Phenol

Phenol

SCHEMBL898454

C=CCOS(=O)(=O)[O-].CCOCC.Oc1ccccc1.[Na+]

nearest known ligand 0.38

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

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 1/20 0.32
ESR2 known ✓ Q92731 1/20 0.32
ESR1 P03372 6/20 0.38
KDM4E B2RXH2 2/20 0.33
CYP3A4 P08684 1/20 0.33
POLB P06746 1/20 0.33
KAT6A Q92794 2/20 0.33
KMT2A Q03164 2/20 0.33
ALDH1A1 P00352 1/20 0.33
TP53 P04637 1/20 0.33
HPGD P15428 1/20 0.33
HSD17B10 Q99714 1/20 0.33
PKM P14618 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
MEN1 O00255 1/20 0.31
CISD1 Q9NZ45 1/20 0.31
FAAH O00519 1/20 0.31

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
Phenol SCHEMBL28240227 0.91 ESR1 (0.43) ESR1KDM4ECYP3A4KAT6AALDH1A1
Phenol SCHEMBL7587323 0.88 ESR1 (0.43) ESR1KDM4ECYP3A4KAT6AALDH1A1
Phenol SCHEMBL728314 0.86 ESR1 (0.37) ESR1KDM4ECYP3A4POLBKAT6A
Phenol SCHEMBL11073236 0.84 ESR1 (0.36) ESR1KDM4ECYP3A4POLBKAT6A
Ether SCHEMBL243398 0.83 RECQL (0.38) POLBKMT2AHPGDMEN1
Ether SCHEMBL10804200 0.81 RECQL (0.34) ALDH1A1HPGD
Phenol SCHEMBL28096986 0.80 ESR1 (0.42) ESR1KMT2AHPGDPTGS2ESR2
Phenol SCHEMBL607067 0.80 ESR1 (0.33) ESR1KDM4ECYP3A4POLBPKM
Ether SCHEMBL6532591 0.80 RECQL (0.34) POLBKMT2AHPGDMEN1
Phenol SCHEMBL3255814 0.78 MEN1 (0.42) ESR1KDM4ECYP3A4POLBKMT2A

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
US-8986467-B2 Method for passivating metallic surfaces with aqueous compositions comprising surfactants BASF SE (DE) 2015-03-24 US disclosed
US-20120080121-A1 METHOD FOR PASSIVATING METALLIC SURFACES WITH AQUEOUS COMPOSITIONS COMPRISING SURFACTANTS BASF SE (DE) 2012-04-05 US disclosed
US-6106940-A ADHESIVE POLYMER AND AS A TACKIFIER OR PLASTICIZER, A ZWITTERIONIC COMPOUND SUCH AS N-(2-HYDROXY-3-SULFOPROPYL)-N,N-DIMETHYL-N-(3-BUTYLOXY-2-HYDROXYPROPYL) -AMMONIUM BETAINE; ADHESIVE TAPES 3M INNOVATIVE PROPERTIES COMPANY (US) 2000-08-22 US disclosed
EP-0739929-A2 Improved physical properties from directly emulsified silicone latices through appropriate surfactant selection DOW CORNING CORPORATION (US) 1996-10-30 EP disclosed