SCHEMBL157493

SCHEMBL157493

Cc1ccc(S(=O)(=O)OCO[PH](=O)OCOS(=O)(=O)c2ccc(C)cc2)cc1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 2/20 0.42
STAT3 P40763 1/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
KMT2A Q03164 2/20 0.41
ALDH1A1 P00352 3/20 0.40
CYP3A4 P08684 1/20 0.40
CYP2C9 P11712 1/20 0.40
CYP2C19 P33261 1/20 0.40
CA1 P00915 3/20 0.39
CA9 Q16790 3/20 0.39
CA12 O43570 2/20 0.39
CA2 P00918 2/20 0.39
CA3 P07451 1/20 0.39
CA6 P23280 1/20 0.39
CA5A P35218 1/20 0.39
CA7 P43166 1/20 0.39
CA5B Q9Y2D0 1/20 0.39
VDR P11473 1/20 0.39
TLR9 Q9NR96 1/20 0.38
CYP2D6 P10635 2/20 0.38

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
SCHEMBL4960150 0.88 GAA (0.41) GAASTAT3SMN1; SMN2KMT2AALDH1A1
SCHEMBL16020729 0.87 BCHE (0.44) GAAKMT2AALDH1A1CYP3A4CYP2C9
SCHEMBL157494 0.86 STAT3 (0.43) GAASTAT3SMN1; SMN2KMT2AALDH1A1
SCHEMBL3315459 0.85 GAA (0.52) GAASTAT3SMN1; SMN2KMT2AALDH1A1
Fluoride SCHEMBL31533364 0.83 GAA (0.50) GAASTAT3SMN1; SMN2KMT2AALDH1A1
Butane SCHEMBL1393934 0.82 STAT3 (0.40) GAASTAT3SMN1; SMN2KMT2AALDH1A1
SCHEMBL8758128 0.82 EEF2K (0.43) SMN1; SMN2KMT2AALDH1A1CYP3A4CA1
SCHEMBL28684539 0.81 PARL (0.42) GAASMN1; SMN2KMT2AALDH1A1CA1
SCHEMBL9905506 0.81 C5AR1 (0.38) GAASTAT3SMN1; SMN2KMT2AALDH1A1
SCHEMBL11604749 0.81 GAA (0.48) GAASTAT3SMN1; SMN2KMT2AALDH1A1

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
US-5733896-A VIRICIDE FOR RETROVIRUS INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY OF THE ACADEMY OF SCIENCES OF THE CZECH REPUBLIC (CZ) 1998-03-31 US claimed
EP-0253412-A2 N-Phosphonylmethoxyalkyl derivatives of pyrimidine and purine bases, methods for their preparation and pharmaceutical compositions therefrom with antiviral activity Ceskoslovenska akademie ved (CS) 1988-01-20 EP claimed
CN-120022913-A Method for using high-stability copper-based catalyst in hydrochlorination of acetylene 中盐吉兰泰氯碱化工有限公司 2025-05-23 CN disclosed
EP-3020720-B1 PHOSPHONATE ESTER DERIVATIVES AND METHODS OF SYNTHESIS THEREOF CHIMERIX INC (US) 2018-09-19 EP disclosed
CN-105998039-A Phosphonate ester derivatives and methods of synthesis thereof 奇默里克斯公司 2016-10-12 CN disclosed
EP-2611818-B1 PHOSPHONATE ESTER DERIVATIVES AND METHODS OF SYNTHESIS THEREOF CHIMERIX INC (US) 2016-08-24 EP disclosed
CN-103209985-B Phosphonate derivatives and methods of synthesis thereof 奇默里克斯公司 2016-08-24 CN disclosed
EP-3020720-A1 PHOSPHONATE ESTER DERIVATIVES AND METHODS OF SYNTHESIS THEREOF Chimerix, Inc. (US) 2016-05-18 EP disclosed
US-9303051-B2 Phosphonate ester derivatives and methods of synthesis thereof CHIMERIX INC. (US) 2016-04-05 US disclosed
CN-105218580-A Phosphate derivatives and synthetic method thereof CHIMERIX INC 2016-01-06 CN disclosed
US-20150329575-A1 PHOSPHONATE ESTER DERIVATIVES AND METHODS OF SYNTHESIS THEREOF EMERGENT BIODEFENSE OPERATIONS LANSING LLC 2015-11-19 US disclosed
US-20120058976-A1 Phosphonate Ester Derivatives and Methods of Synthesis Thereof CHIMERIX, INC. (US) 2012-03-08 US disclosed
EP-2086990-A2 NOVEL NUCLEOTIDE ANALOGUES AS PERCURSOR MOLECULES FOR ANTIVIRALS Centre National De La Recherche Scientifique-CNRS (FR) 2009-08-12 EP disclosed
EP-2016062-A2 ANTI-VIRAL AGENTS THAT ACTIVATE RNASE L The Cleveland Clinic Foundation (US) 2009-01-21 EP disclosed
US-7388002-B2 Nucleosides, preparation thereof and use as inhibitors of RNA viral polymerases BIOCRYST PHARMACEUTICALS, INC. (US) 2008-06-17 US disclosed
WO-2008056264-A2 NOVEL NUCLEOTIDE ANALOGUES AS PERCURSOR MOLECULES FOR ANTIVIRALS CENTRE NATIONAL DE RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2008-05-15 WO disclosed
WO-2007127212-A2 ANTI-VIRAL AGENTS THAT ACTIVATE RNASE L THE CLEVELAND CLINIC FOUNDATION (US) 2007-11-08 WO disclosed
WO-2006076015-A2 1-[2-(PHOSPHONOMETHOXY)ETHYL]-CYTOSINE AND ANALOGS THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2006-07-20 WO disclosed
US-20060122391-A1 Nucleosides, preparation thereof and use as inhibitors of RNA viral polymerases BIOCRYST PHARMACEUTICALS, INC. (US) 2006-06-08 US disclosed
WO-2005087788-A2 METHODS FOR PREPARATION OF NUCLEOSIDE PHOSPHONATE ESTERS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2005-09-22 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 (3 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-20060122391-A1 Nucleosides, preparation thereof and use as inhibitors of RNA viral polymerases POLR2H, NSUN2, POLR2E GAA 2605/4885STAT3 2322/4885SMN1; SMN2 655/4885
US-20120058976-A1 Phosphonate Ester Derivatives and Methods of Synthesis Thereof PHOSPHO1, PIK3CA, PNP GAA 507/4885STAT3 3774/4885SMN1; SMN2 2752/4885
US-20150329575-A1 PHOSPHONATE ESTER DERIVATIVES AND METHODS OF SYNTHESIS THEREOF PHOSPHO1, PIK3CA, PNP GAA 507/4885STAT3 3774/4885SMN1; SMN2 2752/4885

“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.