SCHEMBL1012743

SCHEMBL1012743

COC(=O)C1(c2ccccc2)CC2CCC(C1)N2C

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 P23975 1/20 0.48
SLC6A4 P31645 1/20 0.48
SLC6A3 Q01959 1/20 0.48
OPRL1 P41146 8/20 0.47
OPRM1 P35372 7/20 0.47
HTR3E A5X5Y0 1/20 0.47
HTR3B O95264 1/20 0.47
CHRNA7 P36544 1/20 0.47
HTR3A P46098 1/20 0.47
HTR3D Q70Z44 1/20 0.47
HTR3C Q8WXA8 1/20 0.47
HSD11B1 P28845 1/20 0.45
CHRM3 P20309 3/20 0.45
CHRM2 P08172 2/20 0.45
CHRM4 P08173 2/20 0.45
CHRM5 P08912 2/20 0.45
CHRM1 P11229 2/20 0.45
CYP2C9 P11712 2/20 0.44
OPRD1 P41143 1/20 0.44
OPRK1 P41145 1/20 0.44

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
SCHEMBL7464514 1.00 SLC6A2 (0.48) SLC6A2SLC6A4SLC6A3OPRL1OPRM1
SCHEMBL1012066 0.86 SLC6A4 (0.43) SLC6A2SLC6A4SLC6A3OPRM1
SCHEMBL3656139 0.86 ALDH1A1 (0.47) SLC6A2SLC6A4SLC6A3OPRL1OPRM1
SCHEMBL5730907 0.86 OPRM1 (0.40) OPRL1OPRM1HTR3EHTR3BCHRNA7
SCHEMBL7568500 0.86 CYP2D6 (0.48) SLC6A2SLC6A4SLC6A3OPRL1OPRM1
SCHEMBL11173935 0.84 OPRL1 (0.60) SLC6A2SLC6A4SLC6A3OPRL1OPRM1
SCHEMBL11173936 0.84 OPRL1 (0.60) SLC6A2SLC6A4SLC6A3OPRL1OPRM1
SCHEMBL7157429 0.84 OPRK1 (0.46) SLC6A2SLC6A4SLC6A3OPRL1OPRM1
SCHEMBL4591523 0.84 OPRM1 (0.47) SLC6A4SLC6A3OPRL1OPRM1
SCHEMBL8347022 0.83 HRH3 (0.37) SLC6A2SLC6A4SLC6A3OPRL1OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050215571-A1 Therapeutic combination for cognititon enhancement and psychotic disorders PFIZER INC. 2005-09-29 US claimed
US-11766429-B1 Nicotinic receptor antagonists and pioglitazone as therapeutic agents for Covid-19 UNIVERSITY OF SOUTH FLORIDA (US) 2023-09-26 US disclosed
EP-1118674-B1 PROCESS FOR PRODUCING OPTICALLY ACTIVE TROPINONE MONOCARBOXYLIC ACID DERIVATIVE NIHON MEDIPHYSICS CO LTD (JP) 2011-01-05 EP disclosed
EP-1011678-B1 USE OF MECAMYLAMINE FOR THE TREATMENT OF NICOTINE-RESPONSIVE NEUROPSYCHIATRIC DISORDERS UNIV SOUTH FLORIDA (US) 2007-12-19 EP disclosed
EP-1699488-A2 THERAPEUTIC COMBINATION FOR COGNITION ENHANCEMENT AND PSYCHOTIC DISORDERS Pfizer Products Incorporated (US) 2006-09-13 EP disclosed
US-6979698-B1 Method of treating cognitive deficits in learning and memory TARGACEPT, INC. (US) 2005-12-27 US disclosed
US-20050215571-A1 Therapeutic combination for cognititon enhancement and psychotic disorders PFIZER INC. 2005-09-29 US disclosed
WO-2005063296-A2 THERAPEUTIC COMBINATION FOR COGNITION ENHANCEMENT AND PSYCHOTIC DISORDERS PFIZER PRODUCTS INC. (US) 2005-07-14 WO disclosed
EP-1011678-A4 NICOTINE ANTAGONISTS FOR NICOTINE-RESPONSIVE NEUROPSYCHIATRIC DISORDERS UNIV SOUTH FLORIDA (US) 2004-01-14 EP disclosed
US-6537522-B1 Metabolically stable cocaine analogs such as 2-carbometh-oxy-3-(4-iodophenyl)-tropane; chemical intermediates for compounds having high affinities for dopamine and serotonin reuptake sites in brain AMERSHAM PLC (GB) 2003-03-25 US disclosed
WO-1999007378-A1 NICOTINE ANTAGONISTS FOR NICOTINE-RESPONSIVE NEUROPSYCHIATRIC DISORDERS THE UNIVERSITY OF SOUTH FLORIDA A Corporation of the State of Florida (US) 1999-02-18 WO disclosed
US-5750089-A Halogenated neuroprobe for mapping monoamine reuptake sites NEURO IMAGING TECHNOLOGIES, LLC (US) 1998-05-12 US disclosed
EP-0831941-A1 IODINATED NEUROPROBES FOR MAPPING MONOAMINE REUPTAKE SITES Research Biochemicals, Limited Paternership, doing business as Research biochemicals International (US) 1998-04-01 EP disclosed
US-5698179-A Iodinated neuroprobe for mapping monoamine reuptake sites NEURO IMAGING TECHNOLOGIES, LLC (US) 1997-12-16 US disclosed
WO-1996039198-A1 IODINATED NEUROPROBES FOR MAPPING MONOAMINE REUPTAKE SITES RESEARCH BIOCHEMICALS, LIMITED PARTNERSHIP, doing business as RESEARCH BIOCHEMICALS INTERNATIONAL, A MASSACHUSETTS LIMITED PARTNERSHIP, WHOSE SOLE GENERAL PARTNER IS RBI MANAGEMENT, INC. (US) 1996-12-12 WO disclosed
EP-0703791-A4 AN IODINATED NEUROPROBE FOR MAPPING MONOAMINE REUPTAKE SITES RES BIOMED LP (US) 1996-05-22 EP disclosed
EP-0703791-A1 AN IODINATED NEUROPROBE FOR MAPPING MONOAMINE REUPTAKE SITES RESEARCH BIOMEDICALS LIMITED PARTNERSHIP (US) 1996-04-03 EP disclosed
US-5439666-A Central nervous system RESEARCH BIOCHEMICALS LIMITED PARTNERSHIP (US) 1995-08-08 US disclosed
WO-1995001184-A1 AN IODINATED NEUROPROBE FOR MAPPING MONOAMINE REUPTAKE SITES RESEARCH BIOCHEMICALS LIMITED PARTNERSHIP (US) 1995-01-12 WO disclosed
US-5310912-A Ester-substituted nortropane RESEARCH BIOCHEMICALS LIMITED PARTNERSHIP (US) 1994-05-10 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 (1 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-20050215571-A1 Therapeutic combination for cognititon enhancement and psychotic disorders CHRNA3, CHRNA7, CHRNA2 SLC6A2 131/4885SLC6A4 172/4885SLC6A3 51/4885

“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.