Cytidine

Cytidine

SCHEMBL376514

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

nearest known ligand 0.90

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

POLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PRIM1PRIM2

The experimentally established mechanism targets of Cytidine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.90
MTOR P42345 2/20 0.90
THRB P10828 1/20 0.90
MDM2 Q00987 1/20 0.90
NCOA1 Q15788 1/20 0.90
NCOA3 Q9Y6Q9 1/20 0.90
ALDH1A1 P00352 2/20 0.59
GMNN O75496 1/20 0.59
TP53 P04637 1/20 0.59
NFKB1 P19838 1/20 0.59
DNMT1 P26358 1/20 0.59
THPO P40225 1/20 0.59
HTT P42858 1/20 0.59
RAB9A P51151 1/20 0.59
BLM P54132 1/20 0.59
HBB P68871 1/20 0.59
PMP22 Q01453 1/20 0.59
P2RY2 P41231 1/20 0.59
NT5E P21589 1/20 0.57
TSHR P16473 1/20 0.56

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
Cytidine SCHEMBL1201153 1.00 LMNA (0.90) LMNAMTORTHRBMDM2NCOA1
Cytarabine SCHEMBL28898416 1.00 LMNA (0.90) LMNAMTORTHRBMDM2NCOA1
Cytarabine SCHEMBL458337 1.00 LMNA (0.90) LMNAMTORTHRBMDM2NCOA1
Cytarabine SCHEMBL9007590 1.00 LMNA (0.90) LMNAMTORTHRBMDM2NCOA1
Cytidine SCHEMBL39902 1.00 LMNA (0.90) LMNAMTORTHRBMDM2NCOA1
Cytarabine SCHEMBL285195 1.00 LMNA (0.90) LMNAMTORTHRBMDM2NCOA1
Cytidine SCHEMBL104628 1.00 LMNA (0.90) LMNAMTORTHRBMDM2NCOA1
Cytidine SCHEMBL6672407 0.99 LMNA (0.88) LMNAMTORTHRBMDM2NCOA1
Cytarabine SCHEMBL29084328 0.99 LMNA (0.88) LMNAMTORTHRBMDM2NCOA1
Cytidine SCHEMBL2370482 0.99 LMNA (0.88) 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 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1644394-B1 SYNTHESIS AND COMPOSITIONS OF 2 -TERMINATOR NUCLEOTIDES ROCHE DIAGNOSTICS GMBH (DE) 2018-05-09 EP disclosed
EP-1641943-B1 2'-TERMINATOR NUCLEOTIDE-RELATED METHODS AND SYSTEMS ROCHE DIAGNOSTICS GMBH (DE) 2013-03-20 EP disclosed
US-8163487-B2 2′-terminator nucleotide-related methods and systems ROCHE MOLECULAR SYSTEMS, INC. (US) 2012-04-24 US disclosed
EP-2076606-B1 2'-TERMINATOR RELATED PYROPHOSPHOROLYSIS ACTIVATED POLYMERIZATION ROCHE DIAGNOSTICS GMBH (DE) 2012-01-25 EP disclosed
US-20110201002-A1 2'-Terminator Nucleotide-Related Methods and Systems ROCHE MOLECULAR SYSTEMS, INC. (US) 2011-08-18 US disclosed
US-7947817-B2 Nucleotide blocked with sugar compound; biosynthesis of nucleic acids ROCHE MOLECULAR SYSTEMS, INC. (US) 2011-05-24 US disclosed
US-7928207-B2 use of 2'-terminator nucleotides to effect chain termination; kits; incubating a template nucleic acid with a nucleotide incorporating biocatalyst, and a 2'-terminator nucleotide ROCHE MOLECULAR SYSTEMS, INC (US) 2011-04-19 US disclosed
US-7919249-B2 use of 2'-terminator nucleotides to effect chain termination; kits; incubating a template nucleic acid with a nucleotide incorporating biocatalyst, and a 2'-terminator nucleotide ROCHE MOLECULAR SYSTEMS, INC. (US) 2011-04-05 US disclosed
US-7745125-B2 2′-terminator related pyrophosphorolysis activated polymerization ROCHE MOLECULAR SYSTEMS, INC. (US) 2010-06-29 US disclosed
EP-2195327-A2 SYNTHESIS AND COMPOSITIONS OF NUCLEIC ACIDS COMPRISING 2'-TERMINATOR NUCLEOTIDES Roche Diagnostics GmbH (DE) 2010-06-16 EP disclosed
WO-2008046609-A2 SYNTHESIS AND COMPOSITIONS OF NUCLEIC ACIDS COMPRISING 2'-TERMINATOR NUCLEOTIDES ROCHE DIAGNOSTICS GMBH (DE) 2008-04-24 WO disclosed
US-20070219361-A1 Synthesis and compositions of nucleic acids comprising 2'-terminator nucleotides ROCHE MOLECULAR SYSTEMS, INC. (US) 2007-09-20 US disclosed
US-20070154914-A1 2'-Terminator related pyrophosphorolysis activated polymerization ROCHE MOLECULAR SYSTEMS, INC. (US) 2007-07-05 US disclosed
EP-1644394-A2 SYNTHESIS AND COMPOSITIONS OF 2 -TERMINATOR NUCLEOTIDES Roche Diagnostics GmbH (DE) 2006-04-12 EP disclosed
EP-1641943-A2 2'-TERMINATOR NUCLEOTIDE-RELATED METHODS AND SYSTEMS Roche Diagnostics GmbH (DE) 2006-04-05 EP disclosed
WO-2005026184-A9 SYNTHESIS AND COMPOSITIONS OF 2'-TERMINATOR NUCLEOTIDES ROCHE DIAGNOSTICS GMBH (DE) 2006-03-02 WO disclosed
WO-2005026184-A2 SYNTHESIS AND COMPOSITIONS OF 2'-TERMINATOR NUCLEOTIDES ROCHE DIAGNOSTICS GMBH (DE) 2005-03-24 WO disclosed
US-20050037398-A1 2'-terminator nucleotide-related methods and systems ROCHE MOLECULAR SYSTEMS, INC. (US) 2005-02-17 US disclosed
US-20050037991-A1 Synthesis and compositions of 2'-terminator nucleotides ROCHE MOLECULAR SYSTEMS, INC. (US) 2005-02-17 US disclosed
WO-2005005667-A2 2'-TERMINATOR NUCLEOTIDE-RELATED METHODS AND SYSTEMS ROCHE DIAGNOSTICS GMBH (DE) 2005-01-20 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 (2 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-20050037991-A1 Synthesis and compositions of 2'-terminator nucleotides RNGTT, NT5C3B, NSUN2 LMNA 1378/4885MTOR 3329/4885THRB 1065/4885
US-20070219361-A1 Synthesis and compositions of nucleic acids comprising 2'-terminator nucleotides RNGTT, POLRMT, NT5C3B LMNA 684/4885MTOR 4854/4885THRB 683/4885

“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.