SCHEMBL609272

SCHEMBL609272

O=C(NC1CCC(O)CC1)[C@H]1CCCN(S(=O)(=O)c2cccc(Oc3ccc(F)cc3)c2)C1

nearest known ligand 0.62

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 6/20 0.62
POLB P06746 1/20 0.55
TSHR P16473 2/20 0.53
MAPT P10636 3/20 0.50
LMNA P02545 3/20 0.50
RAB9A P51151 2/20 0.50
GAA P10253 2/20 0.50
NPC1 O15118 1/20 0.50
ATM Q13315 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
HTT P42858 1/20 0.50
MEN1 O00255 3/20 0.48
HCRTR1 O43613 1/20 0.48
ALDH1A1 P00352 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
EPHX2 P34913 1/20 0.48
DPP4 P27487 1/20 0.47
KDM4E B2RXH2 1/20 0.47
HSD17B10 Q99714 1/20 0.47

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
SCHEMBL609271 1.00 KMT2A (0.62) KMT2APOLBTSHRMAPTLMNA
SCHEMBL612158 0.93 TSHR (0.54) KMT2APOLBTSHRRAB9AGAA
SCHEMBL612159 0.93 TSHR (0.54) KMT2APOLBTSHRRAB9AGAA
SCHEMBL610190 0.87 POLB (0.72) KMT2APOLBTSHRMAPTLMNA
SCHEMBL4960549 0.87 POLB (0.72) KMT2APOLBTSHRMAPTLMNA
SCHEMBL610191 0.87 POLB (0.72) KMT2APOLBTSHRMAPTLMNA
SCHEMBL610278 0.87 RAB9A (0.58) KMT2APOLBTSHRRAB9ANPC1
SCHEMBL610279 0.87 RAB9A (0.58) KMT2APOLBTSHRRAB9ANPC1
SCHEMBL4967726 0.87 RAB9A (0.58) KMT2APOLBTSHRRAB9ANPC1
SCHEMBL610984 0.86 KMT2A (0.54) KMT2APOLBTSHRLMNARAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8288417-B2 N-substituted piperidines and their use as pharmaceuticals INCYTE CORPORATION (US) 2012-10-16 US claimed
US-20120040964-A1 N-SUBSTITUTED PIPERIDINES AND THEIR USE AS PHARMACEUTICALS INCYTE CORPORATION (US) 2012-02-16 US claimed
US-20060004049-A1 N-substituted piperidines and their use as pharrmaceuticals INCYTE CORPORATION 2006-01-05 US claimed
US-8288417-B2 N-substituted piperidines and their use as pharmaceuticals INCYTE CORPORATION (US) 2012-10-16 US disclosed
US-20120040964-A1 N-SUBSTITUTED PIPERIDINES AND THEIR USE AS PHARMACEUTICALS INCYTE CORPORATION (US) 2012-02-16 US disclosed
US-8071624-B2 N-substituted piperidines and their use as pharmaceuticals INCYTE CORPORATION (US) 2011-12-06 US disclosed
EP-1758580-A4 N-SUBSTITUTED PIPERIDINES AND THEIR USE AS PHARMACEUTICALS INCYTE CORP (US) 2008-01-16 EP disclosed
EP-1758580-A2 N-SUBSTITUTED PIPERIDINES AND THEIR USE AS PHARMACEUTICALS Incyte Corporation (US) 2007-03-07 EP disclosed
WO-2006012226-A2 N-SUBSTITUTED PIPERIDINES AND THEIR USE AS PHARMACEUTICALS INCYTE CORPORATION (US) 2006-02-02 WO disclosed
US-20060004049-A1 N-substituted piperidines and their use as pharrmaceuticals INCYTE CORPORATION 2006-01-05 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-20120040964-A1 N-SUBSTITUTED PIPERIDINES AND THEIR USE AS PHARMACEUTICALS HSD11B1, CYP11B1, HSD3B1 KMT2A 2726/4885POLB 1184/4885TSHR 1143/4885
US-20060004049-A1 N-substituted piperidines and their use as pharrmaceuticals HSD11B1, HSD3B1, HSD11B2 KMT2A 3003/4885POLB 1100/4885TSHR 1444/4885

“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.