SCHEMBL3549500

SCHEMBL3549500

Oc1ccc2[nH]cc(C3CCNCC3)c2c1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.68
CYP3A4 P08684 1/20 0.68
CYP2D6 P10635 1/20 0.68
CYP2C9 P11712 1/20 0.68
THPO P40225 1/20 0.68
HTR2C P28335 2/20 0.62
ADRB2 P07550 1/20 0.62
APP P05067 3/20 0.60
MAPT P10636 1/20 0.56
BLM P54132 1/20 0.56
NPSR1 Q6W5P4 1/20 0.56
NOS3 P29474 1/20 0.51
NOS1 P29475 1/20 0.51
NMT2 O60551 1/20 0.50
NMT1 P30419 1/20 0.50
HTR6 P50406 1/20 0.49
SLC6A4 P31645 1/20 0.48
GABRP O00591 2/20 0.47
GABRD O14764 2/20 0.47
GABRA1 P14867 2/20 0.47

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
Oxalic Acid SCHEMBL6956302 0.93 NPSR1 (0.60) CYP1A2CYP3A4CYP2D6CYP2C9THPO
SCHEMBL18622640 0.86 CYP1A2 (0.69) CYP1A2CYP3A4CYP2D6CYP2C9THPO
SCHEMBL4674995 0.83 CYP2C9 (0.66) CYP1A2CYP3A4CYP2D6CYP2C9THPO
SCHEMBL3546634 0.82 CYP1A2 (0.58) CYP1A2CYP3A4CYP2D6CYP2C9THPO
SCHEMBL2781047 0.81 HTR2C (0.62) HTR2CADRB2APPNOS3NOS1
SCHEMBL2781509 0.81 HTR2C (0.62) HTR2CADRB2APPNMT2NMT1
SCHEMBL7459828 0.81 HTR2C (0.62) CYP1A2CYP3A4CYP2D6CYP2C9THPO
SCHEMBL7482397 0.81 HTR1D (0.68) CYP1A2CYP3A4CYP2D6CYP2C9THPO
SCHEMBL3832948 0.81 HTR2C (0.62) CYP1A2CYP3A4CYP2D6CYP2C9THPO
SCHEMBL30908918 0.81 CYP1A2 (1.00) CYP1A2CYP3A4CYP2D6CYP2C9THPO

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220193082-A1 COMBINATION TREATMENT OF SPECIFIC FORMS OF EPILEPSY ZOGENIX INTERNATIONAL LIMITED (GB) 2022-06-23 US disclosed
US-20170071949-A1 COMBINATION TREATMENT OF SPECIFIC FORMS OF EPILEPSY ZOGENIX INTERNATIONAL LIMITED (GB) 2017-03-16 US disclosed
CN-102796075-B Benzocycloheptenes derivative as well as preparation method and medical application thereof INST PHARM & TOXICOLOGY AMMS 2014-03-12 CN disclosed
CN-101481323-B Benzocycloheptenes derivatives, preparation method and medical application thereof POISON MED INST PLA MED ACAD 2013-11-20 CN disclosed
CN-102796075-A Benzocycloheptenes derivative as well as preparation method and medical application thereof INST PHARM & TOXICOLOGY AMMS 2012-11-28 CN disclosed
WO-2010107605-A1 CGRP RECEPTOR ANTAGONISTS MERCK SHARP & DOHME CORP. (US) 2010-09-23 WO disclosed
US-7741343-B2 6H-oxazolo[4,5 e]indole derivatives as nicotinic acetylcholine receptor ligands and/or serotonergic ligands MERCK PATENT GMBH (DE) 2010-06-22 US disclosed
CN-101481323-A Benzocycloheptenes derivatives, preparation method and medical application thereof POISON MED INST PLA MED ACAD (CN) 2009-07-15 CN disclosed
EP-0958287-B2 SULFAMIDE-METALLOPROTEASE INHIBITORS HOFFMANN LA ROCHE (CH) 2008-04-09 EP disclosed
US-20080051394-A1 6H-Oxazolo[4,5 e]indole derivatives as nicotinic acetylcholine receptor ligands and/or serotonergic ligands SCHIEMANN KAI 2008-02-28 US disclosed
EP-0958287-A1 SULFAMIDE-METALLOPROTEASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 1999-11-24 EP disclosed
EP-0683166-B1 3-Indolylpiperidines MERCK PATENT GMBH (DE) 1998-10-28 EP disclosed
WO-1998032748-A1 SULFAMIDE-METALLOPROTEASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 1998-07-30 WO disclosed
US-5693655-A 3-indolylpiperidines MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1997-12-02 US disclosed
WO-1997038692-A1 BISINDOLES FOR TREATING PAIN OR NOCICEPTION ELI LILLY AND COMPANY (US) 1997-10-23 WO disclosed
CN-1114651-A 3-indolylpiperidine MERCK PATENT GMBH (DE) 1996-01-10 CN disclosed
EP-0683166-A1 3-Indolylpiperidines MERCK PATENT GmbH (DE) 1995-11-22 EP disclosed
CN-85105804-A Contain 1 of 1H-indol-3-yl, 3-dimethyl-1H-purine-2, the preparation method of 6-diketone 1986-10-22 CN disclosed
EP-0177087-A2 1H-Indol-3-yl containing 1,3-dimethyl-1H-purine-2,6-diones JANSSEN PHARMACEUTICA N.V. (BE) 1986-04-09 EP disclosed
US-4548939-A 1H-Indol-3-yl containing 1,3-dimethyl-1H-purine-2,6-diones JANSSEN PHARMACEUTICA N. V. (BE) 1985-10-22 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 (3 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-20080051394-A1 6H-Oxazolo[4,5 e]indole derivatives as nicotinic acetylcholine receptor ligands and/or serotonergic ligands CHRM1, CHRNA5, CHRNA4 CYP1A2 1291/4885CYP3A4 1193/4885CYP2D6 2008/4885
US-20220193082-A1 COMBINATION TREATMENT OF SPECIFIC FORMS OF EPILEPSY HTR2B, HTR3B, HTR5A CYP1A2 346/4885CYP3A4 496/4885CYP2D6 547/4885
US-20170071949-A1 COMBINATION TREATMENT OF SPECIFIC FORMS OF EPILEPSY HTR2B, HTR3B, HTR5A CYP1A2 346/4885CYP3A4 496/4885CYP2D6 547/4885

“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.