SCHEMBL6301269

SCHEMBL6301269

COc1cccc(C(CCO)c2ccccc2)c1

nearest known ligand 0.63

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MTNR1A P48039 5/20 0.63
MTNR1B P49286 5/20 0.63
CASR P41180 2/20 0.52
MEN1 O00255 2/20 0.52
KMT2A Q03164 2/20 0.52
ALDH1A1 P00352 1/20 0.52
LMNA P02545 1/20 0.52
ALPL P05186 1/20 0.52
MAPT P10636 1/20 0.52
ALOX12 P18054 1/20 0.52
HTT P42858 1/20 0.52
AOC3 Q16853 2/20 0.49
L3MBTL1 Q9Y468 1/20 0.48
ROCK2 O75116 1/20 0.46
ROCK1 Q13464 1/20 0.46
GRIN2B Q13224 1/20 0.46
TDP1 Q9NUW8 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
SCHEMBL9392741 0.97 MTNR1A (0.58) MTNR1AMTNR1BCASRMEN1KMT2A
SCHEMBL17295959 0.86 MTNR1A (0.58) MTNR1AMTNR1BCASRMEN1KMT2A
SCHEMBL9658024 0.85 MTNR1A (0.49) MTNR1AMTNR1BCASRMEN1KMT2A
SCHEMBL7857706 0.83 HRH1 (0.60) MTNR1AMTNR1BCASRMEN1KMT2A
SCHEMBL6302107 0.83 MTNR1A (0.59) MTNR1AMTNR1BCASRMEN1KMT2A
SCHEMBL6301200 0.83 MTNR1A (0.67) MTNR1AMTNR1BCASRMEN1KMT2A
SCHEMBL8661020 0.82 AOC3 (0.54) MTNR1AMTNR1BCASRLMNAAOC3
SCHEMBL6490320 0.81 AOC3 (0.62) MTNR1AMTNR1BAOC3L3MBTL1ROCK2
SCHEMBL11174933 0.81 AOC3 (0.50) MTNR1AMTNR1BCASRAOC3L3MBTL1
SCHEMBL6774246 0.81 OPRD1 (0.59)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1310924-C Chiral copper complex and production processes thereof and using the same SUMITOMO CHEMICAL CO (JP) 2007-04-18 CN disclosed
CN-1246299-C Chiral copper complex, preparation method and application thereof SUMITOMO CHEMICAL CO (JP) 2006-03-22 CN disclosed
US-6943183-B2 5-substituted tetralones as inhibitors of ras farnesyl transferase PFIZER INC (US) 2005-09-13 US disclosed
CN-1616465-A Chiral copper complex and production processes thereof and using the same SUMITOMO CHEMICAL CO (JP) 2005-05-18 CN disclosed
CN-1182915-C Chiral copper complex catalyst composition and method for asymmetrical preparation ס�ѻ�ѧ��ҵ��ʽ���� 2005-01-05 CN disclosed
US-20040044057-A1 5- substituted tetralones as inhibitors of ras farnesyl trransferase WARNER-LAMBERT COMPANY 2004-03-04 US disclosed
EP-1276725-A2 5-SUBSTITUTED TETRALONES AS INHIBITORS OF RAS FARNESYL TRANSFERASE WARNER-LAMBERT COMPANY (US) 2003-01-22 EP disclosed
WO-2001079180-A2 5-SUBSTITUTED TETRALONES AS INHIBITORS OF RAS FARNESYL TRANSFERASE WARNER-LAMBERT COMPANY (US) 2001-10-25 WO disclosed
CN-1314209-A Chiral copper complex catalyst composition and method for asymmetrical preparation SUMITOMO CHEMICAL CO (JP) 2001-09-26 CN disclosed
CN-1313277-A Chiral copper complex, preparation method and application thereof SUMITOMO CHEMICAL CO (JP) 2001-09-19 CN 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-20040044057-A1 5- substituted tetralones as inhibitors of ras farnesyl trransferase PTAR1, FNTA, GGPS1 MTNR1A 2828/4885MTNR1B 3212/4885CASR 2450/4885

“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.