SCHEMBL515359

SCHEMBL515359

C1CCN2CCCCN2C1

nearest known ligand 0.39

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
MGLL Q99685 1/20 0.33
CTSL P07711 1/20 0.31
CTSB P07858 1/20 0.31
CTSS P25774 1/20 0.31
CTSK P43235 1/20 0.31

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
SCHEMBL78337 1.00 MGLL (0.33) MGLLCTSLCTSBCTSSCTSK
SCHEMBL14084740 0.94 MGLL (0.40) MGLL
SCHEMBL2457046 0.94 MGLL (0.40) MGLL
Hydrochloric Acid SCHEMBL17260829 0.94 MGLL (0.31) MGLL
SCHEMBL3658220 0.94 MGLL (0.40) MGLL
SCHEMBL726729 0.94 MGLL (0.40) MGLL
SCHEMBL6926105 0.94 MGLL (0.40) MGLL
SCHEMBL513824 0.94
Bromide SCHEMBL15740961 0.94 MGLL (0.31) MGLL
SCHEMBL42220 0.94 MGLL (0.40) MGLL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025065089-A1 METHOD OF SYNTHESIZING A 1,6-DIAZABICYCLO[4.4.4]TETRADECAN-1,6-IUM CATIONIC STRUCTURE, USE OF SAID CATIONIC STRUCTURE IN ELECTROCHEMICAL APPLICATIONS, AND POLYMERS COMPRISING SAID CATIONIC STRUCTURE SIMON FRASER UNIVERSITY (CA) 2025-04-03 WO claimed
WO-2025065089-A1 METHOD OF SYNTHESIZING A 1,6-DIAZABICYCLO[4.4.4]TETRADECAN-1,6-IUM CATIONIC STRUCTURE, USE OF SAID CATIONIC STRUCTURE IN ELECTROCHEMICAL APPLICATIONS, AND POLYMERS COMPRISING SAID CATIONIC STRUCTURE SIMON FRASER UNIVERSITY (CA) 2025-04-03 WO disclosed
US-9849196-B2 Methods and compositions for altering photophysical properties of fluorophores via proximal quenching CORNELL UNIVERSITY (US) 2017-12-26 US disclosed
US-9631096-B2 Dye compositions, methods of preparation, conjugates thereof, and methods of use CORNELL UNIVERSITY (US) 2017-04-25 US disclosed
US-20150328340-A1 METHODS AND COMPOSITIONS FOR ALTERING PHOTOPHYSICAL PROPERTIES OF FLUOROPHORES VIA PROXIMAL QUENCHING CORNELL UNIVERSITY (US) 2015-11-19 US disclosed
US-8945515-B2 Methods and compositions for altering photophysical properties of fluorophores via proximal quenching CORNELL UNIVERSITY (US) 2015-02-03 US disclosed
US-20150011731-A1 DYE COMPOSITIONS, METHODS OF PREPARATION, CONJUGATES THEREOF, AND METHODS OF USE CORNELL UNIVERSITY (US) 2015-01-08 US disclosed
WO-2013109859-A1 DYE COMPOSITIONS, METHODS OF PREPARATION, CONJUGATES THEREOF, AND METHODS OF USE CORNELL UNIVERSITY (US) 2013-07-25 WO disclosed
EP-1865030-B1 DYE-CONTAINING HARDENABLE COMPOSITION, AND COLOR FILTER AND PROCESS FOR PRODUCING THE SAME FUJIFILM CORP (JP) 2013-06-26 EP disclosed
US-8124304-B2 Dye-containing curable composition, color filter and method for producing the same FUJIFILM CORPORATION (JP) 2012-02-28 US disclosed
US-7193068-B2 Pyridone azo compound, tautomer thereof, and colorant-containing curable composition, color filter and manufacturing method thereof FUJI PHOTO FILM CO., LTD. (JP) 2007-03-20 US disclosed
US-20070049650-A1 Colorant-containing curable composition, color filter and manufacturing method thereof FUJI PHOTO FILM CO., LTD. 2007-03-01 US disclosed
US-20070049650-A1 Colorant-containing curable composition, color filter and manufacturing method thereof FUJI PHOTO FILM CO., LTD. 2007-03-01 US disclosed
US-7169516-B2 Dye-containing curable composition, color filter and method of manufacturing the same FUJI PHOTO FILM CO., LTD. (JP) 2007-01-30 US disclosed
US-7169516-B2 Dye-containing curable composition, color filter and method of manufacturing the same FUJI PHOTO FILM CO., LTD. (JP) 2007-01-30 US disclosed
EP-1739134-A1 AZO COMPOUND Fuji Photo Film Co., Ltd. (JP) 2007-01-03 EP disclosed
EP-0850930-B1 A process for producing alicyclic hydrazine derivatives. JAPAN HYDRAZINE CO LTD (JP) 2001-10-31 EP disclosed
US-6194577-B1 OXIDIZING 1-AMINOPYRROLIDINE IN PRESENCE OF INORGANIC BASE WITH AIR, OXYGEN OR AQUEOUS HYDROGEN PEROXIDE AS AN OXIDIZING AGENT TO FORM TETRAHYDROPYRIDAZINE JAPAN HYDRAZINE CO., LTD. (JP) 2001-02-27 US disclosed
US-5977360-A Process for producing cyclic hydrazine derivatives, tetra-hydropyridazine and hexahydropyridazine JAPAN HYDRAZINE CO., LTD. (JP) 1999-11-02 US disclosed
EP-0850930-A2 A process for producing alicyclic hydrazine derivatives, tetra-hydropyridazine and hexahydropyridazine JAPAN HYDRAZINE CO., LTD. (JP) 1998-07-01 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-20150328340-A1 METHODS AND COMPOSITIONS FOR ALTERING PHOTOPHYSICAL PROPERTIES OF FLUOROPHORES VIA PROXIMAL QUENCHING APEX1, ARFGEF1, PRDX3 MGLL 3616/4885CTSL 2959/4885CTSB 577/4885

“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.