SCHEMBL4113771

SCHEMBL4113771

Nc1ccc2cc(S(=O)(=O)[O-])cc(O)c2c1.[Na+]

nearest known ligand 0.71

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. 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
THRB known ✓ P10828 1/20 0.46
NT5E P21589 2/20 0.71
PTPN1 P18031 3/20 0.54
CASP6 P55212 4/20 0.54
NSD2 O96028 3/20 0.54
DUSP3 P51452 2/20 0.54
PTPN5 P54829 2/20 0.54
PTPN11 Q06124 2/20 0.54
SIRT1 Q96EB6 1/20 0.51
PRMT1 Q99873 1/20 0.51
APEX1 P27695 2/20 0.51
DUSP5 Q16690 2/20 0.48
CTDSP1 Q9GZU7 2/20 0.46
ALDH1A1 P00352 1/20 0.45
CYP2C9 P11712 1/20 0.45
CYP2C19 P33261 1/20 0.45
HSD17B10 Q99714 1/20 0.45
PKLR P30613 1/20 0.41
CASP7 P55210 1/20 0.40
HKDC1 Q2TB90 1/20 0.40

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
SCHEMBL29702480 1.00 NT5E (0.71) NT5EPTPN1CASP6NSD2DUSP3
SCHEMBL10623046 1.00 NT5E (0.71) NT5EPTPN1CASP6NSD2DUSP3
Silver SCHEMBL11309326 0.97 NT5E (0.71) NT5EPTPN1CASP6NSD2DUSP3
SCHEMBL4115385 0.87 CASP6 (0.71) NT5EPTPN1CASP6NSD2DUSP3
SCHEMBL11022672 0.85 NT5E (0.78) NT5ECASP6NSD2DUSP3PTPN5
SCHEMBL10623050 0.83 NT5E (1.00) NT5ECASP6NSD2DUSP3PTPN5
SCHEMBL10332181 0.83 NT5E (1.00) NT5ECASP6NSD2DUSP3PTPN5
SCHEMBL156692 0.83 NT5E (1.00) NT5ECASP6NSD2DUSP3PTPN5
SCHEMBL1070219 0.83 PTPN1 (0.58) NT5EPTPN1CASP6NSD2DUSP3
SCHEMBL8008837 0.83 NT5E (0.56) NT5EPTPN1CASP6NSD2DUSP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114539803-B Direct red/direct violet dye compound and preparation method and application thereof 广东省科学院测试分析研究所(中国广州分析测试中心) 2024-08-30 CN claimed
CN-114539803-A Direct red/direct violet dye compound and preparation method and application thereof 广东省科学院测试分析研究所(中国广州分析测试中心) 2022-05-27 CN claimed
CN-102408754-B Brightening disperse red 3B dye composition and preparation method thereof UNIV SOOCHOW 2014-01-08 CN claimed
CN-102408754-A Brightening disperse red 3B dye composition and preparation method thereof UNIV SOOCHOW 2012-04-11 CN claimed
US-20090306132-A1 USE OF DERIVATIVES OF NAPHTHALENESULPHONIC OR QUINOLINESULPHONIC ACID IN THE TREATMENT OF VASOPROLIFERATIVE OCULAR DISEASES ITALFARMACO, S.A. (ES) 2009-12-10 US claimed
US-20090076140-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING SULPHONIC ACID DERIVATIVES ITALFARMACO, S. A. (ES) 2009-03-19 US claimed
EP-1994929-A1 USE OF DERIVATIVES OF NAPHTHALENESULPHONIC OR QUINOLINESULPHONIC ACID IN THE TREATMENT OF VASOPROLIFERATIVE OCULAR DISEASES ITALFARMACO, S.A. (ES) 2008-11-26 EP claimed
US-20060160849-A1 Pharmaceutical compositions containing sulphonic acid derivatives ITALFARMACO, S.A. (ES) 2006-07-20 US claimed
EP-1602644-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING SULPHONIC ACID DERIVATIVES Italfarmaco, S.A. (ES) 2005-12-07 EP claimed
CN-114539803-B Direct red/direct violet dye compound and preparation method and application thereof 广东省科学院测试分析研究所(中国广州分析测试中心) 2024-08-30 CN disclosed
US-11735719-B2 Reduced graphene oxide/manganese(IV) oxide nanocomposite and electrode comprising same, method of manufacture of various graphene material/metal oxide nanocomposites INSTITUT NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CA) 2023-08-22 US disclosed
CN-114539803-A Direct red/direct violet dye compound and preparation method and application thereof 广东省科学院测试分析研究所(中国广州分析测试中心) 2022-05-27 CN disclosed
US-20210159490-A1 REDUCED GRAPHENE OXIDE/MANGANESE(IV) OXIDE NANOCOMPOSITE AND ELECTRODE COMPRISING SAME, METHOD OF MANUFACTURE OF VARIOUS GRAPHENE MATERIAL/METAL OXIDE NANOCOMPOSITES INSTITUT NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CA) 2021-05-27 US disclosed
CN-102408754-B Brightening disperse red 3B dye composition and preparation method thereof UNIV SOOCHOW 2014-01-08 CN disclosed
EP-1602644-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING SULPHONIC ACID DERIVATIVES Italfarmaco, S.A. (ES) 2005-12-07 EP disclosed
US-6001934-A HEAT OXIDATION CROSSLINKING OF POLYARYLENE SULFIDE RESIN TONEN CHEMICAL CO. (JP) 1999-12-14 US disclosed
EP-0900817-A2 Process for the preparation of a functional group-containing polyarylene sulfide resin Tonen Chemical Corporation (JP) 1999-03-10 EP disclosed
US-5256199-A Cement admixture KAO CORPORATION (JP) 1993-10-26 US disclosed
EP-0469625-A2 Cement admixture Kao Corporation (JP) 1992-02-05 EP disclosed
US-4973672-A Water-soluble aminonaphthol disazo dyestuffs, their preparation and their use CASSELLA AKTIENGESELLSCHAFT (DE) 1990-11-27 US 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 (3 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-20090306132-A1 USE OF DERIVATIVES OF NAPHTHALENESULPHONIC OR QUINOLINESULPHONIC ACID IN THE TREATMENT OF VASOPROLIFERATIVE OCULAR DISEASES NQO2, SQLE, SQOR THRB 4784/4885NT5E 1438/4885PTPN1 892/4885
US-20090076140-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING SULPHONIC ACID DERIVATIVES SUCNR1, NR1H4, CYP2B6 THRB 2224/4885NT5E 3737/4885PTPN1 1567/4885
US-20060160849-A1 Pharmaceutical compositions containing sulphonic acid derivatives SUCNR1, NR1H4, CYP2B6 THRB 2260/4885NT5E 3754/4885PTPN1 1571/4885

“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.