Doxifluridine

Doxifluridine

SCHEMBL8094

C[C@H]1O[C@@H](n2cc(F)c(=O)[nH]c2=O)[C@H](O)[C@@H]1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TYMS

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

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 1.00
SMN1; SMN2 Q16637 2/20 1.00
MAPT P10636 2/20 1.00
TSHR P16473 1/20 1.00
PMP22 Q01453 1/20 1.00
HBB P68871 1/20 1.00
P2RY6 Q15077 2/20 0.54
P2RY14 Q15391 2/20 0.54
NT5E P21589 1/20 0.54
PYGM P11217 3/20 0.46
ESR1 P03372 1/20 0.45
TK2 O00142 2/20 0.43

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
Doxifluridine SCHEMBL28690558 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL10079621 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL4932137 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL14291576 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL14564897 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL12932255 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL98005 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL8095 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL15060572 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22
Doxifluridine SCHEMBL13300971 1.00 LMNA (1.00) LMNASMN1; SMN2MAPTTSHRPMP22

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

Appears in 57837 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4748859-A2 CHEMICALLY AND PHOTOCHEMICALLY INITIATED CELL MEMBRANE BLEBBING TO INDUCE CELL VESICLE PRODUCTION, MODIFICATIONS THEREOF, AND USES THEREOF The Regents of the University of California (US) 2026-05-27 EP claimed
EP-4743490-A1 HUMANIZED ANTI-CD7 ANTIBODY Christian-Albrechts-Universität zu Kiel (DE) 2026-05-20 EP claimed
WO-2026099502-A1 NOVEL DRUG CONJUGATES FOR TESTING CELLULAR DRUG UPTAKE Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts (DE) 2026-05-15 WO claimed
CN-122028934-A Combination of CLDN18_2 antibody and chemotherapeutic drug and application thereof 江苏奥赛康生物医药有限公司 2026-05-12 CN claimed
US-20260116861-A1 ISOXAZOLE HYDROXAMIC ACIDS AS HISTONE DEACETYLASE 6 INHIBITORS THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2026-04-30 US claimed
US-20260115305-A1 LINKERS, CONJUGATES AND APPLICATIONS THEREOF GENEQUANTUM HEALTHCARE SUZHOU CO LTD (CN) 2026-04-30 US claimed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 US claimed
EP-3790536-B1 NANOCONTAINERS FOR TRANSPORTING NONPOLAR, LIPOPHILIC SUBSTANCES SUCH AS ANTIBIOTICS KARLSRUHER INST TECHNOLOGIE (DE) 2026-04-22 EP claimed
EP-4727979-A2 COMPOSITIONS AND METHODS FOR TARGETING EXTRACELLULAR DNA Caris Science, Inc. (US) 2026-04-22 EP claimed
US-12600696-B2 Aromatic compounds Xeniopro GmbH (DE) 2026-04-14 US claimed
EP-0454773-A1 NOVEL PRODRUG DERIVATIVES OF BIOLOGICALLY ACTIVE AGENTS CONTAINING HYDROXYL GROUPS OR NH-ACIDIC GROUPS Bundgaard, Hans (DK) 1991-11-06 EP claimed
EP-0443028-A1 NON-INJECTION CARCINOSTATIC AGENT FOR SUPPRESSING OCCURRENCE OF INFLAMMATION DUE TO 5-FLUOROURACIL AND METHOD FOR CURING CANCER OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1991-08-28 EP claimed
EP-0393575-A1 Neoplasia treatment compositions containing antineoplastic agent and side-effect reducing protective agent G.D. Searle & Co. (US) 1990-10-24 EP claimed
WO-1990008128-A1 NOVEL PRODRUG DERIVATIVES OF BIOLOGICALLY ACTIVE AGENTS CONTAINING HYDROXYL GROUPS OR NH-ACIDIC GROUPS BUNDGAARD HANS (DK) 1990-07-26 WO claimed
EP-0189755-B1 PHARMACEUTICAL COMPOSITION F. HOFFMANN-LA ROCHE AG (CH) 1990-01-03 EP claimed
EP-0189755-A1 Pharmaceutical composition F. HOFFMANN-LA ROCHE AG (CH) 1986-08-06 EP claimed
EP-0180188-A2 A composition for increasing the anti-cancer activity of an anti-cancer compound OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1986-05-07 EP claimed
EP-0021231-B1 PROCESS FOR THE PREPARATION OF 5'-DEOXY-5-FLUORO URIDINE AND INTERMEDIATES IN THIS PROCESS F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1983-10-05 EP claimed
EP-0021231-A2 Process for the preparation of 5'-deoxy-5-fluoro uridine and intermediates in this process F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1981-01-07 EP claimed
US-4071680-A ANTITUMOR AGENTS HOFFMANN-LA ROCHE INC. (US) 1978-01-31 US claimed