SCHEMBL145408

SCHEMBL145408

CCCCN1C(=O)CC(=O)N(CCCC)C1=S

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.46
SMN1; SMN2 Q16637 5/20 0.44
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
PTGS1 P23219 3/20 0.39
PTGS2 P35354 3/20 0.39
MGLL Q99685 3/20 0.39
FAAH O00519 2/20 0.39
MEN1 O00255 5/20 0.38
KMT2A Q03164 5/20 0.38
GAA P10253 3/20 0.38
MAPT P10636 3/20 0.38
ALDH1A1 P00352 2/20 0.38
THRB P10828 1/20 0.38
CYP19A1 P11511 1/20 0.37
USP2 O75604 2/20 0.36
POLB P06746 2/20 0.36
MAPK1 P28482 1/20 0.36
HTT P42858 1/20 0.36
TDP1 Q9NUW8 1/20 0.36

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
SCHEMBL12101786 0.96 MGLL (0.46) KDM4ESMN1; SMN2NPC1RAB9APTGS1
SCHEMBL8652814 0.94 MGLL (0.47) KDM4ESMN1; SMN2NPC1RAB9APTGS1
SCHEMBL5570285 0.92 MGLL (0.50) KDM4EPTGS1PTGS2MGLLFAAH
SCHEMBL11868886 0.90 KDM4E (0.43) KDM4ESMN1; SMN2NPC1RAB9APTGS1
SCHEMBL3142849 0.88 KDM4E (0.42) KDM4ESMN1; SMN2NPC1RAB9APTGS1
SCHEMBL3142469 0.88 MGLL (0.40) KDM4ESMN1; SMN2NPC1RAB9APTGS1
SCHEMBL6162730 0.87 MAPT (0.35) KDM4ESMN1; SMN2NPC1RAB9AMEN1
SCHEMBL3420629 0.83 MAPT (0.49) KDM4ESMN1; SMN2PTGS1PTGS2MGLL
SCHEMBL9466598 0.81 KDM4E (0.51) KDM4ESMN1; SMN2PTGS1PTGS2MGLL
SCHEMBL9432000 0.80 SMN1; SMN2 (0.61) SMN1; SMN2NPC1RAB9APTGS1PTGS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1610126-B1 A system for determining the electrical potential across a membrane UNIV CALIFORNIA (US) 2014-04-30 EP disclosed
US-20120059163-A1 Non-linear opticaly active molecules, their synthesis, and use OPTIMER PHOTONICS, INC. (US) 2012-03-08 US disclosed
EP-1409456-B1 DETECTION OF TRANSMEMBRANE POTENTIALS BY OPTICAL METHODS UNIV CALIFORNIA (US) 2012-02-08 EP disclosed
EP-0977035-B2 A system for determining the electrical potential across a membrane UNIV CALIFORNIA (US) 2010-07-21 EP disclosed
US-7687282-B2 Detection of transmembrane potentials by optical methods THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2010-03-30 US disclosed
EP-1688466-B1 Ink composition, ink jet recording method, printed material, method of producing planographic printing plate, and planographic printing plate FUJIFILM CORP (JP) 2008-11-26 EP disclosed
US-20080004415-A1 Non-linear optically active molecules, their synthesis, and use OPTIMER PHOTONICS, INC. (US) 2008-01-03 US disclosed
US-20070259903-A1 ANTI-VIRAL USES FOR ANALOGS OF BARBITURIC ACID GULLIYA KIRPAL S 2007-11-08 US disclosed
US-7173130-B2 Detection of transmembrane potentials by optical methods THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2007-02-06 US disclosed
US-20070026384-A1 Detection of transmembrane potentials by optical methods THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2007-02-01 US disclosed
EP-0977035-A2 A system for determining the electrical potential across a membrane REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2000-02-02 EP disclosed
EP-0834074-B1 DETECTION OF TRANSMEMBRANE POTENTIALS BY OPTICAL METHODS UNIV CALIFORNIA (US) 1999-11-03 EP disclosed
US-5869494-A ADMINISTERING AS ANTITUMOR AGENTS, IMMUNE SYSTEM MODULATORS AND ANTIDEPRESSANTS GULLIYA KIRPAL S (US) 1999-02-09 US disclosed
EP-0834074-A1 DETECTION OF TRANSMEMBRANE POTENTIALS BY OPTICAL METHODS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1998-04-08 EP disclosed
US-5674870-A Anti-cancer uses for barbituric acid analogs GULLIYA KIRPAL S (US) 1997-10-07 US disclosed
US-5661035-A Voltage sensing by fluorescence resonance energy transfer THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1997-08-26 US disclosed
WO-1996041166-A2 DETECTION OF TRANSMEMBRANE POTENTIALS BY OPTICAL METHODS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1996-12-19 WO disclosed
EP-0591786-B1 Photosensitive composition FUJI PHOTO FILM CO LTD (JP) 1996-05-15 EP disclosed
EP-0591786-A2 Photosensitive composition FUJI PHOTO FILM CO., LTD. (JP) 1994-04-13 EP disclosed
US-4636459-A PHOTOINITIATOR AND UNSATURATED MONOMER; PRINTING PLATES FUJI PHOTO FILM CO., LTD. (JP) 1987-01-13 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 (4 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-20070259903-A1 ANTI-VIRAL USES FOR ANALOGS OF BARBITURIC ACID SARS1, SLC6A1, BAK1 KDM4E 1150/4885SMN1; SMN2 2131/4885NPC1 1320/4885
US-20120059163-A1 Non-linear opticaly active molecules, their synthesis, and use INCENP, CYBA, ADCY5 KDM4E 2422/4885SMN1; SMN2 4522/4885NPC1 4051/4885
US-20070026384-A1 Detection of transmembrane potentials by optical methods MBOAT1, TRPM4, NME4 KDM4E 4599/4885SMN1; SMN2 4297/4885NPC1 335/4885
US-20080004415-A1 Non-linear optically active molecules, their synthesis, and use INCENP, CYBA, PAICS KDM4E 2483/4885SMN1; SMN2 4430/4885NPC1 3846/4885

“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.