SCHEMBL210468

SCHEMBL210468

Nc1ccn(C(=O)c2ccccc2)c(=O)n1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 3/20 0.51
L3MBTL1 Q9Y468 2/20 0.51
TSHR P16473 1/20 0.51
KMT2A Q03164 4/20 0.43
NPC1 O15118 2/20 0.43
MEN1 O00255 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
PKM P14618 2/20 0.41
KDM4E B2RXH2 2/20 0.41
LMNA P02545 1/20 0.41
MAPT P10636 2/20 0.40
HPGD P15428 2/20 0.40
F2 P00734 1/20 0.40
DYRK1A Q13627 1/20 0.39
ELANE P08246 2/20 0.39
GSK3A P49840 1/20 0.38
GSK3B P49841 1/20 0.38
NOS1 P29475 1/20 0.37
SLC22A12 Q96S37 1/20 0.37
F12 P00748 1/20 0.37

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
SCHEMBL16756982 0.84 F2 (0.51) RAB9AKMT2ANPC1SMN1; SMN2PKM
SCHEMBL17541934 0.82 PLA2G7 (0.46) TSHRKMT2AMEN1SMN1; SMN2HPGD
SCHEMBL10679054 0.80 LMNA (0.38) TSHRLMNAMAPT
SCHEMBL5983023 0.80 KMT2A (0.55) RAB9AKMT2ANPC1MEN1SMN1; SMN2
SCHEMBL1387674 0.78 L3MBTL1 (0.47) RAB9AL3MBTL1TSHRKMT2ANPC1
SCHEMBL27819780 0.77 PARP1 (0.43) LMNAMAPT
SCHEMBL5694141 0.75 DYRK1A (0.47) RAB9AL3MBTL1TSHRKMT2ANPC1
SCHEMBL21186 0.75 NOTUM (0.43) LMNAMAPTGSK3A
SCHEMBL10348675 0.75 MEN1 (0.57) RAB9AL3MBTL1TSHRKMT2ANPC1
SCHEMBL10348640 0.75 RAB9A (0.46) RAB9AL3MBTL1TSHRNPC1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260103737-A1 ENZYMATIC METHODS TO GENERATE HIGH YIELDS OF SEQUENCE SPECIFIC RNA OLIGONUCLEOTIDES WITH EXTREME PRECISION UNIV MASSACHUSETTS (US) 2026-04-16 US claimed
US-11987599-B2 Solid support for synthesizing nucleic acid sequences and methods for making and using UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2024-05-21 US claimed
US-20230271998-A1 SOLID SUPPORT FOR SYNTHESIZING NUCLEIC ACID SEQUENCES AND METHODS FOR MAKING AND USING UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2023-08-31 US claimed
US-20220195497-A1 HYBRIDIZING all-LNA OLIGONUCLEOTIDES ROCHE DIAGNOSTICS OPERATIONS, INC. 2022-06-23 US claimed
EP-3980554-A1 HYBRIDIZING ALL-LNA OLIGONUCLEOTIDES F. Hoffmann-La Roche AG (CH) 2022-04-13 EP claimed
WO-2022005988-A2 SOLID SUPPORT FOR SYNTHESIZING NUCLEIC ACID SEQUENCES AND METHODS FOR MAKING AND USING UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2022-01-06 WO claimed
WO-2020245377-A1 HYBRIDIZING ALL-LNA OLIGONUCLEOTIDES F. HOFFMANN-LA ROCHE AG (CH) 2020-12-10 WO claimed
CN-108409818-B Method for synthesizing cytosine nucleoside 新乡拓新药业股份有限公司 2020-09-11 CN claimed
EP-3004131-B1 PHOSPHORAMIDITE BUILDING BLOCKS FOR SUGAR-CONJUGATED OLIGONUCLEOTIDES AM CHEMICALS LLC (US) 2020-07-22 EP claimed
CN-106905398-B Synthetic method of sofosbuvir ZHEJIANG A & F UNIVERSITY (CN) 2019-12-10 CN claimed
EP-0570514-A4 METHYLENE PHOSPHONATE NUCLEOSIDE ANALOGS AND OLIGONUCLEOTIDE ANALOGS MADE THEREFROM GILEAD SCIENCES INC (US) 1994-08-17 EP claimed
WO-1994015622-A1 NUCLEOSIDE DERIVATIVES AND THEIR USE AS EXCITATORY AMINO ACID ANTAGONISTS CAMBRIDGE NEUROSCIENCE (US) 1994-07-21 WO claimed
WO-1994001445-A1 BASE-PROTECTED NUCLEOTIDE ANALOGS WITH PROTECTED THIOL GROUPS RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1994-01-20 WO claimed
EP-0574386-A1 NOVEL PROCESS FOR THE PREPARATION OF NUCLEOTIDES INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY OF THE ACADEMY OF SCIENCES OF THE CZECH REPUBLIC (CZ) 1993-12-22 EP claimed
EP-0570514-A1 METHYLENE PHOSPHONATE NUCLEOSIDE ANALOGS AND OLIGONUCLEOTIDE ANALOGS MADE THEREFROM GILEAD SCIENCES, INC. (US) 1993-11-24 EP claimed
EP-0574386-A4 NOVEL PROCESS FOR THE PREPARATION OF NUCLEOTIDES. BRISTOL MYERS SQUIBB CO (US) 1993-10-27 EP claimed
WO-1992013869-A1 METHYLENE PHOSPHONATE NUCLEOSIDE ANALOGS AND OLIGONUCLEOTIDE ANALOGS MADE THEREFROM GILEAD SCIENCES, INC. (US) 1992-08-20 WO claimed
WO-1992002511-A1 NOVEL PROCESS FOR THE PREPARATION OF NUCLEOTIDES BRISTOL-MYERS SQUIBB COMPANY (US) 1992-02-20 WO claimed
EP-0121112-B1 2'-DEOXY-3-PHOSPHONYLMETHYL NUCLEOSIDES AND METHOD FOR THEIR PREPARATION Gesellschaft für Biotechnologische Forschung mbH (GBF) (DE) 1987-05-13 EP claimed
EP-0121112-A1 2'-Deoxy-3-phosphonylmethyl nucleosides and method for their preparation Gesellschaft für Biotechnologische Forschung mbH (GBF) (DE) 1984-10-10 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-20260103737-A1 ENZYMATIC METHODS TO GENERATE HIGH YIELDS OF SEQUENCE SPECIFIC RNA OLIGONUCLEOTIDES WITH EXTREME PRECISION RNGTT, POLRMT, POLM RAB9A 4388/4885L3MBTL1 191/4885TSHR 1953/4885
US-11987599-B2 Solid support for synthesizing nucleic acid sequences and methods for making and using RNGTT, NSUN2, POLN RAB9A 3828/4885L3MBTL1 950/4885TSHR 3625/4885
US-20230271998-A1 SOLID SUPPORT FOR SYNTHESIZING NUCLEIC ACID SEQUENCES AND METHODS FOR MAKING AND USING RNGTT, NSUN2, POLN RAB9A 3828/4885L3MBTL1 950/4885TSHR 3625/4885

“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.