Phenolsulfonic Acid

Phenolsulfonic Acid

SCHEMBL560246

O.O.O=S(=O)(O)c1ccc(O)cc1

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Phenolsulfonic Acid. 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
MEN1 known ✓ O00255 1/20 0.44
THRB known ✓ P10828 1/20 0.44
ESR1 known ✓ P03372 2/20 0.43
LMNA P02545 2/20 0.94
ALDH1A1 P00352 5/20 0.56
CA2 P00918 4/20 0.56
CA12 O43570 3/20 0.56
CA9 Q16790 3/20 0.56
TSHR P16473 2/20 0.56
CA1 P00915 2/20 0.56
NT5E P21589 1/20 0.56
ENPP2 Q13822 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.55
TDP1 Q9NUW8 1/20 0.50
HSD17B10 Q99714 4/20 0.47
HPGD P15428 3/20 0.47
KDM4E B2RXH2 3/20 0.47
POLB P06746 1/20 0.46
CYP2D6 P10635 1/20 0.46
GAA P10253 1/20 0.45

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
Phenolsulfonic Acid SCHEMBL687364 1.00 LMNA (0.94) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL28288398 0.97 LMNA (0.90) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL710821 0.97 LMNA (0.90) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL1115419 0.97 LMNA (0.90) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL18275 0.97 LMNA (1.00) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL29965481 0.97 LMNA (1.00) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL10622999 0.97 LMNA (1.00) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL2518117 0.94 LMNA (0.94) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL20815893 0.94 LMNA (0.94) LMNAALDH1A1CA2CA12CA9
Phenolsulfonic Acid SCHEMBL9682015 0.94 LMNA (0.94) LMNAALDH1A1CA2CA12CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3091053-B1 OPTICAL FLUORESCENT IMAGING USING CYANINE DYES LI COR INC (US) 2020-12-23 EP disclosed
EP-3091053-A1 OPTICAL FLUORESCENT IMAGING USING CYANINE DYES LI-COR, INC. (US) 2016-11-09 EP disclosed
US-20160280650-A1 NOVEL BENZENESULFONAMIDE COMPOUNDS, METHOD FOR SYNTHESIZING SAME, AND USE THEREOF IN MEDICINE AS WELL AS IN COSMETICS GALDERMA RESEARCH & DEVELOPMENT (FR) 2016-09-29 US disclosed
US-9365529-B2 Benzenesulfonamide compounds, method for synthesizing same, and use thereof in medicine as well as in cosmetics GALDERMA RESEARCH & DEVLOPMENT (FR) 2016-06-14 US disclosed
EP-2035505-B1 OPTICAL FLUORESCENT IMAGING USING CYANINE DYES LI COR INC (US) 2016-03-16 EP disclosed
EP-2968314-A2 NOVEL BENZENESULFONAMIDE COMPOUNDS, METHOD FOR SYNTHESIZING SAME, AND USE THEREOF IN MEDICINE AS WELL AS IN COSMETICS Galderma Research & Development (FR) 2016-01-20 EP disclosed
CN-105228624-A Novel benzenesulfonamide compounds, method for the synthesis thereof and use thereof in medicine and cosmetics GALDERMA RES & DEV 2016-01-06 CN disclosed
US-9110069-B2 Luminescent compounds SETA BIOMEDICALS, LLC (US) 2015-08-18 US disclosed
CN-103059640-B Inkjet ink, inkjet recording method, ink cartridge, recording unit, and inkjet recording apparatus CANON KK 2015-06-24 CN disclosed
US-20150158834-A1 NOVEL BENZENESULFONAMIDE COMPOUNDS, METHOD FOR SYNTHESIZING SAME, AND USE THEREOF IN MEDICINE AS WELL AS IN COSMETICS GALDERMA RESEARCH & DEVELOPMENT (FR) 2015-06-11 US disclosed
EP-1202961-A1 ARYLSULFONAMIDO-SUBSTITUTED HYDROXAMIC ACID DERIVATIVES Novartis AG (CH) 2002-05-08 EP disclosed
WO-2002024815-A1 CYANINE DYES LI-COR, INC. (US) 2002-03-28 WO disclosed
WO-2001010827-A1 ARYLSULFONAMIDO-SUBSTITUTED HYDROXAMIC ACID DERIVATIVES NOVARTIS AG (CH) 2001-02-15 WO disclosed
EP-0979104-A1 SONODYNAMIC THERAPY USING AN ULTRASOUND SENSITIZER COMPOUND NYCOMED IMAGING A/S (NO) 2000-02-16 EP disclosed
WO-1998052609-A1 SONODYNAMIC THERAPY USING AN ULTRASOUND SENSITIZER COMPOUND NYCOMED IMAGING AS (NO) 1998-11-26 WO disclosed
EP-0383995-B1 Aromatic thermosetting resins and preparation thereof SUMIKIN CHEMICAL (JP) 1997-10-15 EP disclosed
US-5536626-A CYCLOALKENYLENE CONTAINING CYANINE DYE E. I. DU PONT DE NEMOURS AND COMPANY (US) 1996-07-16 US disclosed
US-5519145-A CATIONIC INDOLIUM DYES FOR PHOTOGRAPHY E. I. DU PONT DE NEMOURS AND COMPANY (US) 1996-05-21 US disclosed
US-5017683-A Organic acid catalyst SUMIKIN CHEMICAL CO., LTD. (JP) 1991-05-21 US disclosed
EP-0383995-A2 Aromatic thermosetting resins and preparation thereof SUMIKIN CHEMICAL CO., LTD. (JP) 1990-08-29 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20160280650-A1 NOVEL BENZENESULFONAMIDE COMPOUNDS, METHOD FOR SYNTHESIZING SAME, AND USE THEREOF IN MEDICINE AS WELL AS IN COSMETICS TYR, ARSA, NISCH MEN1 2111/4885THRB 4458/4885ESR1 3085/4885
US-20150158834-A1 NOVEL BENZENESULFONAMIDE COMPOUNDS, METHOD FOR SYNTHESIZING SAME, AND USE THEREOF IN MEDICINE AS WELL AS IN COSMETICS TYR, ARSA, NISCH MEN1 2111/4885THRB 4458/4885ESR1 3085/4885

“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.