SCHEMBL526505

SCHEMBL526505

CC(C)S(=O)(=O)Nc1cccc(-c2ccc(C3CC3N)cc2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
KDM1A O60341 14/20 1.00
GRIA2 P42262 6/20 0.57
KCNH2 Q12809 5/20 0.57
MAOA P21397 2/20 0.53
MAOB P27338 1/20 0.53
HDAC6 Q9UBN7 1/20 0.50

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
SCHEMBL526506 1.00 KDM1A (1.00) KDM1AGRIA2KCNH2MAOAMAOB
SCHEMBL15136917 1.00 KDM1A (1.00) KDM1AGRIA2KCNH2MAOAMAOB
Hydrochloric Acid SCHEMBL527300 0.99 KDM1A (0.98) KDM1AGRIA2KCNH2MAOAMAOB
Hydrochloric Acid SCHEMBL527301 0.99 KDM1A (0.98) KDM1AGRIA2KCNH2MAOAMAOB
SCHEMBL15136959 0.86 KDM1A (1.00) KDM1AGRIA2KCNH2MAOAMAOB
SCHEMBL15137074 0.86 KDM1A (1.00) KDM1AGRIA2KCNH2MAOAMAOB
SCHEMBL15136544 0.86 KDM1A (1.00) KDM1AGRIA2KCNH2MAOAMAOB
Hydrochloric Acid SCHEMBL15136418 0.85 KDM1A (0.97) KDM1AGRIA2KCNH2MAOAMAOB
Hydrochloric Acid SCHEMBL15136417 0.85 KDM1A (0.97) KDM1AGRIA2KCNH2MAOAMAOB
SCHEMBL15136922 0.84 KDM1A (1.00) KDM1AMAOAMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2598480-B1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS ORYZON GENOMICS SA (ES) 2019-04-24 EP claimed
US-9676701-B2 Cyclopropylamine derivatives useful as LSD1 inhibitors ORYZON GENOMICS, S.A. (ES) 2017-06-13 US claimed
US-20160052865-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS ORYZON GENOMICS S.A. 2016-02-25 US claimed
US-20130197013-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS ORYZON GENOMICS S.A. (ES) 2013-08-01 US claimed
EP-3430015-B1 METHODS TO DETERMINE KDM1A TARGET ENGAGEMENT AND CHEMOPROBES USEFUL THEREFOR ORYZON GENOMICS SA (ES) 2025-08-06 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
EP-3013424-B1 LSD INHIBITORS FOR MODULATING CANCER STEM CELLS EPIAXIS THERAPEUTICS PTY LTD (AU) 2024-09-25 EP disclosed
US-20220389478-A1 METHODS TO DETERMINE KDM1A TARGET ENGAGEMENT AND CHEMOPROBES USEFUL THEREFOR ORYZON GENOMICS SA (ES) 2022-12-08 US disclosed
WO-2021195723-A1 \"METHODS FOR TREATMENT OF CORONAVIRUS INFECTIONS\ THE COUNCIL OF THE QUEENSLAND INSTITUTE OF MEDICAL RESEARCH (AU) 2021-10-07 WO disclosed
US-20210186905-A1 ENHANCING T-CELL FUNCTION AND TREATING A T-CELL DYSFUNCTIONAL DISORDER WITH A COMBINATION OF AN LSD INHIBITOR AND A PD-1 BINDING ANTAGONIST EPIAXIS THERAPEUTICS PTY LTD (AU) 2021-06-24 US disclosed
US-11034991-B2 Methods to determine KDM1A target engagement and chemoprobes useful therefor ORYZON GENOMICS S.A. (ES) 2021-06-15 US disclosed
US-20210121496-A1 METHODS AND COMPOSITIONS FOR MODULATING CANCER STEM CELLS EpiAxis Therapeutics Pty Ltd. (AU) 2021-04-29 US disclosed
EP-3013424-A1 METHODS AND COMPOSITIONS FOR MODULATING CANCER STEM CELLS University of Canberra (AU) 2016-05-04 EP disclosed
WO-2016029262-A1 COMPOSITIONS FOR MODULATING CANCER STEM CELLS AND USES THEREFOR UNIVERSITY OF CANBERRA (AU) 2016-03-03 WO disclosed
US-20160052865-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS ORYZON GENOMICS S.A. 2016-02-25 US disclosed
US-9006449-B2 Cyclopropylamine derivatives useful as LSD1 inhibitors ORYZON GENOMICS, S.A. (ES) 2015-04-14 US disclosed
WO-2014205511-A1 METHODS AND COMPOSITIONS FOR MODULATING CANCER STEM CELLS UNIVERSITY OF CANBERRA (AU) 2014-12-31 WO disclosed
US-20130197013-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS ORYZON GENOMICS S.A. (ES) 2013-08-01 US disclosed
EP-2598480-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS Oryzon Genomics, S.A. (ES) 2013-06-05 EP disclosed
WO-2012013727-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS ORYZON GENOMICS S.A. (ES) 2012-02-02 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 (7 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-20220389478-A1 METHODS TO DETERMINE KDM1A TARGET ENGAGEMENT AND CHEMOPROBES USEFUL THEREFOR KDM1B, KDM1A, KDM7A KDM1A 2/4885GRIA2 2646/4885KCNH2 2570/4885
US-20210186905-A1 ENHANCING T-CELL FUNCTION AND TREATING A T-CELL DYSFUNCTIONAL DISORDER WITH A COMBINATION OF AN LSD INHIBITOR AND A PD-1 BINDING ANTAGONIST PDCD1, CD274, PDCD1LG2 KDM1A 8/4885GRIA2 3014/4885KCNH2 1947/4885
US-12195783-B2 Methods to determine KDM1A target engagement and chemoprobes useful therefor KDM1B, KDM1A, KDM7A KDM1A 2/4885GRIA2 2646/4885KCNH2 2570/4885
US-20210121496-A1 METHODS AND COMPOSITIONS FOR MODULATING CANCER STEM CELLS BMI1, KDM1B, KDM6B KDM1A 6/4885GRIA2 3200/4885KCNH2 4016/4885
US-20160052865-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS KDM1B, KDM1A, KDM3A KDM1A 2/4885GRIA2 620/4885KCNH2 1391/4885
US-20130197013-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS LSD1 INHIBITORS KDM1B, KDM1A, KDM3A KDM1A 2/4885GRIA2 620/4885KCNH2 1391/4885
US-11034991-B2 Methods to determine KDM1A target engagement and chemoprobes useful therefor KDM1B, KDM1A, KDM7A KDM1A 2/4885GRIA2 2646/4885KCNH2 2570/4885

“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.