SCHEMBL547063

SCHEMBL547063

NOC1C(O)[C@H](CO)O[C@@H]1n1ccc(=O)[nH]c1=O

nearest known ligand 0.73

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
▸ SLC28A1 O00337 1/20 0.73
▸ SLC28A2 O43868 1/20 0.73
▸ SLC29A1 Q99808 1/20 0.73
▸ SLC28A3 Q9HAS3 1/20 0.73
▸ P2RY2 P41231 10/20 0.52
▸ P2RY6 Q15077 7/20 0.52
▸ P2RY14 Q15391 6/20 0.52
▸ P2RY4 P51582 3/20 0.51

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
SCHEMBL13737068 1.00 SLC28A1 (0.73) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL6141707 1.00 SLC28A1 (0.73) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL7520137 0.90 SLC28A1 (0.73) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL12987975 0.89 SLC28A1 (0.70) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL12987977 0.89 SLC28A1 (0.70) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL24359130 0.88 SLC28A1 (0.73) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL19894397 0.88 SLC28A1 (0.73) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL2580965 0.88 SLC28A1 (0.73) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL14389708 0.88 SLC28A1 (0.73) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2
SCHEMBL20732056 0.88 SLC28A1 (0.73) SLC28A1SLC28A2SLC29A1SLC28A3P2RY2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4601656-A1 MODIFIED OLIGONUCLEOTIDES Pharmorage Pty Limited (AU) 2025-08-20 — — EP claimed
US-20240191231-A1 SPINAL MUSCULAR ATROPHY (SMA) TREATMENT VIA TARGETING OF SMN2 SPLICE SITE INHIBITORY SEQUENCES UNIV MASSACHUSETTS (US) 2024-06-13 — — US claimed
WO-2024077351-A1 MODIFIED OLIGONUCLEOTIDES Pharmorage Pty Limited (AU) 2024-04-18 — — WO claimed
WO-2023154964-A1 METHODS AND COMPOSITIONS FOR TARGETING EFEMP1 ALLOY THERAPEUTICS, INC. (US) 2023-08-17 — — WO claimed
US-20220112494-A1 IN VIVO GENE SILENCING BY CHEMICALLY MODIFIED AND STABLE siRNA UNIVERSITY OF MASSACHUSETTS 2022-04-14 — — US claimed
US-20220090071-A1 SPINAL MUSCULAR ATROPHY (SMA) TREATMENT VIA TARGETING OF SMN2 SPLICE SITE INHIBITORY SEQUENCES UNIV MASSACHUSETTS (US) 2022-03-24 — — US claimed
US-11136578-B2 In vivo gene silencing by chemically modified and stable siRNA UNIVERSITY OF MASSACHUSETTS (US) 2021-10-05 — — US claimed
US-11053503-B2 Methods and means of generating IL-17 associated antitumor effector cells by inhibition of NR2F6 inhibition KCL THERAPEUTICS, INC 2021-07-06 — — US claimed
US-20190292540-A1 SPINAL MUSCULAR ATROPHY (SMA) TREATMENT VIA TARGETING OF SMN2 SPLICE SITE INHIBITORY SEQUENCES UNIV MASSACHUSETTS (US) 2019-09-26 — — US claimed
US-10266822-B2 Spinal muscular atrophy (SMA) treatment via targeting of SMN2 splice site inhibitory sequences UNIVERSITY OF MASSACHUSETTS (US) 2019-04-23 — — US claimed
EP-1212416-A2 NUCLEIC ACID BASED MODULATORS OF GENE EXPRESSION RIBOZYME PHARMACEUTICALS, INC. (US) 2002-06-12 — — EP claimed
JP-2002512794-A — — 2002-05-08 — — JP claimed
EP-1178051-A2 PROCESS FOR SELECTIVELY PRODUCING 1-PHOSPHORYLATED SUGAR DERIVATIVE ANOMER AND PROCESS FOR PRODUCING NUCLEOSIDE Mitsui Chemicals, Inc. (JP) 2002-02-06 — — EP claimed
JP-2001525667-A — — 2001-12-11 — — JP claimed
WO-2001016312-A2 NUCLEIC ACID BASED MODULATORS OF GENE EXPRESSION RIBOZYME PHARMACEUTICALS, INC. (US) 2001-03-08 — — WO claimed
EP-1073732-A2 NUCLEOSIDE TRIPHOSPHATES AND THEIR INCORPORATION INTO RIBOZYMES RIBOZYME PHARMACEUTICALS, INC. (US) 2001-02-07 — — EP claimed
US-6127535-A FOR THE INCORPORATION OF MODIFIED (NON-STANDARD) AND UNMODIFIED NUCLEOTIDES INTO NUCLEIC ACIDS RIBOZYME PHARMACEUTICALS, INC. (US) 2000-10-03 — — US claimed
EP-0980424-A2 ENZYMATIC NUCLEIC ACIDS: SYNTHESIS, SELECTION AND USE RIBOZYME PHARMACEUTICALS, INC. (US) 2000-02-23 — — EP claimed
WO-1999055857-A2 NUCLEOSIDE TRIPHOSPHATES AND THEIR INCORPORATION INTO RIBOZYMES RIBOZYME PHARMACEUTICALS, INC. (US) 1999-11-04 — — WO claimed
WO-1998050530-A2 ENZYMATIC NUCLEIC ACIDS: SYNTHESIS, SELECTION AND USE RIBOZYME PHARMACEUTICALS, INC. (US) 1998-11-12 — — 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 (2 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-20220112494-A1 IN VIVO GENE SILENCING BY CHEMICALLY MODIFIED AND STABLE siRNA SNRPE, AGO2, NSUN2 SLC28A1 670/4885SLC28A2 743/4885SLC29A1 268/4885
US-11136578-B2 In vivo gene silencing by chemically modified and stable siRNA SNRPE, AGO2, NSUN2 SLC28A1 670/4885SLC28A2 743/4885SLC29A1 268/4885

“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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