Ethylene Glycol

Ethylene Glycol

SCHEMBL8677488

CN(C)c1cccc(C(=O)O)c1.CN(C)c1cccc(C(=O)O)c1.OCCO

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.56
L3MBTL1 Q9Y468 1/20 0.56
KDM4E B2RXH2 5/20 0.50
RAB9A P51151 4/20 0.50
NPC1 O15118 3/20 0.50
SMN1; SMN2 Q16637 2/20 0.50
LMNA P02545 2/20 0.50
HSD17B10 Q99714 2/20 0.50
GFER P55789 1/20 0.50
TMEM97 Q5BJF2 1/20 0.49
SIGMAR1 Q99720 1/20 0.49
POLB P06746 4/20 0.48
ALDH1A1 P00352 3/20 0.47
MEN1 O00255 2/20 0.47
HPGD P15428 2/20 0.47
MAPT P10636 1/20 0.47
ALOX15 P16050 1/20 0.47
GAA P10253 1/20 0.46
KLF5 Q13887 1/20 0.46
CA12 O43570 1/20 0.46

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
SCHEMBL222176 0.93 KMT2A (0.58) KMT2AL3MBTL1KDM4ERAB9ANPC1
SCHEMBL29625195 0.93 KMT2A (0.58) KMT2AL3MBTL1KDM4ERAB9ANPC1
SCHEMBL27761399 0.91 KMT2A (0.57) KMT2AL3MBTL1KDM4ERAB9ANPC1
Pyrrole SCHEMBL28037854 0.86 KMT2A (0.54) KMT2AL3MBTL1KDM4ERAB9ANPC1
Isophthalic Acid SCHEMBL3867184 0.80 CA12 (0.60) L3MBTL1HSD17B10HPGDCA12CA1
SCHEMBL11108445 0.80 KMT2A (0.58) KMT2AL3MBTL1KDM4ERAB9ANPC1
SCHEMBL7056764 0.79 HPGD (0.59) KMT2AL3MBTL1KDM4ERAB9ANPC1
SCHEMBL28555578 0.79 KMT2A (0.47) KMT2AL3MBTL1KDM4ERAB9ANPC1
SCHEMBL31412787 0.79 CYP2C19 (0.46) LMNAHSD17B10ALDH1A1HPGDCA12
SCHEMBL31412786 0.79 CYP2C19 (0.46) LMNAHSD17B10ALDH1A1HPGDCA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5707559-A PROVIDING A STABLE 1,2-DIOXETANE WHICH FORMS INTERMEDIATE UNSTABLE COMPOUNDS WHEN TRIGGERED TO REMOVE BLOCKING GROUPS BY ACTIVATING AGENT SO THAT UNSTABLE COMPOUND DECOMPOSES TO FORM LIGHT AND TWO CARBONYL COMPOUNDS TROPIX, INC. (US) 1998-01-13 US disclosed
EP-0595369-B1 Alkene compounds TROPIX INC (US) 1996-12-04 EP disclosed
US-5386017-A Can be converted to stable aryl substituted 1,2-dioxetanes which decompose when activated to produce light and carbonyl compounds BOARD OF GOVERNORS OF WAYNE STATE UNIVERSITY (US) 1995-01-31 US disclosed
EP-0254051-B1 Chemiluminescent 1,2-dioxetane compounds UNIV WAYNE STATE (US) 1994-08-31 EP disclosed
EP-0595369-A1 Alkene compounds TROPIX, INC. (US) 1994-05-04 EP disclosed
US-4962192-A Chemiluminescent 1,2-dioxetane compounds BOARD OF GOVERNORS OF WAYNE STATE UNIVERSITY (US) 1990-10-09 US disclosed
US-4857652-A Chemiluminescent 1,2-dioxetane compounds BOARD OF GOVERNORS OF WAYNE STATE UNIVERSITY (US) 1989-08-15 US disclosed
EP-0254051-A2 Chemiluminescent 1,2-dioxetane compounds THE BOARD OF GOVERNORS OF WAYNE STATE UNIVERSITY (US) 1988-01-27 EP disclosed