SCHEMBL6718903

SCHEMBL6718903

CCC(C)OCCCCCO

nearest known ligand 0.47

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.40
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
ALDH1A1 P00352 2/20 0.40
HSD17B10 Q99714 1/20 0.40
TSHR P16473 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.36
THRB P10828 1/20 0.35
HTT P42858 1/20 0.35
MAPT P10636 1/20 0.35
ACHE P22303 6/20 0.35
DNM1 Q05193 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
SCHEMBL6720544 1.00 LMNA (0.40) LMNAMEN1KMT2AALDH1A1HSD17B10
SCHEMBL223965 0.98 SMN1; SMN2 (0.38) LMNAMEN1KMT2AALDH1A1HSD17B10
SCHEMBL28099249 0.93 SMN1; SMN2 (0.35) LMNAMEN1KMT2AALDH1A1HSD17B10
SCHEMBL5792847 0.91
SCHEMBL222917 0.91
Ethylene Glycol SCHEMBL28161259 0.87 MEN1 (0.47) LMNAMEN1KMT2AALDH1A1HSD17B10
SCHEMBL16615781 0.85 DNM1 (0.36) LMNATSHRDNM1
SCHEMBL16615645 0.85 DNM1 (0.36) LMNATSHRDNM1
Ethylene Glycol SCHEMBL27905296 0.84 MEN1 (0.43) LMNAMEN1KMT2AALDH1A1HSD17B10
Ethylene Glycol SCHEMBL8210958 0.82 TSHR (0.44) LMNAMEN1KMT2AALDH1A1HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20180126731-A1 INK DISCHARGE DEVICE AND INK DISCHARGE METHOD RICOH COMPANY, LTD. (JP) 2018-05-10 US disclosed
US-20150353518-A1 CATALYST AND CATALYTIC PROCESS FOR THE ETHERIFICATION/REDUCTION OF FURFURYL DERIVATIVES TO TETRAHYDROFURFURYL ETHERS UNIVERSITAT POLITECNICA DE VALENCIA (ES) 2015-12-10 US disclosed
EP-2913328-A1 CATALYST AND CATALYTIC PROCESS FOR THE ETHERIFICATION/REDUCTION OF FURFURYL DERIVATIVES TO TETRAHYDROFURFURYL ETHERS Consejo Superior De Investigaciones Científicas (CSIC) (ES) 2015-09-02 EP disclosed
US-9109129-B2 Inkjet ink, inkjet recording method, and inkjet recording apparatus RICOH COMPANY, LTD. (JP) 2015-08-18 US disclosed
US-9062217-B2 Liquid composition, recording method, and recorded matter RICOH COMPANY, LTD. (JP) 2015-06-23 US disclosed
US-9033484-B2 Inkjet treatment liquid and inkjet recording apparatus RICOH COMPANY, LTD. (JP) 2015-05-19 US disclosed
US-9011588-B2 Inkjet treatment liquid and image forming method using treatment liquid RICOH COMPANY, LTD. (JP) 2015-04-21 US disclosed
US-8980408-B2 Liquid composition, recording method, and recorded matter RICOH COMPANY, LTD. (JP) 2015-03-17 US disclosed
US-8820875-B2 Image forming method and inkjet recording device using the same RICOH COMPANY, LTD. (JP) 2014-09-02 US disclosed
US-20140240391-A1 INKJET INK, INKJET RECORDING METHOD, AND INKJET RECORDING APPARATUS RICOH COMPANY, LTD. (JP) 2014-08-28 US disclosed
US-20120128949-A1 IMAGE FORMING METHOD, AND IMAGE FORMED MATTER RICOH COMPANY, LTD. (JP) 2012-05-24 US disclosed
US-20110318543-A1 LIQUID COMPOSITION, RECORDING METHOD, AND RECORDED MATTER RICOH COMPANY, LTD. (JP) 2011-12-29 US disclosed
US-20040097728-A1 Method for producing anellated tetrahydro-{1h}-triazoles BASF AKTIENGESELLSCHAFT (DE) 2004-05-20 US disclosed
US-6737544-B1 HEATING ABOVE MELTING POINT BASF AKTIENGESELLSCHAFT (DE) 2004-05-18 US disclosed
US-6639070-B1 4-substituted 1,3,4-oxadiazines; herbicides BASF AKTIENGESELLSCHAFT (DE) 2003-10-28 US disclosed
EP-1187819-B1 N-SUBSTITUTED PERHYDRO DIAZINE BASF AG (DE) 2003-07-23 EP disclosed
US-6525000-B1 N-aminoureas are reacted with formaldehyde to give methyleneimino ureas, cyclizing these to give tetrahydro-4H-1,3,4-oxa(or thia)diazines, and cyclizing the fused triazoles using phosgene; herbicides BASF AKTIENGESELLSCHAFT (DE) 2003-02-25 US disclosed
EP-1095045-B1 METHOD FOR PRODUCING ANELLATED TRIAZOLES AND NEW ANELLATED TRIAZOLES AND THEIR USE BASF AG (DE) 2003-01-15 EP disclosed
EP-0835248-B1 1-AMINO-3-BENZYLURACILS BASF AG (DE) 2001-02-21 EP disclosed
US-6150303-A Substituted 3-phenylisoxazolines BASF AKTIENGESELLSCHAFT (DE) 2000-11-21 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 (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-20040097728-A1 Method for producing anellated tetrahydro-{1h}-triazoles CBR1, CBR3, QSOX1 LMNA 3553/4885MEN1 4291/4885KMT2A 1521/4885
US-20150353518-A1 CATALYST AND CATALYTIC PROCESS FOR THE ETHERIFICATION/REDUCTION OF FURFURYL DERIVATIVES TO TETRAHYDROFURFURYL ETHERS ADH1A, ADH1C, ADH5 LMNA 3240/4885MEN1 1678/4885KMT2A 356/4885

“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.