SCHEMBL547089

SCHEMBL547089

Nc1nc(=O)n([C@@H]2O[C@H](CO)C(O)C2O)cc1F

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.62
MTOR P42345 2/20 0.62
ALDH1A1 P00352 2/20 0.62
THRB P10828 1/20 0.62
MDM2 Q00987 1/20 0.62
NCOA1 Q15788 1/20 0.62
NCOA3 Q9Y6Q9 1/20 0.62
GMNN O75496 1/20 0.62
TP53 P04637 1/20 0.62
NFKB1 P19838 1/20 0.62
DNMT1 P26358 1/20 0.62
THPO P40225 1/20 0.62
HTT P42858 1/20 0.62
RAB9A P51151 1/20 0.62
BLM P54132 1/20 0.62
HBB P68871 1/20 0.62
PMP22 Q01453 1/20 0.62
ALB P02768 1/20 0.54
NT5E P21589 1/20 0.53
HIF1A Q16665 1/20 0.53

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
SCHEMBL3363487 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL18870816 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL207772 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL1230711 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL5697575 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL2583898 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL16805415 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL4286246 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL21423108 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2
SCHEMBL30694436 1.00 LMNA (0.62) LMNAMTORALDH1A1THRBMDM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-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
WO-2021117122-A1 PROPHYLACTIC OR THERAPEUTIC AGENT FOR LYSOSOMAL ACID LIPASE DEFICIENCY SYNDROME 株式会社リボルナバイオサイエンス 2021-06-17 WO 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
US-20190085328-A1 IN VIVO SILENCING BY CHEMICALLY MODIFIED AND STABLE siRNA UNIVERSITY OF MASSACHUSETTS 2019-03-21 US claimed
EP-0653439-B1 Stabilized oligonucleotids and the use thereof AVENTIS PHARMA GMBH (DE) 2004-04-28 EP claimed
WO-2004029212-A2 IN VIVO GENE SILENCING BY CHEMICALLY MODIFIED AND STABLE SIRNA UNIVERSITY OF MASSACHUSETTS (US) 2004-04-08 WO claimed
EP-0983290-B1 METHOD FOR PRODUCING POLYMERS HAVING NUCLEO-BASES AS SIDE-GROUPS MORPHOCHEM AG (DE) 2004-03-03 EP claimed
JP-2002500643-A 2002-01-08 JP claimed
EP-0594667-B1 TREATMENT OF CHEMOTHERAPEUTIC AGENT AND ANTIVIRAL AGENT TOXICITY WITH ACYLATED PYRIMIDINE NUCLEOSIDES PRO NEURON INC (US) 2001-09-19 EP claimed
EP-0350287-B1 Lipid derivatives of antiviral nucleosides, liposomal incorporation and method of use CHIMERIX INC (US) 2000-09-27 EP claimed
EP-0983290-A1 METHOD FOR PRODUCING POLYMERS HAVING NUCLEO-BASES AS SIDE-GROUPS Morphochem AG (DE) 2000-03-08 EP claimed
WO-1998051697-A2 METHOD FOR PRODUCING POLYMERS HAVING NUCLEO-BASES AS SIDE-GROUPS MORPHOCHEM AG (DE) 1998-11-19 WO claimed
EP-0653439-A2 Stabilized oligonucleotids and the use thereof HOECHST AKTIENGESELLSCHAFT (DE) 1995-05-17 EP claimed
EP-0595133-A2 Prodrugs, their preparation and use as medicaments BEHRINGWERKE Aktiengesellschaft (DE) 1994-05-04 EP 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 (3 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-20190085328-A1 IN VIVO SILENCING BY CHEMICALLY MODIFIED AND STABLE siRNA AGO2, SNRPE, NSUN2 LMNA 2205/4885MTOR 2815/4885ALDH1A1 2569/4885
US-20220112494-A1 IN VIVO GENE SILENCING BY CHEMICALLY MODIFIED AND STABLE siRNA SNRPE, AGO2, NSUN2 LMNA 2786/4885MTOR 3352/4885ALDH1A1 2194/4885
US-11136578-B2 In vivo gene silencing by chemically modified and stable siRNA SNRPE, AGO2, NSUN2 LMNA 2786/4885MTOR 3352/4885ALDH1A1 2194/4885

“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.