SCHEMBL3457693

SCHEMBL3457693

CC[n+]1c(C)n(C)c2ccccc21

nearest known ligand 0.49

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 11/20 0.49
APOBEC3A P31941 3/20 0.44
APOBEC3G Q9HC16 3/20 0.44
PTPN1 P18031 1/20 0.40
SMN1; SMN2 Q16637 4/20 0.36
PABPC1 P11940 1/20 0.36
ERAP1 Q9NZ08 1/20 0.36
GPR3 P46089 1/20 0.35
ALDH1A1 P00352 3/20 0.35
HTT P42858 2/20 0.35
CTDSP1 Q9GZU7 1/20 0.35
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35
MAPT P10636 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
LMNA P02545 1/20 0.34
RAB9A P51151 1/20 0.34
TP53 P04637 1/20 0.33

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
SCHEMBL15156667 0.85 MEN1 (0.44) KDM4EAPOBEC3AAPOBEC3GPTPN1SMN1; SMN2
SCHEMBL15157507 0.82 PTPN1 (0.56) KDM4EAPOBEC3AAPOBEC3GPTPN1SMN1; SMN2
Iodide SCHEMBL5143882 0.81 PTPN1 (0.58) KDM4EAPOBEC3AAPOBEC3GPTPN1SMN1; SMN2
Iodide SCHEMBL22390070 0.80 PTPN1 (0.47) KDM4EAPOBEC3AAPOBEC3GPTPN1SMN1; SMN2
SCHEMBL3834206 0.79 APOBEC3A (0.40) KDM4EAPOBEC3AAPOBEC3GPTPN1ERAP1
SCHEMBL13822580 0.79 APOBEC3A (0.40) KDM4EAPOBEC3AAPOBEC3GPTPN1SMN1; SMN2
SCHEMBL10325415 0.78 APOBEC3A (0.43) KDM4EAPOBEC3AAPOBEC3GPTPN1SMN1; SMN2
SCHEMBL18807748 0.75 ERAP1 (0.36) KDM4EPTPN1ERAP1GPR3ALDH1A1
Bromide SCHEMBL11582745 0.75 MAPT (0.44) KDM4EAPOBEC3AAPOBEC3GSMN1; SMN2PABPC1
Fluoride Ion SCHEMBL18784476 0.74 ERAP1 (0.35) KDM4EPTPN1ERAP1GPR3ALDH1A1

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2809739-B1 IONIC LIQUIDS FOR COOLING IN HIGH TEMPERATURE ENVIRONMENT PROIONIC GMBH (AT) 2020-12-09 EP disclosed
US-10677532-B2 Ionic liquids for cooling in high temperature environment PROIONIC GMBH (AT) 2020-06-09 US disclosed
EP-2698802-B1 Electrolytic capacitor PANASONIC IP MAN CO LTD (JP) 2018-05-16 EP disclosed
EP-1808875-B1 ELECTROLYTE FOR ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR UTILIZING THE SAME PANASONIC IP MAN CO LTD (JP) 2017-11-08 EP disclosed
US-20160138876-A1 IONIC LIQUIDS FOR COOLING IN HIGH TEMPERATURE ENVIRONMENT PROIONIC GMBH (AT) 2016-05-19 US disclosed
US-20150007963-A1 IONIC LIQUIDS FOR COOLING IN HIGH TEMPERATURE ENVIRONMENT VTU HOLDING GMBH (AT) 2015-01-08 US disclosed
EP-2809739-A1 IONIC LIQUIDS FOR COOLING IN HIGH TEMPERATURE ENVIRONMENT VTU Holding GmbH (AT) 2014-12-10 EP disclosed
EP-2698802-A1 Electrolytic capacitor comprising a separtor comprising a conductive polymer containing a p-dopant on its surface Panasonic Corporation (JP) 2014-02-19 EP disclosed
WO-2013113461-A1 IONIC LIQUIDS FOR COOLING IN HIGH TEMPERATURE ENVIRONMENT VTU HOLDING GMBH (AT) 2013-08-08 WO disclosed
US-7859828-B2 supresses increase in the ESR (equivalent series resistance) with the elapse of time in an electrolytic capacitor is suppressed PANASONIC CORPORATION (JP) 2010-12-28 US disclosed
US-20100321863-A1 ACTIVATED CARBON AND PROCESS FOR PRODUCING THE SAME SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-12-23 US disclosed
US-7785495-B2 Activated carbon prepared by carbonizing and activating a calixarene containing dihydroxybenzene rings; especially calcining at 400 degrees C. or less in the presence of an oxidative gas, calcining at 1500 degrees or less in an inactive gas, and then further calcining at 200-1500 degrees in H2O or CO2 SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-08-31 US disclosed
EP-2093191-A1 ACTIVATED CARBON AND METHOD FOR PRODUCING THE SAME Sumitomo Chemical Company, Limited (JP) 2009-08-26 EP disclosed
US-20090103241-A1 Activated carbon prepared by carbonizing and activating a calixarene containing dihydroxybenzene rings; especially calcining at 400 degrees C. or less in the presence of an oxidative gas, calcining at 1500 degrees or less in an inactive gas, and then further calcining at 200-1500 degrees in H2O or CO2 SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-04-23 US disclosed
US-20080316679-A1 Electrolytic Solution for Electrolytic Capacitor, and Electrolytic Capacitor Using the Same PANASONIC CORPORATION (JP) 2008-12-25 US disclosed
EP-1905740-A1 ELECTRIC DOUBLE LAYER CAPACITOR Sumitomo Chemical Company, Limited (JP) 2008-04-02 EP disclosed
EP-1808875-A1 ELECTROLYTE FOR ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR UTILIZING THE SAME MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 2007-07-18 EP disclosed
US-5198573-A Reaction of carbon monoxide with dialkoxy-3-butene in the presence of palladium catalysts RHONE-POULENC CHIMIE (FR) 1993-03-30 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-20090103241-A1 Activated carbon prepared by carbonizing and activating a calixarene containing dihydroxybenzene rings; especially calcining at 400 degrees C. or less in the presence of an oxidative gas, calcining at 1500 degrees or less in an inactive gas, and then further calcining at 200-1500 degrees in H2O or CO2 CBR1, CYP24A1, CALU KDM4E 2457/4885APOBEC3A 3809/4885APOBEC3G 4252/4885

“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.