SCHEMBL2283152

SCHEMBL2283152

NCCCCNC(c1ccccc1)(c1ccccc1)c1ccccc1

nearest known ligand 0.74

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
KIF11 P52732 8/20 0.74
KCNN4 O15554 2/20 0.50
DUT P33316 1/20 0.44
MAOA P21397 1/20 0.42
GRIN2D O15399 1/20 0.39
GRIN3B O60391 1/20 0.39
GRIA1 P42261 1/20 0.39
GRIA2 P42262 1/20 0.39
GRIA3 P42263 1/20 0.39
GRIA4 P48058 1/20 0.39
GRIN1 Q05586 1/20 0.39
GRIN2A Q12879 1/20 0.39
GRIN2B Q13224 1/20 0.39
GRIN2C Q14957 1/20 0.39
GRIN3A Q8TCU5 1/20 0.39
CHRM2 P08172 1/20 0.38

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
SCHEMBL15160759 0.98 KIF11 (0.71) KIF11KCNN4DUTMAOAGRIN2D
SCHEMBL1105545 0.85 KIF11 (1.00) KIF11KCNN4DUT
SCHEMBL12264133 0.85 KIF11 (0.68) KIF11KCNN4DUT
SCHEMBL12049184 0.84 KIF11 (0.58) KIF11KCNN4CHRM2
Bromide SCHEMBL5339582 0.83 KIF11 (0.96) KIF11KCNN4DUT
SCHEMBL31229179 0.83 KIF11 (0.61) KIF11KCNN4DUT
SCHEMBL3136435 0.83 KIF11 (0.61) KIF11KCNN4DUT
SCHEMBL9617559 0.82 KIF11 (0.78) KIF11KCNN4DUT
SCHEMBL4801600 0.82 KIF11 (0.59) KIF11KCNN4DUTMAOAGRIN1
SCHEMBL12264131 0.80 KIF11 (0.74) KIF11KCNN4DUT

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
US-9732378-B2 Fluorophore chelated lanthanide luminescent probes with improved quantum efficiency RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2017-08-15 US disclosed
US-20160194690-A1 FLUOROPHORE CHELATED LANTHANIDE LUMINESCENT PROBES WITH IMPROVED QUANTUM EFFICIENCY RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2016-07-07 US disclosed
US-9358300-B2 Transfection reagents Life Technologies Corporation (US) 2016-06-07 US disclosed
US-9358300-B2 Transfection reagents Life Technologies Corporation (US) 2016-06-07 US disclosed
US-9221759-B2 Fluorophore chelated lanthanide luminescent probes with improved quantum efficiency RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2015-12-29 US disclosed
US-20150190522-A1 TRANSFECTION REAGENTS LIFE TECHNOLOGIES CORP (US) 2015-07-09 US disclosed
US-20150190522-A1 TRANSFECTION REAGENTS LIFE TECHNOLOGIES CORP (US) 2015-07-09 US disclosed
US-8785200-B2 Transfection reagents Life Technologies Corporation (US) 2014-07-22 US disclosed
US-8785200-B2 Transfection reagents Life Technologies Corporation (US) 2014-07-22 US disclosed
US-20130202536-A1 FLUOROPHORE CHELATED LANTHANIDE LUMINESCENT PROBES WITH IMPROVED QUANTUM EFFICIENCY NEW JERSEY INSTITUTE OF TECHNOLOGY (US) 2013-08-08 US disclosed
US-20070202598-A1 NEW TRANSFECTION REAGENTS INVITROGEN CORPORATION (US) 2007-08-30 US disclosed
US-7173154-B2 Transfection reagents INVITROGEN CORP. (US) 2007-02-06 US disclosed
US-7173154-B2 Transfection reagents INVITROGEN CORP. (US) 2007-02-06 US disclosed
US-7166745-B1 Transfection reagents INVITROGEN CORPORATION (US) 2007-01-23 US disclosed
US-7166745-B1 Transfection reagents INVITROGEN CORPORATION (US) 2007-01-23 US disclosed
CN-1146552-C Azulene hydroxamic acid derivatives as metalloprotein inhibitors �������ŵ˹�ٿ�˹�������ι�˾ 2004-04-21 CN disclosed
CN-1281444-A Azulene hydroxamic acid derivatives as metalloprotein inhibitors ROTSCHIDEIGNOSTIKS AG (DE) 2001-01-24 CN disclosed
EP-1054878-A1 AZULENE HYDROXAMIC ACID DERIVATIVES AS METALLOPROTEIN INHIBITORS Roche Diagnostics GmbH (DE) 2000-11-29 EP disclosed
US-6121322-A ANTIINFLAMMATORY AGENTS BOEHRINGER MANNHEIM GMBH (DE) 2000-09-19 US disclosed
WO-1999031078-A1 AZULENE HYDROXAMIC ACID DERIVATIVES AS METALLOPROTEIN INHIBITORS ROCHE DIAGNOSTICS GMBH (DE) 1999-06-24 WO 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-20070202598-A1 NEW TRANSFECTION REAGENTS PHAX, CPS1, HNRNPH3 KIF11 4690/4885KCNN4 1659/4885DUT 628/4885
US-20150190522-A1 TRANSFECTION REAGENTS CPS1, PHAX, HNRNPH3 KIF11 4536/4885KCNN4 1855/4885DUT 490/4885
US-20130202536-A1 FLUOROPHORE CHELATED LANTHANIDE LUMINESCENT PROBES WITH IMPROVED QUANTUM EFFICIENCY CLTA, LARS1, SSB KIF11 839/4885KCNN4 1857/4885DUT 87/4885
US-20160194690-A1 FLUOROPHORE CHELATED LANTHANIDE LUMINESCENT PROBES WITH IMPROVED QUANTUM EFFICIENCY CLTA, LARS1, SSB KIF11 839/4885KCNN4 1857/4885DUT 87/4885

“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.