SCHEMBL522210

SCHEMBL522210

O=C1c2cc(Cl)c(Cl)cc2C(=O)N1c1ccc([C](c2ccc(N3C(=O)c4cc(Cl)c(Cl)cc4C3=O)cc2)c2ccc(N3C(=O)c4cc(Cl)c(Cl)cc4C3=O)cc2)cc1

nearest known ligand 0.75

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
CA9 Q16790 11/20 0.75
CA1 P00915 7/20 0.75
CA12 O43570 6/20 0.75
CA2 P00918 4/20 0.58
ESR1 P03372 2/20 0.49
ESR2 Q92731 2/20 0.49
SCN2A Q99250 1/20 0.47
MEN1 O00255 1/20 0.47
KMT2A Q03164 1/20 0.47
CA4 P22748 1/20 0.44

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
SCHEMBL383638 0.93 CA9 (0.71) CA9CA1CA12CA2ESR1
SCHEMBL5647824 0.83 ESR1 (0.70) CA9CA1CA12CA2ESR1
SCHEMBL5198978 0.79 ALDH1A1 (0.64) CA9CA1CA12CA2ESR1
SCHEMBL27475071 0.79 CA9 (0.62) CA9CA1CA12CA2ESR1
SCHEMBL2357830 0.79 CA9 (0.61) CA9CA1CA12CA2ESR1
SCHEMBL29710383 0.79 CA9 (0.66) CA9CA1CA12CA2ESR1
SCHEMBL9633890 0.79 CA9 (0.66) CA9CA1CA12CA2ESR1
SCHEMBL374398 0.78 CA9 (0.60) CA9CA1CA12CA2ESR1
SCHEMBL3626463 0.76 CA9 (0.58) CA9CA1CA12CA2ESR1
SCHEMBL7921955 0.76 CA9 (0.57) CA9CA1CA12CA2ESR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-2004011474-A1 UNIVERSAL SUPPORT MEDIA FOR SYNTHESIS OF OLIGOMERIC COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 2004-02-05 WO claimed
US-6124484-A Recovery of triarylmethyl halide protecting groups cleaved during oligonucleotide synthesis ISIS PHARMACEUTICALS, INC. (US) 2000-09-26 US 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 (5 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 CA9 3036/4885CA1 2308/4885CA12 2383/4885
US-20050059066-A1 Gapped oligomeric compounds having linked bicyclic sugar moieties at the termini OGG1, UNG, PCNA CA9 4009/4885CA1 4569/4885CA12 4189/4885
US-20050053981-A1 Gapped oligomeric compounds having linked bicyclic sugar moieties at the termini OGG1, UNG, PCNA CA9 4009/4885CA1 4569/4885CA12 4189/4885
US-20050208588-A1 Supports for oligomer synthesis ILK, NOP2, PFAS CA9 3036/4885CA1 2308/4885CA12 2383/4885
US-20040242897-A1 Universal support media for synthesis of oligomeric compounds NEFM, POLRMT, POLM CA9 4492/4885CA1 3113/4885CA12 3583/4885

“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.