SCHEMBL338162

SCHEMBL338162

[CH2]C(S)C(=O)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 3/20 0.52
L3MBTL1 Q9Y468 2/20 0.52
CES1 P23141 4/20 0.50
CES2 O00748 3/20 0.50
LMNA P02545 3/20 0.50
CA12 O43570 1/20 0.48
CA1 P00915 1/20 0.48
CA2 P00918 1/20 0.48
CA3 P07451 1/20 0.48
CA4 P22748 1/20 0.48
CA6 P23280 1/20 0.48
CA5A P35218 1/20 0.48
CA7 P43166 1/20 0.48
CA9 Q16790 1/20 0.48
CA13 Q8N1Q1 1/20 0.48
CA14 Q9ULX7 1/20 0.48
CA5B Q9Y2D0 1/20 0.48
MDM2 Q00987 1/20 0.47
TSHR P16473 2/20 0.46
ALDH1A1 P00352 2/20 0.46

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
SCHEMBL28960147 0.80 TDP1 (0.56) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL8445181 0.80 CES1 (0.60) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL2417683 0.80 TDP1 (0.56) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL4380823 0.78 CES1 (0.58) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL1167722 0.76 L3MBTL1 (0.52) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL11377658 0.76 TDP1 (0.52) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL9211939 0.76 TDP1 (0.52) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL7207824 0.76 TDP1 (0.52) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL932126 0.76 TDP1 (0.52) TDP1L3MBTL1CES1CES2LMNA
SCHEMBL5274104 0.76 TDP1 (0.52) TDP1L3MBTL1CES1CES2LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100311960-A1 Phosphinoamidite Carboxylates and Analogs Thereof in the Synthesis of Oligonucleotide Having Reduced Internucleotide Charge LIEVRE CORNU LLC (US) 2010-12-09 US claimed
US-7745591-B2 phosphinocarboxylate and phosphonocarboxylate oligonucleotides having enhanced nuclease resistance Lievre Cornu, LLC (US) 2010-06-29 US claimed
US-7427679-B2 Precursors for two-step polynucleotide synthesis AGILENT TECHNOLOGIES, INC. (US) 2008-09-23 US claimed
US-7417139-B2 Method for polynucleotide synthesis AGILENT TECHNOLOGIES, INC. (US) 2008-08-26 US claimed
US-7385050-B2 Cleavable linker for polynucleotide synthesis AGILENT TECHNOLOGIES, INC. (US) 2008-06-10 US claimed
US-7193077-B2 Exocyclic amine triaryl methyl protecting groups in two-step polynucleotide synthesis AGILENT TECHNOLOGIES, INC. (US) 2007-03-20 US claimed
EP-1334111-A4 PHOSPHINOAMIDITE CARBOXYLATES AND ANALOGS THEREOF IN THE SYNTHESIS OF OLIGONUCLEOTIDES HAVING REDUCED INTERNUCLEOTIDE CHARGE DELLINGER DOUGLAS J (US) 2007-01-24 EP claimed
US-20060293511-A1 phosphinocarboxylate and phosphonocarboxylate oligonucleotides having enhanced nuclease resistance LIEVRE CORNU LLC (US) 2006-12-28 US claimed
US-7067641-B2 Phosphinoamidite carboxylates and analogs thereof in the synthesis of oligonucleotides having reduced internucleotide charge LIEVRE CORNU LLC (US) 2006-06-27 US claimed
US-20050048497-A1 Cleavable linker for polynucleotide synthesis THE REGENTS OF THE UNIVERSITY OF COLORADO 2005-03-03 US claimed
US-20050048601-A1 Method for polynucleotide synthesis REGENTS OF THE UNIVERSITY OF COLORADO, THE 2005-03-03 US claimed
EP-1510523-A1 Precurors for two-step polynucleotide synthesis Agilent Technologies Inc (US) 2005-03-02 EP claimed
EP-1334111-A2 PHOSPHINOAMIDITE CARBOXYLATES AND ANALOGS THEREOF IN THE SYNTHESIS OF OLIGONUCLEOTIDES HAVING REDUCED INTERNUCLEOTIDE CHARGE Dellinger, Douglas J. (US) 2003-08-13 EP claimed
WO-2002032912-A2 PHOSPHINOAMIDITE CARBOXYLATES AND ANALOGS THEREOF IN THE SYNTHESIS OF OLIGONUCLEOTIDES HAVING REDUCED INTERNUCLEOTIDE CHARGE DELLINGER DOUGLAS J (US) 2002-04-25 WO claimed
WO-2024006953-A2 MONOMERS AND METHODS FOR SYNTHESIS OF MODIFIED OLIGONUCLEOTIDES ALNYLAM PHARMACEUTICALS, INC. (US) 2024-01-04 WO disclosed
CN-110461858-A Acyl nucleosides phosphonate ester, its prodrug and its purposes as drug UNIV MONTPELLIER 2019-11-15 CN disclosed
US-8097711-B2 nucleoside monomers protected with thioether substituted aryl carbonate protecting groups; oligonucleotides, using such protected nucleoside monomer monomers, as well as nucleic acids AGILENT TECHNOLOGIES, INC. (US) 2012-01-17 US disclosed
WO-2002032912-A2 PHOSPHINOAMIDITE CARBOXYLATES AND ANALOGS THEREOF IN THE SYNTHESIS OF OLIGONUCLEOTIDES HAVING REDUCED INTERNUCLEOTIDE CHARGE DELLINGER DOUGLAS J (US) 2002-04-25 WO disclosed
EP-1051419-A1 DEPROTECTION AND RECRYSTALLIZATION PROCESSES BRISTOL-MYERS SQUIBB COMPANY (US) 2000-11-15 EP disclosed
WO-1999035145-A1 DEPROTECTION AND RECRYSTALLIZATION PROCESSES BRISTOL-MYERS SQUIBB COMPANY (US) 1999-07-15 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-20050048601-A1 Method for polynucleotide synthesis POLN, RNGTT, NSUN2 TDP1 155/4885L3MBTL1 905/4885CES1 3226/4885
US-20100311960-A1 Phosphinoamidite Carboxylates and Analogs Thereof in the Synthesis of Oligonucleotide Having Reduced Internucleotide Charge NSUN2, POLL, DUT TDP1 485/4885L3MBTL1 46/4885CES1 3049/4885
US-20050048497-A1 Cleavable linker for polynucleotide synthesis TYMP, POLN, CPSF1 TDP1 53/4885L3MBTL1 2004/4885CES1 2420/4885
US-20060293511-A1 phosphinocarboxylate and phosphonocarboxylate oligonucleotides having enhanced nuclease resistance NSUN2, ADAR, POLL TDP1 199/4885L3MBTL1 42/4885CES1 1866/4885

“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.