SCHEMBL880655

SCHEMBL880655

CN(C)C(=O)N1CCC(N)CC1

nearest known ligand 0.55

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.53
MEN1 O00255 2/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
MAPT P10636 3/20 0.51
GAA P10253 1/20 0.47
HSD17B10 Q99714 1/20 0.46
GNAI3 P08754 1/20 0.43
GNAO1 P09471 1/20 0.43
GNAI1 P63096 1/20 0.43
NPSR1 Q6W5P4 1/20 0.42
ALDH1A1 P00352 1/20 0.36
L3MBTL3 Q96JM7 1/20 0.35
DRD2 P14416 1/20 0.35
DRD3 P35462 1/20 0.35
RXFP1 Q9HBX9 1/20 0.35

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
Hydrochloric Acid SCHEMBL853922 0.98 KMT2A (0.51) KMT2AMEN1SMN1; SMN2MAPTGAA
SCHEMBL2687539 0.88 MEN1 (0.46) KMT2AMEN1SMN1; SMN2MAPTGAA
SCHEMBL25306284 0.88 MEN1 (0.46) KMT2AMEN1SMN1; SMN2MAPTGAA
SCHEMBL14275538 0.88 MEN1 (0.46) KMT2AMEN1SMN1; SMN2MAPTGAA
Hydrochloric Acid SCHEMBL31727051 0.86 MEN1 (0.45) KMT2AMEN1SMN1; SMN2MAPTGAA
SCHEMBL6586735 0.85 MAPT (0.44) KMT2AMEN1SMN1; SMN2MAPTGAA
SCHEMBL616596 0.82 KMT2A (0.56) KMT2AMEN1SMN1; SMN2MAPTGAA
SCHEMBL3807935 0.81 GNAI3 (0.42) KMT2AMEN1SMN1; SMN2MAPTGAA
SCHEMBL22549806 0.80 GNAI3 (0.39) KMT2AMEN1SMN1; SMN2MAPTGAA
SCHEMBL10274875 0.80 MEN1 (0.55) KMT2AMEN1SMN1; SMN2MAPTGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240246964-A1 SUBSTITUTED 1-ARYL-1’-HETEROARYL COMPOUNDS, SUBSTITUTED 1,1’-BIHETEROARYL COMPOUNDS, AND METHODS USING SAME ARBUTUS BIOPHARMA CORPORATION (CA) 2024-07-25 US disclosed
EP-4313968-A2 SUBSTITUTED 1-ARYL-1'-HETEROARYL COMPOUNDS, SUBSTITUTED 1,1'-BIHETEROARYL COMPOUNDS, AND METHODS USING SAME Arbutus Biopharma Corporation (CA) 2024-02-07 EP disclosed
WO-2022208269-A2 SUBSTITUTED 1-ARYL-1'-HETEROARYL COMPOUNDS, SUBSTITUTED 1,1'-BIHETEROARYL COMPOUNDS, AND METHODS USING SAME ARBUTUS BIOPHARMA CORPORATION (CA) 2022-10-06 WO disclosed
EP-3027604-B1 NOVEL QUINAZOLINONES AS BROMODOMAIN INHIBITORS ZENITH EPIGENETICS LTD (CA) 2019-02-20 EP disclosed
US-20180092924-A1 NOVEL QUINAZOLINONES AS BROMODOMAIN INHIBITORS RVX THERAPEUTICS INC. (CA) 2018-04-05 US disclosed
US-9855271-B2 Quinazolinones as bromodomain inhibitors ZENITH EPIGENETICS LTD. (CA) 2018-01-02 US disclosed
US-20160193218-A1 NOVEL QUINAZOLINONES AS BROMODOMAIN INHIBITORS ZENITH EPIGENETICS LTD. (CA) 2016-07-07 US disclosed
US-8901315-B2 Thienopyrazole derivative having PDE7 inhibitory activity DAIICHI SANKYO COMPANY, LIMITED (JP) 2014-12-02 US disclosed
US-8901315-B2 Thienopyrazole derivative having PDE7 inhibitory activity DAIICHI SANKYO COMPANY, LIMITED (JP) 2014-12-02 US disclosed
US-20140073799-A1 THIENOPYRAZOLE DERIVATIVE HAVING PDE7 INHIBITORY ACTIVITY DAIICHI SANKYO COMPANY, LIMITED (JP) 2014-03-13 US disclosed
US-20120114739-A1 PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS MERCK SHARP & DOHME LLC 2012-05-10 US disclosed
EP-2433943-A1 Thienopyrazole derivatives having PDE7 inhibitory activity Daiichi Sankyo Company, Limited (JP) 2012-03-28 EP disclosed
US-20110166343-A1 THIENOPYRAZOLE DERIVATIVE HAVING PDE7 INHIBITORY ACTIVITY DAIICHI SANKYO COMPANY, LIMITED (JP) 2011-07-07 US disclosed
US-20110166343-A1 THIENOPYRAZOLE DERIVATIVE HAVING PDE7 INHIBITORY ACTIVITY DAIICHI SANKYO COMPANY, LIMITED (JP) 2011-07-07 US disclosed
US-7932250-B2 Thienopyrazole derivative having PDE7 inhibitory activity DAIICHI SANKYO COMPANY, LIMITED (JP) 2011-04-26 US disclosed
US-7932250-B2 Thienopyrazole derivative having PDE7 inhibitory activity DAIICHI SANKYO COMPANY, LIMITED (JP) 2011-04-26 US disclosed
US-20090131413-A1 Thienopyrazole Derivative Having PDE7 Inhibitory Activity ASUBIO PHARMA CO., LTD. (JP) 2009-05-21 US disclosed
US-20090131413-A1 Thienopyrazole Derivative Having PDE7 Inhibitory Activity ASUBIO PHARMA CO., LTD. (JP) 2009-05-21 US disclosed
US-7332509-B2 Heterocyclic amides, a process for their preparation, compositions comprising them and their use MERIAL LIMITED (US) 2008-02-19 US disclosed
EP-1775298-A1 THIENOPYRAZOLE DERIVATIVE HAVING PDE7 INHIBITORY ACTIVITY Daiichi Asubio Pharma Co., Ltd. (JP) 2007-04-18 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 (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-20140073799-A1 THIENOPYRAZOLE DERIVATIVE HAVING PDE7 INHIBITORY ACTIVITY PDE7A, PDE7B, PDE3B KMT2A 3266/4885MEN1 3519/4885SMN1; SMN2 4191/4885
US-20110166343-A1 THIENOPYRAZOLE DERIVATIVE HAVING PDE7 INHIBITORY ACTIVITY PDE7A, PDE7B, PDE3B KMT2A 3266/4885MEN1 3519/4885SMN1; SMN2 4191/4885
US-20090131413-A1 Thienopyrazole Derivative Having PDE7 Inhibitory Activity PDE7A, PDE7B, PDE3B KMT2A 3266/4885MEN1 3519/4885SMN1; SMN2 4191/4885
US-20180092924-A1 NOVEL QUINAZOLINONES AS BROMODOMAIN INHIBITORS BRD4, BRD3, BRDT KMT2A 825/4885MEN1 3523/4885SMN1; SMN2 4266/4885
US-20240246964-A1 SUBSTITUTED 1-ARYL-1’-HETEROARYL COMPOUNDS, SUBSTITUTED 1,1’-BIHETEROARYL COMPOUNDS, AND METHODS USING SAME HAVCR2, HDGF, HCCS KMT2A 933/4885MEN1 1254/4885SMN1; SMN2 4097/4885
US-20160193218-A1 NOVEL QUINAZOLINONES AS BROMODOMAIN INHIBITORS BRD4, BRD3, BRDT KMT2A 825/4885MEN1 3523/4885SMN1; SMN2 4266/4885
US-20120114739-A1 PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS MTOR, RICTOR, RPTOR KMT2A 2825/4885MEN1 1398/4885SMN1; SMN2 1798/4885

“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.