SCHEMBL5220384

SCHEMBL5220384

COCCOC1C(O)[C@H](n2cnc3c(N)ncnc32)O[C@@H]1CO

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ADORA3 P0DMS8 4/20 0.69
▸ ADORA1 P30542 3/20 0.69
▸ SMN1; SMN2 Q16637 2/20 0.69
▸ DPP4 P27487 1/20 0.69
▸ MEN1 O00255 1/20 0.69
▸ SLC28A1 O00337 1/20 0.69
▸ MAP3K7 O43318 1/20 0.69
▸ SLC28A2 O43868 1/20 0.69
▸ GAPDH P04406 1/20 0.69
▸ MAPK1 P28482 1/20 0.69
▸ ADORA2A P29274 1/20 0.69
▸ ADORA2B P29275 1/20 0.69
▸ STAT6 P42226 1/20 0.69
▸ PI4KA P42356 1/20 0.69
▸ KMT2A Q03164 1/20 0.69
▸ PI4K2B Q8TCG2 1/20 0.69
▸ DOT1L Q8TEK3 1/20 0.69
▸ SLC29A1 Q99808 1/20 0.69
▸ PI4K2A Q9BTU6 1/20 0.69
▸ SLC28A3 Q9HAS3 1/20 0.69

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
SCHEMBL5220374 1.00 ADORA3 (0.69) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL31139492 1.00 ADORA3 (0.69) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL1060584 0.92 ADORA1 (0.72) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL26370816 0.92 ADORA1 (0.72) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL29408565 0.92 ADORA1 (0.72) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL1060588 0.92 ADORA1 (0.72) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL28680450 0.92 ADORA1 (0.72) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL24264106 0.90 ADORA1 (0.61) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL13777063 0.90 ADORA3 (0.72) ADORA3ADORA1SMN1; SMN2DPP4MEN1
SCHEMBL21418864 0.89 ADORA3 (0.75) ADORA3ADORA1SMN1; SMN2DPP4MEN1

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070292875-A1 Human RNase H1 oligonucleotide compositions thereof ISIS PHARMACEUTICALS, INC. (US) 2007-12-20 — — US 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
US-7119184-B2 Oligonucleotides having A-DNA form and B-DNA form conformational geometry ISIS PHARMACEUTICALS, INC. (US) 2006-10-10 — — US disclosed
EP-1222309-B1 HUMAN RNASE H AND OLIGONUCLEOTIDE COMPOSITIONS THEREOF ISIS PHARMACEUTICALS INC (US) 2005-12-07 — — EP disclosed
US-20040102618-A1 Human RNase H1 and oligonucleotide compositions thereof ISIS PHARMACEUTICALS, INC. 2004-05-27 — — US 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-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-6617442-B1 Divided into two portions, one of which supports cleavage of target RNA; use in enhancing antisense therapies ISIS PHARMACEUTICALS, INC. 2003-09-09 — — 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
WO-2000066609-A1 OLIGONUCLEOTIDES HAVING A-DNA FORM AND B-DNA FORM CONFORMATIONAL GEOMETRY ISIS PHARMACEUTICALS, INC. (US) 2000-11-09 — — 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 (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-20030105311-A1 Oligonucleotides having A-DNA form and B-DNA form conformational geometry RNGTT, RNASEH1, ADAR ADORA3 159/4885ADORA1 268/4885SMN1; SMN2 1822/4885
US-20070292875-A1 Human RNase H1 oligonucleotide compositions thereof RNASEH1, RNASE1, RNASEL ADORA3 1318/4885ADORA1 1753/4885SMN1; SMN2 582/4885
US-20030096979-A1 Oligonucleotides having A-DNA form and B-DNA form conformational geometry RNGTT, RNASEH1, ADAR ADORA3 159/4885ADORA1 268/4885SMN1; SMN2 1822/4885
US-20040102618-A1 Human RNase H1 and oligonucleotide compositions thereof RNASEH1, RNASE1, RNASEL ADORA3 1033/4885ADORA1 1431/4885SMN1; SMN2 556/4885
US-20070123702-A1 Oligonucleotdies having A-DNA form and B-DNA form conformational geometry RNASEH1, RNGTT, ADAR ADORA3 171/4885ADORA1 275/4885SMN1; SMN2 1824/4885

“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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