SCHEMBL3356420

SCHEMBL3356420

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

nearest known ligand 0.50

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
KDM1A O60341 1/20 0.46
CNR1 P21554 1/20 0.46
CNR2 P34972 1/20 0.46
RORC P51449 3/20 0.45
HDAC2 Q92769 2/20 0.45
HDAC1 Q13547 1/20 0.45
KMT2A Q03164 4/20 0.43
MEN1 O00255 2/20 0.43
LMNA P02545 2/20 0.43
POLB P06746 1/20 0.43
JAK2 O60674 1/20 0.42
JAK1 P23458 1/20 0.42
TACR1 P25103 1/20 0.42

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
SCHEMBL4633896 0.90 KDM1A (0.46) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL4634342 0.89 HDAC2 (0.46) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL5674689 0.87 MEN1 (0.45) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL3353600 0.85 RORC (0.46) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL5672759 0.85 CNR1 (0.45) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL4635507 0.85 KDM1A (0.43) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL5672765 0.85 KDM1A (0.48) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL4634695 0.85 HDAC2 (0.48) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL14357682 0.85 KDM1A (0.48) KDM1ACNR1CNR2RORCHDAC2
SCHEMBL16986971 0.85 GPR119 (0.52) HDAC1KMT2AMEN1JAK2JAK1

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 77 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-20150225394-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-20150225401-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-20150225375-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION (US) 2015-08-13 US disclosed
US-20100152160-A1 NOVEL BENZODIOXANE AND BENZOXAZINE DERIVATIVES USEFUL AS CC CHEMOKINE RECEPTOR LIGANDS KHAMRAI UTTAM 2010-06-17 US disclosed
US-20100152160-A1 NOVEL BENZODIOXANE AND BENZOXAZINE DERIVATIVES USEFUL AS CC CHEMOKINE RECEPTOR LIGANDS KHAMRAI UTTAM 2010-06-17 US disclosed
WO-2010068881-A1 NOVEL BENZODIOXANE AND BENZOXAZINE DERIVATIVES USEFUL AS CC CHEMOKINE RECEPTOR LIGANDS FOREST LABORATORIES HOLDINGS LIMITED (BM) 2010-06-17 WO disclosed
US-20100152160-A1 NOVEL BENZODIOXANE AND BENZOXAZINE DERIVATIVES USEFUL AS CC CHEMOKINE RECEPTOR LIGANDS KHAMRAI UTTAM 2010-06-17 US disclosed
WO-2010068881-A1 NOVEL BENZODIOXANE AND BENZOXAZINE DERIVATIVES USEFUL AS CC CHEMOKINE RECEPTOR LIGANDS FOREST LABORATORIES HOLDINGS LIMITED (BM) 2010-06-17 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 (8 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-20100152160-A1 NOVEL BENZODIOXANE AND BENZOXAZINE DERIVATIVES USEFUL AS CC CHEMOKINE RECEPTOR LIGANDS CCR1, CCR4, CCR5 KDM1A 1463/4885CNR1 27/4885CNR2 53/4885
US-11155532-B2 Cyclopropylamines as LSD1 inhibitors KDM1B, KDM1A, KDM2A KDM1A 2/4885CNR1 658/4885CNR2 766/4885
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.