SCHEMBL3082641

SCHEMBL3082641

Nc1ccc(-c2nc(-c3ccc(-c4ccccc4)c(C(F)(F)F)c3)no2)cc1

nearest known ligand 0.73

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
S1PR1 P21453 14/20 0.73
S1PR3 Q99500 4/20 0.73
BCHE P06276 1/20 0.52
ACHE P22303 1/20 0.52
NR1H4 Q96RI1 3/20 0.49
NPC1 O15118 1/20 0.46
NFKB1 P19838 1/20 0.46
RAB9A P51151 1/20 0.46
NFKB2 Q00653 1/20 0.46
RELA Q04206 1/20 0.46
ALOX15 P16050 1/20 0.46
S1PR5 Q9H228 1/20 0.46

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
SCHEMBL4617232 0.95 S1PR1 (0.78) S1PR1S1PR3BCHEACHENR1H4
SCHEMBL16592606 0.86 S1PR1 (0.58) S1PR1S1PR3BCHEACHENR1H4
SCHEMBL13417223 0.85 S1PR1 (1.00) S1PR1S1PR3
SCHEMBL13417221 0.82 S1PR1 (1.00) S1PR1S1PR3NPC1NFKB1RAB9A
SCHEMBL13417080 0.82 S1PR1 (0.78) S1PR1S1PR3NPC1NFKB1RAB9A
SCHEMBL3103302 0.82 S1PR1 (0.64) S1PR1S1PR3NPC1NFKB1RAB9A
SCHEMBL14329013 0.82 S1PR1 (0.62) S1PR1S1PR3NPC1
SCHEMBL3813299 0.81 S1PR1 (0.76) S1PR1S1PR3NR1H4NPC1RAB9A
SCHEMBL4617647 0.81 NPC1 (0.62) S1PR1S1PR3NPC1NFKB1RAB9A
SCHEMBL13417068 0.81 S1PR1 (1.00) S1PR1S1PR3NPC1NFKB1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1981858-B1 3,5-DI(ARYL OR HETEROARYL)ISOXAZOLES AND 1,2,4-OXADIAZOLES AS S1P1 RECEPTOR AGONISTS, IMMUNOSUPPRESSSIVE AND ANTI-INFLAMMATORY AGENTS NOVARTIS AG (CH) 2010-06-16 EP claimed
EP-2233473-A1 3,5-di(aryl or heteroaryl)isoxazoles and 1,2,4-oxadiazoles as S1P1 receptor agonists, immunosuppresssive and anti-inflammatory agents Novartis AG (CH) 2010-09-29 EP disclosed
EP-2233473-A1 3,5-di(aryl or heteroaryl)isoxazoles and 1,2,4-oxadiazoles as S1P1 receptor agonists, immunosuppresssive and anti-inflammatory agents Novartis AG (CH) 2010-09-29 EP disclosed
US-7799812-B2 Reverse isoxazoles NOVARTIS AG (CH) 2010-09-21 US disclosed
US-7799812-B2 Reverse isoxazoles NOVARTIS AG (CH) 2010-09-21 US disclosed
US-7799812-B2 Reverse isoxazoles NOVARTIS AG (CH) 2010-09-21 US disclosed
EP-1981858-B1 3,5-DI(ARYL OR HETEROARYL)ISOXAZOLES AND 1,2,4-OXADIAZOLES AS S1P1 RECEPTOR AGONISTS, IMMUNOSUPPRESSSIVE AND ANTI-INFLAMMATORY AGENTS NOVARTIS AG (CH) 2010-06-16 EP disclosed
US-20090137636-A1 Reverse Isoxazoles NOVARTIS AG 2009-05-28 US disclosed
US-20090137636-A1 Reverse Isoxazoles NOVARTIS AG 2009-05-28 US disclosed
US-20090137636-A1 Reverse Isoxazoles NOVARTIS AG 2009-05-28 US disclosed
CN-101374821-A 3,5-di(aryl or heteroaryl)isoxazoles and 1,2,4-oxadiazoles as S1P1 receptor agonists, immunosuppresssive and anti-inflammatory agents NOVARTIS AG (CH) 2009-02-25 CN disclosed
WO-2007085451-A2 3,5-DI (ARYL OR HETEROARYL) ISOXAZOLES AND 1, 2, 4-OXADIAZOLES AS S1P1 RECEPTOR AGONISTS, IMMUNOSUPPRESSSIVE AND ANTI -INFLAMMATORY AGENTS NOVARTIS AG (CH) 2007-08-02 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 (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-20090137636-A1 Reverse Isoxazoles CYP3A7, CYP3A4, TBXA2R S1PR1 3804/4885S1PR3 2578/4885BCHE 2638/4885

“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.