SCHEMBL488506

SCHEMBL488506

Nc1ncccc1OCc1ccccc1C(F)(F)F

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LTA4H P09960 1/20 0.56
▸ MAPK14 Q16539 1/20 0.56
▸ IDO1 P14902 2/20 0.53
▸ SGMS2 Q8NHU3 1/20 0.50
▸ MAOB P27338 4/20 0.49
▸ NPC1 O15118 3/20 0.49
▸ RAB9A P51151 3/20 0.49
▸ HTT P42858 1/20 0.49
▸ SMN1; SMN2 Q16637 1/20 0.49
▸ MAPT P10636 1/20 0.46
▸ MAP4K3 Q8IVH8 1/20 0.45
▸ MAOA P21397 1/20 0.44
▸ SLC6A4 P31645 1/20 0.42
▸ FFAR1 O14842 1/20 0.42
▸ FFAR4 Q5NUL3 1/20 0.42
▸ PLK1 P53350 2/20 0.40
▸ MAP4K4 O95819 1/20 0.40
▸ CSF1R P07333 1/20 0.40
▸ PIM1 P11309 1/20 0.40
▸ KDR P35968 1/20 0.40

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
SCHEMBL6079375 0.80 LTA4H (0.61) LTA4HMAPK14IDO1SGMS2MAOB
SCHEMBL488609 0.78 MAP4K3 (0.52) IDO1SGMS2MAOBMAP4K3MAOA
SCHEMBL488757 0.77 LTA4H (0.61) LTA4HMAPK14IDO1SGMS2MAOB
SCHEMBL9746554 0.77 LTA4H (0.61) LTA4HMAPK14SGMS2NPC1RAB9A
SCHEMBL9125515 0.77 LTA4H (0.61) LTA4HMAPK14SGMS2NPC1RAB9A
SCHEMBL488805 0.77 LTA4H (0.61) LTA4HMAPK14IDO1NPC1RAB9A
SCHEMBL6080009 0.77 NPC1 (0.61) LTA4HMAPK14IDO1SGMS2NPC1
SCHEMBL488499 0.77 KMT2A (0.56) IDO1SGMS2NPC1RAB9AHTT
SCHEMBL2123624 0.76 LTA4H (0.54) LTA4HMAPK14NPC1RAB9AHTT
SCHEMBL2292699 0.75 IDO1 (0.54) IDO1SGMS2MAOBMAOASLC6A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1603570-B9 AMINOHETEROARYL COMPOUNDS AS PROTEIN KINASE INHIBITORS SUGEN INC (US) 2013-10-23 — — EP disclosed
EP-1603570-B1 AMINOHETEROARYL COMPOUNDS AS PROTEIN KINASE INHIBITORS SUGEN INC (US) 2013-01-23 — — EP disclosed
EP-2476667-A2 Aminoheteroaryl compounds as protein kinase inhibitors Sugen, Inc. (US) 2012-07-18 — — EP disclosed
US-8106197-B2 Aminoheteroaryl compounds as protein kinase inhibitors PFIZER INC. (US) 2012-01-31 — — US disclosed
US-7230098-B2 2-amino- pyridines and pyrazines additionally substituted witn one or more carbocyclic or heterocyclic groups, e.g., 4-[6-amino-5-(2,6-dichloro-benzyloxy)-pyridin-3-yl]-phenol, for treating many kinds of cancer SUGEN, INC. (US) 2007-06-12 — — US disclosed
US-20070072874-A1 Aminoheteroaryl compounds as protein kinase inhibitors SUGEN, INC. 2007-03-29 — — US disclosed
US-7105534-B2 Imidazo[1,2-α]pyridine ether compounds as ion channel modulators CARDIOME PHARMA CORP. (CA) 2006-09-12 — — US disclosed
EP-1603570-A2 AMINOHETEROARYL COMPOUNDS AS PROTEIN KINASE INHIBITORS Sugen, Inc. (US) 2005-12-14 — — EP disclosed
US-20050009840-A1 2-amino- pyridines and pyrazines additionally substituted witn one or more carbocyclic or heterocyclic groups, e.g., 4-[6-amino-5-(2,6-dichloro-benzyloxy)-pyridin-3-yl]-phenol, for treating many kinds of cancer SUGEN, INC. 2005-01-13 — — US disclosed
WO-2004076412-A2 AMINOHETEROARYL COMPOUNDS AS PROTEIN KINASE INHIBITORS SUGEN, INC. (US) 2004-09-10 — — WO disclosed
US-20040048885-A1 Imidazo[1,2,-A]pyridine ether compounds as ion channel modulators CORREVIO CANADA CORP. (CA) 2004-03-11 — — US disclosed
WO-2001096335-A1 IMIDAZO[1,2-A]PYRIDINE ETHER COMPOUNDS AS ION CHANNEL MODULATORS CARDIOME PHARMA CORP. (CA) 2001-12-20 — — WO disclosed
US-5409943-A [(alkoxy)pyridinyl]amine compounds which are useful in the treatment of gastrointestinal disorders SMITHKLINE BEECHAM INTERCREDIT B.V. (NL) 1995-04-25 — — US disclosed
EP-0625143-A1 PYRIDINE DERIVATIVES, THEIR PREPARATION AND USE AS MEDICINES SMITHKLINE BEECHAM INTERCREDIT B.V. (NL) 1994-11-23 — — EP disclosed
WO-1993015055-A1 PYRIDINE DERIVATIVES, THEIR PREPARATION AND USE AS MEDICINES SMITHKLINE BEECHAM INTERCREDIT B.V. (NL) 1993-08-05 — — WO disclosed
US-4831041-A ANTIULCER AGENTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1989-05-16 — — US disclosed
EP-0268989-A1 Imidazopyridine compounds and processes for preparation thereof FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1988-06-01 — — 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 (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-20050009840-A1 2-amino- pyridines and pyrazines additionally substituted witn one or more carbocyclic or heterocyclic groups, e.g., 4-[6-amino-5-(2,6-dichloro-benzyloxy)-pyridin-3-yl]-phenol, for treating many kinds of cancer MET, ERBB2, CDK4 LTA4H 4259/4885MAPK14 210/4885IDO1 2061/4885
US-20070072874-A1 Aminoheteroaryl compounds as protein kinase inhibitors MET, MAP4K1, MAP4K2 LTA4H 3789/4885MAPK14 152/4885IDO1 3603/4885
US-20040048885-A1 Imidazo[1,2,-A]pyridine ether compounds as ion channel modulators KCNJ2, KCNH2, KCNA1 LTA4H 3402/4885MAPK14 2384/4885IDO1 1028/4885

“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.

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