SCHEMBL15411012

SCHEMBL15411012

CC(C)(C)OC(=O)N1CCCC(CN[C@@H]2C[C@H]2c2ccccc2)CC1

nearest known ligand 0.58

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.58
PKM P14618 1/20 0.58
KDM1A O60341 19/20 0.57
MAOB P27338 3/20 0.57
HDAC6 Q9UBN7 8/20 0.52
DRD2 P14416 1/20 0.52
HTR2A P28223 1/20 0.52
SLC6A4 P31645 1/20 0.52
SCN5A Q14524 1/20 0.52
HDAC1 Q13547 1/20 0.49
HDAC8 Q9BY41 1/20 0.49

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
SCHEMBL15425023 1.00 KDM4E (0.58) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL15411011 1.00 KDM4E (0.58) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL12965573 1.00 KDM4E (0.58) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL12813366 0.96 KDM4E (0.62) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL21101170 0.96 KDM4E (0.62) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL19513593 0.96 KDM4E (0.62) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL12965568 0.96 KDM4E (0.62) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL21100965 0.96 KDM4E (0.62) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL12813368 0.96 KDM4E (0.62) KDM4EPKMKDM1AMAOBHDAC6
SCHEMBL12813626 0.96 KDM4E (0.62) KDM4EPKMKDM1AMAOBHDAC6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9346840-B2 Cyclopropylamines as LSD1 inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO. 2) LIMITED (GB) 2016-05-24 US claimed
US-20140371176-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2014-12-18 US claimed
US-12576083-B2 Combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2026-03-17 US disclosed
US-20240342178-A1 COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH P21 ACTIVATORS IN THE TREATMENT OF CANCER ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2024-10-17 US disclosed
US-11918580-B2 Use of a combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2024-03-05 US disclosed
EP-2688568-B1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS GLAXOSMITHKLINE IP NO 2 LTD (GB) 2019-06-19 EP disclosed
US-10064854-B2 Cyclopropylamines as LSD1 inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2018-09-04 US disclosed
US-20180000805-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2018-01-04 US disclosed
US-9795597-B2 Cyclopropylamines as LSD1 inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2017-10-24 US disclosed
US-20160220547-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2016-08-04 US disclosed
US-9346840-B2 Cyclopropylamines as LSD1 inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO. 2) LIMITED (GB) 2016-05-24 US disclosed
US-20140371176-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO.2) LIMITED (GB) 2014-12-18 US disclosed
US-8853408-B2 Cyclopropylamines as LSD1 inhibitors GLAXOSMITHKLINE INTELLECTUAL PROPERTY (NO. 2) LIMITED (GB) 2014-10-07 US disclosed
US-20140018393-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS Glaxo Smith Kline LLC 2014-01-16 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 (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-10064854-B2 Cyclopropylamines as LSD1 inhibitors KDM1B, KDM1A, KDM3B KDM4E 13/4885PKM 739/4885KDM1A 2/4885
US-20160220547-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM3B KDM4E 13/4885PKM 739/4885KDM1A 2/4885
US-20140018393-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM3B KDM4E 13/4885PKM 739/4885KDM1A 2/4885
US-11918580-B2 Use of a combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer CDK6, KDM1B, KDM6B KDM4E 18/4885PKM 719/4885KDM1A 7/4885
US-12576083-B2 Combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer CDK3, CDKN1A, CDKL3 KDM4E 69/4885PKM 1268/4885KDM1A 26/4885
US-20180000805-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM3B KDM4E 13/4885PKM 739/4885KDM1A 2/4885
US-20240342178-A1 COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH P21 ACTIVATORS IN THE TREATMENT OF CANCER KDM1B, DOT1L, EZH2 KDM4E 27/4885PKM 914/4885KDM1A 10/4885
US-20140371176-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM3B KDM4E 13/4885PKM 739/4885KDM1A 2/4885

“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.