SCHEMBL970943

SCHEMBL970943

O=C1C(Nc2ccccc2)=CC(=O)c2ncccc21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 1.00
SMN1; SMN2 Q16637 4/20 1.00
ALDH1A1 P00352 3/20 1.00
MEN1 O00255 2/20 1.00
KMT2A Q03164 2/20 1.00
TDP1 Q9NUW8 2/20 1.00
GUCY1B2 O75343 1/20 1.00
GUCY1A2 P33402 1/20 1.00
GUCY1A1 Q02108 1/20 1.00
GUCY1B1 Q02153 1/20 1.00
RAB9A P51151 3/20 0.64
LMNA P02545 3/20 0.64
HTT P42858 3/20 0.64
L3MBTL1 Q9Y468 3/20 0.64
MAPK1 P28482 3/20 0.64
NPC1 O15118 2/20 0.64
NFKB1 P19838 1/20 0.64
NFKB2 Q00653 1/20 0.64
RELA Q04206 1/20 0.64
NQO1 P15559 2/20 0.62

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
SCHEMBL29401747 1.00 MAPT (1.00) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL8651660 0.88 MAPT (0.78) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL31238099 0.88 MEN1 (0.78) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL13940470 0.87 MAPT (0.77) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL8656092 0.87 MAPT (0.77) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL10506584 0.84 MAPT (0.71) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL10506975 0.84 ALDH1A1 (0.71) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL10504983 0.84 MAPT (0.71) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL8368653 0.83 MAPT (0.70) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL8656023 0.81 MAPT (0.68) MAPTSMN1; SMN2ALDH1A1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2016040650-A1 SOLUBLE GUANYLYL CYCLASE INHIBITION EFFECTS ON LYMPHATIC VASCULATURE UNIVERSITY OF ROCHESTER (US) 2016-03-17 WO claimed
US-8026217-B2 Compositions and methods for treating neural anoxia and spreading depression FLORIDA ATLANTIC UNIVERSITY (US) 2011-09-27 US claimed
US-7858579-B2 Thermoprotective compositions of pkg pathway inhibitors and method of use thereof DAWSON-SCULLY KENNETH 2010-12-28 US claimed
US-20090124558-A1 COMPOSITIONS AND METHODS FOR TREATING NEURAL ANOXIA AND SPREADING DEPRESSION FLORIDA ATLANTIC UNIVERSITY (US) 2009-05-14 US claimed
WO-2009046322-A2 COMPOSITIONS AND METHODS FOR TREATING NEURAL ANOXIA AND SPREADING DEPRESSION FLORIDA ATLANTIC UNIVERSITY (US) 2009-04-09 WO claimed
WO-2008076370-A9 P21 COMPOSITIONS AND METHODS FOR THE TREATMENT OF HIV GEN HOSPITAL CORP (US) 2008-08-21 WO claimed
WO-2008076370-A2 P21 COMPOSITIONS AND METHODS FOR THE TREATMENT OF HIV THE GENERAL HOSPITAL CORPORATION (US) 2008-06-26 WO claimed
US-20070184044-A1 Thermoprotective compositions of PKG pathway inhibitors and method of use thereof DAWSON-SCULLY KENNETH 2007-08-09 US claimed
US-20060194769-A1 Small molecules that reduce fungal growth UNIVERSITY OF VERMONT AND STATE AGRICULTURAL COLLEGE (US) 2006-08-31 US claimed
WO-2006081327-A2 SMALL MOLECULES THAT REDUCE FUNGAL GROWTH UNIVERSITY OF VERMONT AND STATE AGRICULTURAL COLLEGE (US) 2006-08-03 WO claimed
WO-2004098601-A1 AS A PKC INHIBITOR, INHIBITOR FOR ANGIOGENESIS CONTAINING 6-ANILINOQUINOLINE-5,8-QUINONE AS AN EFFECTIVE INGREDIENT CHEMON INC. (KR) 2004-11-18 WO claimed
EP-1451211-A2 COMPOSITIONS AND METHODS FOR MODULATING GUANYLYL CYCLASE SIGNALING RECEPTOR (GC-C) ACTIVITY AND FOR TREATING MENIERE'S DISEASE University of Copenhagen (DK) 2004-09-01 EP claimed
US-20040152868-A1 Compositions and methods for modulating guanylyl cyclase signaling receptor (gc-c) activity and for treating meniere's disease UNIVERSITY OF COPENHAGEN (DK) 2004-08-05 US claimed
EP-1398031-A1 Use of 6-amino-quinoline-5,8-quinones and nucleic acids associated with senescence for the treatment of tumors Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2004-03-17 EP claimed
WO-2002079235-A2 COMPOSITIONS AND METHODS FOR MODULATING GUANYLYL CYCLASE SIGNALING RECEPTOR (GC-C) ACTIVITY AND FOR TREATING MENIERE'S DISEASE UNIVERSITY OF COPENHAGEN (US) 2002-10-10 WO claimed
WO-2000030630-A1 COMBINATION PRODUCTS OF A GUANYLATE CYCLASE INHIBITOR AND A LOCAL ANESTHETIC FOR PAIN RELIEF LINDEN BIOTECHNOLOGY, INC. (US) 2000-06-02 WO claimed
EP-0866692-A1 USE OF BICYCLIC MONO- OR DIKETONE DERIVATIVES, RESULTING COMPOUNDS, AND USE THEREOF AS A DRUG FOR TREATING INFLAMMATION, MIGRAINE AND SHOCK LABORATOIRE INNOTHERA Société Anonyme (FR) 1998-09-30 EP claimed
WO-1997021432-A1 USE OF BICYCLIC MONO- OR DIKETONE DERIVATIVES, RESULTING COMPOUNDS, AND USE THEREOF AS A DRUG FOR TREATING INFLAMMATION, MIGRAINE AND SHOCK LABORATOIRE INNOTHERA, S.A. (FR) 1997-06-19 WO claimed
US-5298506-A Use of guanylate cyclase inhibitors in the treatment of shock BRIGHAM AND WOMEN'S HOSPITAL (US) 1994-03-29 US claimed
US-4492704-A ANTHISTAMINES ELI LILLY AND COMPANY (US) 1985-01-08 US claimed

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-20060194769-A1 Small molecules that reduce fungal growth ERG28, DPM1, CYP51A1 MAPT 1481/4885SMN1; SMN2 4868/4885ALDH1A1 2931/4885
US-20040152868-A1 Compositions and methods for modulating guanylyl cyclase signaling receptor (gc-c) activity and for treating meniere's disease PDE7A, PDE6C, PDE9A MAPT 4187/4885SMN1; SMN2 2367/4885ALDH1A1 4193/4885

“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.