SCHEMBL256566

SCHEMBL256566

c1cncc(N2CCOCC2)c1

nearest known ligand 0.62

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CHRNB2 P17787 5/20 0.59
CHRNA4 P43681 5/20 0.59
LMNA P02545 1/20 0.59
PLOD2 O00469 1/20 0.56
PLOD3 O60568 1/20 0.56
PLOD1 Q02809 1/20 0.56
TP53 P04637 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
CHRNA7 P36544 1/20 0.51
MEN1 O00255 1/20 0.48
NPC1 O15118 1/20 0.48
ALDH1A1 P00352 1/20 0.48
CYP1A2 P05177 1/20 0.48
MAPT P10636 1/20 0.48
HTT P42858 1/20 0.48
RAB9A P51151 1/20 0.48
KMT2A Q03164 1/20 0.48

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
SCHEMBL29442130 1.00 CHRNB2 (0.59) CHRNB2CHRNA4LMNAPLOD2PLOD3
SCHEMBL4350327 0.98 LMNA (0.62) CHRNB2CHRNA4LMNAPLOD2PLOD3
SCHEMBL28722657 0.85 PLOD2 (0.57) CHRNB2CHRNA4PLOD2PLOD3PLOD1
SCHEMBL28139563 0.84 CYP3A4 (0.55) CHRNB2CHRNA4PLOD2PLOD3PLOD1
SCHEMBL28288593 0.84 PLOD2 (0.47) CHRNB2CHRNA4LMNAPLOD2PLOD3
SCHEMBL2376409 0.83 AKR1C3 (0.57) CHRNB2CHRNA4PLOD2PLOD3PLOD1
SCHEMBL11544331 0.82 CHRNB2 (0.76) CHRNB2CHRNA4CHRNA7
SCHEMBL29959593 0.82 CHRNB2 (0.76) CHRNB2CHRNA4CHRNA7
SCHEMBL161236 0.82 CHRNB2 (0.76) CHRNB2CHRNA4CHRNA7
SCHEMBL16437214 0.81 TRPV6 (0.60) CHRNB2CHRNA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7442800-B2 Nucleophilic heterocyclic carbene derivatives of Pd(acac)2 for cross-coupling reactions PROMERUS LLC (US) 2008-10-28 US claimed
CN-101184711-A Nucleophilic heterocyclic carbene derivatives of pd(acac)2 for cross-coupling reactions PROMERUS LLC (US) 2008-05-21 CN claimed
EP-1885669-A1 NUCLEOPHILIC HETEROCYCLIC CARBENE DERIVATIVES OF PD(ACAC)2 FOR CROSS-COUPLING REACTIONS Promerus LLC (US) 2008-02-13 EP claimed
US-20060287544-A1 Nucleophilic heterocyclic carbene derivatives of Pd(acac)2 for cross-coupling reactions PROMERUS LLC (US) 2006-12-21 US claimed
WO-2006128097-A1 NUCLEOPHILIC HETEROCYCLIC CARBENE DERIVATIVES OF PD(ACAC)2 FOR CROSS-COUPLING REACTIONS PROMERUS LLC (US) 2006-11-30 WO claimed
US-12392042-B2 Alternating current (AC) transition-metal catalysis YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2025-08-19 US disclosed
CN-119371410-A Chromone spiro compound and preparation method and application thereof 中国药科大学 2025-01-28 CN disclosed
US-20240327410-A1 Monoacylglycerol Lipase Modulators JANSSEN PHARMACEUTICA NV (BE) 2024-10-03 US disclosed
US-12036208-B2 Methods for treating neurodegenerative disorders ALZHEON, INC. (US) 2024-07-16 US disclosed
US-11993601-B2 Monoacylglycerol lipase modulators JANSSEN PHARMACEUTICA NV 2024-05-28 US disclosed
US-11912708-B2 Macrocyclic heterocycles and uses thereof KUMQUAT BIOSCIENCES INC. (US) 2024-02-27 US disclosed
US-20230407492-A1 ALTERNATING CURRENT (AC) TRANSITION-METAL CATALYSIS YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2023-12-21 US disclosed
WO-2005055953-A2 METHODS OF PREVENTING AND TREATING GASTROINTESTINAL DYSFUNCTION ADOLOR CORPORATION (US) 2005-06-23 WO disclosed
WO-2005056011-A1 METHODS OF PREVENTING AND TREATING NON-OPIOID INDUCED GASTROINTESTINAL DYSFUNCTION ADOLOR CORPORATION (US) 2005-06-23 WO disclosed
US-20050124657-A1 Administering aryl piperidine compound before surgery to treat gastrointestinal disorders and to relieve stress associated with surgery MERCK SHARP & DOHME LLC 2005-06-09 US disclosed
WO-2004082623-A2 SUBSTITUTED PIPERIDINE COMPOUNDS ADOLOR CORPORATION (US) 2004-09-30 WO disclosed
US-20040186135-A1 Substituted piperidine compounds CUBIST PHARMACEUTICALS, INC. 2004-09-23 US disclosed
EP-1354887-A1 Ligands for metals and improved metal-catalyzed processes based thereon Massachusetts Insitute of Technology (US) 2003-10-22 EP disclosed
EP-1097158-A2 LIGANDS FOR METALS AND METAL-CATALYZED PROCESSES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2001-05-09 EP disclosed
WO-2000002887-A2 LIGANDS FOR METALS AND METAL-CATALYZED PROCESSES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2000-01-20 WO 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-20040186135-A1 Substituted piperidine compounds OPRK1, OPRD1, OPRM1 CHRNB2 274/4885CHRNA4 78/4885LMNA 4262/4885
US-11912708-B2 Macrocyclic heterocycles and uses thereof HRAS, KRAS, TP53 CHRNB2 4663/4885CHRNA4 4859/4885LMNA 2455/4885
US-12036208-B2 Methods for treating neurodegenerative disorders NLN, CLN6, SNCA CHRNB2 67/4885CHRNA4 127/4885LMNA 542/4885
US-20050124657-A1 Administering aryl piperidine compound before surgery to treat gastrointestinal disorders and to relieve stress associated with surgery PNMT, VIP, PREP CHRNB2 3838/4885CHRNA4 2129/4885LMNA 4388/4885
US-11993601-B2 Monoacylglycerol lipase modulators MGLL, LPL, PNLIP CHRNB2 388/4885CHRNA4 459/4885LMNA 1845/4885
US-20060287544-A1 Nucleophilic heterocyclic carbene derivatives of Pd(acac)2 for cross-coupling reactions NDC1, DDC, PDCD1LG2 CHRNB2 1610/4885CHRNA4 2812/4885LMNA 4016/4885
US-20240327410-A1 Monoacylglycerol Lipase Modulators MGLL, LPL, PNLIP CHRNB2 388/4885CHRNA4 459/4885LMNA 1845/4885

“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.