SCHEMBL1660396

SCHEMBL1660396

N#CC1CCCCN1c1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
USP30 Q70CQ3 1/20 0.50
AR P10275 1/20 0.50
DPP7 Q9UHL4 3/20 0.44
PREP P48147 2/20 0.41
MBTD1 Q05BQ5 1/20 0.40
L3MBTL3 Q96JM7 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
DPP4 P27487 7/20 0.39
DPP8 Q6V1X1 1/20 0.39
DPP9 Q86TI2 1/20 0.39
MAPT P10636 2/20 0.39
NPSR1 Q6W5P4 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.38
CPT1A P50416 1/20 0.37
SLC18A3 Q16572 1/20 0.37

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
SCHEMBL28414703 0.95 AR (0.55) USP30ARDPP7PREPDPP4
SCHEMBL28210486 0.82 USP30 (0.43) USP30MBTD1L3MBTL3L3MBTL1MAPT
SCHEMBL6674309 0.79 DPP4 (0.45) ARDPP7L3MBTL1DPP4DPP8
SCHEMBL3767117 0.76 KMT2A (0.44) USP30ARMBTD1L3MBTL3L3MBTL1
SCHEMBL3767119 0.76 KMT2A (0.44) USP30ARMBTD1L3MBTL3L3MBTL1
SCHEMBL28851318 0.76 AR (0.40) USP30ARDPP7PREPDPP4
SCHEMBL2926923 0.76 MBTD1 (0.43) USP30MBTD1L3MBTL3L3MBTL1MAPT
SCHEMBL1773499 0.75 USP30 (0.49) USP30ARDPP7DPP4DPP8
SCHEMBL28515773 0.75 DPP4 (0.47) ARDPP7L3MBTL1DPP4DPP8
SCHEMBL138440 0.72 LMNA (0.43) USP30ARMAPTNPSR1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113264881-B Synthetic method of alpha-cyanide 南昌大学 2022-12-02 CN disclosed
CN-113264881-A Synthetic method of alpha-cyanide 南昌大学 2021-08-17 CN disclosed
EP-2488028-B1 SUBSTITUTED PIPERIDINES THAT INCREASE P53 ACTIVITY AND THE USES THEREOF MERCK SHARP & DOHME (US) 2020-08-19 EP disclosed
CN-104945382-B Substituted piperidines that increase p53 activity and uses thereof 默沙东公司 2020-02-07 CN disclosed
US-20140336222-A1 SUBSTITUTED PIPERIDINES THAT INCREASE p53 ACTIVITY AND THE USES THEREOF MERCK SHARP & DOHME (US) 2014-11-13 US disclosed
US-8859776-B2 Substituted piperidines that increase p53 activity and the uses thereof MERCK SHARP & DOHME CORP. (US) 2014-10-14 US disclosed
EP-2488028-A1 SUBSTITUTED PIPERIDINES THAT INCREASE p53 ACTIVITY AND THE USES THEREOF Merck Sharp & Dohme Corp. (US) 2012-08-22 EP disclosed
US-20120208844-A1 SUBSTITUTED PIPERIDINES THAT INCREASE P53 ACTIVITY AND THE USES THEREOF MERCK SHARP & DOHME LLC 2012-08-16 US disclosed
CN-102239158-A Method for preparing a spiroindoline and a precursor thereof GLAXO GROUP LTD 2011-11-09 CN disclosed
EP-2370423-A1 METHOD FOR PREPARING A SPIROINDOLINE AND A PRECURSOR THEREOF Glaxo Group Limited (GB) 2011-10-05 EP disclosed
WO-2010065704-A1 METHOD FOR PREPARING A SPIROINDOLINE AND A PRECURSOR THEREOF GLAXO GROUP LIMITED (GB) 2010-06-10 WO disclosed
CN-1675209-A Dihydropyrazolopyridine compounds MITSUBISHI PHARMA CORP (JP) 2005-09-28 CN disclosed
EP-1174419-B1 A method for producing an alpha-aminonitrile from a tertiary amine and a cyanide through oxidation with oxygen by using a transition metal catalyst UNIV OSAKA (JP) 2004-10-06 EP disclosed
US-6486340-B2 Method for producing an α-aminonitrile from a tertiary anime and a cyanide through oxidation with oxygen by using a transition metal catalyst OSAKA UNIVERSITY (JP) 2002-11-26 US disclosed
US-20020042534-A1 Method for producing an alpha-aminonitrile from a tertiary anime and a cyanide through oxidation with oxygen by using a transition metal catalyst OSAKA UNIVERSITY (JP) 2002-04-11 US disclosed
EP-1174419-A1 A method for producing an alpha-aminonitrile from a tertiary amine and a cyanide through oxidation with oxygen by using a transition metal catalyst OSAKA UNIVERSITY (JP) 2002-01-23 EP disclosed
US-5756748-A ALKYLATING 4-CYANO-4-PHENYLPIPERIDINE, PRECIPITATING AS HYDROCHLORIDE SALT, HYDROLYZING TO ACID, REACTING WITH OXALYL CHLORIDE OR THIONYL CHLORIDE AND ETHYLMETHYLAMINE TO FORM AMIDE ASTRA AB (SE) 1998-05-26 US disclosed
EP-0799203-A1 NEW PROCESS FOR THE PREPARATION OF SAMERIDINE Astra Aktiebolag (SE) 1997-10-08 EP disclosed
WO-1996019453-A1 NEW PROCESS FOR THE PREPARATION OF SAMERIDINE ASTRA AKTIEBOLAG (SE) 1996-06-27 WO disclosed
US-4093620-A Process for producing 2-cyano N-substituted heterocyclic compounds and products produced thereby PHILIP MORRIS INCORPORATED (US) 1978-06-06 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 (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-20140336222-A1 SUBSTITUTED PIPERIDINES THAT INCREASE p53 ACTIVITY AND THE USES THEREOF TP53, TP53BP1, MDM2 USP30 1254/4885AR 2820/4885DPP7 425/4885
US-20120208844-A1 SUBSTITUTED PIPERIDINES THAT INCREASE P53 ACTIVITY AND THE USES THEREOF TP53, MDM2, TP53BP1 USP30 1122/4885AR 2819/4885DPP7 350/4885

“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.