Lifarizine

Lifarizine

SCHEMBL9494261

Cc1ccc(-c2nc(CN3CCN(C(c4ccccc4)c4ccccc4)CC3)c(C)[nH]2)cc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.85

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CHRM1CHRM2CHRM3CHRM4ESR1ESR2GABRA1GABRB1GABRG2GBA1HRH1HTR1DHTR2AOPRD1OPRK1OPRM1SLC6A2SLC6A3TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Lifarizine. 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 known ✓ P08172 1/20 0.43
ADRA2A known ✓ P08913 1/20 0.43
CHRM1 known ✓ P11229 1/20 0.43
ADRA2C known ✓ P18825 1/20 0.43
SLC6A2 known ✓ P23975 1/20 0.43
HTR2A known ✓ P28223 1/20 0.43
ADRA1A known ✓ P35348 1/20 0.43
HRH1 known ✓ P35367 1/20 0.43
OPRM1 known ✓ P35372 1/20 0.43
OPRK1 known ✓ P41145 1/20 0.43
SLC6A3 known ✓ Q01959 1/20 0.43
CYP3A4 P08684 3/20 0.50
CYP2C19 P33261 2/20 0.50
DRD2 P14416 2/20 0.50
DRD4 P21917 2/20 0.50
DRD3 P35462 2/20 0.50
CYP2C9 P11712 1/20 0.50
ATM Q13315 3/20 0.45
CTSS P25774 3/20 0.45
CACNA2D1 P54289 1/20 0.43

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
Lifarizine SCHEMBL676318 0.92 DRD2 (0.57) CYP3A4CYP2C19DRD2DRD4DRD3
Lifarizine SCHEMBL8963776 0.91 DRD2 (0.56) CYP3A4CYP2C19DRD2DRD4DRD3
SCHEMBL9424741 0.89 DRD3 (0.55) CYP3A4CYP2C19DRD2DRD4DRD3
SCHEMBL8963644 0.87 DRD3 (0.56) CYP3A4CYP2C19DRD2DRD4DRD3
SCHEMBL8964084 0.87 DRD2 (0.52) CYP3A4CYP2C19DRD2DRD4DRD3
SCHEMBL8963668 0.87 DRD2 (0.64) CYP3A4CYP2C19DRD2DRD4DRD3
SCHEMBL8963501 0.85 CTSS (0.52) CYP3A4CYP2C19DRD2DRD4DRD3
SCHEMBL8963661 0.83 CYP3A4 (0.49) CYP3A4CYP2C19DRD2DRD4DRD3
SCHEMBL8963974 0.83 DRD3 (0.59) CYP3A4CYP2C19DRD2DRD4DRD3
SCHEMBL8963806 0.83 CYP3A4 (0.56) CYP3A4CYP2C19DRD2DRD4DRD3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0365363-B1 Parenteral formulations of 1-diphenylmethyl-4-[(2-(4-methylphenyl)-5-methyl-1H-imidazol-4-yl)methyl]piperazine SYNTEX PHARMACEUTICALS LTD. (GB) 1993-04-14 EP disclosed
US-5063220-A Strokes SYNTEX PHARMACEUTICALS, LTD. (GB) 1991-11-05 US disclosed
US-4973591-A SALT FORMATION IN SITU, TREATMENT OF STROKES SYNTEX PHARMACEUTICALS, LTD. (GB) 1990-11-27 US disclosed
EP-0365363-A1 Parenteral formulations of 1-diphenylmethyl-4-[(2-(4-methylphenyl)-5-methyl-1H-imidazol-4-yl)methyl]piperazine SYNTEX PHARMACEUTICALS LTD. (GB) 1990-04-25 EP disclosed