DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2001-09-11 US disclosed
US-6184390-B1 Catalyst for bisalkoxycarbonylation of olefins, and method for production of succinate derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2001-02-06 US disclosed
US-6159891-A Catalyst for bisalkoxycarbonylation of olefins, and method for production of succinate derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2000-12-12 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-20020091273-A1 Method for the regioselective preparation of substituted benzo[g]quinoline3-carbonitriles and benzo[g]quinazolines PDXK, PKD1, PFKP WDR5 3327/4885ALDH1A1 3804/4885HSD17B10 3378/4885
US-20250074925-A1 RARE EARTH COMPLEX L1CAM, CHRM1, NPM1 WDR5 3107/4885ALDH1A1 2286/4885HSD17B10 3020/4885

“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.