SCHEMBL187006

SCHEMBL187006

O=C(O)c1ccc(-c2ccc(Cl)nn2)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NAPRT Q6XQN6 1/20 0.48
RXRA P19793 1/20 0.47
RXRB P28702 1/20 0.47
TSHR P16473 2/20 0.47
ALOX15 P16050 1/20 0.47
RAB9A P51151 6/20 0.46
NPC1 O15118 5/20 0.46
SMN1; SMN2 Q16637 4/20 0.46
KDM4E B2RXH2 4/20 0.46
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46
ALDH1A1 P00352 1/20 0.45
TP53 P04637 2/20 0.44
LDHA P00338 1/20 0.44
CTRC Q99895 1/20 0.42
POLB P06746 1/20 0.42
GAA P10253 1/20 0.42
HTT P42858 1/20 0.42
BCL2L1 Q07817 1/20 0.42
BAD Q92934 1/20 0.42

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
SCHEMBL29129885 0.88 TP53 (0.57) TSHRRAB9ANPC1SMN1; SMN2KDM4E
SCHEMBL181195 0.85 NAPRT (0.40) NAPRTRAB9ANPC1SMN1; SMN2KDM4E
SCHEMBL8110752 0.78 RAB9A (0.50) RXRARXRBTSHRRAB9ANPC1
SCHEMBL28680918 0.78 RAB9A (0.45) TSHRRAB9ANPC1SMN1; SMN2KDM4E
SCHEMBL18653550 0.76 LDHA (0.51) TSHRRAB9ANPC1SMN1; SMN2KDM4E
SCHEMBL9254659 0.76 LMNA (0.47) ALDH1A1
SCHEMBL2314305 0.76 MAPT (0.45) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL13458074 0.76 SMN1; SMN2 (0.47) RAB9ANPC1SMN1; SMN2KDM4EMEN1
SCHEMBL180516 0.76 POLB (0.39) KDM4EPOLB
SCHEMBL240423 0.76 RAB9A (0.50) RAB9ANPC1SMN1; SMN2KDM4EMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20150065517-A1 NEW COMPOUNDS NOVARTIS AG (CH) 2015-03-05 US disclosed
US-8912208-B2 (4-{4-[5-(benzooxazol-2-ylamino)-pyridin-2-yl]-phenyl}-cyclohexyl)-acetic acid useful for treating or preventing conditions or disorders associated with DGAT1 activity NOVARTIS AG (CH) 2014-12-16 US disclosed
US-8835451-B2 Compounds NOVARTIS AG (CH) 2014-09-16 US disclosed
EP-2418202-B1 (4-[4-[5-(substituted amino)-pyridin-2-yl]phenyl]-cyclohexyl)-acetic acid derivatives as DGAT inhibitors NOVARTIS AG (CH) 2014-01-29 EP disclosed
CN-103288721-A (4-(4-[6-(trifluoromethyl-pyridin-3-ylamino)-n-containing-heteroaryl]-phenyl)-cyclohexyl)-acetic acid derivatives and pharmaceutical uses thereof NOVARTIS AG 2013-09-11 CN disclosed
CN-101415683-B Novel compounds NOVARTIS AG 2013-07-17 CN disclosed
US-20130018074-A1 NEW COMPOUNDS NOVARTIS AG (CH) 2013-01-17 US disclosed
US-20130018054-A1 NEW COMPOUNDS NOVARTIS AG (CH) 2013-01-17 US disclosed
EP-2418202-A1 New compounds Novartis AG (CH) 2012-02-15 EP disclosed
EP-2404905-A1 New compounds Novartis AG (CH) 2012-01-11 EP disclosed
EP-2301923-A1 New compounds Novartis AG (CH) 2011-03-30 EP disclosed
US-20090247534-A1 NEW COMPOUNDS NOVARTIS AG (CH) 2009-10-01 US disclosed
CN-101415683-A Novel compounds NOVARTIS AG (CH) 2009-04-22 CN disclosed
US-7504412-B2 Imidazopyridine derivatives BANYU PHARMACEUTICALS, CO., LTD. (JP) 2009-03-17 US disclosed
EP-2004607-A2 NEW COMPOUNDS Novartis AG (CH) 2008-12-24 EP disclosed
CN-100418965-C Imidazopyridine derivatives BANYU PHARMA CO LTD (JP) 2008-09-17 CN disclosed
US-20080200494-A1 Imidazopyridine Derivatives MSD K.K. (JP) 2008-08-21 US disclosed
WO-2007126957-A2 NEW COMPOUNDS NOVARTIS AG (CH) 2007-11-08 WO disclosed
CN-1835950-A Imidazopyridine derivatives BANYU PHARMA CO LTD (JP) 2006-09-20 CN disclosed
EP-1657242-A1 IMIDAZOPYRIDINE DERIVATIVES Banyu Pharmaceutical Co., Ltd. (JP) 2006-05-17 EP 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 (5 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-20150065517-A1 NEW COMPOUNDS DGAT1, DGAT2, GBA1 NAPRT 2127/4885RXRA 631/4885RXRB 670/4885
US-20090247534-A1 NEW COMPOUNDS DGAT1, DGAT2, GBA1 NAPRT 2127/4885RXRA 631/4885RXRB 670/4885
US-20080200494-A1 Imidazopyridine Derivatives MC1R, MC3R, MC5R NAPRT 3584/4885RXRA 972/4885RXRB 1157/4885
US-20130018054-A1 NEW COMPOUNDS DGAT1, DGAT2, GBA1 NAPRT 2136/4885RXRA 608/4885RXRB 638/4885
US-20130018074-A1 NEW COMPOUNDS DGAT1, DGAT2, GBA1 NAPRT 2136/4885RXRA 608/4885RXRB 638/4885

“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.