SCHEMBL9694491

SCHEMBL9694491

O=C1c2ccccc2C(=O)N1OCc1ccc(Cl)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 6/20 1.00
KMT2A Q03164 6/20 1.00
MAPT P10636 1/20 1.00
GAA P10253 3/20 0.69
POLB P06746 1/20 0.69
L3MBTL1 Q9Y468 1/20 0.69
ATM Q13315 1/20 0.54
GRM5 P41594 1/20 0.50
ALDH1A1 P00352 4/20 0.49
HTT P42858 1/20 0.49
CES2 O00748 1/20 0.47
BCHE P06276 1/20 0.47
CES1 P23141 1/20 0.47
CA12 O43570 1/20 0.45
CA1 P00915 1/20 0.45
CA9 Q16790 1/20 0.45
CYP1A2 P05177 1/20 0.45
CYP2C9 P11712 1/20 0.45

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
SCHEMBL10914237 0.86 MEN1 (0.76) MEN1KMT2AMAPTGAAPOLB
SCHEMBL6524461 0.85 KMT2A (0.74) MEN1KMT2AMAPTGAAPOLB
SCHEMBL29367470 0.85 KMT2A (0.74) MEN1KMT2AMAPTGAAPOLB
SCHEMBL9671952 0.85 MEN1 (0.73) MEN1KMT2AMAPTGAAPOLB
SCHEMBL10912874 0.85 MEN1 (0.73) MEN1KMT2AMAPTGAAPOLB
SCHEMBL5528619 0.84 MEN1 (0.73) MEN1KMT2AMAPTGAAPOLB
SCHEMBL9396061 0.83 KMT2A (0.71) MEN1KMT2AMAPTGAAPOLB
SCHEMBL26497888 0.83 KMT2A (0.71) MEN1KMT2AMAPTGAAPOLB
SCHEMBL9671323 0.83 MEN1 (0.71) MEN1KMT2AMAPTGAAPOLB
SCHEMBL9671233 0.82 MEN1 (0.69) MEN1KMT2AMAPTGAAPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7157205-B2 Intermediate layer composition for multilayer resist process, pattern-forming process using the same, and laminate FUJI PHOTO FILM CO., LTD. (JP) 2007-01-02 US disclosed
US-5120849-A Reacting cyclic imidoether with aminoalcohol BASF AKTIENGESELLSCHAFT (DE) 1992-06-09 US disclosed
EP-0244786-B1 PROCESS FOR PREPARING 0-SUBSTITUTED HYDROXYLAMINES BASF Aktiengesellschaft (DE) 1991-03-06 EP disclosed
EP-0244786-A1 Process for preparing 0-substituted hydroxylamines BASF Aktiengesellschaft (DE) 1987-11-11 EP disclosed