Levemopamil

Levemopamil

SCHEMBL51113

CC(C)[C@@](C#N)(CCCN(C)CCc1ccccc1)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SIGMAR1 Q99720 6/20 1.00
EBP Q15125 3/20 1.00
ABCB1 P08183 6/20 0.59
CYP3A4 P08684 5/20 0.59
ABCC1 P33527 4/20 0.59
KCNH2 Q12809 3/20 0.59
TSHR P16473 3/20 0.59
LMNA P02545 3/20 0.59
MEN1 O00255 3/20 0.59
KMT2A Q03164 3/20 0.59
SLC6A4 P31645 3/20 0.59
CYP2C19 P33261 2/20 0.59
ABCB11 O95342 2/20 0.59
CACNA1F O60840 2/20 0.59
HTR1A P08908 2/20 0.59
ADRA2A P08913 2/20 0.59
DRD2 P14416 2/20 0.59
ADRA2C P18825 2/20 0.59
HTR2A P28223 2/20 0.59
HTR2C P28335 2/20 0.59

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
Emopamil SCHEMBL93921 1.00 SIGMAR1 (1.00) SIGMAR1EBPABCB1CYP3A4ABCC1
Levemopamil SCHEMBL8668419 0.99 SIGMAR1 (0.97) SIGMAR1EBPABCB1CYP3A4ABCC1
Emopamil SCHEMBL30127166 0.99 SIGMAR1 (0.97) SIGMAR1EBPABCB1CYP3A4ABCC1
SCHEMBL7965554 0.92 SIGMAR1 (0.84) SIGMAR1EBPABCB1CYP3A4ABCC1
SCHEMBL10453393 0.92 SIGMAR1 (0.84) SIGMAR1EBPABCB1CYP3A4ABCC1
SCHEMBL7956324 0.92 SIGMAR1 (0.84) SIGMAR1EBPABCB1CYP3A4ABCC1
SCHEMBL7971207 0.92 SIGMAR1 (0.84) SIGMAR1EBPABCB1CYP3A4ABCC1
SCHEMBL9490836 0.92 SIGMAR1 (0.84) SIGMAR1EBPABCB1CYP3A4ABCC1
SCHEMBL7969360 0.92 SIGMAR1 (0.84) SIGMAR1EBPABCB1CYP3A4ABCC1
SCHEMBL9493517 0.89 SIGMAR1 (0.79) SIGMAR1EBPABCB1CYP3A4ABCC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103432091-A Improved-performance tablet and preparation method thereof ZHONG SHUGUANG 2013-12-11 CN claimed
CN-101919822-B Tablet with improved combination properties and preparation method thereof ZHONG SHUGUANG 2013-10-23 CN claimed
US-20100316678-A1 COMBINATION METHODS AND COMPOSITIONS FOR TREATMENT OF NEUROPATHIC PAIN CNSBIO PTY LTD. (AU) 2010-12-16 US claimed
US-20100311697-A1 Methods and Compositions for the Treatment of CNS-Related Conditions ADAMAS PHARMACEUTICALS, INC. (US) 2010-12-09 US claimed
EP-2175886-A1 COMBINATION METHODS AND COMPOSITIONS FOR TREATMENT OF NEUROPATHIC PAIN CNSBio Pty Ltd (AU) 2010-04-21 EP claimed
US-20100074955-A1 Combination of NMDA-Receptor Ligand and a Compound With 5-HT6 Receptor Affinity LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2010-03-25 US claimed
US-20100029665-A1 Methods and Compositions for Treating Migraine Pain MEYERSON LAURENCE R 2010-02-04 US claimed
CN-101563106-A Combination of nmda- receptor ligand and a compound with 5-HT6 receptor affinity ESTEVE LABOR DR (ES) 2009-10-21 CN claimed
US-20090253728-A1 Methods and Compositions for Treating Nociceptive Pain MEYERSON LAURENCE R 2009-10-08 US claimed
EP-2081600-A1 COMBINATION OF NMDA- RECEPTOR LIGAND AND A COMPOUND WITH 5-HT6 RECEPTOR AFFINITY Laboratorios Del. Dr. Esteve, S.A. (ES) 2009-07-29 EP claimed
EP-0858334-A4 ANALGESIC IMMEDIATE AND CONTROLLED RELEASE PHARMACEUTICAL COMPOSITION FAULDING F H & CO LTD (AU) 2000-08-09 EP claimed
EP-0858334-A1 ANALGESIC IMMEDIATE AND CONTROLLED RELEASE PHARMACEUTICAL COMPOSITION F.H. FAULDING & CO. LIMITED (AU) 1998-08-19 EP claimed
WO-1997014415-A1 ANALGESIC IMMEDIATE AND CONTROLLED RELEASE PHARMACEUTICAL COMPOSITION F.H. FAULDING & CO. LIMITED (AU) 1997-04-24 WO claimed
US-5496818-A OIL-IN-WATER TYPE; DISPERSED LIPID PHASE OF VEGETABLE OIL, PHOSPHOLIPID EMULSIFIER AND STRONGLY BASIC HYDROPHOBIC PHARMACEUTICAL; AQUEOUS PHASE WITH BUFFER AND SMALL AMOUNT OF IONIZED PHARMACEUTICAL; POSITIVE CHARGE AT EMULSION INTERFACE KNOLL AKTIENGESELLSCHAFT (DE) 1996-03-05 US claimed
EP-0456106-B1 Stable emulsion for pharmaceutical administration, process for its preparation and use thereof as pharmaceutical KNOLL AG (DE) 1994-12-07 EP claimed
EP-0557290-A1 TREATMENT OF AIDS DEMENTIA, MYELOPATHY, PERIPHERAL NEUROPATHY, AND VISION LOSS The Children's Medical Center Corporation (US) 1993-09-01 EP claimed
EP-0557290-A4 TREATMENT OF AIDS DEMENTIA, MYELOPATHY, PERIPHERAL NEUROPATHY, AND VISION LOSS. CHILDRENS MEDICAL CENTER (US) 1993-07-14 EP claimed
EP-0502418-A1 Use of levemopamil for the manufacture of a medicament for the treatment of alcohol abuse BASF CORPORATION (US) 1992-09-09 EP claimed
WO-1992003137-A1 TREATMENT OF AIDS DEMENTIA, MYELOPATHY, PERIPHERAL NEUROPATHY, AND VISION LOSS THE CHILDREN'S MEDICAL CENTER CORPORATION (US) 1992-03-05 WO claimed
EP-0456106-A2 Stable emulsion for pharmaceutical administration, process for its preparation and use thereof as pharmaceutical KNOLL AG (DE) 1991-11-13 EP claimed

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-20100074955-A1 Combination of NMDA-Receptor Ligand and a Compound With 5-HT6 Receptor Affinity GRM6, GRIN3B, GRIN3A SIGMAR1 118/4885EBP 4275/4885ABCB1 1077/4885

“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.