Ethylene Glycol

Ethylene Glycol

SCHEMBL3402355

OCCO.Oc1ccc(Oc2ccc(O)cc2)cc1

nearest known ligand 0.78

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MEN1 O00255 2/20 0.78
▸ KMT2A Q03164 2/20 0.78
▸ ESR1 P03372 1/20 0.78
▸ ESR2 Q92731 1/20 0.78
▸ LTA4H P09960 7/20 0.64
▸ NR1H2 P55055 1/20 0.64
▸ BAX Q07812 1/20 0.64
▸ PARP10 Q53GL7 1/20 0.52
▸ CA2 P00918 2/20 0.46
▸ LMNA P02545 2/20 0.44
▸ HIF1A Q16665 2/20 0.44
▸ KDM4E B2RXH2 1/20 0.44
▸ NPC1 O15118 1/20 0.44
▸ CA12 O43570 1/20 0.44
▸ GMNN O75496 1/20 0.44
▸ ALDH1A1 P00352 1/20 0.44
▸ CA1 P00915 1/20 0.44
▸ CA3 P07451 1/20 0.44
▸ CYP3A4 P08684 1/20 0.44
▸ MAPT P10636 1/20 0.44

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
SCHEMBL3175106 0.88 ESR2 (1.00) MEN1KMT2AESR1ESR2LTA4H
SCHEMBL249169 0.88 ESR2 (1.00) MEN1KMT2AESR1ESR2LTA4H
SCHEMBL7811939 0.88 ESR2 (1.00) MEN1KMT2AESR1ESR2LTA4H
SCHEMBL18198 0.88 ESR2 (1.00) MEN1KMT2AESR1ESR2LTA4H
Di(Hydroxyethyl)Ether SCHEMBL2471329 0.85 MEN1 (0.64) MEN1KMT2AESR1ESR2LTA4H
Hydrogen Sulfide SCHEMBL27529439 0.85 MEN1 (0.93) MEN1KMT2AESR1ESR2LTA4H
Water SCHEMBL8862151 0.85 MEN1 (0.93) MEN1KMT2AESR1ESR2LTA4H
Bromide SCHEMBL11037542 0.82 MEN1 (0.88) MEN1KMT2AESR1ESR2LTA4H
SCHEMBL5124930 0.82 LTA4H (0.68) MEN1KMT2AESR1ESR2LTA4H
Hydroquinone SCHEMBL10547720 0.82 ALDH1A1 (0.67) MEN1KMT2AESR1ESR2NR1H2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12577391-B2 Chemically-resistant flame retardant compositions SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2026-03-17 — — US disclosed
US-20250002717-A1 THERMOPLASTIC COMPOSITIONS AND USES THEREOF SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2025-01-02 — — US disclosed
US-20240101819-A1 CURABLE COMPOSITION CONTAINING CYCLIC MULTIFUNCTIONAL MONOMER TOKUYAMA CORPORATION (JP) 2024-03-28 — — US disclosed
US-20240101751-A1 HOLLOW MICROBALLOON TOKUYAMA CORPORATION (JP) 2024-03-28 — — US disclosed
US-20240084067-A1 NOVEL CURABLE COMPOSITION CONTAINING CYCLIC MONOMER TOKUYAMA CORPORATION (JP) 2024-03-14 — — US disclosed
US-20230390890-A1 POLYMERIZABLE FUNCTIONAL GROUP-CONTAINING MICROBALLOON TOKUYAMA CORPORATION (JP) 2023-12-07 — — US disclosed
EP-4286435-A1 NOVEL CURABLE COMPOSITION CONTAINING CYCLIC MONOMER Tokuyama Corporation (JP) 2023-12-06 — — EP disclosed
EP-4286439-A1 HOLLOW MICROBALLOON Tokuyama Corporation (JP) 2023-12-06 — — EP disclosed
EP-4286442-A1 CURABLE COMPOSITION CONTAINING CYCLIC MULTIFUNCTIONAL MONOMER Tokuyama Corporation (JP) 2023-12-06 — — EP disclosed
WO-2023167294-A1 METHOD FOR PRODUCING HOLLOW MICROPARTICLES USING SUPERCRITICAL LIQUID 株式会社トクヤマ 2023-09-07 — — WO disclosed
US-4743676-A Method for preparing polycarbonate of controlled molecular weight from aromatic bischloroformate GENERAL ELECTRIC COMPANY (US) 1988-05-10 — — US disclosed
EP-0264835-A2 Cyclic polyester oligomers and methods for their preparation and use GENERAL ELECTRIC COMPANY (US) 1988-04-27 — — EP disclosed
US-4740583-A Method for converting cyclic polycarbonate oligomer mixtures to linear polycarbonate, and composition resulting therefrom GENERAL ELECTRIC COMPANY (US) 1988-04-26 — — US disclosed
EP-0263432-A1 Method for preparing aromatic bischloroformate compositions and polycarbonates GENERAL ELECTRIC COMPANY (US) 1988-04-13 — — EP disclosed
US-4737573-A USING PHOSGENE, DIHYDROXY COMPOUND, WATER AND AN INERT ORGANIC LIQUID AT A BASIC PH, FOLLOWED BY INTERFACIAL CATALYTIC POLYMERIZATION GENERAL ELECTRIC COMPANY (US) 1988-04-12 — — US disclosed
US-4736016-A HIGH GLASS TRANSITION TEMPERATURE GENERAL ELECTRIC COMPANY (US) 1988-04-05 — — US disclosed
EP-0257467-A2 Composition and method for controlling polymerization rate of cyclic polycarbonate oligomers GENERAL ELECTRIC COMPANY (US) 1988-03-02 — — EP disclosed
EP-0254995-A1 Cyclic polycarbonate oligomers from spirobiindane bisphenols GENERAL ELECTRIC COMPANY (US) 1988-02-03 — — EP disclosed
US-4722994-A Method of preparing cyclic oligomeric polycarbonates GENERAL ELECTRIC COMPANY (US) 1988-02-02 — — US disclosed
US-4696998-A Cyclic heterocarbonates and methods for their preparation and use GENERAL ELECTRIC COMPANY (US) 1987-09-29 — — 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-12577391-B2 Chemically-resistant flame retardant compositions RPL3, RPL4, UFM1 MEN1 4095/4885KMT2A 2027/4885ESR1 1778/4885

“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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