SCHEMBL338709

SCHEMBL338709

Nc1ccn([C@@H]2O[C@H](COP(N)O)[C@@H](O)[C@H]2O)c(=O)n1

nearest known ligand 0.70

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.70
THRB P10828 1/20 0.70
MTOR P42345 1/20 0.70
MDM2 Q00987 1/20 0.70
NCOA1 Q15788 1/20 0.70
NCOA3 Q9Y6Q9 1/20 0.70
L3MBTL1 Q9Y468 1/20 0.58
TSHR P16473 1/20 0.57
GLA P06280 1/20 0.57
P2RY2 P41231 1/20 0.57
ST6GAL1 P15907 7/20 0.55

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
SCHEMBL7026416 0.92 LMNA (0.72) LMNATHRBMTORMDM2NCOA1
SCHEMBL28403435 0.92 LMNA (0.72) LMNATHRBMTORMDM2NCOA1
SCHEMBL7919827 0.91 LMNA (0.58) LMNATHRBMTORMDM2NCOA1
SCHEMBL584613 0.91 LMNA (0.70) LMNATHRBMTORMDM2NCOA1
SCHEMBL1683180 0.88 LMNA (0.55) LMNATHRBMTORMDM2NCOA1
SCHEMBL8740127 0.88 LMNA (0.66) LMNATHRBMTORMDM2NCOA1
SCHEMBL366600 0.87 LMNA (0.75) LMNATHRBMTORMDM2NCOA1
SCHEMBL4946508 0.87 LMNA (0.75) LMNATHRBMTORMDM2NCOA1
SCHEMBL5491562 0.87 LMNA (0.75) LMNATHRBMTORMDM2NCOA1
SCHEMBL30924912 0.86 LMNA (0.53) LMNATHRBMTORMDM2NCOA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107474091-A The synthesis and application of 5 aldehyde radical cytidine phosphoramidite monomers of photosensitive protective group protection and preparation method thereof and oligonucleotide 南开大学 2017-12-15 CN claimed
CN-104011209-A Inhibition Of Viral Gene Expression UNIV WITWATERSRAND JHB 2014-08-27 CN claimed
US-20260043027-A1 LINKER, COMPOUND INCLUDING LINKER, METHOD OF PREPARING COMPOUND, USE OF LINKER, AND METHOD OF DELIVERING OLIGONUCLEOTIDES THROUGH LINKER SYNERK BIOTECH LTD (HK) 2026-02-12 US disclosed
EP-3765476-B1 MODIFIED OLIGONUCLEOTIDES FOR USE IN TREATMENT OF TAUOPATHIES JANSSEN PHARMACEUTICA NV (BE) 2025-11-26 EP disclosed
US-12428441-B2 Modified nucleoside phosphoramidites Janssen Biopharma, Inc. (US) 2025-09-30 US disclosed
US-20250092400-A1 Modified Oligonucleotides and Methods of Use JANSSEN PHARMACEUTICA NV (BE) 2025-03-20 US disclosed
US-20240309040-A1 Modified Nucleoside Phosphoramidites Janssen Biopharma, Inc. (US) 2024-09-19 US disclosed
US-12077757-B2 Modified oligonucleotides and methods of use JANSSEN PHARMACEUTICA NV (BE) 2024-09-03 US disclosed
US-12030907-B2 Modified nucleoside phosphoramidites Janssen Biopharma, Inc. (US) 2024-07-09 US disclosed
CN-118265801-A Compositions and methods for improving 5-hydroxymethylated cytosine resolution in nucleic acid sequencing 福瑞诺姆控股公司 2024-06-28 CN disclosed
US-20240011029-A1 MODIFIED OLIGONUCLEOTIDES FOR USE IN TREATMENT OF TAUOPATHIES JANSSEN PHARMACEUTICA NV (BE) 2024-01-11 US disclosed
EP-0724447-A1 DERIVATIZED OLIGONUCLEOTIDES HAVING IMPROVED UPTAKE AND OTHER PROPERTIES ISIS PHARMACEUTICALS, INC. (US) 1996-08-07 EP disclosed
EP-0724447-A4 DERIVATIZED OLIGONUCLEOTIDES HAVING IMPROVED UPTAKE AND OTHER PROPERTIES ISIS PHARMACEUTICALS INC (US) 1996-01-22 EP disclosed
EP-0651759-A4 NOVEL 2'-O-ALKYL NUCLEOSIDES AND PHOSPHORAMIDITES PROCESSES FOR THE PREPARATION AND USES THEREOF. ISIS PHARMACEUTICALS INC (US) 1995-10-25 EP disclosed
EP-0653438-A2 Oligonucleotide compounds, their production and use TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1995-05-17 EP disclosed
EP-0651759-A1 NOVEL 2'-O-ALKYL NUCLEOSIDES AND PHOSPHORAMIDITES PROCESSES FOR THE PREPARATION AND USES THEREOF ISIS PHARMACEUTICALS, INC. (US) 1995-05-10 EP disclosed
EP-0618983-A1 INSERTION ELEMENTS AND AMPLIFIABLE NUCLEIC ACIDS AMOCO CORPORATION (US) 1994-10-12 EP disclosed
WO-1994009159-A2 INSERTION ELEMENTS AND AMPLIFIABLE NUCLEIC ACIDS AMOCO CORPORATION (US) 1994-04-28 WO disclosed
WO-1994002501-A1 NOVEL 2'-O-ALKYL NUCLEOSIDES AND PHOSPHORAMIDITES PROCESSES FOR THE PREPARATION AND USES THEREOF ISIS PHARMACEUTICALS, INC. (US) 1994-02-03 WO disclosed
WO-1993007883-A1 DERIVATIZED OLIGONUCLEOTIDES HAVING IMPROVED UPTAKE AND OTHER PROPERTIES ISIS PHARMACEUTICALS, INC. (US) 1993-04-29 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 (7 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-12030907-B2 Modified nucleoside phosphoramidites PNP, TYMP, NSUN2 LMNA 1464/4885THRB 2641/4885MTOR 2704/4885
US-12077757-B2 Modified oligonucleotides and methods of use NSUN2, ADAR, POLM LMNA 754/4885THRB 1735/4885MTOR 4770/4885
US-12428441-B2 Modified nucleoside phosphoramidites MTAP, PNP, NT5C3B LMNA 957/4885THRB 4590/4885MTOR 2804/4885
US-20260043027-A1 LINKER, COMPOUND INCLUDING LINKER, METHOD OF PREPARING COMPOUND, USE OF LINKER, AND METHOD OF DELIVERING OLIGONUCLEOTIDES THROUGH LINKER SSU72, NSUN2, RNMT LMNA 275/4885THRB 1016/4885MTOR 4566/4885
US-20240011029-A1 MODIFIED OLIGONUCLEOTIDES FOR USE IN TREATMENT OF TAUOPATHIES MAPT, PSEN2, NSUN2 LMNA 505/4885THRB 1861/4885MTOR 4786/4885
US-20250092400-A1 Modified Oligonucleotides and Methods of Use NSUN2, ADAR, POLM LMNA 808/4885THRB 1856/4885MTOR 4787/4885
US-20240309040-A1 Modified Nucleoside Phosphoramidites MTAP, PNP, NT5C3B LMNA 957/4885THRB 4590/4885MTOR 2804/4885

“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.