SCHEMBL3067341

SCHEMBL3067341

CC(C)OC(=O)NC(N)=O

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.43
CRBN Q96SW2 1/20 0.43
HPGD P15428 2/20 0.38
CYP2C9 P11712 2/20 0.38
CYP1A2 P05177 2/20 0.38
NPC1 O15118 1/20 0.38
CYP2D6 P10635 1/20 0.38
CYP2C19 P33261 1/20 0.38
RAB9A P51151 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
KDM4E B2RXH2 1/20 0.36
GLA P06280 1/20 0.35
ALOX15 P16050 2/20 0.35
HCAR2 Q8TDS4 1/20 0.34
HTT P42858 1/20 0.34
GAA P10253 1/20 0.33
LMNA P02545 2/20 0.32
CHRM2 P08172 1/20 0.32
CHRM4 P08173 1/20 0.32
CHRM5 P08912 1/20 0.32

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
SCHEMBL11437545 0.86 TSHR (0.50) TSHRHPGDCYP2C9CYP1A2NPC1
SCHEMBL6272695 0.83 TAS2R38 (0.46) TSHRCRBNHPGDCYP2C9CYP1A2
SCHEMBL19509181 0.82 TSHR (0.42) TSHRCRBNHPGDCYP2C9CYP1A2
SCHEMBL23059563 0.80 LAP3 (0.39) TSHRCRBNCYP2C9LMNACHRM2
SCHEMBL26363428 0.80 CRBN (0.36) TSHRCRBNCYP2C9RAB9AGLA
SCHEMBL13063715 0.79 TSHR (0.50) TSHRCRBNHPGDCYP2C9CYP1A2
SCHEMBL24268019 0.79 TSHR (0.43) TSHRHPGDCYP2C9CYP1A2NPC1
SCHEMBL1134094 0.76
SCHEMBL441968 0.76 TSHR (0.46) TSHRHPGDCYP2C9CYP1A2NPC1
SCHEMBL3067343 0.75 TSHR (0.40) TSHRCRBNCYP2C9GLAHCAR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9683082-B2 Process to produce polycarbamate using a gradient feed of urea DOW GLOBAL TECHNOLOGIES LLC (US) 2017-06-20 US disclosed
US-9683082-B2 Process to produce polycarbamate using a gradient feed of urea DOW GLOBAL TECHNOLOGIES LLC (US) 2017-06-20 US disclosed
US-20160177033-A1 PROCESS TO PRODUCE POLYCARBAMATE USING A GRADIENT FEED OF UREA DOW GLOBAL TECHNOLOGIES LLC 2016-06-23 US disclosed
US-9006379-B2 Process to produce polycarbamate using a gradient feed of urea DOW GLOBAL TECHNOLOGIES LLC (US) 2015-04-14 US disclosed
US-20150038669-A1 Process to Produce Polycarbamate Using a Gradient Feed of Urea DOW GLOBAL TECHNOLOGIES LLC (US) 2015-02-05 US disclosed
US-20150038669-A1 Process to Produce Polycarbamate Using a Gradient Feed of Urea DOW GLOBAL TECHNOLOGIES LLC (US) 2015-02-05 US disclosed
US-7833331-B2 Non-toxic corrosion-protection pigments based on cobalt UNIVERSITY OF DAYTON (US) 2010-11-16 US disclosed
US-7789958-B2 Non-toxic corrosion-protection pigments based on manganese UNIVERSITY OF DAYTON (US) 2010-09-07 US disclosed
US-20100028300-A1 MACROCYCLIC PEPTIDES ACTIVE AGAINST THE HEPATITIS C VIRUS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2010-02-04 US disclosed
US-20100028300-A1 MACROCYCLIC PEPTIDES ACTIVE AGAINST THE HEPATITIS C VIRUS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2010-02-04 US disclosed
US-20040020568-A1 Non-toxic corrosion-protection conversion coats based on rare earth elements DAYTON, UNIVERSITY OF 2004-02-05 US disclosed
US-20040016910-A1 Non-toxic corrosion-protection rinses and seals based on rare earth elements DAYTON, UNIVERSITY OF 2004-01-29 US disclosed
US-20040011252-A1 Non-toxic corrosion-protection pigments based on manganese UNIVERSITY OF DAYTON 2004-01-22 US disclosed
US-20030234063-A1 Non-toxic corrosion-protection conversion coats based on cobalt DAYTON, UNIVERSITY OF 2003-12-25 US disclosed
US-20030230363-A1 Non-toxic corrosion-protection rinses and seals based on cobalt UNIVERSITY OF DAYTON 2003-12-18 US disclosed
WO-2003060192-A1 NON-TOXIC CORROSION-PROTECTION RINSES AND SEALS BASED ON COBALT UNIVERSITY OF DAYTON (US) 2003-07-24 WO disclosed
WO-2003060019-A1 NON-TOXIC CORROSION PROTECTION PIGMENTS BASED ON COBALT UNIVERSITY OF DAYTON (US) 2003-07-24 WO disclosed
EP-0588785-A1 UREA BASED LIPOXYGENASE INHIBITING COMPOUNDS ABBOTT LABORATORIES (US) 1994-03-30 EP disclosed
EP-0588785-A4 UREA BASED LIPOXYGENASE INHIBITING COMPOUNDS. ABBOTT LAB (US) 1991-12-30 EP disclosed
WO-1990012008-A1 UREA BASED LIPOXYGENASE INHIBITING COMPOUNDS ABBOTT LABORATORIES (US) 1990-10-18 WO 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 (1 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-20100028300-A1 MACROCYCLIC PEPTIDES ACTIVE AGAINST THE HEPATITIS C VIRUS CTRL, RPP30, RNASE1 TSHR 1719/4885CRBN 2248/4885HPGD 3244/4885

“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.