SCHEMBL1771966

SCHEMBL1771966

N#Cc1cccc(-c2cccc(-c3cccc(C#N)n3)n2)n1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTSS P25774 3/20 0.53
IDH1 O75874 1/20 0.44
SOS2 Q07890 1/20 0.44
NPY5R Q15761 1/20 0.43
CTSK P43235 2/20 0.42
CCR1 P32246 2/20 0.41
CCR8 P51685 2/20 0.41
KDM4E B2RXH2 1/20 0.41
LMNA P02545 1/20 0.41
TP53 P04637 1/20 0.41
ALPL P05186 1/20 0.41
HSP90AA1 P07900 1/20 0.41
ALPI P09923 1/20 0.41
ALPG P10696 1/20 0.41
ALOX15 P16050 1/20 0.41
MAPK1 P28482 1/20 0.41
HTT P42858 1/20 0.41
CCR5 P51681 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
TDP1 Q9NUW8 1/20 0.41

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
SCHEMBL9220648 0.97 CTSS (0.55) CTSSIDH1SOS2NPY5RCTSK
SCHEMBL29988787 0.97 CTSS (0.55) CTSSIDH1SOS2NPY5RCTSK
SCHEMBL8406858 0.86 IDH1 (0.53) CTSSIDH1SOS2NPY5RCTSK
SCHEMBL19194999 0.85 CTSS (0.50) CTSSIDH1SOS2NPY5RCTSK
SCHEMBL995983 0.84 SOS2 (0.50) CTSSIDH1SOS2NPY5RCTSK
SCHEMBL994386 0.83 KDM4E (0.63) CTSSCCR1CCR8KDM4ELMNA
SCHEMBL317148 0.82 KMT2A (0.60) CTSSCTSKKDM4ELMNAMAPK1
SCHEMBL14007665 0.82 CTSS (0.51) CTSSCTSKKDM4ELMNASMN1; SMN2
SCHEMBL18423239 0.80 CTSS (0.43) CTSSIDH1SOS2NPY5RCTSK
SCHEMBL12598663 0.79 CTSS (0.46) CTSSCTSKKDM4ELMNATP53

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-2025084975-A1 A BI-PHASIC ELECTROLYSIS CELL FOR CARBON DIOXIDE CAPTURE, ELECTROCATALYSTS FOR USE IN THE CELL, RELATED METHODS AND A PRODUCTION FACILITY USING THE ELECTROLYSIS CELL AND THE ELECTROCATALYSTS CarbGen AB (SE) 2025-04-24 WO disclosed
EP-2188620-B1 COMPOUNDS USEFUL AS LIGANDS AND PARTICULARLY AS ORGANIC CHROMOPHORES FOR COMPLEXING LANTHANIDES AND APPLICATIONS THEREOF COMMISSARIAT L ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2017-08-23 EP disclosed
EP-2188620-B1 COMPOUNDS USEFUL AS LIGANDS AND PARTICULARLY AS ORGANIC CHROMOPHORES FOR COMPLEXING LANTHANIDES AND APPLICATIONS THEREOF COMMISSARIAT L ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2017-08-23 EP disclosed
US-9040689-B2 Compounds useful as ligands and particularly as organic chromophores for complexing lanthanides and applications thereof COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 2015-05-26 US disclosed
US-9040689-B2 Compounds useful as ligands and particularly as organic chromophores for complexing lanthanides and applications thereof COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 2015-05-26 US disclosed
US-9040689-B2 Compounds useful as ligands and particularly as organic chromophores for complexing lanthanides and applications thereof COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 2015-05-26 US disclosed
US-8709129-B2 Compounds useful as ligands of actinides, their synthesis and their uses COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2014-04-29 US disclosed
EP-2456766-B1 COMPOUNDS SUITABLE FOR USE AS ACTINIDE LIGANDS, SYNTHESIS AND USES THEREOF COMMISSARIAT ENERGIE ATOMIQUE (FR) 2013-11-06 EP disclosed
EP-2456766-B1 COMPOUNDS SUITABLE FOR USE AS ACTINIDE LIGANDS, SYNTHESIS AND USES THEREOF COMMISSARIAT ENERGIE ATOMIQUE (FR) 2013-11-06 EP disclosed
US-20120186396-A1 COMPOUNDS USEFUL AS LIGANDS OF ACTINIDES, THEIR SYNTHESIS AND THEIR USES UNIVERSITE DE NANTES (FR) 2012-07-26 US disclosed
EP-2188620-A1 COMPOUNDS USEFUL AS LIGANDS AND PARTICULARLY AS ORGANIC CHROMOPHORES FOR COMPLEXING LANTHANIDES AND APPLICATIONS THEREOF Commissariat à l'énergie atomique et aux énergies alternatives (FR) 2010-05-26 EP disclosed
WO-2009037277-A1 COMPOUNDS USEFUL AS LIGANDS AND PARTICULARLY AS ORGANIC CHROMOPHORES FOR COMPLEXING LANTHANIDES AND APPLICATIONS THEREOF COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 2009-03-26 WO disclosed
WO-2009037277-A1 COMPOUNDS USEFUL AS LIGANDS AND PARTICULARLY AS ORGANIC CHROMOPHORES FOR COMPLEXING LANTHANIDES AND APPLICATIONS THEREOF COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 2009-03-26 WO disclosed
EP-0403593-B1 TERPYRIDINE DERIVATIVES WALLAC OY (FI) 1997-03-19 EP disclosed
US-5539117-A 2-acetyl-6-cyanopyridines and their use as intermediates in the synthesis of oligo-2,6-pyridines GE HEALTHCARE AS (NO) 1996-07-23 US disclosed
US-5457186-A Immunoassay WALLAC OY (FI) 1995-10-10 US disclosed
EP-0649020-A1 Luminescent lanthanide chelates with decreased non-radiative energy loss WALLAC OY (FI) 1995-04-19 EP disclosed
US-5350696-A 2-acetyl-6-cyanopyridines and their use as intermediates in the synthesis of oligo-2,6-pyridines STERLING WINTHROP, INC. (US) 1994-09-27 US disclosed
US-5324825-A Terpyridine derivatives WALLAC OY (FI) 1994-06-28 US disclosed
US-5202423-A Terpyridine derivatives WALLAC OY 1993-04-13 US 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-20120186396-A1 COMPOUNDS USEFUL AS LIGANDS OF ACTINIDES, THEIR SYNTHESIS AND THEIR USES AHR, ARNT, HRH3 CTSS 1760/4885IDH1 1367/4885SOS2 3164/4885

“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.