SCHEMBL16010056

SCHEMBL16010056

N[C@H]1CC[C@@H](N[C@@H]2C[C@H]2c2ccc(-c3cccc(NS(=O)(=O)N4CCNCC4)c3)cc2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
KDM1A O60341 20/20 1.00
MAOB P27338 15/20 1.00
MAOA P21397 14/20 1.00
KDM1B Q8NB78 1/20 0.45
RCOR1 Q9UKL0 1/20 0.45

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
SCHEMBL29357786 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL14882286 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL29357857 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL16009812 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL14882283 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL16010546 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL16009813 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL29357936 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL16009931 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1
SCHEMBL18333284 1.00 KDM1A (1.00) KDM1AMAOBMAOAKDM1BRCOR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3495349-B1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS SA (ES) 2023-06-28 EP claimed
EP-4074695-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS Oryzon Genomics, S.A. (ES) 2022-10-19 EP claimed
EP-3495349-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS Oryzon Genomics, S.A. (ES) 2019-06-12 EP claimed
EP-2776394-B1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS SA (ES) 2018-12-26 EP claimed
US-20160368857-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS SA (ES) 2016-12-22 US claimed
US-20150119396-A9 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS S.A. (ES) 2015-04-30 US claimed
US-20140256729-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS SA (ES) 2014-09-11 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
EP-3941465-B1 METHODS OF TREATING ATTENTION DEFICIT HYPERACTIVITY DISORDER USING KDM1A INHIBITORS SUCH AS THE COMPOUND VAFIDEMSTAT ORYZON GENOMICS SA (ES) 2025-09-17 EP disclosed
EP-3430015-B1 METHODS TO DETERMINE KDM1A TARGET ENGAGEMENT AND CHEMOPROBES USEFUL THEREFOR ORYZON GENOMICS SA (ES) 2025-08-06 EP disclosed
EP-4512473-A2 METHODS OF TREATING BEHAVIOR ALTERATIONS Oryzon Genomics, S.A. (ES) 2025-02-26 EP disclosed
US-12195783-B2 Methods to determine KDM1A target engagement and chemoprobes useful therefor ORYZON GENOMICS S.A. (ES) 2025-01-14 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-20160368857-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS SA (ES) 2016-12-22 US disclosed
US-9469597-B2 (Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors ORYZON GENOMICS S.A. (ES) 2016-10-18 US disclosed
US-9469597-B2 (Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors ORYZON GENOMICS S.A. (ES) 2016-10-18 US disclosed
US-20150119396-A9 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS S.A. (ES) 2015-04-30 US disclosed
US-20150119396-A9 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS S.A. (ES) 2015-04-30 US disclosed
US-20140256729-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS SA (ES) 2014-09-11 US disclosed
US-20140256729-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS ORYZON GENOMICS SA (ES) 2014-09-11 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 (6 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-20160368857-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS KDM1B, KDM1A, KDM2A KDM1A 2/4885MAOB 147/4885MAOA 135/4885
US-20150119396-A9 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS KDM1A, KDM1B, KDM3B KDM1A 1/4885MAOB 186/4885MAOA 175/4885
US-20140256729-A1 (HETERO)ARYL CYCLOPROPYLAMINE COMPOUNDS AS LSD1 INHIBITORS KDM1A, KDM1B, KDM3B KDM1A 1/4885MAOB 186/4885MAOA 175/4885
US-12195783-B2 Methods to determine KDM1A target engagement and chemoprobes useful therefor KDM1B, KDM1A, KDM7A KDM1A 2/4885MAOB 3928/4885MAOA 4155/4885
US-12576083-B2 Combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer CDK3, CDKN1A, CDKL3 KDM1A 26/4885MAOB 2453/4885MAOA 3373/4885
US-20240342178-A1 COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH P21 ACTIVATORS IN THE TREATMENT OF CANCER KDM1B, DOT1L, EZH2 KDM1A 10/4885MAOB 2291/4885MAOA 2144/4885

“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.