Ether

Ether

SCHEMBL907948

CC(C)=O.CCOCC.CO

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 8/20 0.50
TSHR P16473 2/20 0.50
LMNA P02545 2/20 0.47
HSD17B10 Q99714 1/20 0.47
THRB P10828 1/20 0.42
TDP1 Q9NUW8 2/20 0.41
ALOX15 P16050 1/20 0.38
MGAM O43451 1/20 0.38
GAA P10253 1/20 0.38
SI P14410 1/20 0.38
MGAM2 Q2M2H8 1/20 0.38
SOAT1 P35610 1/20 0.38
TRPA1 O75762 1/20 0.35
GLO1 Q04760 1/20 0.35
FFAR3 O14843 1/20 0.33
CES2 O00748 1/20 0.33

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
Ether SCHEMBL7531159 0.96 ALDH1A1 (0.52) ALDH1A1TSHRLMNAHSD17B10THRB
Ether SCHEMBL1234081 0.96 ALDH1A1 (0.52) ALDH1A1TSHRLMNAHSD17B10THRB
Ether SCHEMBL3336965 0.96 ALDH1A1 (0.52) ALDH1A1TSHRLMNAHSD17B10THRB
Ether SCHEMBL9353265 0.96 ALDH1A1 (0.52) ALDH1A1TSHRLMNAHSD17B10THRB
Ether SCHEMBL164114 0.96
Ether SCHEMBL8865297 0.93 ALDH1A1 (0.50) ALDH1A1TSHRLMNAHSD17B10THRB
Ether SCHEMBL10836087 0.93 ALDH1A1 (0.50) ALDH1A1TSHRLMNAHSD17B10THRB
Ether SCHEMBL11301526 0.93 ALDH1A1 (0.50) ALDH1A1TSHRLMNAHSD17B10THRB
Ether SCHEMBL4686512 0.90 ALDH1A1 (0.48) ALDH1A1TSHRLMNAHSD17B10THRB
Ether SCHEMBL6524630 0.90 ALDH1A1 (0.48) ALDH1A1TSHRLMNAHSD17B10THRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160008322-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF CARDIOME PHARMA CORP (CA) 2016-01-14 US disclosed
US-20140314685-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF CARDIOME PHARMA CORP. (CA) 2014-10-23 US disclosed
US-20130171077-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF CARDIOME PHARMA CORP. (CA) 2013-07-04 US disclosed
US-8008342-B2 Ion channel modulating compounds and uses thereof CARDIOME PHARMA CORP. (CA) 2011-08-30 US disclosed
US-20110207730-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF CARDIOME PHARMA CORP. (CA) 2011-08-25 US disclosed
US-7875611-B2 (+)-trans-[2-(4-morpholinyl)-1-[2-(2-naphthoxy)ethoxy)]; (1R,2R)/(1S,2S)-2-[1,4-dioxa-7-azaspiro[4.4]non-7-yl]-1-(1-naphthenethoxy)cyclohexanecyclohexane; treatment of arrhythmia and the production of analgesia and local anesthesia CARDIOME PHARMA CORP. (CA) 2011-01-25 US disclosed
US-20100056603-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF CARDIOME PHARMA CORP. (CA) 2010-03-04 US disclosed
US-20100029639-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF CARDIOME PHARMA CORP. (CA) 2010-02-04 US disclosed
US-7534790-B2 Ion channel modulating compounds and uses thereof CARDIOME PHARMA CORP. (CA) 2009-05-19 US disclosed
US-7524879-B2 Ion channel modulating compounds and uses thereof CARDIOME PHARMA CORP. (CA) 2009-04-28 US disclosed
EP-0375351-B1 Phosphonic acid substituted steroids as steroid 5alpha-reductase inhibitors SMITHKLINE BEECHAM CORP (US) 1994-08-31 EP disclosed
EP-0375349-B1 Phosphinic acid substituted steroids as inhibitors of steroid 5alpha-reductase SMITHKLINE BEECHAM CORP (US) 1994-08-31 EP disclosed
WO-1993015080-A1 AZABICYCLO COMPOUNDS AS CALCIUM CHANNEL ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 1993-08-05 WO disclosed
WO-1993015073-A1 AZABRICYCLIC COMPOUNDS AS CALCIUM CHANNEL ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 1993-08-05 WO disclosed
US-5026882-A Phosphinic acid substituted steroids as inhibitors of steroid 5α-reductase SMITHKLINE BEECHAM CORPORATION (US) 1991-06-25 US disclosed
US-4946834-A ACRYLATE ANALOGUES OF STEROIDAL SYNTHETIC COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 1990-08-07 US disclosed
EP-0375351-A1 Phosphonic acid substituted steroids as steroid 5alpha-reductase inhibitors SMITHKLINE BEECHAM CORPORATION (US) 1990-06-27 EP disclosed
EP-0375349-A1 Phosphinic acid substituted steroids as inhibitors of steroid 5alpha-reductase SMITHKLINE BEECHAM CORPORATION (US) 1990-06-27 EP disclosed
US-4338453-A Aminoalkyl-1,2,4-triazoles THE UPJOHN COMPANY (US) 1982-07-06 US disclosed
US-3991207-A TETRAHYDRONAPHTHYLAMINES AND L-3,4-DIHYDROXYPHENYL-ALANINE PFIZER INC. (US) 1976-11-09 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 (6 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-20130171077-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF TRPV1, TRPA1, KCNN2 ALDH1A1 1319/4885TSHR 2898/4885LMNA 2669/4885
US-20110207730-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF TRPV1, TRPA1, KCNN2 ALDH1A1 1319/4885TSHR 2898/4885LMNA 2669/4885
US-20100056603-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF TRPV1, TRPA1, KCNN2 ALDH1A1 1319/4885TSHR 2898/4885LMNA 2669/4885
US-20160008322-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF TRPV1, TRPA1, KCNN2 ALDH1A1 1319/4885TSHR 2898/4885LMNA 2669/4885
US-20140314685-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF TRPV1, TRPA1, KCNN2 ALDH1A1 1319/4885TSHR 2898/4885LMNA 2669/4885
US-20100029639-A1 ION CHANNEL MODULATING COMPOUNDS AND USES THEREOF TRPV1, TRPA1, KCNN2 ALDH1A1 1319/4885TSHR 2898/4885LMNA 2669/4885

“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.