SCHEMBL3316338

SCHEMBL3316338

O=[N+]([O-])c1ccc(F)cc1OCc1cccnc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP11B1 P15538 3/20 0.53
CYP11B2 P19099 3/20 0.53
MAPT P10636 7/20 0.49
ALDH1A1 P00352 4/20 0.49
CYP19A1 P11511 1/20 0.48
RAB9A P51151 3/20 0.47
GAA P10253 2/20 0.47
MEN1 O00255 1/20 0.47
KMT2A Q03164 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47
MGMT P16455 1/20 0.47
HTR1A P08908 1/20 0.46
DRD2 P14416 1/20 0.46
LRRK2 Q5S007 1/20 0.46
HTT P42858 2/20 0.45
NPSR1 Q6W5P4 1/20 0.45
SGMS2 Q8NHU3 1/20 0.45
TDP1 Q9NUW8 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
CYP1A2 P05177 1/20 0.43

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
SCHEMBL2038318 0.90 LRRK2 (0.48) CYP11B1CYP11B2MAPTALDH1A1CYP19A1
SCHEMBL17323483 0.85 CYP11B1 (0.53) CYP11B1CYP11B2MAPTALDH1A1CYP19A1
SCHEMBL14988688 0.85 RAB9A (0.57) CYP11B1CYP11B2MAPTALDH1A1CYP19A1
SCHEMBL29447092 0.84 MAPT (0.59) CYP11B1CYP11B2MAPTALDH1A1RAB9A
SCHEMBL564270 0.84 MAPT (0.59) CYP11B1CYP11B2MAPTALDH1A1RAB9A
SCHEMBL2038846 0.82 LRRK2 (0.46) CYP11B1CYP11B2ALDH1A1CYP19A1SMN1; SMN2
SCHEMBL17630123 0.82 CYP11B1 (0.50) CYP11B1CYP11B2MAPTCYP19A1RAB9A
SCHEMBL3585058 0.80 MGMT (0.52) CYP11B1CYP11B2MAPTALDH1A1CYP19A1
SCHEMBL7900848 0.80 RAB9A (0.51) CYP11B1CYP11B2MAPTALDH1A1CYP19A1
SCHEMBL2035674 0.79 KMT2A (0.55) CYP11B1CYP11B2MAPTALDH1A1CYP19A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100105683-A1 COMPOUNDS USEFUL FOR INHIBITING CHK1 KEEGAN KATHLEEN S 2010-04-29 US disclosed
US-7608618-B2 Urea or thiourea substituted 1,4-pyrazine compounds useful as anti-cancer agents and for inhibiting Chk1 ICOS CORPORATION (US) 2009-10-27 US disclosed
US-7067506-B2 Compounds useful for inhibiting Chk1 ICOS CORPORATION (US) 2006-06-27 US disclosed
US-20050245525-A1 Compounds useful for inhibiting CHK1 ICOS CORPORATION (US) 2005-11-03 US disclosed
US-20030069284-A1 Compounds useful for inhibiting Chk1 ICOS CORPORATION (A WASHINGTON CORPORATION) 2003-04-10 US 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-20100105683-A1 COMPOUNDS USEFUL FOR INHIBITING CHK1 CHEK1, PCNA, CHEK2 CYP11B1 3367/4885CYP11B2 3622/4885MAPT 3233/4885
US-20050245525-A1 Compounds useful for inhibiting CHK1 CHEK1, PCNA, CHEK2 CYP11B1 3367/4885CYP11B2 3622/4885MAPT 3233/4885
US-20030069284-A1 Compounds useful for inhibiting Chk1 CHEK1, PCNA, CHEK2 CYP11B1 3367/4885CYP11B2 3622/4885MAPT 3233/4885

“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.