SCHEMBL1367390

SCHEMBL1367390

O=C(CCl)c1ccc2c(c1)CN(C(=O)C(F)(F)F)CC2

nearest known ligand 0.64

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 5/20 0.64
ESR2 Q92731 5/20 0.64
PKM P14618 1/20 0.49
HDAC6 Q9UBN7 5/20 0.46
HDAC8 Q9BY41 2/20 0.46
ALDH1A1 P00352 2/20 0.45
MAPT P10636 2/20 0.45
SMN1; SMN2 Q16637 2/20 0.45
ABHD6 Q9BV23 3/20 0.44
KDM4E B2RXH2 1/20 0.43
LMNA P02545 1/20 0.43
RAB9A P51151 1/20 0.43
MCHR1 Q99705 1/20 0.41
KDM1A O60341 1/20 0.38
CYP3A4 P08684 1/20 0.38
CYP2D6 P10635 1/20 0.38
HPGD P15428 1/20 0.38
CYP2C19 P33261 1/20 0.38

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
SCHEMBL1366408 0.92 ESR1 (0.52) ESR1ESR2PKMHDAC6HDAC8
SCHEMBL1366031 0.89 ESR1 (0.48) ESR1ESR2PKMHDAC6HDAC8
SCHEMBL1367533 0.87 ESR1 (0.64) ESR1ESR2PKMHDAC6HDAC8
SCHEMBL3292015 0.87 ESR1 (0.64) ESR1ESR2PKMHDAC6HDAC8
Hydrochloric Acid SCHEMBL6193455 0.85 ESR1 (0.61) ESR1ESR2PKMHDAC6HDAC8
SCHEMBL5418343 0.85 ESR1 (0.61) ESR1ESR2PKMHDAC6HDAC8
SCHEMBL14101079 0.84 ESR1 (0.70) ESR1ESR2PKMHDAC6HDAC8
SCHEMBL31670429 0.83 ESR1 (0.68) ESR1ESR2PKMHDAC6HDAC8
SCHEMBL4704441 0.83 ESR1 (0.68) ESR1ESR2PKMHDAC6HDAC8
SCHEMBL28631452 0.82 ESR1 (0.57) ESR1ESR2PKMHDAC6HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8173648-B2 1,2,3,4-tetrahydroisoquinoline derivatives, preparation process therefor and pharmaceutical composition containing the same NATIONAL DEFENSE MEDICAL CENTER (TW) 2012-05-08 US claimed
US-20100016309-A1 1,2,3,4-Tetrahydroisoquinoline Derivatives, Preparation Process therefor and Pharmaceutical Composition Containing the Same NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-01-21 US claimed
EP-2069327-B1 NEW PYRIDONE DERIVATIVES WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS BOEHRINGER INGELHEIM INT (DE) 2013-10-16 EP disclosed
US-8173648-B2 1,2,3,4-tetrahydroisoquinoline derivatives, preparation process therefor and pharmaceutical composition containing the same NATIONAL DEFENSE MEDICAL CENTER (TW) 2012-05-08 US disclosed
US-20120010185-A1 NEW PYRIDONE DERIVATES WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-01-12 US disclosed
US-8067590-B2 Melanin-concentrating hormone (MCH) receptor antagonists; treating obesity, eating disorders, affective disorders, drug dependency; compounds are amino-functional pyridazin-3-one, 1H-pyridin-2-one or 3H-pyrimidin-4-one BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2011-11-29 US disclosed
EP-2383259-A1 New pyridone derivatives with MCH antagonistic activity and medicaments comprising these compounds Boehringer Ingelheim International GmbH (DE) 2011-11-02 EP disclosed
US-20100016309-A1 1,2,3,4-Tetrahydroisoquinoline Derivatives, Preparation Process therefor and Pharmaceutical Composition Containing the Same NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-01-21 US disclosed
US-20100016309-A1 1,2,3,4-Tetrahydroisoquinoline Derivatives, Preparation Process therefor and Pharmaceutical Composition Containing the Same NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-01-21 US disclosed
WO-2009103478-A1 PYRIDONE AND PYRIDAZINONE DERIVATIVES AS MCH ANTAGONISTS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2009-08-27 WO disclosed
US-20080255083-A1 NEW PYRIDONE DERIVATES WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2008-10-16 US disclosed
EP-1701954-A1 N-SUBSTITUTED PIPERIDINE AND PIPERAZINE DERIVATIVES Warner-Lambert Company LLC (US) 2006-09-20 EP disclosed
WO-2005066165-A1 N-SUBSTITUTED PIPERIDINE AND PIPERAZINE DERIVATIVES WARNER-LAMBERT COMPANY LLC (US) 2005-07-21 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 (3 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-20120010185-A1 NEW PYRIDONE DERIVATES WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS MCHR1, MCHR2, GPR119 ESR1 2249/4885ESR2 1432/4885PKM 230/4885
US-20080255083-A1 NEW PYRIDONE DERIVATES WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS MCHR1, MCHR2, GPR119 ESR1 2249/4885ESR2 1432/4885PKM 230/4885
US-20100016309-A1 1,2,3,4-Tetrahydroisoquinoline Derivatives, Preparation Process therefor and Pharmaceutical Composition Containing the Same APP, BACE1, PSEN1 ESR1 2972/4885ESR2 3287/4885PKM 1467/4885

“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.