SCHEMBL2474840

SCHEMBL2474840

COc1ccc(CCNC(=O)CCc2ccc(C(F)(F)F)cc2)cc1OC

nearest known ligand 0.74

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.74
MEN1 O00255 3/20 0.74
ALDH1A1 P00352 3/20 0.62
MAPT P10636 2/20 0.58
SMN1; SMN2 Q16637 1/20 0.58
POLB P06746 1/20 0.57
PTGER1 P34995 1/20 0.57
LMNA P02545 1/20 0.56
CA12 O43570 1/20 0.56
CA1 P00915 1/20 0.56
CA2 P00918 1/20 0.56
CA9 Q16790 1/20 0.56

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
SCHEMBL3659341 0.92 KMT2A (0.63) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2
SCHEMBL4022887 0.89 KMT2A (0.87) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2
SCHEMBL4027607 0.87 KMT2A (0.59) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2
SCHEMBL4023394 0.86 KMT2A (0.79) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2
SCHEMBL6375210 0.85 KMT2A (0.81) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2
SCHEMBL5899116 0.83 CA1 (0.61) KMT2AMEN1CA12CA1CA2
SCHEMBL2959611 0.83 KMT2A (0.64) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2
SCHEMBL4028185 0.83 KMT2A (0.73) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2
SCHEMBL23417617 0.82 ALDH1A1 (0.77) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2
SCHEMBL23392535 0.82 MAPT (0.77) KMT2AMEN1ALDH1A1MAPTSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2227454-B1 PROCESS FOR THE PREPARATION OF AN ENANTIOMERIC TRISUBSTITUTED 3,4-DIHYDRO-ISOQUINOLINE DERIVATIVE ACTELION PHARMACEUTICALS LTD (CH) 2015-09-30 EP disclosed
EP-2227454-B1 PROCESS FOR THE PREPARATION OF AN ENANTIOMERIC TRISUBSTITUTED 3,4-DIHYDRO-ISOQUINOLINE DERIVATIVE ACTELION PHARMACEUTICALS LTD (CH) 2015-09-30 EP disclosed
EP-1751111-B1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVES ACTELION PHARMACEUTICALS LTD (CH) 2014-12-31 EP disclosed
EP-1751111-B1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVES ACTELION PHARMACEUTICALS LTD (CH) 2014-12-31 EP disclosed
US-8314238-B2 Process for the preparation of an enantiomeric trisubstituted 3,4-dihydro-isoquinoline derivative ACTELION PHARMACEUTICALS LTD. (CH) 2012-11-20 US disclosed
US-8314238-B2 Process for the preparation of an enantiomeric trisubstituted 3,4-dihydro-isoquinoline derivative ACTELION PHARMACEUTICALS LTD. (CH) 2012-11-20 US disclosed
US-8314238-B2 Process for the preparation of an enantiomeric trisubstituted 3,4-dihydro-isoquinoline derivative ACTELION PHARMACEUTICALS LTD. (CH) 2012-11-20 US disclosed
US-8247560-B2 Trisubstituted 3,4-dihydro-1H-isoquinolin compound, process for its preparation, and its use ACTELION PHARMACEUTICALS LTD. (CH) 2012-08-21 US disclosed
US-8247560-B2 Trisubstituted 3,4-dihydro-1H-isoquinolin compound, process for its preparation, and its use ACTELION PHARMACEUTICALS LTD. (CH) 2012-08-21 US disclosed
US-8247560-B2 Trisubstituted 3,4-dihydro-1H-isoquinolin compound, process for its preparation, and its use ACTELION PHARMACEUTICALS LTD. (CH) 2012-08-21 US disclosed
US-20070191424-A1 Substituted 1,2,3,4-tetrahydroisoquinoline derivatives IDORSIA PHARMACEUTICALS LTD (CH) 2007-08-16 US disclosed
CN-1926109-A Substituted 1,2,3, 4-tetrahydroisoquinoline derivatives ACTELION PHARMACEUTICALS LTD (CH) 2007-03-07 CN disclosed
EP-1751111-A1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVES Actelion Pharmaceuticals Ltd. (CH) 2007-02-14 EP disclosed
US-20060178515-A1 Tetrahydroisoquinolyl acetamide derivatives for use as orexin receptor antagonists ACTELION PHARMACEUTICALS, LTD. (CH) 2006-08-10 US disclosed
CN-1764647-A Tetrahydroisoquinolyl acetamide derivatives for use as orexin receptor antagonists ACTELION PHARMACEUTICALS LTD (CH) 2006-04-26 CN disclosed
EP-1611104-A1 TETRAHYDROISOQUINOLYL ACETAMIDE DERIVATIVES FOR USE AS OREXIN RECEPTOR ANTAGONISTS Actelion Pharmaceuticals Ltd. (CH) 2006-01-04 EP disclosed
WO-2005118548-A1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVES ACTELION PHARMACEUTICALS LTD (CH) 2005-12-15 WO disclosed
WO-2005118548-A1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVES ACTELION PHARMACEUTICALS LTD (CH) 2005-12-15 WO disclosed
WO-2004085403-A1 TETRAHYDROISOQUINOLYL ACETAMIDE DERIVATIVES FOR USE AS OREXIN RECEPTOR ANTAGONISTS ACTELION PHARMACEUTICALS LTD (CH) 2004-10-07 WO disclosed
WO-2004085403-A1 TETRAHYDROISOQUINOLYL ACETAMIDE DERIVATIVES FOR USE AS OREXIN RECEPTOR ANTAGONISTS ACTELION PHARMACEUTICALS LTD (CH) 2004-10-07 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 (2 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-20060178515-A1 Tetrahydroisoquinolyl acetamide derivatives for use as orexin receptor antagonists HCRTR2, HCRTR1, OXTR KMT2A 1035/4885MEN1 1135/4885ALDH1A1 1059/4885
US-20070191424-A1 Substituted 1,2,3,4-tetrahydroisoquinoline derivatives CPT1A, NQO1, COQ8A KMT2A 2028/4885MEN1 2601/4885ALDH1A1 1448/4885

“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.