SCHEMBL17287948

SCHEMBL17287948

N[C@@H]1C[C@H]1c1ccc(NC(=O)Cc2ccccc2)cc1

nearest known ligand 0.72

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
KDM1A O60341 16/20 0.72
MAOA P21397 11/20 0.66
MAOB P27338 11/20 0.66
RCOR1 Q9UKL0 8/20 0.64
KDM1B Q8NB78 1/20 0.63
EPHX2 P34913 1/20 0.61
CA12 O43570 1/20 0.56
CA1 P00915 1/20 0.56
CA2 P00918 1/20 0.56
CA5A P35218 1/20 0.56
CA7 P43166 1/20 0.56
CA9 Q16790 1/20 0.56
CA14 Q9ULX7 1/20 0.56
CA5B Q9Y2D0 1/20 0.56

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
SCHEMBL2556963 1.00 KDM1A (0.72) KDM1AMAOAMAOBRCOR1KDM1B
SCHEMBL2561991 0.84 NR1H4 (0.63) KDM1AMAOAMAOBRCOR1KDM1B
SCHEMBL30816610 0.84 NR1H4 (0.63) KDM1AMAOAMAOBRCOR1KDM1B
Hydrochloric Acid SCHEMBL26977347 0.83 NR1H4 (0.62) KDM1AMAOAMAOBRCOR1KDM1B
Hydrochloric Acid SCHEMBL30745120 0.83 NR1H4 (0.62) KDM1AMAOAMAOBRCOR1KDM1B
SCHEMBL15780115 0.82 EPHX2 (0.56) KDM1AEPHX2
SCHEMBL2561238 0.80 KDM1A (1.00) KDM1AMAOAMAOBRCOR1KDM1B
SCHEMBL30816679 0.80 KDM1A (1.00) KDM1AMAOAMAOBRCOR1KDM1B
SCHEMBL30816658 0.79 KMT2A (0.57) KDM1AMAOAMAOBRCOR1KDM1B
SCHEMBL2563538 0.79 KMT2A (0.57) KDM1AMAOAMAOBRCOR1KDM1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2560949-B1 TRANYLCYPROMINE DERIVATIVES AS INHIBITORS OF HISTONE DEMETHYLASE LSD1 AND/OR LSD2 UNIVERSIT DEGLI STUDI DI ROMA LA SAPIENZA (IT) 2015-12-02 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

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-11918580-B2 Use of a combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer CDK6, KDM1B, KDM6B KDM1A 7/4885MAOA 1440/4885MAOB 1514/4885
US-12576083-B2 Combinational therapy of LSD1 inhibitors with P21 activators in the treatment of cancer CDK3, CDKN1A, CDKL3 KDM1A 26/4885MAOA 3373/4885MAOB 2453/4885
US-20240342178-A1 COMBINATIONAL THERAPY OF LSD1 INHIBITORS WITH P21 ACTIVATORS IN THE TREATMENT OF CANCER KDM1B, DOT1L, EZH2 KDM1A 10/4885MAOA 2144/4885MAOB 2291/4885

“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.