Ethylene Glycol

Ethylene Glycol

SCHEMBL206376

C=CC.O.OCCO

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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 SCHEMBL15110 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL3058481 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL9133774 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL3197361 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL3200076 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL4769225 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL5830392 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL3171689 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL9756248 0.96 TSHR (0.46)
Ethylene Glycol SCHEMBL622577 0.96 TSHR (0.46)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113242860-B Alkyl lithium aluminate as transalkylation reagent 优美科股份公司及两合公司 2024-01-02 CN claimed
US-11384102-B2 Lithium alkyl aluminates as alkyl transfer reagents UMICORE AG & CO. KG (DE) 2022-07-12 US claimed
EP-3894419-A1 LITHIUM ALKYL ALUMINATES AS ALKYL TRANSFER REAGENTS UMICORE AG & Co. KG (DE) 2021-10-20 EP claimed
WO-2020120148-A1 LITHIUM ALKYL ALUMINATES AS ALKYL TRANSFER REAGENTS UMICORE AG. & CO. KG. (DE) 2020-06-18 WO claimed
CN-106146446-B Dapagliflozin semihydrate and its crystal form, preparation method and pharmaceutical composition 杭州领业医药科技有限公司 2019-11-08 CN claimed
CN-108516966-A Crystal form of Dapagliflozin and its preparation method and application 浙江海正药业股份有限公司 2018-09-11 CN claimed
WO-2018142422-A1 PROCESS FOR THE PREPARATION OF DAPAGLIFLOZIN INDOCO REMEDIES LIMITED (IN) 2018-08-09 WO claimed
EP-2498759-B1 IMMEDIATE RELEASE TABLET FORMULATIONS ASTRAZENECA AB (SE) 2018-08-01 EP claimed
US-8716251-B2 Pharmaceutical formulations containing an SGLT2 inhibitor BRISTOL-MYERS SQUIBB COMPANY (US) 2014-05-06 US claimed
US-20130129819-A1 Pharmaceutical Formulations Containing An SGLT2 Inhibitor BRISTOL-MYERS SQUIBB COMPANY (US) 2013-05-23 US claimed
US-20130034606-A1 IMMEDIATE RELEASE TABLET FORMULATIONS ASTRAZENECA UK LIMITED (GB) 2013-02-07 US claimed
EP-2498759-A2 IMMEDIATE RELEASE TABLET FORMULATIONS Bristol-Myers Squibb Company (US) 2012-09-19 EP claimed
WO-2011060290-A2 IMMEDIATE RELEASE TABLET FORMULATIONS Bristol-Myer Squibb Company (US) 2011-05-19 WO claimed
EP-4431088-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING DAPAGLIFLOZIN AND METFORMIN Galenicum Health S.L.U. (ES) 2024-09-18 EP disclosed
EP-4427742-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING DAPAGLIFLOZIN AND METFORMIN Galenicum Health S.L.U. (ES) 2024-09-11 EP disclosed
CN-113242860-B Alkyl lithium aluminate as transalkylation reagent 优美科股份公司及两合公司 2024-01-02 CN disclosed
EP-2139494-A1 PHARMACEUTICAL FORMULATIONS CONTAINING DAPAGLIFLOZIN PROPYLENE GLYCOL HYDRATE Bristol-Myers Squibb Company (US) 2010-01-06 EP disclosed
WO-2008116179-A1 PHARMACEUTICAL FORMULATIONS CONTAINING DAPAGLIFLOZIN PROPYLENE GLYCOL HYDRATE BRISTOL-MYERS SQUIBB (US) 2008-09-25 WO disclosed
US-20080234367-A1 Sodium dependent glucose transporter (SGLT2); such as dapagliflozin, dapagliflozin-PGS, a C-glucoside or an O-glucoside BRISTOL-MYERS SQUIBB (US) 2008-09-25 US disclosed
US-20080234366-A1 Dapagliflozin propylene glycol hydrate; diabetes; immediate release; sodium dependent glucose transporter (SGLT2) inhibitor BRISTOL-MYERS SQUIBB (US) 2008-09-25 US disclosed