SCHEMBL9810972

SCHEMBL9810972

O=C1NC(=O)C2(N1)c1cc(Br)ccc1-c1ccc(Br)cc12

nearest known ligand 0.82

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ AKR1B1 P15121 15/20 0.82
▸ AKR1A1 P14550 14/20 0.82
▸ ITGA4 P13612 1/20 0.58
▸ CACNA1F O60840 1/20 0.43
▸ ALDH1A1 P00352 1/20 0.43
▸ MAPT P10636 1/20 0.43
▸ CYP2C9 P11712 1/20 0.43
▸ HTR2A P28223 1/20 0.43
▸ HRH1 P35367 1/20 0.43
▸ SCN1A P35498 1/20 0.43
▸ SCN4A P35499 1/20 0.43
▸ BLM P54132 1/20 0.43
▸ PMP22 Q01453 1/20 0.43
▸ CACNA1D Q01668 1/20 0.43
▸ KCNH2 Q12809 1/20 0.43
▸ CACNA1S Q13698 1/20 0.43
▸ CACNA1C Q13936 1/20 0.43
▸ SCN5A Q14524 1/20 0.43
▸ SCN2A Q99250 1/20 0.43
▸ SCN3A Q9NY46 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
SCHEMBL9810970 0.92 ITGA4 (0.73) AKR1B1AKR1A1ITGA4CACNA1FALDH1A1
SCHEMBL25892565 0.91 AKR1B1 (0.70) AKR1B1AKR1A1ITGA4
SCHEMBL20845832 0.91 AKR1A1 (1.00) AKR1B1AKR1A1ITGA4
SCHEMBL9671558 0.82 AKR1B1 (0.59) AKR1B1AKR1A1ITGA4
Imirestat SCHEMBL49034 0.79 AKR1A1 (1.00) AKR1B1AKR1A1ITGA4
SCHEMBL9811003 0.79 AKR1A1 (0.65) AKR1B1AKR1A1ITGA4CACNA1FALDH1A1
Imirestat SCHEMBL30924520 0.79 AKR1A1 (1.00) AKR1B1AKR1A1ITGA4
SCHEMBL22380780 0.79 AKR1B1 (0.65) AKR1B1AKR1A1ITGA4CACNA1FALDH1A1
SCHEMBL11001789 0.79 AKR1B1 (1.00) AKR1B1AKR1A1ITGA4
SCHEMBL21095587 0.75 AKR1A1 (0.59) AKR1B1AKR1A1ITGA4CACNA1FALDH1A1

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
US-20230190710-A1 COMPOSITIONS AND METHODS OF REDUCING SERUM CHOLESTEROL AND PCSK9 UNIV CASE WESTERN RESERVE (US) 2023-06-22 — — US disclosed
US-20220002552-A1 SUBSTITUTED POLYFLUORENE COMPOUNDS BioLegend, Inc. (US) 2022-01-06 — — US disclosed
US-20220002552-A1 SUBSTITUTED POLYFLUORENE COMPOUNDS BioLegend, Inc. (US) 2022-01-06 — — US disclosed
US-11155714-B2 Substituted polyfluorene compounds BioLegend, Inc. (US) 2021-10-26 — — US disclosed
US-11155714-B2 Substituted polyfluorene compounds BioLegend, Inc. (US) 2021-10-26 — — US disclosed
US-20190203052-A1 SUBSTITUTED POLYFLUORENE COMPOUNDS BIOLEGEND (US) 2019-07-04 — — US disclosed
US-20190203052-A1 SUBSTITUTED POLYFLUORENE COMPOUNDS BIOLEGEND (US) 2019-07-04 — — US disclosed
WO-2019060720-A1 COMPOSITIONS AND METHODS OF REDUCING SERUM CHOLESTEROL AND PCSK9 CASE WESTERN RESERVE UNIVERSITY (US) 2019-03-28 — — WO disclosed
WO-2018009861-A1 SUBSTITUTED POLYFLUORENE COMPOUNDS BIOLEGEND (US) 2018-01-11 — — WO disclosed
EP-0092385-B1 HYDANTOIN DERIVATIVES FOR USE IN INHIBITING ALDOSE REDUCTASE ACTIVITY, COMPOSITIONS THEREFOR AND PROCESS FOR PREPARING SPIRO-FLUOREN COMPOUNDS ALCON LABORATORIES, INC. (US) 1991-06-12 — — EP disclosed
US-4540700-A Treatment of diabetic complications with certain spiro-imidazolidine-diones ALCON LABORATORIES, INC. (US) 1985-09-10 — — US disclosed
US-4436745-A TETRACYCLIC SPIROHYDANTOINS ALCON LABORATORIES, INC. (US) 1984-03-13 — — US disclosed
WO-1983003543-A1 METHOD OF INHIBITING ALDOSE REDUCTASE ACTIVITY, COMPOSITIONS THEREFOR AND PROCESS FOR PREPARING SPIRO-FLUOROFLUOREN AND SPIRO-DIFLUOROFLUOREN COMPOUNDS ALCON LAB INC (US) 1983-10-27 — — WO disclosed
EP-0092385-A2 Hydantoin derivatives for use in inhibiting aldose reductase activity, compositions therefor and process for preparing spiro-fluoren compounds ALCON LABORATORIES, INC. (US) 1983-10-26 — — EP 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-20230190710-A1 COMPOSITIONS AND METHODS OF REDUCING SERUM CHOLESTEROL AND PCSK9 PCSK9, HMGCR, PCSK7 AKR1B1 9/4885AKR1A1 8/4885ITGA4 4832/4885
US-11155714-B2 Substituted polyfluorene compounds PARG, PFAS, PARN AKR1B1 3073/4885AKR1A1 2953/4885ITGA4 2651/4885
US-20220002552-A1 SUBSTITUTED POLYFLUORENE COMPOUNDS PARG, PFAS, PARN AKR1B1 3073/4885AKR1A1 2953/4885ITGA4 2651/4885

“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.

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