Phenolsulfonic Acid

Phenolsulfonic Acid

SCHEMBL710820

O.O.O=S(=O)([O-])c1ccc(O)cc1.[Na+]

nearest known ligand 0.56

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
▸ PTGS1 known ✓ P23219 1/20 0.45
▸ MEN1 known ✓ O00255 1/20 0.42
▸ ESR1 known ✓ P03372 2/20 0.42
▸ LMNA P02545 3/20 0.56
▸ CA2 P00918 5/20 0.54
▸ CA12 O43570 3/20 0.54
▸ CA9 Q16790 3/20 0.54
▸ CA1 P00915 3/20 0.54
▸ ENPP2 Q13822 1/20 0.54
▸ DUSP5 Q16690 3/20 0.45
▸ PTPN1 P18031 2/20 0.45
▸ DUSP6 Q16828 1/20 0.45
▸ GAA P10253 1/20 0.43
▸ PKM P14618 1/20 0.43
▸ CA7 P43166 1/20 0.43
▸ TDP1 Q9NUW8 1/20 0.43
▸ KDM4E B2RXH2 1/20 0.42
▸ NPC1 O15118 1/20 0.42
▸ GMNN O75496 1/20 0.42
▸ ALDH1A1 P00352 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
Phenolsulfonic Acid SCHEMBL2518118 0.97 LMNA (0.59) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL125056 0.97 LMNA (0.59) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL30756570 0.97 LMNA (0.59) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL27472854 0.95 LMNA (0.56) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL10758562 0.95 LMNA (0.56) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL1642911 0.95 LMNA (0.56) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL7671608 0.95 LMNA (0.56) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL11198896 0.95 LMNA (0.56) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL11202643 0.95 LMNA (0.56) LMNACA2CA12CA9CA1
Phenolsulfonic Acid SCHEMBL8764688 0.95 LMNA (0.56) LMNACA2CA12CA9CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119593003-A Preparation method and application of high-activity NiCe (OH) n/NF 浙江工业大学 2025-03-11 — — CN claimed
US-11647590-B2 Systems and methods for etching of metals D-WAVE SYSTEMS INC. (CA) 2023-05-09 — — US claimed
CN-112023726-A Low-energy-consumption high-flux reverse osmosis membrane and preparation method and application thereof 万华化学集团股份有限公司 2020-12-04 — — CN claimed
US-20250243303-A1 DYNAMIC CROSSLINKER FOR CROSSLINKING VARIOUS TYPES OF POLYMERS AND APPLICATIONS THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2025-07-31 — — US disclosed
CN-119593003-A Preparation method and application of high-activity NiCe (OH) n/NF 浙江工业大学 2025-03-11 — — CN disclosed
WO-2024203772-A1 METHOD FOR PRODUCING ALPHA-CYANOACRYLATE 東亞合成株式会社 2024-10-03 — — WO disclosed
US-20240167922-A1 TRANSPARENTIZING REAGENT AND TRANSPARENTIZING METHOD KYOTO UNIVERSITY (JP) 2024-05-23 — — US disclosed
EP-4306927-A1 TRANSPARENTIZING REAGENT AND TRANSPARENTIZING METHOD Kyoto University (JP) 2024-01-17 — — EP disclosed
CN-117295847-A Electroless nickel plating bath and electroless nickel alloy plating bath 株式会社杰希优 2023-12-26 — — CN disclosed
EP-4279522-A1 WATER-DISPERSIBLE POLYISOCYANATES WITH ALDEHYDE BLOCKING AND AQUEOUS COMPOSITIONS OBTAINABLE THEREFROM Covestro Deutschland AG (DE) 2023-11-22 — — EP disclosed
US-11647590-B2 Systems and methods for etching of metals D-WAVE SYSTEMS INC. (CA) 2023-05-09 — — US disclosed
EP-0284132-A2 Quaternary ammonium or phosphonium peroxy carbonic acid precursors and their use in detergent bleach compositions UNILEVER N.V. (NL) 1988-09-28 — — EP disclosed
US-4751015-A LOW TEMPERATURE BLEACH LEVER BROTHERS COMPANY (US) 1988-06-14 — — US disclosed
US-4686061-A BLEACHING ACTIVATOR AKZO NV (NL) 1987-08-11 — — US disclosed
EP-0125641-B1 ALKANOYLOXYBENZENESULFONATE SALT PRODUCTION ETHYL CORPORATION (US) 1987-03-04 — — EP disclosed
EP-0210674-A2 P-sulphophenyl carbonates and detergent compositions containing them AKZO N.V. (NL) 1987-02-04 — — EP disclosed
EP-0195597-A1 Bleach activator compounds and bleaching compositions containing them THE PROCTER & GAMBLE COMPANY (US) 1986-09-24 — — EP disclosed
US-4606838-A FORMED IN SITU FROM ACYL ACTIVATOR THE PROCTER & GAMBLE COMPANY (US) 1986-08-19 — — US disclosed
US-4537724-A Alkanoyloxybenzenesulfonate salt production ETHYL CORPORATION (US) 1985-08-27 — — US disclosed
EP-0125641-A2 Alkanoyloxybenzenesulfonate salt production ETHYL CORPORATION (US) 1984-11-21 — — 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 (1 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-20240167922-A1 TRANSPARENTIZING REAGENT AND TRANSPARENTIZING METHOD TST, TTR, ALB PTGS1 2920/4885MEN1 2865/4885ESR1 4437/4885

“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.

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