SCHEMBL183848

SCHEMBL183848

COCCO[C@@H](C=O)[C@H](O)[C@H](O)CO

nearest known ligand 0.38

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
TDP1 Q9NUW8 1/20 0.33
AKR1B1 P15121 1/20 0.31
KDM4E B2RXH2 2/20 0.31
PDE4A P27815 1/20 0.31

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
SCHEMBL15239341 0.95 LMNA (0.31) LMNAL3MBTL1TDP1
SCHEMBL31386724 0.86 LMNA (0.32) LMNAL3MBTL1TDP1
SCHEMBL234252 0.84 LMNA (0.36) LMNAL3MBTL1TDP1AKR1B1KDM4E
SCHEMBL2559273 0.83 LMNA (0.39) LMNAL3MBTL1TDP1AKR1B1PDE4A
SCHEMBL6256241 0.83 LMNA (0.32) LMNAL3MBTL1TDP1
SCHEMBL999357 0.81 ALDH1A1 (0.35) LMNAL3MBTL1TDP1
SCHEMBL4338288 0.80 LMNA (0.36) LMNAL3MBTL1TDP1AKR1B1PDE4A
SCHEMBL2558960 0.80 LMNA (0.36) LMNAL3MBTL1TDP1AKR1B1PDE4A
SCHEMBL6087524 0.80 LMNA (0.36) LMNAL3MBTL1TDP1AKR1B1PDE4A
SCHEMBL15966786 0.79 LMNA (0.39) LMNAL3MBTL1TDP1AKR1B1KDM4E

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 1013 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119790155-A Threose nucleic acid antisense oligonucleotide and method thereof 豪夫迈·罗氏有限公司 2025-04-08 CN claimed
CN-114025805-B Method for preparing protein-oligonucleotide complex 达因疗法公司 2025-01-24 CN claimed
CN-119185345-A Compositions and methods for treating and preventing amyotrophic lateral sclerosis 渤健马萨诸塞州股份有限公司 2024-12-27 CN claimed
CN-118987017-A Compositions and methods for treating and preventing amyotrophic lateral sclerosis 渤健马萨诸塞州股份有限公司 2024-11-22 CN claimed
CN-118434860-A Threose nucleic acid antisense oligonucleotide and method thereof 豪夫迈·罗氏有限公司 2024-08-02 CN claimed
CN-118339292-A Antisense inhibitors of MIR17HG precursor RNAs as cancer therapeutics 丹娜-法伯癌症研究院 2024-07-12 CN claimed
US-20240229042-A1 COMPOUNDS AND METHODS FOR REDUCING KCNT1 EXPRESSION IONIS PHARMACEUTICALS, INC. (US) 2024-07-11 US claimed
EP-4220360-B1 OLIGONUCLEOTIDES FOR INDUCING PATERNAL UBE3A EXPRESSION HOFFMANN LA ROCHE (CH) 2024-06-26 EP claimed
WO-2024129779-A1 INTERNAL RIBOSOME ENTRY SITES FOR IMPROVED POLYNUCLEOTIDE TRANSLATION MODERNATX, INC. (US) 2024-06-20 WO claimed
US-20240182903-A1 TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS BIOGEN MA INC (US) 2024-06-06 US claimed
EP-1601789-A4 MODULATION OF IMMUNOSTIMULATORY PROPERTIES OF OLIGONUCLEOTIDE-BASED COMPOUNDS BY UTILIZING MODIFIED IMMUNOSTIMULATORY DINUCLEOTIDES IDERA PHARMACEUTICALS INC (US) 2007-10-31 EP claimed
US-7276489-B2 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5′ ends IDERA PHARMACEUTICALS, INC. (US) 2007-10-02 US claimed
EP-1601789-A2 MODULATION OF IMMUNOSTIMULATORY PROPERTIES OF OLIGONUCLEOTIDE-BASED COMPOUNDS BY UTILIZING MODIFIED IMMUNOSTIMULATORY DINUCLEOTIDES HYBRIDON, INC. (US) 2005-12-07 EP claimed
US-20040198685-A1 Modulation of immunostimulatory properties of oligonucleotide-based compounds by utilizing modified immunostimulatory dinucleotides HYBRIDON, INC. 2004-10-07 US claimed
WO-2004064782-A2 MODULATION OF IMMUNOSTIMULATORY PROPERTIES OF OLIGONUCLEOTIDE-BASED COMPOUNDS BY UTILIZING MODIFIED IMMUNOSTIMULATORY DINUCLEOTIDES HYBRIDON, INC. (US) 2004-08-05 WO claimed
WO-2003057822-A9 MODULATION OF IMMUNOSTIMULATORY PROPERTIES OF OLIGONUCLEOTIDE-BASED COMPOUNDS BY OPTIMAL PRESENTATION OF 5' ENDS HYBRIDON INC (US) 2004-07-01 WO claimed
US-20040097719-A1 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5' ends HYBRIDON, INC. 2004-05-20 US claimed
EP-1393745-A1 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5'ends HYBRIDON, INC. (US) 2004-03-03 EP claimed
WO-2003057822-A2 MODULATION OF IMMUNOSTIMULATORY PROPERTIES OF OLIGONUCLEOTIDE-BASED COMPOUNDS BY OPTIMAL PRESENTATION OF 5' ENDS HYBRIDON, INC. (US) 2003-07-17 WO claimed
WO-2003035836-A2 MODULATION OF IMMUNOSTIMULATORY PROPERTIES OF OLIGONUCLEOTIDE-BASED COMPOUNDS BY OPTIMAL PRESENTATION OF 5' ENDS HYBRIDON INC. (US) 2003-05-01 WO 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-20240182903-A1 TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS SOD1, SMN1; SMN2, SOD3 LMNA 801/4885L3MBTL1 261/4885TDP1 53/4885
US-20040198685-A1 Modulation of immunostimulatory properties of oligonucleotide-based compounds by utilizing modified immunostimulatory dinucleotides NT5C2, ENTPD5, TLR5 LMNA 4834/4885L3MBTL1 2327/4885TDP1 410/4885
US-20040097719-A1 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5' ends TLR5, TLR3, ENTPD5 LMNA 4649/4885L3MBTL1 1024/4885TDP1 620/4885

“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.