Sugi Predict

Sugi Predict / Compounds / SCHEMBL1754882

SCHEMBL1754882

SCHEMBL1754882

O=S(=O)(c1ccc(O)cc1)c1cccc(O)c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HSD17B1 P14061 2/20 0.56
▸ HSD17B2 P37059 2/20 0.56
▸ CA2 P00918 4/20 0.54
▸ GAA P10253 4/20 0.52
▸ POLB P06746 2/20 0.52
▸ GFER P55789 1/20 0.52
▸ ABCC9 O60706 1/20 0.51
▸ ABCC8 Q09428 1/20 0.51
▸ KCNJ11 Q14654 1/20 0.51
▸ KCNJ8 Q15842 1/20 0.51
▸ PKM P14618 1/20 0.50
▸ MAPT P10636 1/20 0.48
▸ HTR6 P50406 2/20 0.48
▸ RAPGEF4 Q8WZA2 1/20 0.47
▸ LMNA P02545 2/20 0.47
▸ HTT P42858 1/20 0.46
▸ KMT2A Q03164 1/20 0.46
▸ CA12 O43570 1/20 0.45
▸ CA1 P00915 1/20 0.45
▸ CA9 Q16790 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
SCHEMBL9456691 0.91 GAA (0.53) HSD17B1HSD17B2CA2GAAPOLB
SCHEMBL31146723 0.91 CA2 (0.61) HSD17B1HSD17B2CA2GAAPOLB
SCHEMBL69135 0.91 CA2 (0.61) HSD17B1HSD17B2CA2GAAPOLB
SCHEMBL10340796 0.91 CA2 (0.61) HSD17B1HSD17B2CA2GAAPOLB
SCHEMBL487036 0.89 HTR6 (0.61) HSD17B1HSD17B2CA2GAAPOLB
SCHEMBL10587183 0.89 CA2 (0.59) HSD17B1HSD17B2CA2GAAPOLB
SCHEMBL10860256 0.89 CA2 (0.59) HSD17B1HSD17B2CA2GAAPOLB
SCHEMBL11880694 0.86 ALDH1A1 (0.59) HSD17B1HSD17B2CA2GAAPOLB
Resorcinol SCHEMBL28332324 0.86 GAA (0.53) HSD17B1HSD17B2CA2GAAPOLB
Phenol SCHEMBL28246660 0.85 HTR6 (0.61) HSD17B1HSD17B2CA2GAAPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8163864-B2 Sulfonated polyarylene compounds, membrane material made therefrom, method for the production thereof and use LEIBNIZ-INSTITUT FUER POLYMERFORSCHUNG DRESDEN E.V. (DE) 2012-04-24 — — US claimed
US-20110172317-A1 SULFONATED POLYARYLENE COMPOUNDS, MEMBRANE MATERIAL MADE THEREFROM, METHOD FOR THE PRODUCTION THEREOF AND USE LEIBNIZ-INSTITUT FUER POLYMERFORSCHUNG DRESDEN E.V. (DE) 2011-07-14 — — US claimed
EP-2046491-B1 SULFONATED POLYARYLENE COMPOUNDS, MEMBRANE MATERIAL MADE THEREFROM, METHOD FOR THE PRODUCTION THEREOF, AND USE LEIBNIZ INST POLYMERFORSCHUNG (DE) 2010-05-12 — — EP claimed
JP-2009544831-A — — 2009-12-17 — — JP claimed
EP-2046491-A2 SULFONATED POLYARYLENE COMPOUNDS, MEMBRANE MATERIAL MADE THEREFROM, METHOD FOR THE PRODUCTION THEREOF, AND USE Leibniz-Institut für Polymerforschung Dresden e.V. (DE) 2009-04-15 — — EP claimed
WO-2008012222-A2 SULFONATED POLYARYLENE COMPOUNDS, MEMBRANE MATERIAL MADE THEREFROM, METHOD FOR THE PRODUCTION THEREOF, AND USE LEIBNIZ-INSTITUT FÜR POLYMERFORSCHUNG DRESDEN E.V. (DE) 2008-01-31 — — WO claimed
EP-0141692-B1 BIS-QUATERNARY SALTS AS PHASE TRANSFER CATALYSTS FOR AROMATIC ETHER IMIDE PREPARATION GENERAL ELECTRIC COMPANY (US) 1989-10-25 — — EP claimed
CN-110914383-B Liquid crystal polymer shell material 离子材料第二公司 2024-03-08 — — CN disclosed
US-20240052103-A1 POLYMER AND TRIAZINE COMPOUND TOKYO OHKA KOGYO CO., LTD. (JP) 2024-02-15 — — US disclosed
US-20230344042-A1 LIQUID CRYSTAL POLYMER BATTERY ENCLOSURE MATERIAL IONIC MATERIALS, INC. (US) 2023-10-26 — — US disclosed
EP-4263752-A1 LIQUID CRYSTAL POLYMER COMPOSITE, LIQUID CRYSTAL POLYMER COMPOSITE FILM, AND METAL-CLAD LAMINATE INCLUDING SAME Ionic Materials, Inc. (US) 2023-10-25 — — EP disclosed
CN-116848216-A Liquid crystal polymer composite, liquid crystal polymer composite film, and metal-clad laminate including the same 离子材料公司 2023-10-03 — — CN disclosed
US-11695178-B2 Liquid crystal polymer battery enclosure material IONIC MATERIALS, INC. (US) 2023-07-04 — — US disclosed
US-4550210-A Process for preparing halogen-terminated oligomers useful in the production of acetylene-terminated resins THE UNIVERSITY OF DAYTON (US) 1985-10-29 — — US disclosed
EP-0142835-A2 Bis-aminopyridinium salts and their use as phase transfer catalysts for aromatic ether imide preparation GENERAL ELECTRIC COMPANY (US) 1985-05-29 — — EP disclosed
EP-0141692-A1 Bis-quaternary salts as phase transfer catalysts for aromatic ether imide preparation GENERAL ELECTRIC COMPANY (US) 1985-05-15 — — EP disclosed
US-4440920-A ISOPHTHALIC OR TEREPHTHALIC ACID WITH BIS/HYDROXYPHENYL/ SULFONE AND 2,2-BIS/4-HYDROXYPHENYL/PROPANE MITSUI TOATSU CHEMICALS, INC. (JP) 1984-04-03 — — US disclosed
EP-0077834-A1 AROMATIC POLYESTER MITSUI TOATSU CHEMICALS, Inc. (JP) 1983-05-04 — — EP disclosed
US-4356325-A Process for preparation of acetylene terminated sulfones, oligomers and precursors therefor GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-10-26 — — US disclosed
US-3975322-A CHAIN EXTENDED WITH DIHYDROXYDIPHENYL SULFONE, ESTERIFIED WITH DRYING OIL ACID, PRIMERS WESTINGHOUSE ELECTRIC CORPORATION (US) 1976-08-17 — — 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 (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-20240052103-A1 POLYMER AND TRIAZINE COMPOUND TERT, TERB1, MCM5 HSD17B1 1152/4885HSD17B2 1370/4885CA2 4791/4885

“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.