SCHEMBL223208

SCHEMBL223208

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

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE3A Q14432 3/20 0.54
PDE4D Q08499 1/20 0.54
SLC29A1 Q99808 1/20 0.54
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
SMN1; SMN2 Q16637 2/20 0.40
ALDH1A1 P00352 2/20 0.40
POLB P06746 1/20 0.40
CACNA1F O60840 2/20 0.39
ALB P02768 2/20 0.39
MAPT P10636 2/20 0.39
CACNA1D Q01668 2/20 0.39
CACNA1S Q13698 2/20 0.39
CACNA1C Q13936 2/20 0.39
POLA1 P09884 1/20 0.36
GMNN O75496 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
Hydrochloric Acid SCHEMBL28104164 0.99 PDE3A (0.53) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL23258348 0.92 PDE3A (0.56) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL582792 0.90 PDE3A (0.52) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL350552 0.90 PDE3A (0.52) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL27966727 0.89 PDE3A (0.54) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL28213460 0.87 PDE3A (0.45) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL30514296 0.85 LMNA (0.53) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL30514303 0.84 LMNA (0.50) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL366599 0.84 LMNA (0.52) PDE3APDE4DSLC29A1LMNAMTOR
SCHEMBL22631542 0.84 LMNA (0.52) PDE3APDE4DSLC29A1LMNAMTOR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116333019-B Fluorocytidine compound and preparation method and application thereof 沈阳农业大学 2024-04-02 CN claimed
WO-2023150622-A2 RNAI AGENTS FOR INHIBITING EXPRESSION OF CORONAVIRUS (COV) VIRAL GENOMES, COMPOSITIONS THEREOF, AND METHODS OF USE Arrowhead Pharmaceuticals, Inc. (US) 2023-08-10 WO claimed
CN-116333019-A Fluorocytidine compound and preparation method and application thereof 沈阳农业大学 2023-06-27 CN claimed
WO-2019195494-A1 COMPOSITIONS AND METHODS FOR SYNTHESIS OF PHOSPHORYLATED MOLECULES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2019-10-10 WO claimed
US-20190292540-A1 SPINAL MUSCULAR ATROPHY (SMA) TREATMENT VIA TARGETING OF SMN2 SPLICE SITE INHIBITORY SEQUENCES UNIV MASSACHUSETTS (US) 2019-09-26 US claimed
US-20170096664-A1 SPINAL MUSCULAR ATROPHY (SMA) TREATMENT VIA TARGETING OF SMN2 SPLICE SITE INHIBITORY SEQUENCES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2017-04-06 US claimed
US-9260760-B2 Method for determining complete response to anticancer therapy BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2016-02-16 US claimed
US-20150152504-A1 METHOD FOR DETERMINING COMPLETE RESPONSE TO ANTICANCER THERAPY BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2015-06-04 US claimed
US-8889645-B2 Nucleic acid modulators of glycoprotein VI REGADO BIOSCIENCES, INC. (US) 2014-11-18 US claimed
US-20140128587-A1 NUCLEIC ACID MODULATORS OF GLYCOPROTEIN VI REGADO BIOSCIENCES, INC. (US) 2014-05-08 US claimed
EP-0504279-B1 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES CHEMGEN CORP (US) 1997-07-09 EP claimed
US-5476932-A Process for producing N4-acyl-5'-deoxy-5-fluorocytidine derivatives HOFFMANN-LA ROCHE INC. (US) 1995-12-19 US claimed
US-5453497-A Process for producing N4 -acyl-5'-deoxy-5-fluorocytidine compounds HOFFMANN-LA ROCHE INC. (US) 1995-09-26 US claimed
EP-0637966-A1 BYSTANDER EFFECT TUMORICIDAL THERAPY. US HEALTH (US) 1995-02-15 EP claimed
WO-1993021959-A1 BYSTANDER EFFECT TUMORICIDAL THERAPY THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1993-11-11 WO claimed
US-5213972-A Production of thymidine and deoxyuridine, intermediates for AZT CHEMGEN CORPORATION (US) 1993-05-25 US claimed
EP-0504279-A4 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES 1993-02-17 EP claimed
EP-0504279-A1 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES. CHEMGEN CORP (US) 1992-09-23 EP claimed
WO-1991009130-A1 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES CHEMGEN CORPORATION (US) 1991-06-27 WO claimed
CN-1045791-A Use the cooperative compositions HIV inhibiting of nucleoside derivates ONCOGEN (US) 1990-10-03 CN claimed