SCHEMBL9536563

SCHEMBL9536563

COC(=O)C1(N)CCOc2ccc(F)cc21

nearest known ligand 0.51

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
AKR1B1 P15121 5/20 0.51
AKR1B10 O60218 1/20 0.46
MAPT P10636 1/20 0.46
AKR1A1 P14550 1/20 0.46
RARA P10276 1/20 0.41
RARB P10826 1/20 0.41
RARG P13631 1/20 0.41
APP P05067 1/20 0.40
BACE1 P56817 1/20 0.40
KDM4E B2RXH2 1/20 0.39
ALDH1A1 P00352 1/20 0.39
GAA P10253 1/20 0.39
KIF11 P52732 3/20 0.37
CHRNA7 P36544 1/20 0.37
NPC1 O15118 1/20 0.36
RAB9A P51151 1/20 0.36
MAOB P27338 1/20 0.36
HDAC4 P56524 1/20 0.36

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
SCHEMBL10574215 1.00 AKR1B1 (0.51) AKR1B1AKR1B10MAPTAKR1A1RARA
Hydrochloric Acid SCHEMBL10572120 0.99 AKR1B1 (0.50) AKR1B1AKR1B10MAPTAKR1A1RARA
SCHEMBL10571394 0.86 AKR1B1 (0.51) AKR1B1AKR1B10MAPTAKR1A1APP
SCHEMBL10570941 0.84 RARA (0.39) AKR1B1MAPTRARARARBRARG
SCHEMBL10651444 0.83 AKR1B1 (0.59) AKR1B1AKR1B10MAPTAKR1A1RARA
SCHEMBL10754110 0.83 AKR1B1 (0.56) AKR1B1AKR1B10MAPTAKR1A1KIF11
SCHEMBL10569394 0.83 AKR1B1 (0.59) AKR1B1AKR1B10MAPTAKR1A1RARA
SCHEMBL10919189 0.83 AKR1B1 (0.59) AKR1B1AKR1B10MAPTAKR1A1RARA
SCHEMBL10649371 0.83 AKR1B1 (0.56) AKR1B1AKR1B10MAPTAKR1A1KIF11
SCHEMBL7177095 0.83 AKR1B1 (0.55) AKR1B1AKR1B10MAPTAKR1A1RARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0352959-B1 RESOLUTION PROCESS FOR RACEMIC SPIRO-HYDANTOINS PFIZER INC. (US) 1993-09-01 EP disclosed
US-5206367-A Preparation of optically active spiro-hydantoins PFIZER INC. (US) 1993-04-27 US disclosed
US-5006657-A Intermediates in a resolution process for racemic spiro hydantoins PFIZER INC. (US) 1991-04-09 US disclosed
US-4952694-A Novel resolution process for racemic spiro-hydantoins PFIZER INC. (US) 1990-08-28 US disclosed
EP-0352959-A1 Resolution process for racemic spiro-hydantoins PFIZER INC. (US) 1990-01-31 EP disclosed
US-4841079-A Process for the production of asymmetric hydantoins PFIZER, INC. (US) 1989-06-20 US disclosed
EP-0173522-B1 PROCESS AND INTERMEDIATES FOR SORBINIL PFIZER INC. (US) 1988-12-07 EP disclosed
EP-0172719-B1 PROCESS FOR THE PRODUCTION AS ASYMMETRIC HYDANTOINS PFIZER INC. (US) 1988-09-21 EP disclosed
US-4716113-A Process for the production of an (S)-methyl or (S)-ethyl 4-amino-6-fluorochroman-4-carboxylate PFIZER INC. (US) 1987-12-29 US disclosed
US-4704461-A Processes and intermediates for sorbinil PFIZER INC. (US) 1987-11-03 US disclosed
CN-85105869-A The preparation method of asymmetric glycolylurea 1987-01-28 CN disclosed
US-4620019-A S-6-fluoro-4-aminochroman-4-carboxylic acid derivatives useful as intermediates for sorbinil PFIZER INC. (US) 1986-10-28 US disclosed
EP-0173522-A2 Process and intermediates for sorbinil PFIZER INC. (US) 1986-03-05 EP disclosed
EP-0172719-A1 Process for the production as asymmetric hydantoins PFIZER INC. (US) 1986-02-26 EP disclosed