SCHEMBL3272285

SCHEMBL3272285

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

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 5/20 0.51
MTOR P42345 2/20 0.51
THRB P10828 1/20 0.51
MDM2 Q00987 1/20 0.51
NCOA1 Q15788 1/20 0.51
NCOA3 Q9Y6Q9 1/20 0.51
PDE3A Q14432 3/20 0.48
PDE4D Q08499 1/20 0.48
SLC29A1 Q99808 1/20 0.48
SMN1; SMN2 Q16637 2/20 0.40
ALDH1A1 P00352 2/20 0.40
POLB P06746 1/20 0.40
MAPT P10636 3/20 0.39
CACNA1F O60840 2/20 0.39
ALB P02768 2/20 0.39
CACNA1D Q01668 2/20 0.39
CACNA1S Q13698 2/20 0.39
CACNA1C Q13936 2/20 0.39
GMNN O75496 1/20 0.35
TP53 P04637 1/20 0.35

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
Phosphoric Acid SCHEMBL21645281 0.95 LMNA (0.47) LMNAMTORTHRBMDM2NCOA1
Phosphoric Acid SCHEMBL16655013 0.95 LMNA (0.47) LMNAMTORTHRBMDM2NCOA1
Pyrophosphoric Acid SCHEMBL21248625 0.91 LMNA (0.44) LMNAMTORTHRBMDM2NCOA1
SCHEMBL2180644 0.90 LMNA (0.49) LMNAMTORTHRBMDM2NCOA1
SCHEMBL1896532 0.90 LMNA (0.49) LMNAMTORTHRBMDM2NCOA1
SCHEMBL31070840 0.90 LMNA (0.49) LMNAMTORTHRBMDM2NCOA1
SCHEMBL7775032 0.89 LMNA (0.48) LMNAMTORTHRBMDM2NCOA1
SCHEMBL6385398 0.88 LMNA (0.47) LMNAMTORTHRBMDM2NCOA1
SCHEMBL15239320 0.88 LMNA (0.47) LMNAMTORTHRBMDM2NCOA1
SCHEMBL7196048 0.87 LMNA (0.46) LMNAMTORTHRBMDM2NCOA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024015366-A1 COMPOSITIONS AND METHODS FOR REDUCING METHANE EMISSIONS IN RUMINANT POPULATIONS Arkea Bio Corp. (US) 2024-01-18 WO claimed
US-20230204605-A1 COMPOSITIONS AND METHODS FOR DIAGNOSING AND TREATING CHRONIC KIDNEY DISEASE SOCIETE DES PRODUITS NESTLE S.A. (CH) 2023-06-29 US claimed
WO-2023077156-A1 MODIFIED MRNA THERAPEUTICS SHATTUCK LABS, INC. (US) 2023-05-04 WO claimed
CN-112176043-B Sequencing, enrichment and detection method of modified nucleoside based on chemical marker 北京大学 2022-07-12 CN claimed
EP-3099801-A1 METHODS AND PRODUCTS FOR NUCLEIC ACID PRODUCTION AND DELIVERY Factor Bioscience Inc. (US) 2016-12-07 EP claimed
CN-105940110-A Methods and products for nucleic acid production and delivery 菲克特生物科学股份有限公司 2016-09-14 CN claimed
EP-2914728-A1 METHODS AND PRODUCTS FOR EXPRESSING PROTEINS IN CELLS Factor Bioscience Inc. (US) 2015-09-09 EP claimed
WO-2015117021-A1 METHODS AND PRODUCTS FOR NUCLEIC ACID PRODUCTION AND DELIVERY FACTOR BIOSCIENCE INC. (US) 2015-08-06 WO claimed
WO-2014071219-A1 METHODS AND PRODUCTS FOR EXPRESSING PROTEINS IN CELLS FACTOR BIOSCIENCE INC. (US) 2014-05-08 WO claimed
EP-2691101-A2 DELIVERY AND FORMULATION OF ENGINEERED NUCLEIC ACIDS Moderna Therapeutics, Inc. (US) 2014-02-05 EP claimed
WO-2012135805-A2 DELIVERY AND FORMULATION OF ENGINEERED NUCLEIC ACIDS modeRNA Therapeutics (US) 2012-10-04 WO claimed
US-20260146264-A1 METHODS FOR REPROGRAMMING AND GENE EDITING CELLS FACTOR BIOSCIENCE INC. (US) 2026-05-28 US disclosed
US-20260108554-A1 METHODS FOR REPROGRAMMING AND GENE EDITING CELLS FACTOR BIOSCIENCE INC (US) 2026-04-23 US disclosed
US-12473594-B2 Chemical tagging-based method for modified nucleoside sequencing, enrichment, and measurement PEKING UNIVERSITY (CN) 2025-11-18 US disclosed
WO-2025125630-A1 METHOD FOR BIOPROTAC DESIGN MEDIMMUNE LIMITED (GB) 2025-06-19 WO disclosed
US-5856148-A GENETIC ENGINEERED DNA CODING 3-PHOSPHOGLYCERATE DEHYDROGENASE; STABILITY WACKER CHEMIE GMBH (DE) 1999-01-05 US disclosed
US-5618716-A ENGINEERED DNA ENCODING 3-PHOSPHOGLYCERATE DEHYDROGENASE(PGD) HAS REDUCED SENSITIVITY TO INHIBITION BY SERINE IN COMPARISION TO WILD-TYPE PGD WACKER-CHEMIE GMBH (DE) 1997-04-08 US disclosed
EP-0620853-B1 MATERIALS AND METHODS FOR BIOSYNTHESIS OF SERINE AND SERINE-RELATED PRODUCTS WACKER CHEMIE GMBH (DE) 1996-03-06 EP disclosed
EP-0620853-A1 MATERIALS AND METHODS FOR BIOSYNTHESIS OF SERINE AND SERINE-RELATED PRODUCTS. WACKER CHEMIE GMBH (DE) 1994-10-26 EP disclosed
WO-1993012235-A1 MATERIALS AND METHODS FOR BIOSYNTHESIS OF SERINE AND SERINE-RELATED PRODUCTS WACKER-CHEMIE GMBH (DE) 1993-06-24 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 (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-20260108554-A1 METHODS FOR REPROGRAMMING AND GENE EDITING CELLS B2M, MYADM, CD74 LMNA 407/4885MTOR 4088/4885THRB 1295/4885
US-12473594-B2 Chemical tagging-based method for modified nucleoside sequencing, enrichment, and measurement NT5C3B, BHMT2, NNMT LMNA 2427/4885MTOR 4305/4885THRB 1431/4885
US-20260146264-A1 METHODS FOR REPROGRAMMING AND GENE EDITING CELLS ZMYND8, STING1, DCLRE1A LMNA 2027/4885MTOR 3404/4885THRB 1914/4885

“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.