SCHEMBL75493

SCHEMBL75493

c1ccc(N(c2ccccc2)c2ccc(-c3ccc(N(c4ccc(N(c5ccccc5)c5ccccc5)cc4)c4ccc(N(c5ccccc5)c5ccccc5)cc4)cc3)cc2)cc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 6/20 0.62
▸ TDP1 Q9NUW8 3/20 0.62
▸ L3MBTL1 Q9Y468 2/20 0.62
▸ CYP1A2 P05177 2/20 0.62
▸ CYP3A4 P08684 2/20 0.62
▸ KDM4E B2RXH2 1/20 0.62
▸ CYP2D6 P10635 1/20 0.62
▸ MAPT P10636 1/20 0.62
▸ CYP2C9 P11712 1/20 0.62
▸ CYP2C19 P33261 1/20 0.62
▸ MEN1 O00255 2/20 0.50
▸ KMT2A Q03164 2/20 0.50
▸ CRHBP P24387 1/20 0.50
▸ ATM Q13315 1/20 0.50
▸ CRHR2 Q13324 1/20 0.50
▸ TLR9 Q9NR96 1/20 0.50
▸ APP P05067 2/20 0.46
▸ PKM P14618 1/20 0.44
▸ CA1 P00915 1/20 0.42
▸ CA2 P00918 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
SCHEMBL6013505 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
SCHEMBL101594 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
SCHEMBL13020777 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
SCHEMBL8644338 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
SCHEMBL12593200 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
SCHEMBL2070021 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
SCHEMBL879258 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
SCHEMBL12780851 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
Benzene SCHEMBL14537408 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4
SCHEMBL14018359 1.00 ALDH1A1 (0.62) ALDH1A1TDP1L3MBTL1CYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1182183-B1 ANTHRACENE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICES MADE BY USING THE SAME IDEMITSU KOSAN CO (JP) 2009-12-09 — — EP claimed
EP-4396259-A1 COMPOSITION Merck Patent GmbH (DE) 2024-07-10 — — EP disclosed
WO-2024126635-A1 FORMULATION OF AN ORGANIC FUNCTIONAL MATERIAL MERCK PATENT GMBH (DE) 2024-06-20 — — WO disclosed
WO-2023237458-A1 METHOD OF PRINTING A FUNCTIONAL LAYER OF AN ELECTRONIC DEVICE BY COMBINING INKS MERCK PATENT GMBH (DE) 2023-12-14 — — WO disclosed
EP-3475372-B1 FORMULATION OF AN ORGANIC FUNCTIONAL MATERIAL MERCK PATENT GMBH (DE) 2023-11-22 — — EP disclosed
EP-3387077-B1 FORMULATIONS CONTAINING KETONES COMPRISING NON-AROMATIC CYCLES MERCK PATENT GMBH (DE) 2023-10-18 — — EP disclosed
US-11770971-B2 Esters containing aromatic groups as solvents for organic electronic formulations MERCK PATENT GMBH (DE) 2023-09-26 — — US disclosed
EP-3807367-B1 FORMULATION OF AN ORGANIC FUNCTIONAL MATERIAL MERCK PATENT GMBH (DE) 2023-07-19 — — EP disclosed
EP-3552252-B1 PREPARATION PROCESS FOR AN ELECTRONIC DEVICE MERCK PATENT GMBH (DE) 2023-05-17 — — EP disclosed
EP-3360175-B1 FORMULATIONS COMPRISING AT LEAST TWO ORGANIC SEMICONDUCTING COMPOUNDS AND AT LEAST TWO SOLVENTS MERCK PATENT GMBH (DE) 2023-05-17 — — EP disclosed
US-20040100188-A1 Anthracene derivative and organic electroluminescence device using the derivative IDEMITSU KOSAN CO., LTD. (JP) 2004-05-27 — — US disclosed
US-6660410-B2 Organic luminescence layer having a carbazole derivative with a glass-transition temperature of 110 degrees C. or higher, and a phosphorescent dopant; possible triplet exciton state at room temperature IDEMITSU KOSAN CO., LTD. (JP) 2003-12-09 — — US disclosed
US-20020168544-A1 Organic electroluminescence device emitting white light IDEMITSU KOSAN CO., LTD. (JP) 2002-11-14 — — US disclosed
EP-1205527-A1 ORGANIC ELECTROLUMINESCENCE DEVICE IDEMITSU KOSAN CO., LTD. (JP) 2002-05-15 — — EP disclosed
US-20020048687-A1 Anthracene derivative and organic electroluminescence device using the derivative IDEMITSU KOSAN CO., LTD. (JP) 2002-04-25 — — US disclosed
US-20020045061-A1 Organic luminescence layer having a carbazole derivative with a glass-transition temperature of 110 degrees C. or higher, and a phosphorescent dopant; possible triplet exciton state at room temperature IDEMITSU KOSAN CO., LTD. 2002-04-18 — — US disclosed
EP-1182244-A1 WHITE ORGANIC ELECTROLUMINESCENCE ELEMENT IDEMITSU KOSAN CO., LTD. (JP) 2002-02-27 — — EP disclosed
EP-1182183-A1 ANTHRACENE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICES MADE BY USING THE SAME IDEMITSU KOSAN CO., LTD. (JP) 2002-02-27 — — EP disclosed
EP-0420092-A1 Process for the preparation of 1-hydroxy-imidazole BASF Aktiengesellschaft (DE) 1991-04-03 — — EP disclosed
EP-0420092-A1 Process for the preparation of 1-hydroxy-imidazole BASF Aktiengesellschaft (DE) 1991-04-03 — — EP 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-20040100188-A1 Anthracene derivative and organic electroluminescence device using the derivative ACIN1, KCNQ1, LBR ALDH1A1 200/4885TDP1 1727/4885L3MBTL1 323/4885

“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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