SCHEMBL15766945

SCHEMBL15766945

CC[C@@]1(N)C[C@@H]1c1ccc(OC(F)(F)F)cc1

nearest known ligand 0.97

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
KDM1A O60341 20/20 0.97
RCOR1 Q9UKL0 12/20 0.97
MAOA P21397 8/20 0.57
MAOB P27338 8/20 0.57

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
SCHEMBL15787696 1.00 KDM1A (0.97) KDM1ARCOR1MAOAMAOB
SCHEMBL15766948 1.00 KDM1A (0.97) KDM1ARCOR1MAOAMAOB
Hydrochloric Acid SCHEMBL17223489 0.98 KDM1A (1.00) KDM1ARCOR1MAOAMAOB
Hydrochloric Acid SCHEMBL17223491 0.98 KDM1A (1.00) KDM1ARCOR1MAOAMAOB
SCHEMBL17231234 0.81 KDM1A (0.66) KDM1ARCOR1MAOAMAOB
SCHEMBL15787380 0.80 KDM1A (0.97) KDM1ARCOR1MAOAMAOB
SCHEMBL15767422 0.80 KDM1A (0.97) KDM1ARCOR1MAOAMAOB
SCHEMBL15767423 0.80 KDM1A (0.97) KDM1ARCOR1MAOAMAOB
Hydrochloric Acid SCHEMBL17223530 0.78 KDM1A (1.00) KDM1ARCOR1MAOAMAOB
Hydrochloric Acid SCHEMBL22318600 0.78 KDM1A (1.00) KDM1ARCOR1MAOAMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2928457-B1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A ST EUROPEO DI ONCOLOGIA S R L (IT) 2020-08-12 EP claimed
US-9944589-B2 Cycloproplyamine derivatives useful as inhibitors of histone demethylases KDM1A ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2018-04-17 US claimed
US-20150315126-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2015-11-05 US claimed
EP-2928457-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A Istituto Europeo di Oncologia S.r.l. (IT) 2015-10-14 EP claimed
WO-2014086790-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2014-06-12 WO claimed
EP-2740474-A1 Cyclopropylamine derivatives useful as inhibitors of histone demethylases kdm1a Instituto Europeo di Oncologia S.r.l. (IT) 2014-06-11 EP 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
US-20210100800-A1 USE OF A COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH P21 ACTIVATORS IN THE TREATMENT OF CANCER INSTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2021-04-08 US disclosed
EP-2928457-B1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A ST EUROPEO DI ONCOLOGIA S R L (IT) 2020-08-12 EP disclosed
WO-2018197583-A1 USE OF A COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH P21 ACTIVATORS IN THE TREATMENT OF CANCER ISTITUTO EUROPEO DI ONCOLOGIA (IT) 2018-11-01 WO disclosed
US-20180311245-A1 USE OF A COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH CDK2 INHIBITORS IN THE TREATMENT OF CANCER RASNA THERAPEUTICS LTD (GB) 2018-11-01 US disclosed
US-9944589-B2 Cycloproplyamine derivatives useful as inhibitors of histone demethylases KDM1A ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2018-04-17 US disclosed
WO-2017097865-A9 COMBINATION OF CALORIC RESTRICTION (CR) OR IGF1/INSULIN RECEPTOR INHIBITOR WITH LSD1 INHIBITOR ISTITUTO EUROPEO DI ONCOLOGIA (IT) 2017-08-31 WO disclosed
WO-2017097865-A1 COMBINATION OF CALORIC RESTRICTION (CR) OR IGF1/INSULIN RECEPTOR INHIBITOR WITH LSD1 INHIBITOR ISTITUTO EUROPEO DI ONCOLOGIA (IT) 2017-06-15 WO disclosed
US-20150315126-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2015-11-05 US disclosed
EP-2928457-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A Istituto Europeo di Oncologia S.r.l. (IT) 2015-10-14 EP disclosed
WO-2014086790-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A ISTITUTO EUROPEO DI ONCOLOGIA S.R.L. (IT) 2014-06-12 WO disclosed
EP-2740474-A1 Cyclopropylamine derivatives useful as inhibitors of histone demethylases kdm1a Instituto Europeo di Oncologia S.r.l. (IT) 2014-06-11 EP 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-20180311245-A1 USE OF A COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH CDK2 INHIBITORS IN THE TREATMENT OF CANCER CDK2, EZH2, CDK6 KDM1A 16/4885RCOR1 230/4885MAOA 1955/4885
US-20150315126-A1 CYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A KDM1A, KDM1B, KDM2A KDM1A 1/4885RCOR1 152/4885MAOA 790/4885
US-20210100800-A1 USE OF A COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH P21 ACTIVATORS IN THE TREATMENT OF CANCER CDK6, KDM1B, KDM6B KDM1A 7/4885RCOR1 144/4885MAOA 1440/4885
US-11918580-B2 Use of a combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer CDK6, KDM1B, KDM6B KDM1A 7/4885RCOR1 144/4885MAOA 1440/4885
US-12576083-B2 Combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer CDK3, CDKN1A, CDKL3 KDM1A 26/4885RCOR1 587/4885MAOA 3373/4885
US-20240342178-A1 COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH P21 ACTIVATORS IN THE TREATMENT OF CANCER KDM1B, DOT1L, EZH2 KDM1A 10/4885RCOR1 106/4885MAOA 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.