SCHEMBL69006

SCHEMBL69006

O=[N+]([O-])c1cc(S(=O)(=O)c2ccc(O)c([N+](=O)[O-])c2)ccc1O

nearest known ligand 0.76

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 4/20 0.76
CA1 P00915 4/20 0.76
CA2 P00918 4/20 0.76
CA9 Q16790 4/20 0.76
VCAM1 P19320 2/20 0.61
HPGD P15428 4/20 0.60
MAPK1 P28482 3/20 0.60
SMN1; SMN2 Q16637 3/20 0.60
ALDH1A1 P00352 3/20 0.60
TP53 P04637 2/20 0.60
TSHR P16473 2/20 0.60
GPR35 Q9HC97 1/20 0.60
L3MBTL1 Q9Y468 3/20 0.58
ALOX15 P16050 1/20 0.58
HSD17B10 Q99714 1/20 0.58
ALDH5A1 P51649 1/20 0.55
ABAT P80404 1/20 0.55
MAPT P10636 3/20 0.53
KDM4E B2RXH2 2/20 0.53
LMNA P02545 2/20 0.53

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
SCHEMBL31080938 1.00 CA12 (0.76) CA12CA1CA2CA9VCAM1
SCHEMBL2904332 0.91 CA12 (0.65) CA12CA1CA2CA9VCAM1
SCHEMBL1959737 0.86 CA2 (1.00) CA12CA1CA2CA9VCAM1
SCHEMBL51033 0.86 CA12 (0.73) CA12CA1CA2CA9VCAM1
SCHEMBL51034 0.86 CA12 (0.73) CA12CA1CA2CA9VCAM1
SCHEMBL1055674 0.86 CA12 (0.73) CA12CA1CA2CA9VCAM1
SCHEMBL1059060 0.85 CA12 (0.71) CA12CA1CA2CA9VCAM1
SCHEMBL1055670 0.85 CA12 (0.71) CA12CA1CA2CA9VCAM1
SCHEMBL1268485 0.85 CA12 (0.71) CA12CA1CA2CA9VCAM1
SCHEMBL8150946 0.85 CA12 (0.71) CA12CA1CA2CA9VCAM1

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119504328-A Method for preparing bisphenol nitro compound by using continuous kettle reactor 上海旭流化学科技有限公司 2025-02-25 CN claimed
WO-2025047698-A1 PHOTOSENSITIVE COMPOSITION, CURED PRODUCT, METHOD FOR PRODUCING SAME, LIQUID CRYSTAL DEVICE, SEMICONDUCTOR DEVICE, POLYMER, AND COMPOUND JSR株式会社 2025-03-06 WO disclosed
CN-119504328-A Method for preparing bisphenol nitro compound by using continuous kettle reactor 上海旭流化学科技有限公司 2025-02-25 CN disclosed
CN-117924130-A Preparation method of 3,3 '-diamino-4, 4' -dihydroxydiphenyl sulfone 上海凌凯医药科技有限公司 2024-04-26 CN disclosed
EP-3434705-A1 BISPHENOL BASED RESIN, ELECTRODE, LEAD ACID BATTERY, AND METHOD FOR MANUFACTURING SAME Hitachi Chemical Company, Ltd. (JP) 2019-01-30 EP disclosed
CN-105949094-A Preparation method of bis[4-(2-hydroxyethoxy)phenyl] sulphone and derivative of bis[4-(2-hydroxyethoxy)phenyl] sulphone as well as catalyst of bis[4-(2-hydroxyethoxy)phenyl] sulphone and derivative of bis[4-(2-hydroxyethoxy)phenyl] sulphone 江苏傲伦达科技实业股份有限公司 2016-09-21 CN disclosed
EP-2479203-A1 AROMATIC POLYESTER Muroran Institute of Technology (JP) 2012-07-25 EP disclosed
US-20120172570-A1 AROMATIC POLYESTER NITTA CORPORATION 2012-07-05 US disclosed
US-8129493-B2 Aromatic polyester MURORAN INSTITUTE OF TECHNOLOGY (JP) 2012-03-06 US disclosed
US-20110224343-A1 MODIFIER FOR AROMATIC POLYESTER AND AROMATIC POLYESTER RESIN COMPOSITION COMPRISING THE SAME MURORAN INSTITUTE OF TECHNOLOGY (JP) 2011-09-15 US disclosed
US-20110092662-A1 AROMATIC POLYESTER NITTA CORPORATION (JP) 2011-04-21 US disclosed
JP-2007015967-A HIGH PURITY 3,3'-DIAMINO-4,4'-DIHYDROXYDIPHENYL SULFONE HAVING LOW METAL CONTENT AND METHOD FOR PRODUCING THE SAME NIPPON KAYAKU CO LTD 2007-01-25 JP disclosed
CN-1216851-C Process for producing bis (4-hydroxy-3-nitrophenyl) compound NIPPON KAYAKU KK (JP) 2005-08-31 CN disclosed
US-6608233-B2 Nitrating a bis(4-hydroxyphenyl) bonded to each other or through an electron-donating bridging group, sulfoxide, sulfone or carbonyl group using nitric acid in a solvent and free from other acids NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2003-08-19 US disclosed
CN-1426390-A Process for producing bis (4-hydroxy-3-nitrophenyl) compound NIPPON KAYAKU KK (JP) 2003-06-25 CN disclosed
US-20030055288-A1 Process for producting bis(4-hydroxy-3-nitrophenyl) compound NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2003-03-20 US disclosed
EP-1277727-A1 PROCESS FOR PRODUCING BIS(4-HYDROXY-3-NITROPHENYL) COMPOUND Nippon Kayaku Kabushiki Kaisha (JP) 2003-01-22 EP disclosed
US-5977413-A Method for producing bis(3-amino-4-hydroxyphenyl) compounds NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1999-11-02 US disclosed
EP-0895985-A2 Method for producing bis(3-amino-4-hydroxyphenyl) compounds Nippon Kayaku Kabushiki Kaisha (JP) 1999-02-10 EP disclosed
US-5099057-A Nitration, hydrolysis and reduction THE DOW CHEMICAL COMPANY (US) 1992-03-24 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 (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-20110224343-A1 MODIFIER FOR AROMATIC POLYESTER AND AROMATIC POLYESTER RESIN COMPOSITION COMPRISING THE SAME F12, PHAX, WDR82 CA12 1221/4885CA1 550/4885CA2 612/4885
US-20030055288-A1 Process for producting bis(4-hydroxy-3-nitrophenyl) compound NOS3, NOS2, NOS1 CA12 4411/4885CA1 3152/4885CA2 2055/4885

“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.