SCHEMBL8737704

SCHEMBL8737704

CCOc1ccc(Oc2ccc(C)cc2)cc1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 3/20 0.68
NQO1 P15559 1/20 0.67
TDP1 Q9NUW8 2/20 0.54
TEAD4 Q15561 1/20 0.54
TSHR P16473 1/20 0.54
ALDH1A1 P00352 1/20 0.52
POLB P06746 1/20 0.52
MAPT P10636 1/20 0.52
MAOB P27338 1/20 0.49
NPBWR1 P48145 2/20 0.47
MCHR1 Q99705 2/20 0.47
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46
PARP10 Q53GL7 1/20 0.45
DRD2 P14416 1/20 0.45
DRD4 P21917 1/20 0.45
DRD3 P35462 1/20 0.45
RELA Q04206 1/20 0.45
CA12 O43570 1/20 0.45
CA1 P00915 1/20 0.45

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
SCHEMBL92159 0.93 NQO1 (0.78) LTA4HNQO1TDP1TSHRALDH1A1
Ammonia Solution, Strong SCHEMBL27799297 0.90 NQO1 (0.74) LTA4HNQO1TDP1TSHRALDH1A1
SCHEMBL12476726 0.90 NQO1 (0.82) LTA4HNQO1TDP1TSHRALDH1A1
SCHEMBL6285912 0.90 NQO1 (0.82) LTA4HNQO1TDP1TSHRALDH1A1
SCHEMBL12736285 0.86 NQO1 (0.67) LTA4HNQO1TDP1TSHRALDH1A1
Cyanide SCHEMBL28150915 0.86 NQO1 (0.67) LTA4HNQO1TDP1TSHRALDH1A1
SCHEMBL2492122 0.86 NQO1 (0.67) LTA4HNQO1TDP1TSHRALDH1A1
Phenetole SCHEMBL28299913 0.85 LTA4H (0.72) LTA4HNQO1ALDH1A1MAPTMEN1
SCHEMBL8736875 0.84 LTA4H (0.60) LTA4HNQO1TDP1ALDH1A1MAPT
SCHEMBL1688856 0.83 TEAD4 (0.56) LTA4HTDP1TEAD4ALDH1A1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9271998-B2 Method of inhibiting nonsense-mediated mRNA decay RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2016-03-01 US disclosed
US-20140206637-A1 Inhibition of Nonsense Mediated mRNA Decay by Drugs that Prevent Hypusination of Eukaryotic Initiation Factor 5A RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2014-07-24 US disclosed
US-20140073685-A1 METHOD OF INHIBITING NONSENSE-MEDIATED mRNA DECAY RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2014-03-13 US disclosed
US-20120149706-A1 INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS DUMAS JACQUES (US) 2012-06-14 US disclosed
US-20120149706-A1 INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS DUMAS JACQUES (US) 2012-06-14 US disclosed
US-20120129893-A1 Inhibition Of Raf Kinase Using Substituted Heterocyclic Ureas DUMAS JACQUES (US) 2012-05-24 US disclosed
US-20120129893-A1 Inhibition Of Raf Kinase Using Substituted Heterocyclic Ureas DUMAS JACQUES (US) 2012-05-24 US disclosed
US-20120046290-A1 INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS BAYER HEALTHCARE LLC 2012-02-23 US disclosed
US-20120046290-A1 INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS BAYER HEALTHCARE LLC 2012-02-23 US disclosed
US-20070299043-A1 Anti-scarring drug combinations and use thereof HUNTER WILLIAM L 2007-12-27 US disclosed
US-20070244120-A1 INHIBITION OF RAF KINASE USING SUBSTITUTED HETEROCYCLIC UREAS BAYER HEALTHCARE LLC 2007-10-18 US disclosed
US-20070244120-A1 INHIBITION OF RAF KINASE USING SUBSTITUTED HETEROCYCLIC UREAS BAYER HEALTHCARE LLC 2007-10-18 US disclosed
US-20070208134-A1 Anti-scarring drug combinations and use thereof HUNTER WILLIAM L 2007-09-06 US disclosed
US-20070196421-A1 Soft tissue implants and drug combination compositions, and use thereof ANGIOTECH INTERNATIONAL AG (CH) 2007-08-23 US disclosed
US-20070198063-A1 Electrical devices and anti-scarring drug combinations HUNTER WILLIAM L 2007-08-23 US disclosed
US-20070197957-A1 Implantable sensors, implantable pumps and anti-scarring drug combinations HUNTER WILLIAM L 2007-08-23 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 (9 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-20140073685-A1 METHOD OF INHIBITING NONSENSE-MEDIATED mRNA DECAY EIF5B, RNMT, SARM1 LTA4H 2306/4885NQO1 33/4885TDP1 605/4885
US-20120149706-A1 INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS MAPK1, MAP3K1, MAP3K7 LTA4H 1342/4885NQO1 1264/4885TDP1 1729/4885
US-20120046290-A1 INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS MAPK1, MAP3K1, MAP3K7 LTA4H 1342/4885NQO1 1264/4885TDP1 1729/4885
US-20070244120-A1 INHIBITION OF RAF KINASE USING SUBSTITUTED HETEROCYCLIC UREAS BRAF, RAF1, ARAF LTA4H 4145/4885NQO1 2043/4885TDP1 2205/4885
US-20070208134-A1 Anti-scarring drug combinations and use thereof MMP1, COL2A1, COL1A1 LTA4H 208/4885NQO1 2719/4885TDP1 3275/4885
US-20070196421-A1 Soft tissue implants and drug combination compositions, and use thereof COL2A1, MMP1, FN1 LTA4H 179/4885NQO1 3499/4885TDP1 2902/4885
US-20120129893-A1 Inhibition Of Raf Kinase Using Substituted Heterocyclic Ureas BRAF, RAF1, ARAF LTA4H 4145/4885NQO1 2043/4885TDP1 2205/4885
US-20070299043-A1 Anti-scarring drug combinations and use thereof MMP1, COL2A1, COL1A1 LTA4H 208/4885NQO1 2719/4885TDP1 3275/4885
US-20140206637-A1 Inhibition of Nonsense Mediated mRNA Decay by Drugs that Prevent Hypusination of Eukaryotic Initiation Factor 5A EIF5B, UPF1, NUDT21 LTA4H 1953/4885NQO1 83/4885TDP1 693/4885

“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.