SCHEMBL4948926

SCHEMBL4948926

O=[N+]([O-])c1ccc(Nc2ccccc2S(=O)(=O)O)c([N+](=O)[O-])c1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 4/20 0.63
▸ MEN1 O00255 5/20 0.53
▸ KMT2A Q03164 5/20 0.53
▸ NT5E P21589 1/20 0.51
▸ MAPK1 P28482 4/20 0.50
▸ GUSB P08236 1/20 0.49
▸ GFER P55789 1/20 0.48
▸ ALDH1A1 P00352 4/20 0.47
▸ TDP1 Q9NUW8 2/20 0.47
▸ L3MBTL1 Q9Y468 2/20 0.47
▸ CTDSP1 Q9GZU7 1/20 0.47
▸ CRHBP P24387 1/20 0.47
▸ CRHR2 Q13324 1/20 0.47
▸ POLB P06746 2/20 0.45
▸ CYP1A2 P05177 1/20 0.45
▸ CYP3A4 P08684 1/20 0.45
▸ CYP2D6 P10635 1/20 0.45
▸ CYP2C9 P11712 1/20 0.45
▸ CYP2C19 P33261 1/20 0.45
▸ HIF1A Q16665 1/20 0.45

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
SCHEMBL4948931 1.00 MAPT (0.63) MAPTMEN1KMT2ANT5EMAPK1
SCHEMBL10720749 0.86 MAPT (0.63) MAPTMEN1KMT2AMAPK1GUSB
SCHEMBL10628268 0.84 NT5E (0.52) MAPTMEN1KMT2ANT5EMAPK1
SCHEMBL16147671 0.84 NT5E (0.61) MAPTMEN1KMT2ANT5EMAPK1
SCHEMBL108329 0.84 NT5E (0.61) MAPTMEN1KMT2ANT5EMAPK1
SCHEMBL141078 0.83 NT5E (0.60) MAPTMEN1KMT2ANT5EMAPK1
SCHEMBL141080 0.83 NT5E (0.60) MAPTMEN1KMT2ANT5EMAPK1
SCHEMBL141081 0.83 NT5E (0.60) MAPTMEN1KMT2ANT5EMAPK1
SCHEMBL31715811 0.81 MAPT (0.73) MAPTMEN1KMT2AMAPK1GFER
SCHEMBL9225420 0.80 NT5E (0.67) MAPTMEN1KMT2ANT5EMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1895841-A2 METHODS FOR SELECTIVE N-9 GLYCOSYLATION OF PURINES Brigham Young University (US) 2008-03-12 — — EP disclosed
US-20070123702-A1 Oligonucleotdies having A-DNA form and B-DNA form conformational geometry MANOHARAN MUTHIAH 2007-05-31 — — US disclosed
EP-1743901-A2 Oligonucleotides having A-DNA or B-DNA form ISIS PHARMACEUTICALS, INC. (US) 2007-01-17 — — EP disclosed
WO-2006138396-A2 METHODS FOR SELECTIVE N-9 GLYCOSYLATION OF PURINES BRIGHAM YOUNG UNIVERSITY, TRANSFER TECHNOLOGY OFFICE (US) 2006-12-28 — — WO disclosed
US-7119184-B2 Oligonucleotides having A-DNA form and B-DNA form conformational geometry ISIS PHARMACEUTICALS, INC. (US) 2006-10-10 — — US disclosed
EP-1100809-B1 RNA TARGETED 2'-MODIFIED OLIGONUCLEOTIDES THAT ARE CONFORMATIONALLY PREORGANIZED ISIS PHARMACEUTICALS INC (US) 2004-09-22 — — EP disclosed
US-6737520-B2 FOR USE AS SUBSTRATE FOR RIBONUCLEASE AND CONTROLLING BINDING AFFINITY/NUCLEASE RESISTANCE ISIS PHARMACEUTICALS, INC. 2004-05-18 — — US disclosed
US-20040009938-A1 Methods of enhancing renal uptake of oligonucleotides ISIS PHARMACEUTICAL INC. 2004-01-15 — — US disclosed
US-6673912-B1 2′-O-aminoethyloxyethyl-modified oligonucleotides ISIS PHARMACEUTICALS, INC. 2004-01-06 — — US disclosed
US-6653458-B1 Phosphodiester or phosphorothioate internucleotide linkages at 2',5' positions; substituents at 3'; nuclease resistance and increased binding affinity; use as antisense agents ISIS PHARMACEUTICALS, INC. 2003-11-25 — — US disclosed
US-20030105311-A1 Oligonucleotides having A-DNA form and B-DNA form conformational geometry ISIS PHARMACEUTICALS, INC. 2003-06-05 — — US disclosed
US-20030096979-A1 Oligonucleotides having A-DNA form and B-DNA form conformational geometry ISIS PHARMACEUTICALS, INC. 2003-05-22 — — US disclosed
EP-1180113-A4 OLIGONUCLEOTIDES HAVING A-DNA FORM AND B-DNA FORM CONFORMATIONAL GEOMETRY ISIS PHARMACEUTICALS INC (US) 2002-09-18 — — EP disclosed
US-6369209-B1 AFFINITY AND NUCLEASE RESISTANCE WHILE CONCURRENTLY SERVING AS SUBSTRATES FOR RNASE H WHEN BOUND TO A TARGET RNA STRAND ISIS PHARMACEUTICALS, INC. 2002-04-09 — — US disclosed
EP-1180113-A1 OLIGONUCLEOTIDES HAVING A-DNA FORM AND B-DNA FORM CONFORMATIONAL GEOMETRY ISIS PHARMACEUTICALS, INC. (US) 2002-02-20 — — EP disclosed
US-6271358-B1 FOR INHIBITING SPECIFIC GENE EXPRESSION; HAVING ENHANCED HYBRID BINDING AFFINITY AND/OR INCREASED NUCLEASE RESISTANCE ISIS PHARMACEUTICALS, INC. 2001-08-07 — — US disclosed
EP-1102787-A1 2'-O-AMINOETHYLOXYETHYL-MODIFIED OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 2001-05-30 — — EP disclosed
WO-2000066609-A1 OLIGONUCLEOTIDES HAVING A-DNA FORM AND B-DNA FORM CONFORMATIONAL GEOMETRY ISIS PHARMACEUTICALS, INC. (US) 2000-11-09 — — WO disclosed
US-6043352-A INCREASED HYBRIDIZATION BINDING AFFINITY AND NUCLEASE RESISTANCE ISIS PHARMACEUTICALS, INC. (US) 2000-03-28 — — US disclosed
WO-2000008044-A1 2'-O-AMINOETHYLOXYETHYL-MODIFIED OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 2000-02-17 — — 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-20030105311-A1 Oligonucleotides having A-DNA form and B-DNA form conformational geometry RNGTT, RNASEH1, ADAR MAPT 4326/4885MEN1 2146/4885KMT2A 3376/4885
US-20030096979-A1 Oligonucleotides having A-DNA form and B-DNA form conformational geometry RNGTT, RNASEH1, ADAR MAPT 4326/4885MEN1 2146/4885KMT2A 3376/4885
US-20070123702-A1 Oligonucleotdies having A-DNA form and B-DNA form conformational geometry RNASEH1, RNGTT, ADAR MAPT 4375/4885MEN1 2294/4885KMT2A 2796/4885
US-20040009938-A1 Methods of enhancing renal uptake of oligonucleotides NUDT1, SLC29A2, DUT MAPT 4522/4885MEN1 2516/4885KMT2A 3150/4885

“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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