SCHEMBL522139

SCHEMBL522139

CSCOCc1ccccc1C=O

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.40
KMT2A Q03164 3/20 0.40
TDP1 Q9NUW8 2/20 0.40
MEN1 O00255 1/20 0.40
THRB P10828 1/20 0.40
BLM P54132 1/20 0.40
ALDH1A1 P00352 3/20 0.39
HPGD P15428 1/20 0.39
HTT P42858 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
TSHR P16473 1/20 0.38
CDK4 P11802 1/20 0.35
CCND1 P24385 1/20 0.35
TRIM24 O15164 1/20 0.34
TRIM33 Q9UPN9 1/20 0.34
SRC P12931 2/20 0.34
PTGDR2 Q9Y5Y4 1/20 0.33
GAA P10253 1/20 0.33
CYP1A2 P05177 1/20 0.33
CYP2C9 P11712 1/20 0.33

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
SCHEMBL9166924 0.83 LMNA (0.38) LMNAKMT2ATDP1MEN1THRB
SCHEMBL522410 0.82 LMNA (0.36) LMNAKMT2ATDP1MEN1THRB
SCHEMBL1200922 0.80 LMNA (0.44) LMNAKMT2ATDP1MEN1THRB
SCHEMBL1199895 0.76 LMNA (0.48) LMNAKMT2ATDP1MEN1THRB
SCHEMBL1199445 0.76 LMNA (0.54) LMNAKMT2ATDP1MEN1THRB
SCHEMBL8791743 0.75 TSHR (0.56) LMNAKMT2ATDP1MEN1THRB
SCHEMBL14948694 0.75 ALDH1A1 (0.42) LMNAKMT2ATDP1MEN1THRB
SCHEMBL27939291 0.73 ALDH1A1 (0.41) LMNAKMT2ATDP1MEN1THRB
SCHEMBL1200238 0.73 LMNA (0.44) LMNAKMT2ATDP1MEN1THRB
SCHEMBL10715229 0.72 PTGDR2 (0.56) LMNAKMT2ATDP1MEN1THRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100029513-A1 Methods And Compositions For Generating Mixtures Of Nucleic Acid Molecules AGILENT TECHNOLOGIES, INC. 2010-02-04 US claimed
US-7576119-B2 Supports for oligomer synthesis ISIS PHARMACEUTICALS, INC. (US) 2009-08-18 US claimed
US-20080021224-A1 SUPPORTS FOR OLIGOMER SYNTHESIS ISIS PHARMACEUTICALS, INC. (US) 2008-01-24 US claimed
US-7202264-B2 Supports such as glass and styrene polymers functionalized with tricyclic hetercyclic anhydrides and imides, used in the preparation of oligonucleotides ISIS PHARMACEUTICALS, INC. (US) 2007-04-10 US claimed
EP-1670810-A2 GAPPED OLIGOMERIC COMPOUNDS HAVING LINKED BICYCLI CSUGAR MOIETIES AT THE TERMINI Isis Pharmaceuticals, Inc. (US) 2006-06-21 EP claimed
US-20050208588-A1 Supports for oligomer synthesis ISIS PHARMACEUTICALS, INC. (US) 2005-09-22 US claimed
US-20050059066-A1 Gapped oligomeric compounds having linked bicyclic sugar moieties at the termini IONIS PHARMACEUTICALS, INC. 2005-03-17 US claimed
WO-2005023825-A2 GAPPED OLIGOMERIC COMPOUNDS HAVING LINKED BICYCLIC SUGAR MOIETIES AT THE TERMINI ISIS PHARMACEUTICALS, INC. (US) 2005-03-17 WO claimed
US-20050053981-A1 Gapped oligomeric compounds having linked bicyclic sugar moieties at the termini ISIS PHARMACEUTICALS, INC. 2005-03-10 US claimed
US-20040242897-A1 Universal support media for synthesis of oligomeric compounds ISIS PHARMACEUTICALS, INC. 2004-12-02 US claimed
WO-2000075157-A1 OLIGONUCLEOTIDE SYNTHESIS WITH LEWIS ACIDS AS ACTIVATORS ABBOTT LABORATORIES (US) 2000-12-14 WO claimed
US-5721350-A Deuterated nucleosides CHATTOPADHYAYA JYOTI (SE) 1998-02-24 US claimed
JP-H09510206-A 1997-10-14 JP claimed
US-5623068-A Synthesis of DNA using substituted phenylacetyl-protected nucleotides BECKMAN INSTRUMENTS, INC. (US) 1997-04-22 US claimed
EP-0749436-A1 COMPOSITIONS AND METHODS FOR USE IN THE SYNTHESIS OF OLIGONUCLEOTIDES BECKMAN INSTRUMENTS, INC. (US) 1996-12-27 EP claimed
US-5574146-A Oligonucleotide synthesis with substituted aryl carboxylic acids as activators BECKMAN INSTRUMENTS, INC. (US) 1996-11-12 US claimed
EP-0725787-A1 ACTIVATED NUCLEOSIDE PHOSPHORAMIDITES AND METHODS FOR THE PREPARATION AND USE THEREOF BECKMAN INSTRUMENTS, INC. (US) 1996-08-14 EP claimed
WO-1996006853-A1 ACTIVATED NUCLEOSIDE PHOSPHORAMIDITES AND METHODS FOR THE PREPARATION AND USE THEREOF BECKMAN INSTRUMENTS, INC. (US) 1996-03-07 WO claimed
WO-1995024413-A1 COMPOSITIONS AND METHODS FOR USE IN THE SYNTHESIS OF OLIGONUCLEOTIDES BECKMAN INSTRUMENTS, INC. (US) 1995-09-14 WO claimed
WO-1993025566-A1 DEUTERATED NUCLEOSIDES CHATTOPADHYAYA JYOTI (SE) 1993-12-23 WO claimed

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-20080021224-A1 SUPPORTS FOR OLIGOMER SYNTHESIS ILK, NOP2, PFAS LMNA 1785/4885KMT2A 2924/4885TDP1 1417/4885
US-20100029513-A1 Methods And Compositions For Generating Mixtures Of Nucleic Acid Molecules POLM, RNGTT, POLN LMNA 109/4885KMT2A 1878/4885TDP1 95/4885
US-20050059066-A1 Gapped oligomeric compounds having linked bicyclic sugar moieties at the termini OGG1, UNG, PCNA LMNA 141/4885KMT2A 2982/4885TDP1 103/4885
US-20050053981-A1 Gapped oligomeric compounds having linked bicyclic sugar moieties at the termini OGG1, UNG, PCNA LMNA 141/4885KMT2A 2982/4885TDP1 103/4885
US-20050208588-A1 Supports for oligomer synthesis ILK, NOP2, PFAS LMNA 1785/4885KMT2A 2924/4885TDP1 1417/4885
US-20040242897-A1 Universal support media for synthesis of oligomeric compounds NEFM, POLRMT, POLM LMNA 2165/4885KMT2A 3200/4885TDP1 1169/4885

“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.