SCHEMBL3222136

SCHEMBL3222136

NC(=O)N1CCN(Cc2ccccc2)CC1

nearest known ligand 0.68

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.66
LMNA P02545 4/20 0.66
SMN1; SMN2 Q16637 4/20 0.66
KMT2A Q03164 3/20 0.66
MAPK1 P28482 2/20 0.65
SIGMAR1 Q99720 1/20 0.64
KDM4E B2RXH2 2/20 0.64
MEN1 O00255 2/20 0.62
FAAH O00519 1/20 0.62
TSHR P16473 1/20 0.62
L3MBTL1 Q9Y468 1/20 0.62
PHGDH O43175 1/20 0.60
MGLL Q99685 1/20 0.60
MAPT P10636 1/20 0.59
HTT P42858 2/20 0.57
HPGD P15428 1/20 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
SCHEMBL27791391 0.85 ALDH1A1 (0.70) ALDH1A1LMNASMN1; SMN2KMT2AMAPK1
SCHEMBL2850013 0.85 ALDH1A1 (0.70) ALDH1A1LMNASMN1; SMN2KMT2AMAPK1
SCHEMBL10825084 0.85 ALDH1A1 (0.70) ALDH1A1LMNASMN1; SMN2KMT2AMAPK1
SCHEMBL2784148 0.84 AKR1C3 (0.63) ALDH1A1KMT2ASIGMAR1KDM4EMEN1
SCHEMBL611401 0.84 ALDH1A1 (0.68) ALDH1A1LMNASMN1; SMN2KMT2AMAPK1
SCHEMBL15224104 0.83 FAAH (0.60) ALDH1A1LMNASMN1; SMN2KMT2AMAPK1
Diphenylmethane SCHEMBL28522550 0.83 LTA4H (0.64) ALDH1A1LMNASMN1; SMN2KMT2AMAPK1
SCHEMBL7142559 0.83 CYP2D6 (0.69) ALDH1A1LMNASMN1; SMN2KMT2AMAPK1
SCHEMBL544161 0.83 SIGMAR1 (0.68) ALDH1A1LMNASMN1; SMN2KMT2AMAPK1
SCHEMBL5524549 0.83 MEN1 (0.69) KMT2ASIGMAR1MEN1FAAHTSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2142516-B1 PYRIMIDINE HYDRAZIDE COMPOUNDS AS PGDS INHIBITORS SANOFI SA (FR) 2012-12-26 EP claimed
US-8258130-B2 Pyrimidine hydrazide compounds as PGDS inhibitors SANOFI (FR) 2012-09-04 US claimed
US-20100048568-A1 PYRIMIDINE HYDRAZIDE COMPOUNDS AS PGDS INHIBITORS SANOFI-AVENTIS (FR) 2010-02-25 US claimed
EP-2142516-A1 PYRIMIDINE HYDRAZIDE COMPOUNDS AS PGDS INHIBITORS Sanofi-Aventis (FR) 2010-01-13 EP claimed
EP-1725238-A4 M 3 MUSCARINIC ACETYLCHOLINE RECEPTOR ANTAGONISTS GLAXO GROUP LTD (GB) 2009-04-01 EP claimed
WO-2008121670-A1 PYRIMIDINE HYDRAZIDE COMPOUNDS AS PGDS INHIBITORS SANOFI-AVENTIS (FR) 2008-10-09 WO claimed
EP-1725238-A2 M 3 MUSCARINIC ACETYLCHOLINE RECEPTOR ANTAGONISTS GLAXO GROUP LIMITED (GB) 2006-11-29 EP claimed
WO-2005094251-A2 M3MUSCARINIC ACETYLCHOLINE RECEPTOR ANTAGONISTS GLAXO GROUP LIMITED (GB) 2005-10-13 WO claimed
WO-2001068645-A2 N-CYANOMETHYLCARBOXAMIDES AND THEIR USE AS PROTEASE INHIBITORS AXYS PHARMACEUTICALS, INC. (US) 2001-09-20 WO claimed
EP-0588655-B1 Amidinophenol derivatives ONO PHARMACEUTICAL CO (JP) 1996-12-04 EP claimed
EP-4683909-A2 ATM KINASE INHIBITORS Eberhard Karls Universität Tübingen (DE) 2026-01-28 EP disclosed
US-20260015328-A1 ATM KINASE INHIBITORS EBERHARD KARLS UNIVERSITÄT TÜBINGEN (DE) 2026-01-15 US disclosed
WO-2024194460-A2 ATM KINASE INHIBITORS EBERHARD KARLS UNIVERSITAET TUEBINGEN MEDIZINISCHE FAKULTAET (DE) 2024-09-26 WO disclosed
EP-4434972-A1 ATM KINASE INHIBITORS Eberhard-Karls-Universität Tübingen (DE) 2024-09-25 EP disclosed
US-9309224-B2 N-acyl-N′-(pyridin-2-yl) ureas and analogs exhibiting anti-cancer and anti-proliferative activities DECIPHERA PHARMACEUTICALS, LLC. (US) 2016-04-12 US disclosed
US-5643908-A ANGIOGENESIS INHIBITOR, ANTITUMOR SANKYO COMPANY, LIMITED (JP) 1997-07-01 US disclosed
EP-0759918-A1 PIPERAZINE, PIPERIDINE AND TETRAHYDROPYRIDINE DERIVATIVES OF INDOL-3-YLALKYL AS 5-HT1D-ALPHA AGONISTS MERCK SHARP & DOHME LTD. (GB) 1997-03-05 EP disclosed
WO-1996004269-A1 INDOLINE AND AZAINDOLINE DERIVATIVES AS 5-HT1D ALPHA RECEPTOR AGONISTS MERCK SHARP & DOHME LIMITED (GB) 1996-02-15 WO disclosed
WO-1995032196-A1 PIPERAZINE, PIPERIDINE AND TETRAHYDROPYRIDINE DERIVATIVES OF INDOL-3-YLALKYL AS 5-HT1D-ALPHA AGONISTS MERCK SHARP & DOHME LIMITED (GB) 1995-11-30 WO disclosed
EP-0621270-A1 COLLAGENASE INHIBITOR SANKYO COMPANY LIMITED (JP) 1994-10-26 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 (2 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-20100048568-A1 PYRIMIDINE HYDRAZIDE COMPOUNDS AS PGDS INHIBITORS HRH2, HRH1, HRH4 ALDH1A1 298/4885LMNA 3470/4885SMN1; SMN2 4832/4885
US-20260015328-A1 ATM KINASE INHIBITORS ATM, CHEK2, CHEK1 ALDH1A1 4484/4885LMNA 1399/4885SMN1; SMN2 2346/4885

“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.