SCHEMBL253499

SCHEMBL253499

NC(=O)c1c(C(N)=O)c2c(C(N)=O)ccc3c4cccc5cccc(c(c1C(N)=O)c23)c54

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 6/20 0.39
▸ ALDH1A1 P00352 5/20 0.39
▸ GAA P10253 2/20 0.39
▸ KMT2A Q03164 3/20 0.38
▸ CYP1A2 P05177 3/20 0.38
▸ HSD17B10 Q99714 3/20 0.38
▸ GLA P06280 2/20 0.38
▸ POLB P06746 2/20 0.38
▸ HPGD P15428 2/20 0.38
▸ CYP2D6 P10635 1/20 0.38
▸ SMN1; SMN2 Q16637 1/20 0.37
▸ ATM Q13315 2/20 0.37
▸ PARP1 P09874 3/20 0.35
▸ PDPK1 O15530 1/20 0.35
▸ MEN1 O00255 1/20 0.35
▸ PLK4 O00444 1/20 0.33
▸ CHEK1 O14757 1/20 0.33
▸ AURKA O14965 1/20 0.33
▸ DAPK3 O43293 1/20 0.33
▸ MAP4K4 O95819 1/20 0.33

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
SCHEMBL31738427 1.00 KDM4E (0.39) KDM4EALDH1A1GAAKMT2ACYP1A2
SCHEMBL31218570 0.90 KDM4E (0.36) KDM4EALDH1A1GAAKMT2ACYP1A2
SCHEMBL29452406 0.88 HSD17B10 (0.41) KDM4EALDH1A1GAAKMT2ACYP1A2
SCHEMBL2599500 0.88 HSD17B10 (0.41) KDM4EALDH1A1GAAKMT2ACYP1A2
SCHEMBL4706744 0.88 HSD17B10 (0.41) KDM4EALDH1A1GAAKMT2ACYP1A2
SCHEMBL30436033 0.87 HSD17B10 (0.41) KDM4EALDH1A1GAAKMT2ACYP1A2
Bromide SCHEMBL27831012 0.87 HSD17B10 (0.41) KDM4EALDH1A1GAAKMT2ACYP1A2
SCHEMBL3853000 0.85 PARP1 (0.36) KDM4EALDH1A1GAAKMT2ACYP1A2
SCHEMBL6897520 0.85 HSD17B10 (0.41) KDM4EALDH1A1GAAKMT2ACYP1A2
SCHEMBL4706742 0.85 KDM4E (0.41) KDM4EALDH1A1GAAKMT2AGLA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5725604-A Thermofixing of dyes in presence of polymerizable compound and an initiator CIBA SPECIALTY CHEMICALS CORPORATION (US) 1998-03-10 — — US claimed
EP-0719357-B1 THERMOFIXING OF DYES IN PRESENCE OF POLYMERIZABLE COMPOUND AND AN INITIATOR CIBA GEIGY AG (CH) 1998-01-14 — — EP claimed
EP-0719357-A1 THERMOFIXING OF DYES IN PRESENCE OF POLYMERIZABLE COMPOUND AND AN INITIATOR Ciba SC Holding AG (CH) 1996-07-03 — — EP claimed
WO-1995008018-A1 THERMOFIXING OF DYES IN PRESENCE OF POLYMERIZABLE COMPOUND AND AN INITIATOR CIBA-GEIGY AG (CH) 1995-03-23 — — WO claimed
EP-0126025-B1 PROCESS FOR DYEING SILK OR SILK-CONTAINING FIBROUS MATERIAL BLENDS CIBA-GEIGY AG (CH) 1987-10-07 — — EP claimed
JP-8053626-A — — None — — JP disclosed
US-8501046-B2 Use of rylene derivatives as photosensitizers in solar cells BASF SE (DE) 2013-08-06 — — US disclosed
EP-2589058-A1 PHOTOELECTRIC CONVERSION DEVICE COMPRISING HYDROXAMIC ACID DERIVATIVE OR SALT THEREOF AS ADDITIVE AND PROCESS FOR PRODUCING SAME BASF SE (DE) 2013-05-08 — — EP disclosed
US-20120283432-A1 USE OF RYLENE DERIVATIVES AS PHOTOSENSITIZERS IN SOLAR CELLS MAX-PLANCK-GESEL. ZUR FOERDERUNG DER WISSEN. E.V. (DE) 2012-11-08 — — US disclosed
US-8231809-B2 Solid p-semiconductors may also be used in the inventive dye-sensitized solar cells without increasing the cell resistance, since the rylene derivatives absorb strongly and therefore require only thin n-semiconductor layers BASF AKTIENGESELLSCHAFT (DE) 2012-07-31 — — US disclosed
WO-2012001628-A1 PHOTOELECTRIC CONVERSION DEVICE COMPRISING HYDROXAMIC ACID DERIVATIVE OR SALT THEREOF AS ADDITIVE AND PROCESS FOR PRODUCING SAME BASF SE (DE) 2012-01-05 — — WO disclosed
US-20120000533-A1 PHOTOELECTRIC CONVERSION DEVICE COMPRISING HYDROXAMIC ACID OR A SALT THEREOF AS ADDITIVE AND PROCESS FOR PRODUCING SAME BASF SE (DE) 2012-01-05 — — US disclosed
US-6813182-B2 Diode-and-fuse memory elements for a write-once memory comprising an anisotropic semiconductor sheet HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. 2004-11-02 — — US disclosed
US-20030223270-A1 Diode-and-fuse memory elements for a write-once memory comprising an anisotropic semiconductor sheet SAMSUNG ELECTRONICS CO., LTD. (KR) 2003-12-04 — — US disclosed
US-5725604-A Thermofixing of dyes in presence of polymerizable compound and an initiator CIBA SPECIALTY CHEMICALS CORPORATION (US) 1998-03-10 — — US disclosed
JP-H0853626-A METHOD FOR CONTINUOUS REACTION OF AMINO-CONTAINING ORGANIC DYE WITH TRIFLUOROTRIAZINE HOECHST AG 1996-02-27 — — JP disclosed
EP-0681006-A1 Process for continuously reacting organic dyestuffs containing amino groups with trifluorotriazine HOECHST AKTIENGESELLSCHAFT (DE) 1995-11-08 — — EP disclosed
EP-0511246-B1 WATER-SOLUBLE DYES WHICH REACT WITH FIBRES, PROCESS FOR PRODUCING THEM AND THEIR USE HOECHST AG (DE) 1994-09-07 — — EP disclosed
EP-0511246-A1 WATER-SOLUBLE DYES WHICH REACT WITH FIBRES, PROCESS FOR PRODUCING THEM AND THEIR USE. HOECHST AG (DE) 1992-11-04 — — EP disclosed
WO-1991010709-A1 WATER-SOLUBLE DYES WHICH REACT WITH FIBRES, PROCESS FOR PRODUCING THEM AND THEIR USE HOECHST AKTIENGESELLSCHAFT (DE) 1991-07-25 — — WO 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 (1 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-20120283432-A1 USE OF RYLENE DERIVATIVES AS PHOTOSENSITIZERS IN SOLAR CELLS NR2E3, NR2E1, NR1D2 KDM4E 1373/4885ALDH1A1 4248/4885GAA 4790/4885

“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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