SCHEMBL3467445

SCHEMBL3467445

COC[C@H]1O[C@H](OC)[C@H](OCc2ccccc2)[C@@H](OCc2ccccc2)[C@@H]1OCc1ccccc1

nearest known ligand 0.71

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SSTR5 P35346 5/20 0.67
SSTR1 P30872 4/20 0.67
SSTR2 P30874 4/20 0.67
SSTR4 P31391 4/20 0.67
SSTR3 P32745 4/20 0.67
BCHE P06276 1/20 0.57
PTPN1 P18031 5/20 0.47
PTPN2 P17706 3/20 0.47
GJB2 P29033 1/20 0.44
NT5E P21589 1/20 0.44
CDC25B P30305 2/20 0.44
ADRB2 P07550 1/20 0.43
TACR1 P25103 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
SCHEMBL1772244 1.00 SSTR5 (0.67) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL6879922 0.99 SSTR5 (0.65) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL6879920 0.99 SSTR5 (0.65) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL8152898 0.94 SSTR5 (0.60) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL8152902 0.94 SSTR5 (0.60) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL6383598 0.94 SSTR5 (0.64) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL6893382 0.92 SSTR5 (0.59) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL24122546 0.90 SSTR1 (0.72) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL6298172 0.90 SSTR1 (0.72) SSTR5SSTR1SSTR2SSTR4SSTR3
SCHEMBL7148930 0.90 SSTR1 (0.72) SSTR5SSTR1SSTR2SSTR4SSTR3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11168179-B2 Macromolecular transition metal complexes for treatment of cancer and process for their preparation FACULDADE DE CIÉNCIAS DA UNIVERSIDADE DE LISBOA (PT) 2021-11-09 US disclosed
EP-3227307-B1 MACROMOLECULAR TRANSITION METAL COMPLEXES FOR TREATMENT OF CANCER AND PROCESS FOR THEIR PREPARATION FACULDADE DE CIENCIAS DA UNIV DE LISBOA (PT) 2020-10-21 EP disclosed
US-20180009940-A1 MACROMOLECULAR TRANSITION METAL COMPLEXES FOR TREATMENT OF CANCERAND PROCESS FOR THEIR PREPARATION FACULDADE DE CIÉNCIAS DA UNIVERSIDADE DE LISBOA (PT) 2018-01-11 US disclosed
WO-2010073126-A2 COMPOUNDS USEFUL IN DELIVERING ANTI-NEOPLASTIC THERAPY AND DIAGNOSTIC IMAGING TO HYPOXIC CELLS AND METHODS OF USE THEREOF THE GOVERNORS OF THE UNIVERSITY OF ALBERTA (CA) 2010-07-01 WO disclosed
US-20090275524-A1 NOVEL HYPOCHOLESTEROLEMIC COMPOUNDS LIPIDEON BIOTECHNOLOGY AG 2009-11-05 US disclosed
US-7544667-B2 Hypocholesterolemic compounds LIPIDEON BIOTECHNOLOGY AG (CH) 2009-06-09 US disclosed
US-20080167255-A1 4-BIARYLYL-1-PHENYLAZETIDIN-2-ONES MICROBIA, INC. (US) 2008-07-10 US disclosed
EP-1885694-A2 4-BIARYLYL-1-PHENYLAZETIDIN-2-ONES Microbia, Inc. (US) 2008-02-13 EP disclosed
US-7320972-B2 4-Biarylyl-1-phenylazetidin-2-ones MICROBIA, INC. (US) 2008-01-22 US disclosed
US-20070275909-A1 Useful in the treatment and prevention of atherosclerosis and for the reduction of cholesterol levels; carbohydrate-containing pyrazolidinone or oxazolidinone derivatives, for example LIPIDEON BIOTECHNOLOGY AG (CH) 2007-11-29 US disclosed
US-5097023-A α-glucosidase inhibitors MERRELL DOW PHARMACEUTICALS INC. (US) 1992-03-17 US disclosed
WO-1991018915-A1 NOVEL α-GLUCOSIDASE INHIBITORS MERRELL DOW PHARMACEUTICALS INC. (US) 1991-12-12 WO disclosed
EP-0422975-A1 Alpha-glucosidase inhibitors MERRELL DOW PHARMACEUTICALS INC. (US) 1991-04-17 EP disclosed
EP-0422307-A1 Novel alpha-glucosidase inhibitors MERRELL DOW PHARMACEUTICALS INC. (US) 1991-04-17 EP disclosed
EP-0389723-A1 Novel alpha-glucosidase inhibitors MERRELL DOW PHARMACEUTICALS INC. (US) 1990-10-03 EP disclosed
EP-0390674-A1 Novel alpha-glucosidase inhibitors MERRELL DOW PHARMACEUTICALS INC. (US) 1990-10-03 EP disclosed
EP-0344383-A1 Novel alpha-Glucosidase inhibitors MERRELL DOW PHARMACEUTICALS INC. (US) 1989-12-06 EP disclosed
EP-0345104-A2 Novel Alpha-glucosidase inhibitors MERRELL DOW PHARMACEUTICALS INC. (US) 1989-12-06 EP disclosed
US-4801710-A Regioselective synthesis of 9-substituted purine acyclonucleoside derivatives MERCK & CO., INC. (US) 1989-01-31 US disclosed
EP-0184473-A1 Regioselective synthesis of 9-substituted purine acyclonucleoside derivatives MERCK & CO. INC. (US) 1986-06-11 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 (5 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-20080167255-A1 4-BIARYLYL-1-PHENYLAZETIDIN-2-ONES APOB, CYP46A1, PCSK9 SSTR5 4191/4885SSTR1 4669/4885SSTR2 4097/4885
US-20180009940-A1 MACROMOLECULAR TRANSITION METAL COMPLEXES FOR TREATMENT OF CANCERAND PROCESS FOR THEIR PREPARATION MDH1, SLC11A2, EXOSC9 SSTR5 2621/4885SSTR1 3914/4885SSTR2 3619/4885
US-11168179-B2 Macromolecular transition metal complexes for treatment of cancer and process for their preparation ABCB7, TFRC, IMMT SSTR5 2678/4885SSTR1 3655/4885SSTR2 3583/4885
US-20090275524-A1 NOVEL HYPOCHOLESTEROLEMIC COMPOUNDS CYP46A1, SREBF1, CETP SSTR5 1865/4885SSTR1 3275/4885SSTR2 2571/4885
US-20070275909-A1 Useful in the treatment and prevention of atherosclerosis and for the reduction of cholesterol levels; carbohydrate-containing pyrazolidinone or oxazolidinone derivatives, for example PCSK9, APOB, HMGCR SSTR5 1360/4885SSTR1 3011/4885SSTR2 3074/4885

“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.