Ethylene Glycol

Ethylene Glycol

SCHEMBL241885

Cc1ccc(S(=O)(=O)O)cc1.Cc1ccc(S(=O)(=O)O)cc1.OCCO

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Ethylene Glycol. 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
GAA P10253 2/20 0.52
ALDH1A1 P00352 6/20 0.51
SMN1; SMN2 Q16637 4/20 0.51
LMNA P02545 2/20 0.51
KDM4E B2RXH2 1/20 0.51
MAPT P10636 1/20 0.51
HTT P42858 1/20 0.51
TDP1 Q9NUW8 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
RECQL P46063 1/20 0.50
SNCA P37840 1/20 0.49
CA1 P00915 2/20 0.48
CA2 P00918 2/20 0.48
CYP2C9 P11712 2/20 0.48
MMP1 P03956 1/20 0.48
MMP2 P08253 1/20 0.48
MMP9 P14780 1/20 0.48
MMP8 P22894 1/20 0.48
MMP13 P45452 1/20 0.48
CYP3A4 P08684 1/20 0.48

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
Ethylene Glycol SCHEMBL4370506 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL1617251 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL6046437 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL6046435 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL1617625 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL1936216 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL6046494 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL1247518 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL3283790 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E
Ethylene Glycol SCHEMBL19210022 1.00 GAA (0.52) GAAALDH1A1SMN1; SMN2LMNAKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120020119-A Process for preparing N- (2-substituted ethyl) amides and N-vinyl amides 中国石油化工股份有限公司 2025-05-20 CN claimed
CN-117865858-A Novel PET imaging agent targeting cannabinoid type 2 receptor, preparation method and application thereof 浙江大学 2024-04-12 CN claimed
CN-114989166-B Tumor KRAS G12C mutation targeting positron tracer agent, preparation method and application 中国人民解放军空军军医大学 2023-10-10 CN claimed
CN-114989166-A Tumor KRAS G12C mutation targeted positron tracer, preparation method and application 中国人民解放军空军军医大学 2022-09-02 CN claimed
CN-108017593-B Simple, convenient and efficient 1-oxo-4, 5-diazepane synthesis method 东南大学 2021-05-11 CN claimed
CN-110734426-A Acetylcholinesterase degradation compound and preparation method and application thereof 浙江省医学科学院 2020-01-31 CN claimed
US-20160096820-A1 INHIBITORS OF INV(16) LEUKEMIA UNIVERSITY OF VIRGINIA PATENT FOUNDATION 2016-04-07 US claimed
US-6776930-B2 POLYMER BONDED TO DYE EASTMAN KODAK COMPANY 2004-08-17 US claimed
US-20010023938-A1 Polymer bonded to dye ALLEN MAX (US) 2001-09-27 US claimed
US-12404269-B2 Aminoquinazolinone and aminoisoquinolinone derivatives and application thereof ZHEJIANG UNIVERSITY (CN) 2025-09-02 US disclosed
CN-116283955-B Compound for targeted degradation of HDAC7, and preparation method and application thereof 浙江大学 2025-06-17 CN disclosed
CN-120020119-A Process for preparing N- (2-substituted ethyl) amides and N-vinyl amides 中国石油化工股份有限公司 2025-05-20 CN disclosed
CN-115819193-B Synthesis method of binary symmetrical hydrofluoroether 浙江诺亚氟化工有限公司 2024-09-10 CN disclosed
CN-118065133-A Unsaturated ion phosphonate composition and preparation method thereof 江苏海洋大学 2024-05-24 CN disclosed
EP-0747448-A2 Rigidized monomethine cyanine dyes CARNEGIE-MELLON UNIVERSITY (US) 1996-12-11 EP disclosed
US-5545785-A Process for preparing biscyclopentadienyl compounds WITCO GMBH (DE) 1996-08-13 US disclosed
EP-0343897-A1 Seawater-insoluble hydrolysable polymers and marine anti-fouling paint containing them COURTAULDS COATINGS (HOLDINGS) LIMITED (GB) 1989-11-29 EP disclosed
US-4492788-A Partially deacylated ultra-high molecular weight poly(N-propionylethylenimines) ALLIED CORPORATION (US) 1985-01-08 US disclosed
US-4137080-A POLYFUNCTIONAL COUPLER AND DEVELOPER KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1979-01-30 US disclosed
US-4064260-A Anti-inflammatory diarylimidazothiazoles and their corresponding S-oxides E. I. DU PONT DE NEMOURS AND COMPANY (US) 1977-12-20 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-12404269-B2 Aminoquinazolinone and aminoisoquinolinone derivatives and application thereof PIK3R5, PIK3CA, PIK3R1 GAA 1385/4885ALDH1A1 2788/4885SMN1; SMN2 4463/4885
US-20160096820-A1 INHIBITORS OF INV(16) LEUKEMIA FLI1, MCL1, CBFB GAA 4210/4885ALDH1A1 4339/4885SMN1; SMN2 760/4885

“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.