SCHEMBL391667

SCHEMBL391667

O=S(=O)([O-])c1ccc2cc(/N=N/c3cc(S(=O)(=O)[O-])c4cccnc4c3O)ccc2c1.[Na+].[Na+]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 2/20 0.47
PTPN11 Q06124 3/20 1.00
PTPN7 P35236 2/20 1.00
PTPRC P08575 1/20 0.76
ALOX15 P16050 1/20 0.76
PTPN1 P18031 1/20 0.76
PTPN6 P29350 1/20 0.76
PTPRJ Q12913 1/20 0.76
HSD17B10 Q99714 1/20 0.76
DUSP26 Q9BV47 1/20 0.76
CYP1A2 P05177 1/20 0.53
HPGD P15428 1/20 0.53
HIF1A Q16665 1/20 0.53
GLO1 Q04760 3/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
NPC1 O15118 1/20 0.46
RAB9A P51151 1/20 0.46
CASP6 P55212 1/20 0.46
ATM Q13315 1/20 0.46

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
SCHEMBL31186847 1.00 PTPN11 (1.00) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL2401970 1.00 PTPN11 (1.00) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL14154415 0.86 PTPN11 (1.00) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL13738903 0.86 PTPN11 (1.00) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL2401972 0.86 PTPN11 (1.00) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL29391398 0.86 PTPN11 (1.00) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL30542884 0.86 PTPN11 (1.00) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL13738901 0.86 PTPN11 (1.00) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL2401966 0.85 PTPN11 (0.98) PTPN11PTPN7PTPRCALOX15PTPN1
SCHEMBL29624127 0.83 PTPN11 (0.71) PTPN11PTPN7PTPRCALOX15PTPN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8100020-B2 Compliant and wireless health monitoring sensors for composite structures Lumimove, Inc., a Missouri Corporation (US) 2012-01-24 US claimed
JP-2011525240-A 2011-09-15 JP claimed
EP-2297559-A2 COMPLIANT AND WIRELESS HEALTH MONITORING SENSORS FOR COMPOSITE STRUCTURES Lumimove, Inc., Dba Crosslink (US) 2011-03-23 EP claimed
US-20100095781-A1 COMPLIANT AND WIRELESS HEALTH MONITORING SENSORS FOR COMPOSITE STRUCTURES LUMIMOVE, INC., D/B/A CROSSLINK (US) 2010-04-22 US claimed
WO-2009155367-A2 COMPLIANT AND WIRELESS HEALTH MONITORING SENSORS FOR COMPOSITE STRUCTURES LUMIMOVE, INC., D/B/A CROSSLINK (US) 2009-12-23 WO claimed
WO-2009140215-A2 METHOD FOR TREATING DRUG-RESISTANT BACTERIAL AND OTHER INFECTIONS WITH CLIOQUINOL, PHANQUINONE, AND RELATED COMPOUNDS GERAGHTY, ERIN (US) 2009-11-19 WO claimed
CN-117838863-B Nucleic acid molecule for inhibiting D2HGDH, inhibitor and application thereof 厦门大学 2025-03-11 CN disclosed
WO-2024092274-A2 ENDOCYTIC AGENTS BIOVENTURES, LLC (US) 2024-05-02 WO disclosed
CN-117838863-A Nucleic acid molecule for inhibiting D2HGDH, inhibitor and application thereof 厦门大学 2024-04-09 CN disclosed
CN-116212048-A Cell surface coupling of nanoparticles 麻省理工学院 2023-06-06 CN disclosed
US-20220185860-A1 CELL SURFACE COUPLING OF NANOPARTICLES IRVINE, DARRELL 2022-06-16 US disclosed
US-20220151921-A1 MONOCYTE-SELECTIVE DRUG DELIVERY SYSTEM USING SINGLE-WALLED CARBON NANOTUBES TO INDUCE EFFEROCYTOSIS THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2022-05-19 US disclosed
US-11261226-B2 Cell surface coupling of nanoparticles MASSACHUSETTS INSTITUTE OF TECHNOLOGY (MITN1) (US) 2022-03-01 US disclosed
US-5160457-A Dopes, fibers, films, moldings, sheets ALLIED-SIGNAL INC. (US) 1992-11-03 US disclosed
WO-1992018572-A2 METHOD OF PROCESSING NEUTRAL POLYANILINES IN SOLVENT AND SOLVENT MIXTURES ALLIED-SIGNAL INC. (US) 1992-10-29 WO disclosed
WO-1992015632-A1 THERMALLY INDUCED CHAIN COUPLING IN SOLID STATE POLYANILINE ALLIED-SIGNAL INC. (US) 1992-09-17 WO disclosed
WO-1992011644-A1 METHOD OF PROCESSING ELECTRICALLY CONDUCTIVE POLYANILINES IN SOLVENT MIXTURES ALLIED-SIGNAL INC. (US) 1992-07-09 WO disclosed
WO-1992011645-A1 METHOD FOR PROCESSING ELECTRICALLY CONDUCTIVE POLYANILINES IN LEWIS-BASE SOLVENTS ALLIED-SIGNAL INC. (US) 1992-07-09 WO disclosed
EP-0461182-A1 THERMALLY STABLE FORMS OF ELECTRICALLY CONDUCTIVE POLYANILINE. ALLIED SIGNAL INC (US) 1991-12-18 EP disclosed
WO-1990010297-A1 THERMALLY STABLE FORMS OF ELECTRICALLY CONDUCTIVE POLYANILINE ALLIED-SIGNAL INC. (US) 1990-09-07 WO 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-20220185860-A1 CELL SURFACE COUPLING OF NANOPARTICLES EPCAM, CD47, CD63 THRB 1171/4885PTPN11 142/4885PTPN7 131/4885
US-11261226-B2 Cell surface coupling of nanoparticles EPCAM, CD47, CD63 THRB 1171/4885PTPN11 142/4885PTPN7 131/4885

“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.