Di(Hydroxyethyl)Ether

Di(Hydroxyethyl)Ether

SCHEMBL11211981

CC(=O)O.CC(=O)OOC(C)=O.OCCOCCO

nearest known ligand 0.50

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Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Di(Hydroxyethyl)Ether. 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
ADRB2 known ✓ P07550 1/20 0.31
CHRNB4 known ✓ P30926 1/20 0.30
CHRNA3 known ✓ P32297 1/20 0.30
TSHR P16473 5/20 0.50
MAPK1 P28482 1/20 0.50
MEN1 O00255 2/20 0.48
KMT2A Q03164 2/20 0.48
ALDH1A1 P00352 6/20 0.42
THRB P10828 1/20 0.38
HTT P42858 1/20 0.38
MAPT P10636 1/20 0.38
FFAR3 O14843 1/20 0.35
LCK P06239 1/20 0.35
FYN P06241 1/20 0.35
LMNA P02545 1/20 0.31
HSD17B10 Q99714 1/20 0.31
ADRB3 P13945 1/20 0.31
GALR3 O60755 1/20 0.30
PGR P06401 1/20 0.30
CHRM2 P08172 1/20 0.30

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
Di(Hydroxyethyl)Ether SCHEMBL4528960 0.89 TSHR (0.62) TSHRMAPK1MEN1KMT2AALDH1A1
Di(Hydroxyethyl)Ether SCHEMBL27615302 0.89 TSHR (0.62) TSHRMAPK1MEN1KMT2AALDH1A1
Di(Hydroxyethyl)Ether SCHEMBL8642258 0.89 TSHR (0.62) TSHRMAPK1MEN1KMT2AALDH1A1
Di(Hydroxyethyl)Ether SCHEMBL36022 0.89 TSHR (0.62) TSHRMAPK1MEN1KMT2AALDH1A1
Di(Hydroxyethyl)Ether SCHEMBL9325783 0.89 TSHR (0.62) TSHRMAPK1MEN1KMT2AALDH1A1
Di(Hydroxyethyl)Ether SCHEMBL28435040 0.89 TSHR (0.62) TSHRMAPK1MEN1KMT2AALDH1A1
Di(Hydroxyethyl)Ether SCHEMBL271069 0.89 TSHR (0.62) TSHRMAPK1MEN1KMT2AALDH1A1
Triethylene Glycol SCHEMBL994880 0.87 MEN1 (0.65) TSHRMAPK1MEN1KMT2AALDH1A1
Acetic Acid SCHEMBL21878939 0.87 MEN1 (0.65) TSHRMAPK1MEN1KMT2AALDH1A1
Acetic Acid SCHEMBL21878891 0.87 MEN1 (0.65) TSHRMAPK1MEN1KMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4330376-A RHODIUM COATING ATLANTIC RICHFIELD COMPANY (US) 1982-05-18 US disclosed
US-4321231-A IN TH PRESENCE OF AN ACID, USING A TELLURIUM OR SELENIUM COMPOUND ATLANTIC RICHFIELD COMPANY (US) 1982-03-23 US disclosed
US-4238551-A RHODIUM COATING, ACID RESISTANCE HALCON RESEARCH & DEVELOPMENT CORPORATION (US) 1980-12-09 US disclosed
US-4153806-A Recovery of vicinal glycol esters by plural stage distillation HALCON RESEARCH AND DEVELOPMENT CORP. (US) 1979-05-08 US disclosed