SCHEMBL7530640

SCHEMBL7530640

O=C(O[C@H]1CO[C@H]2[C@@H]1OC[C@H]2OC(=O)c1ccc(O)cc1)c1ccc(O)cc1

nearest known ligand 0.66

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ BCHE P06276 17/20 0.66
▸ PTPN1 P18031 1/20 0.48
▸ HSP90AA1 P07900 1/20 0.44
▸ CA12 O43570 1/20 0.44
▸ CA1 P00915 1/20 0.44
▸ CA2 P00918 1/20 0.44
▸ CA7 P43166 1/20 0.44
▸ CA9 Q16790 1/20 0.44
▸ CA14 Q9ULX7 1/20 0.44

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
SCHEMBL12702984 1.00 BCHE (0.66) BCHEPTPN1HSP90AA1CA12CA1
SCHEMBL9946847 1.00 BCHE (0.66) BCHEPTPN1HSP90AA1CA12CA1
SCHEMBL12411417 1.00 BCHE (0.66) BCHEPTPN1HSP90AA1CA12CA1
SCHEMBL18306889 1.00 BCHE (0.66) BCHEPTPN1HSP90AA1CA12CA1
SCHEMBL13367641 1.00 BCHE (0.66) BCHEPTPN1HSP90AA1CA12CA1
SCHEMBL12411448 0.95 BCHE (0.62) BCHEPTPN1HSP90AA1
SCHEMBL12411488 0.92 BCHE (0.59) BCHEPTPN1HSP90AA1
SCHEMBL12942000 0.92 BCHE (0.59) BCHEPTPN1HSP90AA1
SCHEMBL12411490 0.92 BCHE (0.59) BCHEPTPN1HSP90AA1
SCHEMBL14877911 0.92 BCHE (0.59) BCHEPTPN1HSP90AA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116948376-A Biodegradable polylactic acid composition and production method thereof 江西省隆旭科技有限公司 2023-10-27 — — CN disclosed
US-8507699-B2 Bisphenol polymer structural units and method of making the same SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2013-08-13 — — US disclosed
US-8344175-B2 Liquid crystal compositions, polymer networks derived therefrom and process for making the same E I DU PONT DE NEMOURS AND COMPANY (US) 2013-01-01 — — US disclosed
US-8344175-B2 Liquid crystal compositions, polymer networks derived therefrom and process for making the same E I DU PONT DE NEMOURS AND COMPANY (US) 2013-01-01 — — US disclosed
US-8334393-B2 Chiral compounds and liquid crystal compositions and polymer networks derived therefrom E I DU PONT DE NEMOURS AND COMPANY (US) 2012-12-18 — — US disclosed
US-8334393-B2 Chiral compounds and liquid crystal compositions and polymer networks derived therefrom E I DU PONT DE NEMOURS AND COMPANY (US) 2012-12-18 — — US disclosed
US-20120149923-A1 BISPHENOL POLYMER STRUCTURAL UNITS AND METHOD OF MAKING THE SAME SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2012-06-14 — — US disclosed
US-20110163267-A1 CHIRAL COMPOUNDS AND LIQUID CRYSTAL COMPOSITIONS AND POLYMER NETWORKS DERIVED THEREFROM E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-07-07 — — US disclosed
US-20110163267-A1 CHIRAL COMPOUNDS AND LIQUID CRYSTAL COMPOSITIONS AND POLYMER NETWORKS DERIVED THEREFROM E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-07-07 — — US disclosed
US-20110114885-A1 LIQUID CRYSTAL COMPOSITIONS, POLYMER NETWORKS DERIVED THEREFROM AND PROCESS FOR MAKING THE SAME E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-05-19 — — US disclosed
US-7879256-B2 bis(meth)acrylates with esters linking mesogen to a flexible spacer and polymerizable (meth)acrylates E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-02-01 — — US disclosed
US-7879256-B2 bis(meth)acrylates with esters linking mesogen to a flexible spacer and polymerizable (meth)acrylates E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-02-01 — — US disclosed
US-20070267599-A1 Liquid crystal compositions and polymer networks derived therefrom GOLDFINGER MARC B 2007-11-22 — — US disclosed
US-20070267599-A1 Liquid crystal compositions and polymer networks derived therefrom GOLDFINGER MARC B 2007-11-22 — — US disclosed
WO-2007120458-A1 LIQUID CRYSTAL COMPOSITIONS, POLYMER NETWORKS DERIVED THEREFROM AND PROCESS FOR MAKING THE SAME E. I. DU PONT DE NEMOURS AND COMPANY (US) 2007-10-25 — — WO disclosed
US-20020013482-A1 Process for the preparation of dianhydrohexitol bis(4-acryloyloxy)acylates CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH 2002-01-31 — — US disclosed
US-20020013483-A1 Process for the preparation of dianhydrohexitol bisacylates CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH 2002-01-31 — — US disclosed
EP-0773250-B1 Chiral dianhydro hexite derivative containing liquid-crystalline organosiloxanes CONSORTIUM ELEKTROCHEM IND (DE) 1999-01-27 — — EP disclosed
US-5788880-A Liquid-crystalline organosiloxanes containing chiral dianhydrohexitol derivatives CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) 1998-08-04 — — US disclosed
EP-0773250-A1 Chiral dianhydro hexite derivative containing liquid-crystalline organosiloxanes Consortium für elektrochemische Industrie GmbH (DE) 1997-05-14 — — 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 (6 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-20070267599-A1 Liquid crystal compositions and polymer networks derived therefrom F2, CCNB1, CYP2F1 BCHE 4080/4885PTPN1 1979/4885HSP90AA1 4770/4885
US-20120149923-A1 BISPHENOL POLYMER STRUCTURAL UNITS AND METHOD OF MAKING THE SAME PCBP1, PUF60, FHIT BCHE 3521/4885PTPN1 3080/4885HSP90AA1 2521/4885
US-20110163267-A1 CHIRAL COMPOUNDS AND LIQUID CRYSTAL COMPOSITIONS AND POLYMER NETWORKS DERIVED THEREFROM CCNB1, F2, CYP4F11 BCHE 3686/4885PTPN1 2046/4885HSP90AA1 4811/4885
US-20020013482-A1 Process for the preparation of dianhydrohexitol bis(4-acryloyloxy)acylates HDHD5, ABHD5, HACL2 BCHE 1159/4885PTPN1 4027/4885HSP90AA1 1761/4885
US-20020013483-A1 Process for the preparation of dianhydrohexitol bisacylates G6PD, HSD17B14, PAOX BCHE 1774/4885PTPN1 1286/4885HSP90AA1 4024/4885
US-20110114885-A1 LIQUID CRYSTAL COMPOSITIONS, POLYMER NETWORKS DERIVED THEREFROM AND PROCESS FOR MAKING THE SAME THEM6, NOTUM, WEE1 BCHE 3695/4885PTPN1 1908/4885HSP90AA1 3792/4885

“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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