SCHEMBL1948748

SCHEMBL1948748

Oc1ccccc1/C=N/c1cccc(Br)c1

nearest known ligand 0.62

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
SIRT2 Q8IXJ6 1/20 0.62
CA2 P00918 5/20 0.53
CA9 Q16790 4/20 0.53
CA12 O43570 4/20 0.53
TSHR P16473 1/20 0.53
CA1 P00915 3/20 0.49
LMNA P02545 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
CA7 P43166 1/20 0.46
MAOB P27338 3/20 0.46
MEN1 O00255 1/20 0.46
PLA2G1B P04054 1/20 0.46
MAPT P10636 1/20 0.46
KMT2A Q03164 1/20 0.46
ATG4B Q9Y4P1 1/20 0.46
ALDH1A1 P00352 1/20 0.45
PTK6 Q13882 1/20 0.45
KDM4E B2RXH2 1/20 0.44

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
SCHEMBL1948751 1.00 SIRT2 (0.62) SIRT2CA2CA9CA12TSHR
SCHEMBL2492349 0.88 SIRT2 (0.74) SIRT2CA2CA9CA12TSHR
SCHEMBL2937662 0.88 SIRT2 (0.74) SIRT2CA2CA9CA12TSHR
SCHEMBL2492350 0.88 SIRT2 (0.74) SIRT2CA2CA9CA12TSHR
SCHEMBL15347538 0.84 MAPT (0.63) CA2CA9CA12TSHRCA1
SCHEMBL15347537 0.84 MAPT (0.63) CA2CA9CA12TSHRCA1
SCHEMBL11406841 0.83 SIRT2 (0.67) SIRT2CA2CA9CA12TSHR
SCHEMBL11406860 0.83 SIRT2 (0.67) SIRT2CA2CA9CA12TSHR
SCHEMBL5784155 0.81 SIRT2 (0.81) SIRT2CA2CA9CA12TSHR
SCHEMBL5784154 0.81 SIRT2 (0.81) SIRT2CA2CA9CA12TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2151446-B1 Process for the preparation of bidentate schiff base ruthenium catalysts containing a salicylaldimine-type ligand RIMTEC CORP (JP) 2016-04-13 EP disclosed
EP-2151445-B1 Process for the preparation of bidentate Schiff base ruthenium catalysts containing a salicylaldimine-type ligand RIMTEC CORP (JP) 2015-02-18 EP disclosed
US-8338613-B2 Process for the preparation of bidentate schiff base ruthenium catalysts containing a salicylaldimine-type ligand RIMTEC CORPORATION (JP) 2012-12-25 US disclosed
US-20110137043-A1 Process for the preparation of bidentate schiff base ruthenium catalysts containing a salicylaldimine-type ligand TELENE S.A.S. (FR) 2011-06-09 US disclosed
US-20110065925-A1 Process for the preparation of bidentate schiff base ruthenium catalysts containing a salicylaldimine-type ligand TELENE S.A.S. (FR) 2011-03-17 US disclosed
EP-2151446-A1 Process for the preparation of bidentate schiff base ruthenium catalysts containing a salicylaldimine-type ligand Telene SAS (FR) 2010-02-10 EP disclosed
EP-2151445-A1 Process for the preparation of bidentate Schiff base ruthenium cataysts containing a saliclyldimine-type ligand Telene SAS (FR) 2010-02-10 EP 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-20110137043-A1 Process for the preparation of bidentate schiff base ruthenium catalysts containing a salicylaldimine-type ligand SPR, LIG4, SUCLA2 SIRT2 135/4885CA2 1434/4885CA9 2120/4885
US-20110065925-A1 Process for the preparation of bidentate schiff base ruthenium catalysts containing a salicylaldimine-type ligand SPR, LIG4, SUCLA2 SIRT2 135/4885CA2 1434/4885CA9 2120/4885

“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.