Phenidone

Phenidone

SCHEMBL8470486

O=C1CCN(c2ccccc2)N1.O=C1CCN(c2ccccc2)N1.O=S([O-])[O-].[Na+].[Na+]

nearest known ligand 0.80

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 Phenidone. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
ALOX5 known ✓ P09917 15/20 0.80
PTGS1 known ✓ P23219 1/20 0.80
PTGS2 known ✓ P35354 1/20 0.80
G6PD P11413 1/20 0.80
ALOX15 P16050 1/20 0.80
ALOX12 P18054 1/20 0.80
DDB1 Q16531 1/20 0.45
CRBN Q96SW2 1/20 0.45
GAA P10253 1/20 0.42

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
Phenidone SCHEMBL8470489 1.00 ALOX5 (0.80) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL7999908 0.97 ALOX5 (0.80) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL7999902 0.97 ALOX5 (0.80) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL8470482 0.94 ALOX5 (0.75) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL7999896 0.90 ALOX5 (0.75) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL235192 0.89 ALOX5 (1.00) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL10904906 0.89 ALOX5 (1.00) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL11130362 0.88 ALOX5 (0.83) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL8480957 0.88 ALOX5 (0.96) ALOX5G6PDALOX15ALOX12PTGS1
Phenidone SCHEMBL9281777 0.86 ALOX5 (0.92) ALOX5G6PDALOX15ALOX12PTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5972578-A Yellow dye-containing developing/fixing monobath and method for processing roomlight handleable black-and-white photographic elements EASTMAN KODAK COMPANY (US) 1999-10-26 US disclosed
US-5972581-A COMPRISING BLACK-AND-WHITE DEVELOPING AGENT, SULFITE, FIXING AGENT, PARTICULATE OPACIFYING AGENT; ROOMLIGHT PROCESSING OF RADIOGRAPHIC FILMS EASTMAN KODAK COMPANY (US) 1999-10-26 US disclosed