SCHEMBL4635556

SCHEMBL4635556

CC(C)(C)OC(=O)N1CCC(C=O)(Cc2ccc(F)cc2)CC1

nearest known ligand 0.49

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
KDM1A O60341 1/20 0.46
CNR1 P21554 1/20 0.45
CNR2 P34972 1/20 0.45
HDAC2 Q92769 2/20 0.44
HDAC1 Q13547 2/20 0.44
MEN1 O00255 1/20 0.42
KMT2A Q03164 1/20 0.42
RORC P51449 3/20 0.42
JAK2 O60674 1/20 0.42
JAK1 P23458 1/20 0.42
TACR1 P25103 1/20 0.41
ALOX15 P16050 1/20 0.40
TSHR P16473 1/20 0.40
ATM Q13315 1/20 0.40
OPRD1 P41143 1/20 0.39
OPRK1 P41145 1/20 0.39
HDAC8 Q9BY41 1/20 0.39
HDAC6 Q9UBN7 1/20 0.39
GPR119 Q8TDV5 1/20 0.39

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
SCHEMBL5674643 0.89 KDM1A (0.45) KDM1ACNR1CNR2HDAC2HDAC1
SCHEMBL4024667 0.88 OPRD1 (0.50) TACR1ALOX15TSHRATMOPRD1
SCHEMBL20137495 0.87 SMN1; SMN2 (0.49) KDM1AMEN1KMT2AGPR119
SCHEMBL16987051 0.85 GPR119 (0.51) HDAC1JAK2JAK1TACR1ALOX15
SCHEMBL5672765 0.84 KDM1A (0.48) KDM1ACNR1CNR2HDAC2HDAC1
SCHEMBL14357682 0.84 KDM1A (0.48) KDM1ACNR1CNR2HDAC2HDAC1
SCHEMBL4634695 0.84 HDAC2 (0.48) KDM1ACNR1CNR2HDAC2HDAC1
SCHEMBL4634666 0.83 HDAC2 (0.48) KDM1ACNR1CNR2HDAC2HDAC1
SCHEMBL4634595 0.82 KDM1A (0.46) KDM1ACNR1CNR2HDAC2HDAC1
Hydrochloric Acid SCHEMBL5812318 0.82 HDAC2 (0.47) KDM1ACNR1CNR2HDAC2HDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11247992-B2 Cyclopropylamines as LSD1 inhibitors INCYTE CORPORATION (US) 2022-02-15 US disclosed
US-11247992-B2 Cyclopropylamines as LSD1 inhibitors INCYTE CORPORATION (US) 2022-02-15 US disclosed
US-11155532-B2 Cyclopropylamines as LSD1 inhibitors INCYTE CORPORATION (US) 2021-10-26 US disclosed
US-11155532-B2 Cyclopropylamines as LSD1 inhibitors INCYTE CORPORATION (US) 2021-10-26 US disclosed
EP-3626713-B1 CYCLOPROPYLAMINES FOR USE AS LSD1 INHIBITORS INCYTE CORP (US) 2021-09-29 EP disclosed
EP-3626713-B1 CYCLOPROPYLAMINES FOR USE AS LSD1 INHIBITORS INCYTE CORP (US) 2021-09-29 EP disclosed
US-20210032244-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION 2021-02-04 US disclosed
US-20210032244-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION 2021-02-04 US disclosed
US-20210024487-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION 2021-01-28 US disclosed
US-20210024487-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION 2021-01-28 US disclosed
US-20150225379-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION (US) 2015-08-13 US disclosed
US-20150225401-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION (US) 2015-08-13 US disclosed
US-20150225394-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION (US) 2015-08-13 US disclosed
US-20150225394-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION (US) 2015-08-13 US disclosed
US-20150225375-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION (US) 2015-08-13 US disclosed
US-20150225379-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION (US) 2015-08-13 US disclosed
US-20150225375-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION (US) 2015-08-13 US disclosed
EP-1928829-A1 PIPERIDINE DERIVATIVES AS ANTAGONISTS OF THE CC CHEMOKINE RECEPTOR CCR1 AND THEIR USE AS ANTI-INFLAMMATORY AGENTS Schering Aktiengesellschaft (DE) 2008-06-11 EP disclosed
US-20060167044-A1 Piperidine derivatives and their use as anti-inflammatory agents BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2006-07-27 US disclosed
WO-2006066948-A1 PIPERIDINE DERIVATIVES AS ANTAGONISTS OF THE CC CHEMOKINE RECEPTOR CCR1 AND THEIR USE AS ANTI-INFLAMMATORY AGENTS SCHERING AKTIENGESELLSCHAFT (DE) 2006-06-29 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 (9 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-20150225401-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885
US-20150225375-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885
US-20210024487-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885
US-11155532-B2 Cyclopropylamines as LSD1 inhibitors KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885
US-20150225379-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885
US-20060167044-A1 Piperidine derivatives and their use as anti-inflammatory agents CCR1, CCR2, CCR3 KDM1A 3174/4885CNR1 33/4885CNR2 51/4885
US-11247992-B2 Cyclopropylamines as LSD1 inhibitors KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885
US-20150225394-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885
US-20210032244-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885

“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.