SCHEMBL1201112

SCHEMBL1201112

CC1CC2(NC(=O)NC2=O)c2cc(F)ccc2O1

nearest known ligand 0.69

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
AKR1B1 P15121 13/20 0.69
AKR1B10 O60218 2/20 0.69
AKR1A1 P14550 2/20 0.69
MAPT P10636 1/20 0.61

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
SCHEMBL5925115 1.00 AKR1B1 (0.69) AKR1B1AKR1B10AKR1A1MAPT
SCHEMBL10577770 1.00 AKR1B1 (0.69) AKR1B1AKR1B10AKR1A1MAPT
SCHEMBL2106459 1.00 AKR1B1 (0.69) AKR1B1AKR1B10AKR1A1MAPT
SCHEMBL10575326 1.00 AKR1B1 (0.69) AKR1B1AKR1B10AKR1A1MAPT
SCHEMBL29392626 1.00 AKR1B1 (0.69) AKR1B1AKR1B10AKR1A1MAPT
SCHEMBL10607407 0.86 AKR1B1 (0.74) AKR1B1AKR1B10AKR1A1MAPT
SCHEMBL10575841 0.86 AKR1B1 (0.54) AKR1B1AKR1B10AKR1A1
SCHEMBL10373488 0.85 AKR1B1 (0.63) AKR1B1AKR1B10AKR1A1
SCHEMBL25892734 0.85 AKR1B1 (0.63) AKR1B1AKR1B10AKR1A1
SCHEMBL10574757 0.84 AKR1B1 (0.65) AKR1B1AKR1B10AKR1A1MAPT

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 173 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110092566-A1 Treatment of cancer with aldose reductase inhibitors NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2011-04-21 US claimed
US-20100016404-A1 STRUCTURAL-BASED INHIBITORS OF THE GLUTATHIONE BINDING SITE IN ALDOSE REDUCTASE, METHODS OF SCREENING THEREFOR AND METHODS OF USE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM, THE 2010-01-21 US claimed
EP-2032145-A2 STRUCTURAL-BASED INHIBITORS OF THE GLUTATHIONE BINDING SITE IN ALDOSE REDUCTASE, METHODS OF SCREENING THEREFOR AND METHODS OF USE The Board of Regents of The University of Texas System (US) 2009-03-11 EP claimed
WO-2008002678-A2 STRUCTURAL-BASED INHIBITORS OF THE GLUTATHIONE BINDING SITE IN ALDOSE REDUCTASE, METHODS OF SCREENING THEREFOR AND METHODS OF USE THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2008-01-03 WO claimed
US-20060058310-A1 Remedies for vertebral canal stenosis ONO PHARMACEUTICAL CO., LTD. (JP) 2006-03-16 US claimed
US-20040077671-A1 Sorbitol dehydrogenase inhibitors CHU-MOYER MARGARET Y (US) 2004-04-22 US claimed
US-20030065179-A1 Sorbitol dehydrogenase inhibitors CHU-MOYER MARGARET Y (US) 2003-04-03 US claimed
EP-0175312-A2 Process for preparing optically active hydantoins KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1986-03-26 EP claimed
US-4540704-A Treating complications of diabetes mellitus with hydantoin derivatives EISAI CO., LTD. (JP) 1985-09-10 US claimed
JP-57045185-A None JP disclosed
US-20210085650-A1 COMBINATION THERAPY FOR THE TREATMENT OF CANCER NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2021-03-25 US disclosed
EP-3050593-B1 STRUCTURAL-BASED INHIBITORS OF THE GLUTATHIONE BINDING SITE IN ALDOSE REDUCTASE, METHODS OF SCREENING THEREFOR AND METHODS OF USE UNIV TEXAS (US) 2018-05-16 EP disclosed
EP-2654749-B1 METHODS FOR TREATING COPD UNIV TEXAS (US) 2017-05-10 EP disclosed
EP-3050593-A1 STRUCTURAL-BASED INHIBITORS OF THE GLUTATHIONE BINDING SITE IN ALDOSE REDUCTASE, METHODS OF SCREENING THEREFOR AND METHODS OF USE The Board of Regents of The University of Texas System (US) 2016-08-03 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
EP-0193855-A1 Hydantoin derivatives, processes for preparing them and pharmaceutical compositions containing them Eisai Co., Ltd. (JP) 1986-09-10 EP disclosed
EP-0172719-A1 Process for the production as asymmetric hydantoins PFIZER INC. (US) 1986-02-26 EP disclosed
US-4540704-A Treating complications of diabetes mellitus with hydantoin derivatives EISAI CO., LTD. (JP) 1985-09-10 US disclosed
JP-S5745185-A HYDANTOIN DERIVATIVE AND ITS PREPARATION EISAI CO LTD 1982-03-13 JP 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-20060058310-A1 Remedies for vertebral canal stenosis ALDOA, AKR1B1, AKR1A1 AKR1B1 2/4885AKR1B10 10/4885AKR1A1 3/4885
US-20040077671-A1 Sorbitol dehydrogenase inhibitors SLC5A1, SORD, SLC5A2 AKR1B1 5/4885AKR1B10 24/4885AKR1A1 11/4885
US-20030065179-A1 Sorbitol dehydrogenase inhibitors SLC5A1, SORD, SLC5A2 AKR1B1 5/4885AKR1B10 24/4885AKR1A1 11/4885

“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.