SCHEMBL935060

SCHEMBL935060

CCOC(=O)CCN1CCCC(C(=O)OCC)C1

nearest known ligand 0.63

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.60
KDM4E B2RXH2 4/20 0.60
MAPT P10636 1/20 0.60
L3MBTL1 Q9Y468 1/20 0.60
LMNA P02545 1/20 0.58
MEN1 O00255 1/20 0.57
NPC1 O15118 1/20 0.57
RAB9A P51151 1/20 0.57
KMT2A Q03164 1/20 0.57
POLB P06746 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
TDP1 Q9NUW8 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
SCHEMBL8555290 0.91 LMNA (0.51) ALDH1A1KDM4EMAPTL3MBTL1LMNA
SCHEMBL6667435 0.90 KDM4E (0.53) ALDH1A1KDM4EMAPTL3MBTL1LMNA
SCHEMBL4517151 0.88 ALDH1A1 (0.63) ALDH1A1KDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL4513801 0.88 ALDH1A1 (0.63) ALDH1A1KDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL8872114 0.87 KDM4E (0.66) ALDH1A1KDM4EL3MBTL1LMNAMEN1
SCHEMBL7925245 0.87 ALDH1A1 (0.62) ALDH1A1KDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL4521072 0.87 ALDH1A1 (0.62) ALDH1A1KDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL4514426 0.87 ALDH1A1 (0.62) ALDH1A1KDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL205046 0.85 ALDH1A1 (0.60) ALDH1A1KDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL9342470 0.85 KDM4E (0.60) ALDH1A1KDM4ESMN1; SMN2TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9983218-B2 Indole and indoline derivatives and methods of use thereof ABBVIE INC. (US) 2018-05-29 US disclosed
US-20180024144-A1 INDOLE AND INDOLINE DERIVATIVES AND METHODS OF USE THEREOF ABBVIE INC. (US) 2018-01-25 US disclosed
US-9625475-B2 Indole and indoline derivatives and methods of use thereof ABBVIE INC. (US) 2017-04-18 US disclosed
US-20150353550-A1 INDOLE AND INDOLINE DERIVATIVES AND METHODS OF USE THEREOF ABBVIE INC (US) 2015-12-10 US disclosed
US-9063126-B2 Indole and indoline derivatives and methods of use thereof ABBVIE INC. (US) 2015-06-23 US disclosed
EP-2516440-B1 BRIDGEHEAD AMINE RING-FUSED INDOLES AND INDOLINES USEFUL TO TREAT NEURODEGENERATIVE AND NEUROPSYCHIATRIC DISORDERS ABBVIE INC (US) 2014-07-23 EP disclosed
US-8524703-B2 Bridgehead amine ring-fused indoles and indolines ABBVIE INC. (US) 2013-09-03 US disclosed
EP-2516440-A1 BRIDGEHEAD AMINE RING -FUSED INDOLES AND INDOLINES USEFUL TO TREAT NEURODEGENERATIVE AND NEUROPSYCHIATRY DISORDERS Abbott Laboratories (US) 2012-10-31 EP disclosed
EP-2344505-A2 INDOLE AND INDOLINE DERIVATIVES AND METHODS OF USE THEREOF Abbott Laboratories (US) 2011-07-20 EP disclosed
WO-2011075487-A1 BRIDGEHEAD AMINE RING -FUSED INDOLES AND INDOLINES USEFUL TO TREAT NEURODEGENERATIVE AND NEUROPSYCHIATRY DISORDERS ABBOTT LABORATORIES (US) 2011-06-23 WO disclosed
US-7189852-B2 Preparing renzapride (hydrochloride) on a laboratory or industrial scale by a simplified process of forming the acyl chloride derivative of 2-(methoxy),3-acyamino,5-chlorobenzoic acid by reacting oxalyl or thionyl chloride in a solvent, e.g. dimethylformamide; coupling with 1-diazabicylo(3.3.1)nonane ALIZYME THERAPEUTICS LIMITED (GB) 2007-03-13 US disclosed
EP-1664048-A2 PROCESS FOR THE PREPARATION OF RENZAPRIDE AND INTERMEDIATES THEREOF Alizyme Therapeutics Limited (GB) 2006-06-07 EP disclosed
US-20050137225-A1 Aza-bridged bicyclic amine derivatives for use as novel cholinergic receptor ligands KOHN HAROLD (US) 2005-06-23 US disclosed
US-6875774-B2 Aza-bridged bicyclic amine derivatives for use as novel cholinergic receptor ligands THE UNIVERSITY OF NORTH CAROLINA (US) 2005-04-05 US disclosed
WO-2005023808-A2 PROCESS FOR THE PREPARATION OF RENZAPRIDE AND INTERMEDIATES THEREOF ALIZYME THERAPEUTICS LIMITED (GB) 2005-03-17 WO disclosed
WO-2005023808-A2 PROCESS FOR THE PREPARATION OF RENZAPRIDE AND INTERMEDIATES THEREOF ALIZYME THERAPEUTICS LIMITED (GB) 2005-03-17 WO disclosed
WO-2004013143-A2 AZA-BRIDGED BICYCLIC AMINE DERIVATIVES FOR USE AS NOVEL CHOLINERGIC RECEPTOR LIGANDS UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2004-02-12 WO disclosed
US-20040029911-A1 Aza-bridged bicyclic amine derivatives for use as novel cholinergic receptor ligands NORTH CAROLINA, UNIVERSITY OF, THE 2004-02-12 US disclosed
EP-0337547-B1 Spirocyclic compounds incorporating five-membered rings with two heteroatoms MERCK SHARP & DOHME (GB) 1994-03-02 EP disclosed
EP-0337547-A1 Spirocyclic compounds incorporating five-membered rings with two heteroatoms MERCK SHARP & DOHME LTD. (GB) 1989-10-18 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 (4 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-20050137225-A1 Aza-bridged bicyclic amine derivatives for use as novel cholinergic receptor ligands CHRNA5, CHRNG, CHRNA4 ALDH1A1 1433/4885KDM4E 706/4885MAPT 1737/4885
US-20180024144-A1 INDOLE AND INDOLINE DERIVATIVES AND METHODS OF USE THEREOF IDO1, IDO2, TPH1 ALDH1A1 1307/4885KDM4E 1720/4885MAPT 1916/4885
US-20040029911-A1 Aza-bridged bicyclic amine derivatives for use as novel cholinergic receptor ligands CHRNA5, CHRNG, CHRNA4 ALDH1A1 1433/4885KDM4E 706/4885MAPT 1737/4885
US-20150353550-A1 INDOLE AND INDOLINE DERIVATIVES AND METHODS OF USE THEREOF IDO1, IDO2, TPH1 ALDH1A1 1307/4885KDM4E 1720/4885MAPT 1916/4885

“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.