SCHEMBL6160902

SCHEMBL6160902

CCOC(=O)N1CCN(c2cc[c]cc2)CC1

nearest known ligand 0.72

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MAPT P10636 7/20 0.72
GAA P10253 4/20 0.72
LMNA P02545 3/20 0.72
KDM4E B2RXH2 1/20 0.72
ALDH1A1 P00352 7/20 0.63
SMN1; SMN2 Q16637 3/20 0.63
HTT P42858 2/20 0.61
MAPK1 P28482 1/20 0.61
TSHR P16473 2/20 0.54
HPGD P15428 1/20 0.54
CASP1 P29466 1/20 0.54
NPSR1 Q6W5P4 1/20 0.54
ABL1 P00519 1/20 0.53
POLB P06746 1/20 0.53
RIN1 Q13671 1/20 0.53
TDP1 Q9NUW8 1/20 0.53
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.49

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
SCHEMBL15127501 0.85 MAPT (0.79) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL27610366 0.85 MAPT (0.74) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL5542809 0.84 MAPT (1.00) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL5542804 0.84 MAPT (0.77) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL2581059 0.83 MAPT (0.75) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL27676396 0.82 MAPT (0.53) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL3334981 0.82 LMNA (0.59) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL15009898 0.82 MAPT (0.69) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL28799444 0.82 MAPT (0.50) MAPTGAALMNAKDM4EALDH1A1
SCHEMBL8703730 0.81 MAPT (0.73) MAPTGAALMNAKDM4EALDH1A1

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
CN-103087122-A Preparation method and applications of glucoside compounds SHANGHAI INST ORGANIC CHEM 2013-05-08 CN claimed
US-6417186-B1 TREATING PAIN, URINARY TRACT INFECTIONS, INFLAMMATION, RESPIRATORY DISEASE STATES FROM ALLERGIES OR ASTHMA, EDEMA FORMATION OR HYPOTENSIVE VASCULAR DISEASES. SYNTEX (U.S.A.) LLC 2002-07-09 US claimed
CN-103087122-A Preparation method and applications of glucoside compounds SHANGHAI INST ORGANIC CHEM 2013-05-08 CN disclosed
EP-1339694-B1 SUBSTITUTED 2-PHENYLAMINOIMIDAZOLINE PHENYL KETONE DERIVATIVES AS IP ANTAGONISTS HOFFMANN LA ROCHE (CH) 2005-09-21 EP disclosed
EP-1339694-A1 SUBSTITUTED 2-PHENYLAMINOIMIDAZOLINE PHENYL KETONE DERIVATIVES AS IP ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2003-09-03 EP disclosed
US-20020091147-A1 SUBSTITUTED-PHENYL KETONE DERIVATIVES AS IP ANTAGONISTS SYNTEX (U.S.A.) LLC 2002-07-11 US disclosed
US-6417186-B1 TREATING PAIN, URINARY TRACT INFECTIONS, INFLAMMATION, RESPIRATORY DISEASE STATES FROM ALLERGIES OR ASTHMA, EDEMA FORMATION OR HYPOTENSIVE VASCULAR DISEASES. SYNTEX (U.S.A.) LLC 2002-07-09 US disclosed
WO-2002040453-A1 SUBSTITUTED 2-PHENYLAMINOIMIDAZOLINE PHENYL KETONE DERIVATIVES AS IP ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2002-05-23 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-20020091147-A1 SUBSTITUTED-PHENYL KETONE DERIVATIVES AS IP ANTAGONISTS PTGER1, FFAR1, BDKRB1 MAPT 4409/4885GAA 4466/4885LMNA 4499/4885

“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.