SCHEMBL1521576

SCHEMBL1521576

CSC(=S)O[C@@H]1[C@H]2OC(C)(C)O[C@H]2O[C@@H]1[C@H]1COC(C)(C)O1

nearest known ligand 0.56

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
▸ CA1 P00915 1/20 0.56
▸ CA2 P00918 1/20 0.56
▸ CA9 Q16790 1/20 0.56

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
SCHEMBL17822617 1.00 CA1 (0.56) CA1CA2CA9
SCHEMBL15694522 1.00 CA1 (0.56) CA1CA2CA9
SCHEMBL20457638 1.00 CA1 (0.56) CA1CA2CA9
SCHEMBL26457815 0.82 CA2 (0.64) CA1CA2CA9
SCHEMBL1847432 0.82 CA2 (0.64) CA1CA2CA9
SCHEMBL27174720 0.82 CA2 (0.64) CA1CA2CA9
SCHEMBL14441192 0.82 CA2 (0.64) CA1CA2CA9
SCHEMBL16307847 0.82 CA2 (0.64) CA1CA2CA9
SCHEMBL10883648 0.82 CA2 (0.64) CA1CA2CA9
SCHEMBL15254185 0.82 CA2 (0.64) CA1CA2CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12187759-B2 TLR7 agonists Primmune Therapeutics, Inc. (US) 2025-01-07 — — US disclosed
US-11692005-B2 TLR7 agonists Primmune Therapeutics, Inc. (US) 2023-07-04 — — US disclosed
US-20210155652-A1 TLR7 AGONISTS Primmune Therapeutics, Inc. 2021-05-27 — — US disclosed
US-20200223860-A1 THE TOTAL SYNTHESIS OF GLUCOSEPANE AND RELATED CHEMICAL REACTIONS, COMPOUNDS AND COMPOSITIONS AND OBTAINED THEREFROM AND METHODS OF TREATMENT UNIV YALE (US) 2020-07-16 — — US disclosed
US-7906460-B2 Active-site engineering of nucleotidylyltransferases and general enzymatic methods for the synthesis of natural and “unnatural” UDP- and TDP-nucleotide sugars SLOAN-KETTERING INSTITUTE FOR CANCER (US) 2011-03-15 — — US disclosed
US-20070178487-A1 ACTIVE-SITE ENGINEERING OF NUCLEOTIDYLYLTRANSFERASES AND GENERAL ENZYMATIC METHODS FOR THE SYNTHESIS OF NATURAL AND \"UNNATURAL\" UDP- AND TDP-NUCLEOTIDE SUGARS WISCONSIN ALUMNI RESEARCH FOUNDATION 2007-08-02 — — US disclosed
US-7122359-B2 Active-site engineering of nucleotidylyltransferases and general enzymatic methods for the synthesis of natural and “unnatural” UDP- and TDP-nucleotide sugars SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 2006-10-17 — — US disclosed
US-20030055235-A1 Active-site engineering of nucleotidylyltransferases and general enzymatic methods for the synthesis of natural and \"unnatural\" UDP- and TDP-nucleotide sugars SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH 2003-03-20 — — US disclosed
US-4078139-A Process for deoxygenating secondary alcohols SCHERING CORPORATION (US) 1978-03-07 — — US 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-20210155652-A1 TLR7 AGONISTS TLR7, TLR1, TLR9 CA1 4872/4885CA2 4796/4885CA9 4617/4885
US-20200223860-A1 THE TOTAL SYNTHESIS OF GLUCOSEPANE AND RELATED CHEMICAL REACTIONS, COMPOUNDS AND COMPOSITIONS AND OBTAINED THEREFROM AND METHODS OF TREATMENT PTMS, AGER, GALE CA1 4847/4885CA2 4715/4885CA9 4766/4885
US-20030055235-A1 Active-site engineering of nucleotidylyltransferases and general enzymatic methods for the synthesis of natural and \"unnatural\" UDP- and TDP-nucleotide sugars PNP, NUDT14, ENTPD5 CA1 4383/4885CA2 3438/4885CA9 3993/4885
US-12187759-B2 TLR7 agonists TLR7, TLR1, TLR9 CA1 4872/4885CA2 4796/4885CA9 4617/4885
US-20070178487-A1 ACTIVE-SITE ENGINEERING OF NUCLEOTIDYLYLTRANSFERASES AND GENERAL ENZYMATIC METHODS FOR THE SYNTHESIS OF NATURAL AND \"UNNATURAL\" UDP- AND TDP-NUCLEOTIDE SUGARS PNP, NUDT14, NUDT5 CA1 4342/4885CA2 3133/4885CA9 3963/4885
US-11692005-B2 TLR7 agonists TLR7, TLR1, TLR9 CA1 4872/4885CA2 4796/4885CA9 4617/4885

“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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