SCHEMBL523268

SCHEMBL523268

COC1C[C@H](n2cc(C)c(=O)[nH]c2=O)O[C@@H]1CO

nearest known ligand 0.72

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ RNASE1 P07998 1/20 0.69
▸ TK1 P04183 6/20 0.65
▸ LMNA P02545 2/20 0.63
▸ TSHR P16473 2/20 0.63
▸ ALB P02768 1/20 0.63
▸ PKM P14618 1/20 0.63
▸ BLM P54132 1/20 0.63
▸ PMP22 Q01453 1/20 0.63
▸ CYP2D6 P10635 1/20 0.63

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
SCHEMBL19132672 1.00 RNASE1 (0.69) RNASE1TK1LMNATSHRALB
SCHEMBL12670320 1.00 RNASE1 (0.69) RNASE1TK1LMNATSHRALB
SCHEMBL16359947 1.00 RNASE1 (0.69) RNASE1TK1LMNATSHRALB
SCHEMBL25756080 1.00 RNASE1 (0.69) RNASE1TK1LMNATSHRALB
SCHEMBL523267 1.00 RNASE1 (0.69) RNASE1TK1LMNATSHRALB
SCHEMBL10431982 1.00 RNASE1 (0.69) RNASE1TK1LMNATSHRALB
SCHEMBL8996152 0.91 RNASE1 (0.70) RNASE1TK1LMNATSHRALB
SCHEMBL22992460 0.91 RNASE1 (0.69) RNASE1TK1LMNATSHRALB
SCHEMBL4286458 0.91 RNASE1 (0.69) RNASE1TK1LMNATSHRALB
SCHEMBL2056647 0.91 RNASE1 (0.69) RNASE1TK1LMNATSHRALB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230203484-A1 DOUBLE STRANDED OLIGONUCLEOTIDE COMPOSITIONS AND METHODS RELATING THERETO WAVE LIFE SCIENCES LTD. (SG) 2023-06-29 — — US disclosed
US-20170204152-A1 CHIMERIC POLYNUCLEOTIDES MODERNA THERAPEUTICS, INC. (US) 2017-07-20 — — US disclosed
EP-3165606-A1 METHODS FOR TREATING OR PREVENTING OPHTHALMOLOGICAL DISEASES Ophthotech Corporation (US) 2017-05-10 — — EP disclosed
EP-1730309-B1 COMPOSITIONS AND METHODS FOR OPTIMIZING CLEAVAGE OF RNA BY RNASE H IONIS PHARMACEUTICALS INC (US) 2016-05-04 — — EP disclosed
US-9303055-B2 Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2016-04-05 — — US disclosed
US-20150011001-A1 COMPOSITIONS AND METHODS FOR OPTIMIZING CLEAVAGE OF RNA BY RNASE H ISIS PHARMACEUTICALS, INC. (US) 2015-01-08 — — US disclosed
US-8790919-B2 Compositions and methods for optimizing cleavage of RNA by RNase H ISIS PHARMACEUTICALS, INC. (US) 2014-07-29 — — US disclosed
US-20140179875-A1 SULFURIZATION REAGENTS ON SOLID SUPPORTS GIRINDUS AMERICA, INC. (US) 2014-06-26 — — US disclosed
EP-2700720-A2 Compositions and methods for optimizing cleavage of RNA by RNASE H Isis Pharmaceuticals, Inc. (US) 2014-02-26 — — EP disclosed
US-20130261026-A1 LINKERS AND CO-COUPLING AGENTS FOR OPTIMIZATION OF OLIGONUCLEOTIDE SYNTHESIS AND PURIFICATION ON SOLID SUPPORTS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2013-10-03 — — US disclosed
WO-2002072791-A2 LINKERS AND CO-COUPLING AGENTS FOR OPTIMIZATION OF OLIGONUCLEOTIDE SYNTHESIS AND PURIFICATION ON SOLID SUPPORT THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2002-09-19 — — WO disclosed
US-20020055483-A1 3'-or 2'-hydroxymethyl substituted nucleoside derivatives for treatment of hepatites virus infections PHARMASSET, INC. 2002-05-09 — — US disclosed
WO-2001079246-A2 3'-OR 2'-HYDROXYMETHYL SUBSTITUTED NUCLEOSIDE DERIVATIVES FOR TREATMENT OF HEPATITIS VIRUS INFECTIONS PHARMASSET, LTD. (BB) 2001-10-25 — — WO disclosed
US-6191266-B1 MODIFIED TO COMPRISE SUBSTITUTIONS AT POSITIONS C1', C3', C4' OR C5' OF THE SUGAR MOIETY OF THE NUCLEOSIDE, INCLUDING AN OPTIONAL 3' PHOSPHOROAMIDITE GROUP; USE IN MAKING NUCLEASE RESISTANT OLIGONUCLEOTIDES FOR ANTISENSE THERAPY ICN PHARMACEUTICALS, INC. 2001-02-20 — — US disclosed
EP-0789706-A4 SUGAR MODIFIED NUCLEOSIDES AND THEIR USE FOR SYNTHESIS OF OLIGONUCLEOTIDES ICN PHARMACEUTICALS (US) 1999-08-11 — — EP disclosed
US-5712378-A SUGAR MOLECULE IS SUBSTITUTED WITH HYDROCARBON OR SUBSTITUTED HYDROCARBON GROUPS, ANTISENSE AGENTS ICN PHARMACEUTICALS (US) 1998-01-27 — — US disclosed
EP-0789706-A1 SUGAR MODIFIED NUCLEOSIDES AND THEIR USE FOR SYNTHESIS OF OLIGONUCLEOTIDES ICN PHARMACEUTICALS (US) 1997-08-20 — — EP disclosed
WO-1996014329-A1 SUGAR MODIFIED NUCLEOSIDES AND THEIR USE FOR SYNTHESIS OF OLIGONUCLEOTIDES ICN PHARMACEUTICALS (US) 1996-05-17 — — WO disclosed
EP-0460045-A1 NUCLEOSIDE ANALOGUES UNIVERSITY COLLEGE LONDON (GB) 1991-12-11 — — EP disclosed
WO-1990010012-A1 NUCLEOSIDE ANALOGUES UNIVERSITY COLLEGE LONDON (GB) 1990-09-07 — — WO 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 (4 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-20170204152-A1 CHIMERIC POLYNUCLEOTIDES NSUN3, TRDMT1, NSUN2 RNASE1 116/4885TK1 518/4885LMNA 1098/4885
US-20130261026-A1 LINKERS AND CO-COUPLING AGENTS FOR OPTIMIZATION OF OLIGONUCLEOTIDE SYNTHESIS AND PURIFICATION ON SOLID SUPPORTS PCNA, LIG4, DCLRE1A RNASE1 491/4885TK1 282/4885LMNA 1096/4885
US-20020055483-A1 3'-or 2'-hydroxymethyl substituted nucleoside derivatives for treatment of hepatites virus infections HCCS, HDGF, HMBS RNASE1 265/4885TK1 65/4885LMNA 1253/4885
US-20140179875-A1 SULFURIZATION REAGENTS ON SOLID SUPPORTS OR10J3, RPS8, NSUN2 RNASE1 2182/4885TK1 2907/4885LMNA 3685/4885

“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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