SCHEMBL659091

SCHEMBL659091

COC1C(O)[C@@H](CO)O[C@H]1n1cc(C)c(N)nc1=O

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.47
MTOR P42345 2/20 0.47
ALDH1A1 P00352 2/20 0.47
THRB P10828 1/20 0.47
MDM2 Q00987 1/20 0.47
NCOA1 Q15788 1/20 0.47
NCOA3 Q9Y6Q9 1/20 0.47
GMNN O75496 1/20 0.47
TP53 P04637 1/20 0.47
NFKB1 P19838 1/20 0.47
DNMT1 P26358 1/20 0.47
THPO P40225 1/20 0.47
HTT P42858 1/20 0.47
RAB9A P51151 1/20 0.47
BLM P54132 1/20 0.47
HBB P68871 1/20 0.47
PMP22 Q01453 1/20 0.47
TK2 O00142 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.42
POLB P06746 1/20 0.42

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
SCHEMBL22261563 1.00 LMNA (0.47) LMNAMTORALDH1A1THRBMDM2
SCHEMBL18512865 1.00 LMNA (0.47) LMNAMTORALDH1A1THRBMDM2
SCHEMBL659090 1.00 LMNA (0.47) LMNAMTORALDH1A1THRBMDM2
SCHEMBL16805336 1.00 LMNA (0.47) LMNAMTORALDH1A1THRBMDM2
SCHEMBL15810727 1.00 LMNA (0.47) LMNAMTORALDH1A1THRBMDM2
SCHEMBL28738894 0.92 LMNA (0.46) LMNAMTORALDH1A1THRBMDM2
SCHEMBL23547665 0.91 LMNA (0.37) LMNAMTORALDH1A1THRBMDM2
SCHEMBL21999057 0.91 LMNA (0.47) LMNAMTORALDH1A1THRBMDM2
SCHEMBL23547707 0.91 LMNA (0.47) LMNAMTORALDH1A1THRBMDM2
SCHEMBL21999226 0.91 LMNA (0.47) 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 119 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
WO-2024077351-A1 MODIFIED OLIGONUCLEOTIDES Pharmorage Pty Limited (AU) 2024-04-18 WO claimed
EP-4247393-A1 CONJUGATES OF S-ANTIGEN TRANSPORT INHIBITING OLIGONUCLEOTIDE POLYMERS HAVING ENHANCED LIVER TARGETING Aligos Therapeutics, Inc. (US) 2023-09-27 EP claimed
WO-2022109129-A1 CONJUGATES OF S-ANTIGEN TRANSPORT INHIBITING OLIGONUCLEOTIDE POLYMERS HAVING ENHANCED LIVER TARGETING ALIGOS THERAPEUTICS, INC. (US) 2022-05-27 WO claimed
US-20220160748-A1 CONJUGATES OF S-ANTIGEN TRANSPORT INHIBITING OLIGONUCLEOTIDE POLYMERS HAVING ENHANCED LIVER TARGETING ALIGOS THERAPEUTICS, INC. 2022-05-26 US claimed
US-20090307805-A1 ALTERNATIVE NUCLEOTIDES FOR IMPROVED TARGETED NUCLEOTIDE EXCHANGE KEYGENE N.V 2009-12-10 US claimed
EP-0813539-B1 IMPROVED PROCESS FOR THE SYNTHESIS OF 2'-O-SUBSTITUTED PYRIMIDINES AND OLIGOMERIC COMPOUNDS THEREFROM ISIS PHARMACEUTICALS INC (US) 2006-05-24 EP claimed
US-20050059815-A1 Processes for the synthesis of 2'-O-substituted pyrimidines and oligomeric compounds therefrom COOK PHILLIP DAN (US) 2005-03-17 US claimed
US-20030050454-A1 Process for the synthesis of 2' -O-substituted pyrimidines and oligomeric compounds therefrom ISIS PHARMACEUTICALS, INC. 2003-03-13 US claimed
US-5861493-A ALKYLATING WITH ALCOHOL IN PRESENCE OF LEWIS ACID; PREPARING OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 1999-01-19 US claimed
US-5767270-A PROTECTING EXOCYCLIC AMINO GROUPS ISIS PHARMACEUTICALS, INC. (US) 1998-06-16 US claimed
EP-4720294-A2 MODIFIED UNC13A OLIGONUCLEOTIDES Quralis Corporation (US) 2026-04-08 EP disclosed
US-20260066042-A1 METHODS AND SYSTEMS FOR HIGH-THROUGHPUT MOLECULAR ANALYSIS OPENTRONS LABWORKS INC (US) 2026-03-05 US disclosed
US-20250313889-A1 SAMPLE PREPARATION METHOD OXFORD NANOPORE TECHNOLOGIES PLC (GB) 2025-10-09 US disclosed
US-20250289840-A1 RNA STABILIZING SUBSTANCES AND METHODS OF USE TEAM MEDICAL, LLC 2025-09-18 US disclosed
US-5861493-A ALKYLATING WITH ALCOHOL IN PRESENCE OF LEWIS ACID; PREPARING OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 1999-01-19 US disclosed
US-5767270-A PROTECTING EXOCYCLIC AMINO GROUPS ISIS PHARMACEUTICALS, INC. (US) 1998-06-16 US disclosed
US-5760202-A TREATING 2,2'-ANHYDROPYRIMIDINE NUCLEOSIDE WITH ALCOHOL AND LEWIS ACID ISIS PHARMACEUTICALS, INC. (US) 1998-06-02 US disclosed
EP-0813539-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF 2'-O-SUBSTITUTED PYRIMIDINES AND OLIGOMERIC COMPOUNDS THEREFROM ISIS PHARMACEUTICALS, INC. (US) 1997-12-29 EP disclosed
WO-1996027606-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF 2'-O-SUBSTITUTED PYRIMIDINES AND OLIGOMERIC COMPOUNDS THEREFROM ISIS PHARMACEUTICALS, INC. (US) 1996-09-12 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-20260066042-A1 METHODS AND SYSTEMS FOR HIGH-THROUGHPUT MOLECULAR ANALYSIS POLRMT, POLL, SARS1 LMNA 3119/4885MTOR 1898/4885ALDH1A1 4286/4885
US-20050059815-A1 Processes for the synthesis of 2'-O-substituted pyrimidines and oligomeric compounds therefrom NUDT1, DPYD, UMPS LMNA 3765/4885MTOR 4149/4885ALDH1A1 842/4885
US-20220160748-A1 CONJUGATES OF S-ANTIGEN TRANSPORT INHIBITING OLIGONUCLEOTIDE POLYMERS HAVING ENHANCED LIVER TARGETING HAVCR2, CD74, SLC10A1 LMNA 4002/4885MTOR 4606/4885ALDH1A1 2760/4885
US-20030050454-A1 Process for the synthesis of 2' -O-substituted pyrimidines and oligomeric compounds therefrom ATIC, TYMS, RRM2 LMNA 3797/4885MTOR 4007/4885ALDH1A1 940/4885
US-20250289840-A1 RNA STABILIZING SUBSTANCES AND METHODS OF USE SYNCRIP, SNRPA, RNASE1 LMNA 240/4885MTOR 3099/4885ALDH1A1 1153/4885

“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.