SCHEMBL4070380

SCHEMBL4070380

CONc1ccccc1C(=O)O

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CDC25B P30305 1/20 0.53
▸ CHEK1 O14757 1/20 0.53
▸ PIM1 P11309 1/20 0.53
▸ MAPK8 P45983 1/20 0.53
▸ CLK4 Q9HAZ1 1/20 0.53
▸ FABP4 P15090 3/20 0.52
▸ KMT2A Q03164 4/20 0.51
▸ KDM4E B2RXH2 4/20 0.51
▸ RECQL P46063 2/20 0.51
▸ APAF1 O14727 1/20 0.51
▸ CASP6 P55212 1/20 0.51
▸ CACNA1B Q00975 1/20 0.51
▸ APBA1 Q02410 1/20 0.51
▸ MCL1 Q07820 1/20 0.51
▸ CASP8 Q14790 1/20 0.51
▸ ALDH1A1 P00352 3/20 0.50
▸ MEN1 O00255 2/20 0.50
▸ FABP3 P05413 2/20 0.50
▸ FABP5 Q01469 2/20 0.50
▸ ALOX15 P16050 2/20 0.50

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
SCHEMBL28142654 0.83 HPGD (0.54) MAPK8KDM4EALDH1A1HPGDHSD17B10
SCHEMBL5925582 0.81 KDM4E (0.50) CDC25BCHEK1PIM1MAPK8CLK4
SCHEMBL7523030 0.79 HCAR2 (0.49) CDC25BCHEK1PIM1MAPK8CLK4
SCHEMBL7517565 0.79 KDM4E (0.58) MAPK8FABP4KMT2AKDM4EALDH1A1
SCHEMBL7519507 0.79 FABP4 (0.47) CDC25BCHEK1PIM1MAPK8CLK4
SCHEMBL3629659 0.78 KMT2A (0.57) CHEK1PIM1MAPK8CLK4KMT2A
SCHEMBL11433582 0.78 KMT2A (0.44) KMT2AKDM4EALDH1A1MEN1ALOX15
SCHEMBL7034926 0.77 MAPT (0.74) CDC25BFABP4KMT2AKDM4ERECQL
N-Methylanthranilic Acid SCHEMBL130356 0.77 KDM4E (0.64) FABP4KMT2AKDM4EALDH1A1MEN1
N-Methylanthranilic Acid SCHEMBL29381752 0.77 KDM4E (0.64) FABP4KMT2AKDM4EALDH1A1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024090362-A1 CHARGE-TRANSPORTING COMPOSITION 日産化学株式会社 2024-05-02 — — WO disclosed
EP-2634204-B1 CONDUCTIVE ANILINE POLYMER, METHOD FOR PRODUCING SAME, AND METHOD FOR PRODUCING CONDUCTIVE FILM MITSUBISHI CHEM CORP (JP) 2021-03-31 — — EP disclosed
US-9799420-B2 Conductive aniline polymer, method for producing same, and method for producing conductive film MITSUBISHI CHEMICAL CORPORATION (JP) 2017-10-24 — — US disclosed
US-9679673-B2 Conductive composition, conductor and solid electrolytic capacitor using conductive composition MITSUBISHI RAYON CO., LTD. (JP) 2017-06-13 — — US disclosed
US-20160078978-A1 CONDUCTIVE COMPOSITION, CONDUCTOR AND SOLID ELECTROLYTIC CAPACITOR USING CONDUCTIVE COMPOSITION MITSUBISHI RAYON CO., LTD. (JP) 2016-03-17 — — US disclosed
US-20150179295-A1 CONDUCTIVE ANILINE POLYMER, METHOD FOR PRODUCING SAME, AND METHOD FOR PRODUCING CONDUCTIVE FILM MITSUBISHI RAYON CO., LTD. (JP) 2015-06-25 — — US disclosed
EP-2700676-A1 CONDUCTIVE COMPOSITION, CONDUCTOR USING CONDUCTIVE COMPOSITION, AND SOLID ELECTROLYTIC CAPACITOR Mitsubishi Rayon Co., Ltd. (JP) 2014-02-26 — — EP disclosed
US-20140043731-A1 CONDUCTIVE COMPOSITION, CONDUCTOR AND SOLID ELECTROLYTIC CAPACITOR USING CONDUCTIVE COMPOSITION MITSUBISHI RAYON CO., LTD. (JP) 2014-02-13 — — US disclosed
EP-2634204-A1 CONDUCTIVE ANILINE POLYMER, METHOD FOR PRODUCING SAME, AND METHOD FOR PRODUCING CONDUCTIVE FILM Mitsubishi Rayon Co., Ltd. (JP) 2013-09-04 — — EP disclosed
US-20130209667-A1 CONDUCTIVE ANILINE POLYMER, METHOD FOR PRODUCING SAME, AND METHOD FOR PRODUCING CONDUCTIVE FILM MITSUBISHI RAYON CO., LTD. (JP) 2013-08-15 — — US disclosed
US-20080119470-A1 Neurologically-Active Compounds XOMA TECHNOLOGY LTD. 2008-05-22 — — US disclosed
EP-1737831-A1 NEUROLOGICALLY-ACTIVE COMPOUNDS Prana Biotechnology Limited (AU) 2007-01-03 — — EP disclosed
WO-2005095360-A1 NEUROLOGICALLY-ACTIVE COMPOUNDS PRANA BIOTECHNOLOGY LIMITED (AU) 2005-10-13 — — WO disclosed
EP-0834885-B1 Method for producing soluble conductive polymers having acidic groups MITSUBISHI RAYON CO (JP) 2002-01-02 — — EP disclosed
US-5980784-A SUBJECTING TO ELECTROLYTIC POLYMERIZATION AT LEAST ONE COMPOUND SELECTED FROM THE GROUP CONSISTING OF ACIDIC GROUP SUBSTITUTED ANILINES, PYRROLES, THIOPHENES, FURANS, SELENOPHENES, TELLUROPHENES, ISOTHIANAPHTHENES, IN BASE MITSUBISHI RAYON CO., LTD. (JP) 1999-11-09 — — US disclosed
EP-0834885-A2 Method for producing soluble conductive polymer having acidic groups NITTO CHEMICAL INDUSTRY CO., LTD. (JP) 1998-04-08 — — EP disclosed
EP-0190915-B1 Process for the preparation of 2-alkoxy-N-(1-azabicyclo[2.2.2]octan-3-yl) aminobenzamides SYNTHELABO (FR) 1992-10-28 — — EP disclosed
US-4870181-A AMIDATION OF 3-AMINOQUINUCLIDINE SALT A. H. ROBINS COMPANY, INCORPORATED (US) 1989-09-26 — — US disclosed
CN-1033380-A Compound SMITHKLINE BECKMAN INTERCREDIT (NL) 1989-06-14 — — CN disclosed
EP-0190915-A2 Process for the preparation of 2-alkoxy-N-(1-azabicyclo[2.2.2]octan-3-yl) aminobenzamides SYNTHELABO (FR) 1986-08-13 — — 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-20080119470-A1 Neurologically-Active Compounds ACHE, PSEN1, PSEN2 CDC25B 4382/4885CHEK1 2066/4885PIM1 3819/4885

“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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