5-Fluorouridine

5-Fluorouridine

SCHEMBL668873

O=P(O)(O)O.O=c1[nH]c(=O)n([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)cc1F

nearest known ligand 0.88

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of 5-Fluorouridine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
P2RY6 Q15077 2/20 0.68
P2RY14 Q15391 2/20 0.68
NT5E P21589 1/20 0.68
PYGM P11217 3/20 0.65
LMNA P02545 2/20 0.62
SMN1; SMN2 Q16637 2/20 0.62
TSHR P16473 1/20 0.62
MAPT P10636 1/20 0.62
PMP22 Q01453 1/20 0.62
HBB P68871 1/20 0.62
TK2 O00142 2/20 0.60
P2RY2 P41231 2/20 0.57
DNPH1 O43598 1/20 0.56
SLC28A1 O00337 1/20 0.55
SLC28A2 O43868 1/20 0.55
SLC29A1 Q99808 1/20 0.55
SLC28A3 Q9HAS3 1/20 0.55

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
5-Fluorouridine SCHEMBL148674 1.00 P2RY6 (0.68) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL19901621 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL3385435 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL1682759 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL329381 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL12174049 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL11756887 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL17173362 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL21423048 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA
5-Fluorouridine SCHEMBL214536 0.95 PYGM (0.70) P2RY6P2RY14NT5EPYGMLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2021260322-A1 STRAINS OF CLOSTRIDIUM BACTERIA RESISTANT TO 5-FLUOROURACIL, GENETIC TOOLS AND USES THEREOF IFP Energies Nouvelles (FR) 2021-12-30 WO claimed
EP-0791056-B1 LIPID-CLEAVAGE ENZYME COMPLEX HEIDELBERG PHARMA GMBH (DE) 2005-03-30 EP claimed
US-20030082167-A1 Lapid cleavage enzyme HEIDELBERG PHARMA HOLDING GMBH 2003-05-01 US claimed
US-20020106363-A1 LIPID CLEAVAGE ENZYME HEIDELBERG PHARMA HOLDING GMBH (DE) 2002-08-08 US claimed
EP-0302473-B1 Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells BRISTOL MYERS SQUIBB CO (US) 1995-02-15 EP claimed
US-4975278-A Converting the prodrug at the tumor site to the active drug by means of the conjugate bound to a tumor surface antigen BRISTOL-MYERS COMPANY (US) 1990-12-04 US claimed
EP-0302473-A2 Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells Bristol-Myers Squibb Company (US) 1989-02-08 EP claimed
EP-4696780-A1 METHOD FOR TRANSFORMING BACTERIUM BELONGING TO GENUS BIFIDOBACTERIUM Kabushiki Kaisha Yakult Honsha (JP) 2026-02-18 EP disclosed
EP-4689128-A1 NUCLEIC ACID MOLECULE AND METHODS Forge Genetics Ltd (GB) 2026-02-11 EP disclosed
EP-4689059-A1 MODIFIED CLOSTRIDIUM BACTERIA, GENETIC EDITING TOOL FOR THE PSOL PLASMID OF CLOSTRIDIUM BACTERIA AND USES THEREOF IFP Energies nouvelles (FR) 2026-02-11 EP disclosed
US-12146135-B2 Method for editing filamentous fungal genome through direct introduction of genome-editing protein NATIONAL RESEARCH INSTITUTE OF BREWING (JP) 2024-11-19 US disclosed
WO-2024209201-A1 NUCLEIC ACID MOLECULE AND METHODS THE UNIVERSITY OF NOTTINGHAM (GB) 2024-10-10 WO disclosed
WO-2024200980-A1 MODIFIED CLOSTRIDIUM BACTERIA, GENETIC EDITING TOOL FOR THE PSOL PLASMID OF CLOSTRIDIUM BACTERIA AND USES THEREOF IFP Energies Nouvelles (FR) 2024-10-03 WO disclosed
US-5859295-A Canavanine analogs and their use as chemotherapeutic agents UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 1999-01-12 US disclosed
EP-0540859-B1 Anthracycline prodrugs BRISTOL MYERS SQUIBB CO (US) 1998-01-14 EP disclosed
US-5552440-A Use of L-canavanine as a chemotherapeutic agent for the treatment of pancreatic cancer THE UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 1996-09-03 US disclosed
EP-0302473-B1 Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells BRISTOL MYERS SQUIBB CO (US) 1995-02-15 EP disclosed
EP-0540859-A1 Anthracycline prodrugs Bristol-Myers Squibb Company (US) 1993-05-12 EP disclosed
US-4975278-A Converting the prodrug at the tumor site to the active drug by means of the conjugate bound to a tumor surface antigen BRISTOL-MYERS COMPANY (US) 1990-12-04 US disclosed
EP-0302473-A2 Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells Bristol-Myers Squibb Company (US) 1989-02-08 EP 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-20030082167-A1 Lapid cleavage enzyme LAP3, NAALAD2, ENGASE P2RY6 3635/4885P2RY14 2861/4885NT5E 621/4885
US-20020106363-A1 LIPID CLEAVAGE ENZYME SMPD1, MMEL1, ENGASE P2RY6 3422/4885P2RY14 2684/4885NT5E 528/4885

“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.