Lanperisone

Lanperisone

SCHEMBL9820433

CC(CN1CCCC1)C(=O)c1ccc(C(F)(F)F)cc1.Cc1ccc(S(=O)(=O)[N-]Cl)cc1.[Na+]

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Lanperisone. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM2 P08172 2/20 0.60
ADRA2B P18089 2/20 0.60
DRD3 P35462 2/20 0.60
SIGMAR1 Q99720 2/20 0.60
HRH3 Q9Y5N1 2/20 0.60
ALDH1A1 P00352 3/20 0.58
LMNA P02545 2/20 0.58
CYP2D6 P10635 1/20 0.47
ADRA2C P18825 1/20 0.47
CHRM3 P20309 1/20 0.47
OPRD1 P41143 1/20 0.47
KCNH2 Q12809 1/20 0.47
MC4R P32245 1/20 0.46
SLC6A4 P31645 3/20 0.43
KDM1A O60341 1/20 0.39
MAPT P10636 2/20 0.39
MEN1 O00255 1/20 0.38
MITF O75030 1/20 0.38
RAB9A P51151 1/20 0.38
KMT2A Q03164 1/20 0.38

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
Lanperisone SCHEMBL570832 0.83 CHRM2 (0.68) CHRM2ADRA2BDRD3SIGMAR1HRH3
Lanperisone SCHEMBL5819917 0.83 CHRM2 (0.68) CHRM2ADRA2BDRD3SIGMAR1HRH3
SCHEMBL9720545 0.82 CHRM2 (0.70) CHRM2ADRA2BDRD3SIGMAR1HRH3
Lanperisone SCHEMBL5819985 0.82 ALDH1A1 (0.68) CHRM2ADRA2BDRD3SIGMAR1HRH3
Lanperisone SCHEMBL1987393 0.82 ALDH1A1 (0.68) CHRM2ADRA2BDRD3SIGMAR1HRH3
SCHEMBL9172663 0.78 CHRM2 (0.97) CHRM2ADRA2BDRD3SIGMAR1HRH3
Tolperisone SCHEMBL148499 0.77 CHRM2 (1.00) CHRM2ADRA2BDRD3SIGMAR1HRH3
SCHEMBL21451092 0.77 CHRM2 (1.00) CHRM2ADRA2BDRD3SIGMAR1HRH3
Tolperisone SCHEMBL4516510 0.77 CHRM2 (1.00) CHRM2ADRA2BDRD3SIGMAR1HRH3
Tolperisone SCHEMBL17223884 0.77 CHRM2 (1.00) CHRM2ADRA2BDRD3SIGMAR1HRH3

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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0266577-B1 AN OPTICALLY ACTIVE PROPANONE DERIVATIVE AND PROCESS FOR PRODUCING THE SAME AND USE THEREOF NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1991-09-25 EP claimed