SCHEMBL8728498

SCHEMBL8728498

COc1ccc2c(c1)c(CC(=O)OCCNC(=O)c1cccnc1)c(C)n2C(=O)c1ccc(Cl)cc1

nearest known ligand 0.71

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
▸ PTGS2 P35354 17/20 0.71
▸ CNR2 P34972 1/20 0.65
▸ AKR1C3 P42330 1/20 0.65
▸ HTR1A P08908 1/20 0.62
▸ PKM P14618 1/20 0.62
▸ PTGS1 P23219 1/20 0.62
▸ GLO1 Q04760 1/20 0.62
▸ HIF1A Q16665 1/20 0.62

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
SCHEMBL12989547 0.87 PTGS2 (0.77) PTGS2CNR2AKR1C3HTR1APKM
SCHEMBL9879816 0.86 PTGS2 (0.68) PTGS2CNR2AKR1C3HTR1APKM
Iodide SCHEMBL8724770 0.85 PTGS2 (0.68) PTGS2CNR2AKR1C3HTR1APKM
SCHEMBL11565442 0.84 PTGS2 (0.77) PTGS2CNR2AKR1C3HTR1APKM
SCHEMBL17703439 0.84 PTGS2 (0.81) PTGS2CNR2AKR1C3HTR1APKM
SCHEMBL1394516 0.82 PTGS2 (0.81) PTGS2CNR2AKR1C3HTR1APKM
SCHEMBL11174704 0.81 PTGS2 (0.85) PTGS2CNR2AKR1C3HTR1APKM
SCHEMBL13813542 0.81 PTGS2 (1.00) PTGS2CNR2AKR1C3HTR1APKM
SCHEMBL12742120 0.81 PTGS2 (0.91) PTGS2CNR2AKR1C3HTR1APKM
SCHEMBL30077218 0.81 PTGS2 (0.91) PTGS2CNR2AKR1C3HTR1APKM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0335545-B2 Pharmaceutical formulations for parenteral use UNIV FLORIDA (US) 1998-09-23 — — EP disclosed
EP-0327766-B1 Redox systems for brain-targeted drug delivery UNIV FLORIDA (US) 1998-04-08 — — EP disclosed
US-5024998-A Administering in aqueous solution with cyclodextrin derivative UNIVERSITY OF FLORIDA (US) 1991-06-18 — — US disclosed
US-5002935-A Inclusion Complexing Hydroxypropylcyclodextrin with a Dihydropyridine-substituted Drug UNIVERSITY OF FLORIDA (US) 1991-03-26 — — US disclosed
US-4983586-A Decreasing precipitation at injection site or in lungs or other organs by combining with hydroxypropyl-beta-cyclodextrin UNIVERSITY OF FLORIDA (US) 1991-01-08 — — US disclosed
EP-0335545-A2 Pharmaceutical formulations for parenteral use UNIVERSITY OF FLORIDA (US) 1989-10-04 — — EP disclosed
EP-0327766-A2 Redox systems for brain-targeted drug delivery UNIVERSITY OF FLORIDA (US) 1989-08-16 — — EP disclosed
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