SCHEMBL5344718

SCHEMBL5344718

Cc1cn(C(=O)c2ccccc2)c(=O)nc1N

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 3/20 0.41
TSHR P16473 2/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
KMT2A Q03164 7/20 0.40
NPC1 O15118 2/20 0.40
SMN1; SMN2 Q16637 2/20 0.40
MEN1 O00255 1/20 0.40
DYRK1A Q13627 1/20 0.40
HPGD P15428 3/20 0.39
NPSR1 Q6W5P4 2/20 0.38
MAPK14 Q16539 1/20 0.38
MGAM O43451 1/20 0.38
AMY1A P0DUB6 1/20 0.38
GAA P10253 1/20 0.38
SI P14410 1/20 0.38
MGAM2 Q2M2H8 1/20 0.38
KDM4E B2RXH2 7/20 0.37
F2 P00734 1/20 0.37
CYP1A2 P05177 1/20 0.37
PKM P14618 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
SCHEMBL6880479 0.83 KMT2A (0.52) RAB9AKMT2ANPC1SMN1; SMN2MEN1
SCHEMBL3627806 0.82 DCK (0.43) RAB9ATSHRL3MBTL1KMT2ANPC1
SCHEMBL10348673 0.81 MAPK14 (0.44) RAB9ATSHRL3MBTL1KMT2ANPC1
SCHEMBL8303938 0.78 ABCB1 (0.40) RAB9ATSHRL3MBTL1KMT2ANPC1
SCHEMBL27622346 0.77 RAB9A (0.37) RAB9ATSHRL3MBTL1KMT2ANPC1
SCHEMBL27603628 0.76 PTGS2 (0.36) RAB9ATSHRL3MBTL1KMT2ANPC1
SCHEMBL12882196 0.74 KMT2A (0.48) RAB9AKMT2ANPC1SMN1; SMN2MEN1
SCHEMBL210468 0.73 RAB9A (0.51) RAB9ATSHRL3MBTL1KMT2ANPC1
SCHEMBL5694141 0.72 DYRK1A (0.47) RAB9ATSHRL3MBTL1KMT2ANPC1
SCHEMBL7264255 0.71 RAB9A (0.41) RAB9ATSHRL3MBTL1KMT2ANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104736551-B The method for preparing oligomeric compounds using improved end-blocking scheme IONIS制药公司 2017-07-28 CN claimed
EP-2885312-A1 METHOD OF PREPARING OLIGOMERIC COMPOUNDS USING MODIFIED CAPPING PROTOCOLS Isis Pharmaceuticals, Inc. (US) 2015-06-24 EP claimed
WO-2014028739-A1 METHOD OF PREPARING OLIGOMERIC COMPOUNDS USING MODIFIED CAPPING PROTOCOLS ISIS PHARMACEUTICALS, INC. (US) 2014-02-20 WO claimed
US-6809195-B1 COMPRISES A MODIFIED PHOSPHORAMIDITE PROTOCOL IN WHICH OXIDATION AND CAPPING STEPS ARE COMBINED INTO A SINGLE STEP; INCREASED EFFICIENCY; SOLID PHASE SYNTHESIS ISIS PHARMACEUTICALS, INC. 2004-10-26 US claimed
US-20030229220-A1 Oligomer phosphoramidite compositions and processes for synthesizing the same RAVIKUMAR VASULINGA T (US) 2003-12-11 US claimed
US-6610842-B1 Removing hydroxyl protecting group from compound of given formula and treating with another compound; wide range of diagnostic and therapeutic uses ISIS PHARMACEUTICALS, INC. 2003-08-26 US claimed
EP-1311526-A1 PROCESSES FOR THE PREPARATION OF OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 2003-05-21 EP claimed
EP-1244682-A4 PROCESS FOR THE PREPARATION OF OLIGOMERIC COMPOUNDS ISIS PHARMACEUTICALS INC (US) 2003-02-05 EP claimed
EP-1244682-A1 PROCESS FOR THE PREPARATION OF OLIGOMERIC COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 2002-10-02 EP claimed
EP-1175432-A4 PROCESSES FOR THE SYNTHESIS OF OLIGOMERS USING PHOSPHORAMIDITE COMPOSITIONS ISIS PHARMACEUTICALS INC (US) 2002-09-25 EP claimed
WO-2002014340-A1 PROCESSES FOR THE PREPARATION OF OLIGONUCLEOTIDES_______________ ISIS PHARMACEUTICALS, INC. (US) 2002-02-21 WO claimed
EP-1175432-A1 PROCESSES FOR THE SYNTHESIS OF OLIGOMERS USING PHUSPHORAMIDITE COMPOSITIONS ISIS PHARMACEUTICALS, INC. (US) 2002-01-30 EP claimed
WO-2001049701-A1 PROCESS FOR THE PREPARATION OF OLIGOMERIC COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 2001-07-12 WO claimed
WO-2000068241-A1 PROCESSES FOR THE SYNTHESIS OF OLIGOMERS USING PHUSPHORAMIDITE COMPOSITIONS ISIS PHARMACEUTICALS, INC. (US) 2000-11-16 WO claimed
WO-1995029930-A2 IMPROVED METHOD FOR OLIGONUCLEOTIDE ANALOG SYNTHESIS GILEAD SCIENCES, INC. (US) 1995-11-09 WO claimed
EP-4349846-A1 CHIMERIC NUCLEIC ACID OLIGOMER INCLUDING PHOSPHOROTHIOATE AND BORANOPHOSPHATE, AND METHOD FOR PRODUCING SAME TOKYO UNIVERSITY OF SCIENCE FOUNDATION (JP) 2024-04-10 EP disclosed
WO-2024064858-A2 COMPOUNDS AND METHODS FOR REDUCING MECP2 EXPRESSION IONIS PHARMACEUTICALS, INC. (US) 2024-03-28 WO disclosed
WO-2001002415-A1 C3'-METHYLENE HYDROGEN PHOSPHONATE MONOMERS AND RELATED COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 2001-01-11 WO disclosed
WO-2000068241-A1 PROCESSES FOR THE SYNTHESIS OF OLIGOMERS USING PHUSPHORAMIDITE COMPOSITIONS ISIS PHARMACEUTICALS, INC. (US) 2000-11-16 WO disclosed
WO-2000004034-A2 OLIGONUCLEOTIDES HAVING SITE SPECIFIC CHIRAL PHOSPHOROTHIOATE INTERNUCLEOSIDE LINKAGES ISIS PHARMACEUTICALS, INC. (US) 2000-01-27 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 (1 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-20030229220-A1 Oligomer phosphoramidite compositions and processes for synthesizing the same PHOSPHO1, OSGEP, DTYMK RAB9A 4222/4885TSHR 3963/4885L3MBTL1 2842/4885

“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.